Welcome To Bylands Garden Centre, Bylans

Welcome to Bylands Garden Centre!

Bylands Garden Centre , your local one stop shop for all your garden needs. and much, much more.

Open year round Bylands is considered a destination garden centre in beautiful BC's Okanagan Valley. Bylands offers one of the most diverse and complete mixes of quality hardy plants available in Western Canada together with a great selection of gardening accessories, home decor, jewellery and a full floral design service.

Most of the plants sold at the garden centre are grown by Bylands Nurseries Ltd which is a significant advantage as the plants are acclimatized for the area and the footprint to grow these plants has less impact on our environment.

Bylands invites you and your family to come visit us in West Kelowna and get growing together.

Lifelabs - Medical Centers - 650 41st Avenue, Oakridge, Vancouver, Bc, Canada - Phone Number, Lipela

LifeLabs

I hate phlebotomists. But what can I say. I make an appointment online as not to wait. However there still is the time it takes to enter the info from your requisition into the computer. Hopefully as technology progresses one day their will be no need for these requisition forms that seem to be a problem. People forget to bring them, they have to be entered into the computer, why can't my doctor electronically submit the requisition? It would save so much time and hassle. Another problem, but this is more the doctor. when they forget to tell you to fast, your if they want the "first morning sample".

I can see that continuing to be a hurdle and more a requirement of the patient to ask and be clear with their doctor what they form says and why they are going. I have had the ladies ask me about what my doctor wrote on the form, ask for my address repeatedly, which doctor is supposed to be CC'd on results. I usually cannot wait to get out of there.

Was this review …?

Go to a different LifeLabs if possible. The workers at the Oakridge LifeLabs are simply not competent in handling the volume of being next to so many medical offices. One of my particular experiences involved booking an appointment online ahead of time for 3:25pm. Upon arriving at 3:15, with about 4 people in the clinic already, I registered at the desk and was told to sit down. At 3:30, I mentioned again that I had an appointment, and was told I was in queue. At 3:45, a new person came in to register. They sit down, and immediately get called up. I go up and ask why I haven't been called yet, since there is now no one else around, and their response is 'oops'. If incompetence had a physical home, it would be LifeLabs Oakridge.

Was this review …?

I'm a pansy when it comes to needles. No idea why. Throw me off a bridge attached to a large elastic band or down a river full of rapids. no problemo. But come near me with a tiny needle and I shall be a shaking, whimpering woman-child for the next 30 minutes.

However, sometimes life requires needles and after finding out I was due for some blood work, and after a rather eventful last experience (i'm a fainter - classy right?) I was more then a little nervous.

There was absolutely no wait - which helps with the "anticipation" nerves and the nurse who took my blood was just excellent. When I told her "I'm not good around needles" and "mmaayy have fainted in the hallway the last time" - instead of being overly touchy feely or rolling her eyes, she started telling me stories about other people who had done the same, cracking jokes about the day and asking me about work, etc. She didn't make a big deal of it and that started to put me at ease.

By needle-time, I was ten times better off then my last go round.

But like I said, i'm a pansy - so after, when I got a bit dizzy and that tell tale white-faced, clammy hands syndrome set - she got me an ice pack, a glass of juice. heck she even fanned me. Never making me feel like the large woman-child I knew I was being. It made the whole experience much less embarrassing/nerve-wracking then my last few.

I still hate needles. But when I need to go down that road again - I will definitely go back to that place. Plus - it's in Oakridge Mall so when you survive getting blood drawn, you can reward yourself with shoes and a $7 juice smoothie.

Was this review …?

Delasco - Chlorazol Fungal Stain, Chlorasol

Chlorazol Fungal Stain

Contains chlorazol black E, potassium hydroxide and dimethylsulfoxide in convenient polyethylene drop dispensing containers.

Stains hyphae green against a grey background. May examine with bright or reduced light. Use on scrapings or with Delasco slide adhesive preparations.

1/2 oz bottle = 15 ml 1 oz bottle = 30 ml

More Information

The Material Data Safety Sheet for Chlorazol Fungal Stain.

Supplied in plastic squeeze opaque white dropper bottles, 1/2 oz and 1 oz. Should be stored in a dark place. The Chlorazol stain deteriorates . Continue reading

Shipping Information

1/2 and 1 oz bottles (up to 24) are no longer hazardous by air under the limited quantity exemption. All bottle sizes larger than 1 oz are still subject to hazardous material regulations and fees.

This product is now available for shipment to select international countries by UPS Hazmat air service for an additional $66.25 fee. Contact Delasco for more information.

Buventol Easyhaler - Laakeopas, Buventol

BUVENTOL EASYHALER

Astman oireenmukainen hoito, kun tarvitaan akillisten astmaoireiden poistamista tai ilmaantumisen estamista rasituksen yhteydessa. Myos muiden keuhkoputkien ahtautumisesta johtuvien keuhkosairauksien oireenmukainen hoito.

Laakarin ohjeen mukaan. Otetaan yleensa tarvittaessa astman oirelaakkeena, ei jatkuvana, jokapaivaisena hoitona. Laakkeen keuhkoputkia laajentava vaikutus alkaa nopeasti. Laakkeen annoksen ja ottotiheyden muuttamisesta on aina neuvoteltava laakarin kanssa.

Laaketta otettaessa suoritetaan alusta pitaen voimakas sisaanhengitys ja uloshengittamista inhalaattorin kautta pitaa valttaa. Annosta ja laakkeenottotiheytta saa lisata vain laakarin ohjeen mukaan. Pakkauksessa tarkat ohjeet laakkeen ottamistavasta ja antolaitteen puhdistamisesta ja sailyttamisesta. Jos oirelaakkeen tarve lisaantyy, pitaa ottaa yhteytta hoitavaan laakariin kokonaislaakityksen arvioimiseksi. Lisaantyva kaytto saattaa olla merkki astman vaikeutumisesta

Salbutamoli vahentaa keuhkoputkien lihasjannitysta, laajentaa keuhkoputkia, helpottaa hengitysta ja lievittaa yskaa.

Pakkausseloste: Tietoa kayttajalle

Buventol Easyhaler 100 mikrog/annos inhalaatiojauhe Buventol Easyhaler 200 mikrog/annos inhalaatiojauhe

Lue tama pakkausseloste huolellisesti, ennen kuin aloitat laakkeen kayttamisen, silla se sisaltaa sinulle tarkeita tietoja.

Sailyta tama pakkausseloste. Voit tarvita sita myohemmin.

Jos sinulla on kysyttavaa, kaanny laakarin tai apteekkihenkilokunnan puoleen.

Tama laake on maaratty vain sinulle eika sita tule antaa muiden kayttoon. Se voi aiheuttaa haittaa muille, vaikka heilla olisikin samanlaiset oireet kuin sinulla.

Jos havaitset haittavaikutuksia, kaanny laakarin tai apteekkihenkilokunnan puoleen. Tama koskee myos sellaisia haittavaikutuksia, joita ei ole mainittu tassa pakkausselosteessa. Ks. kohta 4.

Tassa pakkausselosteessa kerrotaan :

Mita Buventol Easyhaler on ja mihin sita kaytetaan

Mita sinun on tiedettava, ennen kuin kaytat Buventol Easyhaler? valmistetta

Miten Buventol Easyhaler? valmistetta kaytetaan

Mahdolliset haittavaikutukset

Buventol Easyhaler? valmisteen sailyttaminen

Pakkauksen sisalto ja muuta tietoa

1. Mita Buventol Easyhaler on ja mihin sita kaytetaan

Buventol Easyhaler on lyhytvaikutteinen keuhkoputkia avaava astmalaake, jonka vaikutus alkaa nopeasti. Vaikuttava aine on salbutamoli. Salbutamoli laajentaa keuhkoputkia, jolloin ilma kulkee niissa vapaammin. Laakkeen avulla astmaan kuuluva kiusallinen yskiminen ja hengityksen vinkuminen vahenevat ja hengenahdistus lievittyy.

Buventol Easyhaler? valmistetta kaytetaan aikuisten ja yli 6?vuotiaiden lasten

astmakohtausten ja astman pahenemisvaiheiden oireenmukaiseen hoitoon

rasitusastman ehkaisyyn

astmakohtauksen ennaltaehkaisyyn ennen altistumista tunnetulle allergian aiheuttajalle, jos altistusta ei voi valttaa.

Buventol Easyhaler? valmistetta kaytetaan aikuisten

astman ja muiden ahtauttavien keuhkosairauksien oireenmukaiseen hoitoon.

Salbutamolijauhe on pakattu Easyhaler? nimiseen antolaitteeseen. Jauhe hengitetaan keuhkoihin antolaitteen suukappaleen kautta.

2. Mita sinun on tiedettava, ennen kuin kaytat Buventol Easyhaler? valmistetta

Ala kayta Buventol Easyhaler? valmistetta

jos olet allerginen salbutamolille tai taman laakkeen jollekin muulle aineelle (lueteltu kohdassa 6) eli laktoosille (joka sisaltaa pienia maaria maitoproteiineja).

Ota yhteys laakariin, jotta laakkeesi voidaan vaihtaa toiseen.

Varoitukset ja varotoimet Neuvottele laakarin kanssa ennen laakkeen kayttoa, jos sinulla on

jokin sydan - tai verisuonisairaus

kilpirauhasen liikatoiminta

alhainen veren kaliumpitoisuus.

Muut laakevalmisteet ja Buventol Easyhaler Kerro laakarille tai apteekkihenkilokunnalle, jos parhaillaan kaytat tai olet askettain kayttanyt tai saatat kayttaa muita laakkeita.

Erityisen tarkeaa on kertoa laakarille, jos kaytat jotain seuraavista laakkeista

digoksiinia (sydanlaake)

teofylliinia (keuhkosairauksien laake)

kortikosteroideja (esim. astman tai erilaisten tulehdussairauksien hoitoon kaytettavia laakkeita)

beetasalpaajia, kuten propranololia esim. verenpaineen hoitoon

nesteenpoistolaakkeita (diureetteja)

masennuslaakkeita (MAO:n estajia tai trisyklisia masennuslaakkeita).

Raskaus ja imetys Jos olet raskaana tai imetat, epailet olevasi raskaana tai jos suunnittelet lapsen hankkimista, kysy laakarilta neuvoa ennen taman laakkeen kayttoa.

Ajaminen ja koneiden kaytto Buventol Easyhaler? valmisteella ei normaaliannoksina ole haitallista vaikutusta ajokykyyn ja koneiden kayttokykyyn.

Buventol Easyhaler sisaltaa laktoosia Tama laake sisaltaa laktoosia (alle 10 mg/annos). Laktoosi-intoleranssista karsivat eivat todennakoisesti saa siita oireita. Jos laakari on kertonut, etta sinulla on jokin sokeri-intoleranssi, keskustele laakarin kanssa ennen taman laakkeen kayttamista.

3. Miten Buventol Easyhaler? valmistetta kaytetaan

Kayta tata laaketta juuri siten kuin laakari on maarannyt. Tarkista ohjeet laakarilta tai apteekista, jos olet epavarma.

Katso kohta ”Nain kaytat Easyhaleria” pakkausselosteen lopussa.

Laakkeen annostus on yksilollinen. Laakari on maarannyt sinulle sopivan laakevahvuuden ja hoitoannoksen. Noudata huolellisesti laakarin antamia ohjeita. Jos sinulle on maaratty hoitava astmalaake, jatka sen kayttoa normaalisti.

Laaketta kaytetaan etenkin pitkaaikaisessa hoidossa yleensa pienina annoksina oireenmukaisesti ja vain tarvittaessa.

Suositeltu annos on aikuisille 1–2 annosta (100–400 mikrogrammaa) tarvittaessa astmakohtauksen hoitoon tai ennen rasitusta. Yleensa enintaan 4 kertaa vuorokaudessa.

Astman oireiden paheneminen hoidon aikana Ota mahdollisimman pian yhteys laakariin, jos

hengityksen vinkuminen tai hengenahdistus pahenee hoidon aikana

joudut kayttamaan keuhkoputkia avaavaa laaketta aiempaa useammin

laakkeesi ei auta yhta hyvin tai yhta pitkaan kuin aiemmin.

Astmasi saattaa olla pahenemassa ja voit tarvita lisahoitoa.

Kaytto lapsille ja nuorille Yli 6?vuotiaat lapset: Suositeltava annos yllapito - tai ehkaisyhoidossa on 1–2 annosta (100–200 mikrogrammaa) 1–4 kertaa vuorokaudessa.

Lasten tulisi kayttaa laitetta vain aikuisten valvonnassa.

Jos kaytat enemman Buventol Easyhaler? valmistetta kuin sinun pitaisi Jos olet ottanut liian suuren laakeannoksen tai vaikkapa lapsi on ottanut laaketta vahingossa, ota aina yhteytta laakariin, sairaalaan tai Myrkytystietokeskukseen (puh. 09 471 977) riskien arvioimiseksi ja lisaohjeiden saamiseksi.

Yliannostus voi aiheuttaa esim. levottomuutta, vapinaa ja sydamen tykytysta.

4. Mahdolliset haittavaikutukset

Kuten kaikki laakkeet, tamakin laake voi aiheuttaa haittavaikutuksia. Kaikki eivat kuitenkaan niita saa. Osa oireista voi johtua liian suuresta laakeannoksesta. Laakari voi tarvittaessa arvioida hoitoannoksesi uudelleen.

Etenkin kayton alkuvaiheessa laake saattaa aiheuttaa joillekin kayttajille levotonta oloa seka vapinaa ja sydamen tykytysta. Nama oireet menevat yleensa ohi laakityksen jatkuessa.

Vakava allerginen reaktio Jos sinulle ilmaantuu pian annoksen ottamisen jalkeen kutinaa, ihottumaa, ihon punoitusta, silmaluomien, huulten, kasvojen tai nielun turvotusta, verenpaineen laskua tai tajunnan menetysta, toimi seuraavasti:

lopeta Buventol Easyhaler? valmisteen kaytto

hakeudu valittomasti laakariin.

Hengenahdistus valittomasti laakkeen oton jalkeen Keuhkoihin hengitettavat laakkeet voivat harvoin lisata hengityksen vinkumista ja hengenahdistusta valittomasti laakkeen oton jalkeen. Jos nain kay:

lopeta Buventol Easyhaler? valmisteen kaytto

hakeudu valittomasti laakariin.

Yleiset (yli 1 potilaalla sadasta)

lieva sydamen sykkeen nousu, sydamen tykytys

vapina.

Melko harvinaiset (alle 1 potilaalla sadasta)

paansarky

yliherkkyysreaktiot (kohtauksittain esiintyva ihon paikallinen turvotus – angioedeema, nokkosrokko, verenpaineen liiallinen lasku, pyortyminen).

Harvinaiset (alle 1 potilaalla tuhannesta)

verenpaineen nousu tai lasku, sydamen rytmihairiot, rasitusrintakipu, sydanlihaksen hapenpuute

pahoinvointi

keuhkoputkien supistelu

yska, suun ja nielun arsytys. Voit ennaltaehkaista naita haittavaikutuksia huuhtelemalla suusi ja nielusi vedella jokaisen laakkeenottokerran jalkeen. Ala niele huuhteluvetta, sylje se pois.

liian alhainen veren kaliumpitoisuus, liian korkea veren sokeripitoisuus

lihaskrampit

yliaktiivisuus, hermostuneisuus, levottomuus, huimaus.

Haittavaikutuksista ilmoittaminen Jos havaitset haittavaikutuksia, kerro niista laakarille tai apteekkihenkilokunnalle. Tama koskee myos sellaisia mahdollisia haittavaikutuksia, joita ei ole mainittu tassa pakkausselosteessa. Voit ilmoittaa haittavaikutuksista myos suoraan (ks. yhteystiedot alla). Ilmoittamalla haittavaikutuksista voit auttaa saamaan enemman tietoa taman laakevalmisteen turvallisuudesta.

www? sivusto: www. fimea. fi Laakealan turvallisuus - ja kehittamiskeskus Fimea Laakkeiden haittavaikutusrekisteri PL 55 00034 FIMEA

5. Buventol Easyhaler? valmisteen sailyttaminen

Ei lasten ulottuville eika nakyville.

Sailytettava huoneenlammossa (15 °C–25 °C).

Laakkeen kestoaika on 6 kuukautta laminaattipussin avaamisen jalkeen.

Ala kayta tata laaketta pakkauksessa mainitun viimeisen kayttopaivamaaran jalkeen. Viimeinen kayttopaivamaara tarkoittaa kuukauden viimeista paivaa.

Laakkeita ei tule heittaa viemariin eika havittaa talousjatteiden mukana. Kysy kayttamattomien laakkeiden havittamisesta apteekista. Nain menetellen suojelet luontoa.

6. Pakkauksen sisalto ja muuta tietoa

Mita Buventol Easyhaler sisaltaa

Vaikuttava aine on salbutamoli, jota on 100 mikrogrammaa/annos tai 200 mikrogrammaa/annos.

Muu aine on laktoosimonohydraatti (sisaltaa maitoproteiinia).

Laakevalmisteen kuvaus ja pakkauskoot Valkoinen tai melkein valkoinen jauhe.

Aloituspakkauksessa mukana suojakotelo. Kaikkia pakkauskokoja ei valttamatta ole myynnissa.

Myyntiluvan haltija ja valmistaja Myyntiluvan haltija Orion Oyj Orionintie 1 02200 Espoo

Valmistaja Orion Pharma Orionintie 1 02200 Espoo

Tama pakkausseloste on tarkistettu viimeksi 7.5.2015

NAIN KAYTAT EASYHALERIA

Buventol Easyhaleria on helppo kayttaa. Lue aluksi seuraavat ohjeet. Niissa kerrotaan, mita sinun tulee tehda ja mihin kiinnittaa huomiota

Easyhaler (Kuva 1) on pakattu laminaattipussiin, jotta jauhe pysyy kuivana.

Ala avaa pussia ennen kuin otat Easyhalerin kayttoon.

Voit kayttaa Easyhaleria suojakotelon kanssa tai ilman sita. Jos et kayta suojakoteloa , siirry kohtaan ”Annoksen ottaminen Buventol Easyhalerista” (katso b-kuvat).

Avaa suojakotelo ja tyonna Easyhaler koteloon (Kuva 2). Varmista, etta suojus on Easyhalerin suukappaleen paalla (se estaa Easyhalerin lataamisen vahingossa).

Jos et kayta Easyhaleria heti, sulje suojakotelo.

ANNOKSEN OTTAMINEN BUVENTOL EASYHALERISTA

Jos kaytat suojakoteloa, avaa se.

Poista suukappaleen suojus .

A) Ravista Ravista Easyhaleriavoimakkaasti ylos ja alas 3–5 kertaa (Kuva 3a tai 3b), jotta jauhe liikkuu kunnolla ja saat oikean annoksen. Pida Easyhaler ravistamisen jalkeen pystyasennossa.

B) Naksauta Paina Easyhaleria kerran peukalon ja etusormen valissa kunnes kuulet naksahduksen (Kuva 4a tai 4b), ja anna laitteen palautua alkuperaiseen asentoon. Jauhe siirtyy suukappaleen sisalla olevaan inhalaatiokanavaan. Pida laite edelleen pystyasennossa.

Jos epailet ladanneesi useamman kuin yhden annoksen, katso kohta HUOM! (kuva 6a tai 6b).

C) Hengita sisaan Istuma-asennossa tai seisten

hengita ulos tavalliseen tapaan (mutta ALA Easyhaleriin)

aseta suukappale suuhun hampaiden valiin ja sulje huulet tiiviisti suukappaleen ymparille

hengita sisaan voimakkaasti ja syvaan Easyhalerin kautta (kuva 5a tai 5b)

ota Easyhaler pois suusta

pidata hengitysta vahintaan 5 sekuntia ja hengita sitten tavalliseen tapaan.

Pida huolta, etta et hengita Easyhaleriin, koska se voi johtaa Easyhalerin tukkeutumiseen. Katso kohta HUOM! (Kuva 6a tai 6b).

Jos sinulle on maaratty enemman kuin yksi annos kerralla, toista kohdat A, B ja C .

Laita suojus takaisin suukappaleen paalle. Jos kaytat suojakoteloa, sulje se.

HUOM! Jos lataat annoksen vahingossa tai useamman kuin yhden annoksen kerrallaan tai jos hengitat Easyhaleriin, poista jauhe koputtamalla suukappaletta poytaa tai kammenta vasten (kuva 6a tai 6b). Nain varmistat oikean annoksen. Aloita taman jalkeen alusta ja toista kohdat A, B ja C.

Puhdista suukappale vahintaan kerran viikossa puhtaalla kuivalla kankaalla tai pehmealla paperipyyhkeella. Ala kayta puhdistukseen vetta tai muuta nestetta, silla jauhe ei saa kostua. Jos kaytat suojakoteloa, voit ottaa Easyhalerin pois kotelosta pyyhkimista varten. Kun laitat sen takaisin suojakoteloon, laita suojus suukappaleen paalle, jotta et vahingossa lataa annosta.

EASYHALERIN VAIHTO UUTEEN

Easyhalerissa on annoslaskuri, josta nakyy montako annosta on jaljella (Kuva 7a tai 7b). Laskuri liikahtaa joka viidennen annoksen lataamisen jalkeen. Laskurin naytto muuttuu punaiseksi, kun jaljella on 20 annosta. Jos sinulla ei viela ole uutta Easyhaleria, ota yhteys laakariin uuden reseptin saamiseksi. Kun laskurissa nakyy 0, Easyhaler on vaihdettava uuteen, vaikka jauhetta viela nakyykin inhalaattorin takaseinassa olevasta kirkkaasta ikkunasta (Kuva 8).

Sailyta suojakotelo seuraavaa Easyhaleria varten.

Ixia Reviews, Ixia

Ixia Reviews

I won't try to 'hype' the company like others here. Working for companies like this should come with competitive pay and perks, and a much stronger vision and sense of inclusion. Toward the end, I saw low morale, although management does try to pump people up. Not sure if it works. There is a pulse that is missing, and it shows. People here work very hard, but it doesn't seem to translate into smiling faces.

Ixia has some winning solutions, but the marketing and execution is lacking. Conservative company that needs someone at the helm who understands how to be a strong advocate for their offerings.

Advice to Management

There is more to life than your stock price and shareholders. Remember the people who are supporting you. Put your people first. And park your ego at the door.

Smart knowledgeable people to work with. Latest cutting edge technologies to work on. No big issues with work/life balance. Pay was above expectations.

Big rush to get new products finished and shipping by a certain date but few customer orders to justify the push. There were no project managers to determine that the timeline was feasible based the tasks and number of resources. No real marketing data to show a demand for the product being developed. Budget is determined at the end of the year and half the time you don't have visibility into what projects are coming up. That leads to underplanning. Poor sales pipeline planning leads to big end of quarter pushes to book and ship product in a quick turn also leads to forecasting issues.

Advice to Management

Get better marketing data so you know you're making a product that will sell immediately. Also helps with adequate forecasting. Get a better handle on sales deals so that a large chunk of quarterly sales aren't done in the last 2 weeks. Hire some project managers to set realistic project timelines. Engineering shouldn't be managing projects.

5dh3 560 - Prysmian Cables - Systems, Cordaflex

PRYSMIAN CABLES & SYSTEMS | 5DH3 560 CORDAFLEX (SM) AWG Portable Reel Cable EP insulation, dual Neoprene jacket with braid enforcement, 90C, 600 V, 12 AWG, 20 conductors, yellow

Description

Cordaflex (SM), extra flexible tinned copper conductors, ozone-resistant EPR insulation, double neoprene jacket with a textile braid between the jacket layers, Kevlar central strength member with EPDM insulation.

Applications

Flexible power and control cable for use on reels and drum systems for connecting movable parts of machine tools, material handling equipment, etc. associated with high mechanical stresses. RS - version for use in vertical reeling application.

Features

Central messenger superior tensile force capabilties

Extra finely stranded tin coated copper conductors with a short length of lay - high durability under constant flexing conditions, highly flexible conductor assembly

PROTOLON EP insulation highly resistant to ozone

Inner jacket locked construction of conductor assembly - resistance to sheave induced corkscrewing water blocked

Wide mesh textile braid reinforcement in a vulcanized bond - high torsion resistance

Extra heavy duty yellow neoprene double extruded jacket - very resistant to deformation and compressive forces highly resistant to oil, flame, and high temperatures

Reinforced RS version available - improved vertical suspension performance

Good conductor geometry promotes long conductor life less spare conductors required

Large standard range with many sizes stocked - readily available

Metric sizes available international jobs

Composite cables with integrated fiber optics available - power and control/data transmission through one single cable no interference on control/data circuits

Specification Description

CONDUCTOR: Tinned or Coated Copper INSULATION: Ethylene Propylene Rubber (EPR) TEMPERATURE: 90C VOLTAGE: 600 V

Shipping and Fulfillment Policy

When you order products from Anixter. com, the order is processed within one to two business days. Orders received during non-business days are processed on the next business day.

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Shipping charges are calculated based on the shipping option you select, and is prepaid by you at the time of shipment.

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In addition, Anixter. com offers Less-Than-A-Truckload “LTL” option for products that cannot be shipped via parcel shipping. For products that will be shipped via LTL, you will be provided with a set of Accessorials to select from to provide Anixter with additional shipping considerations, such as residential delivery, inside delivery, lift gate or limited access.

Residential Delivery - A residential delivery charge applies to shipments to a home or private residence, including locations where a business is operated from a home, or to any shipment in which the shipper has designated the delivery address as a residence.

Inside Delivery - When requested, freight carrier unloads shipments from or to areas that are not next to the trailer, such as shopping malls or office buildings. An Elevator must be available to provide service to floors above or below the trailer.

Liftgate - Freight carrier provides liftgate service, if needed, to load and unload a shipment when loading/unloading docks are not available.

Limited Access Locations - A limited access location is a site where pickup or delivery is restricted or limited.

Shipping charges are calculated based on the shipping option you select, and is prepaid by you at the time of shipment.

Tamona, Tamona

Products

TGstream PMR

TGstream PMR

ATTENTION: In this device fuel injectos emulation is done by relays . it this case you can not use fuel enrichment function.

FCI hermetic connection

Tiny remote control with indication

Standard interface cable for connecting ECU and PC

Sequential Gas Injection

Possibility to operate with multipoint simultaneous petrol injection and monoinjection

Smooth (injector-by-injector) switching from petrol to LPG

Forced starting on gas

Change-over switch K-5

Petrol-gas switch K-5 is applicable for use in automotives on Liquified Petroleum Gas (LPG), with electromagnetic valve gas pressure reducer, carburettor and +12V supply. K-5 has yellow and green LEDs on the front panel.

Change-over switch PG-3

PG-3 is versatile change-over switch for use in vehicles with Liquified Petrolem Gas (LPG) whose parameters to be adjusted during installation. The microprocessor of the switch lets the installer or driver set required configuration. The electronic keys protect PG-3 outputs from possible mistakes in connection. Front panel has 5 LEDs (yellow, red and 3 green) and two control buttons. The switch memorizes last settings.

GAS alarm

GAS alarm

Gas escape sensor

Gas escape sensor GasAlarm is intended for installation onto cars in order to prevent fire which could occur due to broken or defective hoses, reducers and other possible reasons. If gas concentration achieves certain limit within checked area this device blocks active valve, i. e. prevents concentration from dangerous value.

TGstream 4P

TGstream 4P

Device TGstream 4P is 4th generation controller of multipoint gas injection designed for petrol cars.

TGstream-4P and TGstream-6P are identical devices to TGStream-4 and TGstream-6, the only difference is housing, plastic or aluminum.

FCI hermetic connection

Tiny remote control with indication

Standard interface cable for connecting ECU and PC

Sequential Gas Injection

Smooth (injector-by-injector) switching from petrol to LPG

Forced starting on gas

Wireless switch DJ-01

Wireless switch DJ-01

Wireless package of lighting control DJ-01

The package of lighting control DJ-01 is appointed for the lighting control in the room remotely (radio waves). It consists of receiver and one transmitter (controller). Encoded control signal is transmitted from the transmitter to receiver by the radio waves. The relay is toggled in the receiver after the decoding. For receiver to work it’s necessary to record the transmitter of the remote control to the memory of receiver (register). The amount of transmitters is up to 30pc. The receiver is of small dimensions (48x42x22mm), that allow to install it in the lamp corps or aside. The construction of transmitter is constructed as the light switch, which is powered by separate power battery (CR2032) that is why it’s possible to install it (or several transmitters) in any esirable place.

Fors-4-100

Fors-4-100

Injector emulators are used in vehicles on Liquified Petroleum Gas (LPG) with fuel injection of Bosch type for 4-cylinders engines. At switching on LPG emulator does not let burners be open what cuts off petrol feed. At the same time, vehicle diagnostic system does not detect burners cutting off and does not make any changing in engine performance.

Frequency converter SLU

Frequency converter SLU

Universal frequency converter „Solaris SLU“

Variable Frequency Driver „Solaris SLU“ is designed to be used with AC induction motors that are rated from 550W up to 4kW with voltages range 380-400V. VFD is compact, easy to use, ready for many applications. Because of low price „Solaris SLU“ can replace motor soft starting systems or motor protection systems.

Input phase sequence protections, input voltage too low/high protections.

Motor overload, underload, overcurrent protections.

Output frequency from 0.1Hz … 100.0 Hz

Scalar V/f frequency control.

Selectable carrier frequency up to 18kHz

Remote control with 0-10V or 4-20mA signal

TGstream 4/6/8

TGstream 4/6/8

Device TGstream is 4th generation controller of multipoint gas injection designed for petrol cars.

TGstream-4P and TGstream-6P are identical devices to TGStream-4 and TGstream-6, the only difference is housing, plastic or aluminum.

FCI hermetic connection

Tiny remote control with indication

Standard interface cable for connecting ECU and PC

Sequential Gas Injection

Smooth (injector-by-injector) switching from petrol to LPG

Forced starting on gas

TGstream PM

TGstream PM

FCI hermetic connection

Tiny remote control with indication

Standard interface cable for connecting ECU and PC

Sequential Gas Injection

Possibility to operate with multipoint simultaneous petrol injection and monoinjection

Smooth (injector-by-injector) switching from petrol to LPG

Forced starting on gas

ProGas 4P

ProGas 4P

Multipoint Gas Injection system ProGAS

System ProGAS is the controller of multipoint gas injection. It could be installed on to the cars with following types of fuel injection:

Multipoint phased petrol injection into engine manifold.

Multipoint coupled petrol injection into engine manifold.

Multipoint simultaneous petrol injection into engine manifold.

Monoinjection of petrol into engine manifold. ProGAS consists of: main unit which is installed in engine compartment, temperature and pressure sensors, installation kit and remote control which is installed in passenger compartment in handy place. ProGAS memorizes last performance mode: “AUTOMATIC” or “PETROL”. It is provided forced starting on gas. There are light and sound indication of the status and system modes.

USB adapter

USB adapter

ZOND-4

ZOND-4

PRODUCT DESCRIPTION

Change-over switch PG-3

PG-3 is versatile change-over switch for use in vehicles with Liquified Petrolem Gas (LPG) whose parameters to be adjusted during installation. The microprocessor of the switch lets the installer or driver set required configuration. The electronic keys protect PG-3 outputs from possible mistakes in connection. Front panel has 5 LEDs (yellow, red and 3 green) and two control buttons. The switch memorizes last settings.

Commutation of multivalves control with electronic protection

Automatic switching petrol-LPG on pre-set threshold

Smooth adjusting threshold of switching petrol-LPG

Adjusting delay of petrol cut-off at switching onto LPG

Switching petrol-LPG at accelerating or decelerating

Two thresholds of the signal level sensitivity

Indication of LPG level in the tank (0, 25%, 50%, 75%,100 %)

USER MANUAL

2015 TAMONA Sukurta:

Ceo Who Kicked Dog On Viral Video Has New Job Running Frozen Food Firm, Dianben

CEO who kicked dog on viral video has new job running frozen food firm

Des Hague caught on video kicking a friend's dog in an elevator.

Fallen food executive Des Hague has been hired to run a frozen food company, two years after a viral video exposing him abusing a small dog led to his resignation as CEO of top food concessionaire Centerplate .

The 48-year-old Hague, who pleaded guilty in connection to the incident, became an investor and chairman of the board several months ago of his new company Froozer. He was named CEO last week. Colorado-based Froozer sells tubes of frozen fruit and vegetables, an official snack of the U. S. speedskating team.

"I am fully invested in the Froozer brand and its potential," Hague said in a statement last week. His hiring was first reported by The Advocate newspaper in Stamford, Conn.

In an interview with CNBC on Friday, Hague discussed his remorse over the incident with the dog, which he had kicked repeatedly and whose leash he had harshly yanked. He also talked about his desire to do good on the heels of that, his charitable endeavors and his enthusiasm about working with Froozer.

He noted that legendary investor Warren Buffett has been quoted as saying "it takes 20 years to build a reputation and five minutes to ruin it."

"In my case, it was less than a minute in Vancouver two years ago," Hague said. "I made a dreadful mistake one night, but I believe it has not defined me, and I think I have the potential to do good."

"The last two years have been really painful. And the whole situation was self-inflicted," Hague said.

Source: @deshague Twitter

Hague said he was excited to identify an opportunity to invest in Froozer.

"I came across this healthy food that's good for athletes, kids and more. It's really simple and a great product," Hague said.

Hague said that one positive side effect from the case is the fact that "it has allowed me to spend more time recently with family and friends." He also said he's learned a lot about himself "from my mistake," and gotten healthier physically, acknowledging that the stress of running Centerplate "got to me."

Hague's Twitter feed shows him looking relaxed, and trimmer than his days at Centerplate. His Twitter bio calls him a "Dealmaker. Investor. Optimist. Philanthropist," and an "imperfect human being working to better myself."

This week, the Connecticut resident had updated his Twitter followers about a vacation in the Bahamas, where a photo Hague posted Thursday shows him swimming with pigs. Other recent images he posted show him feeding sharks and heading into the pricey sushi restaurant Nobu.

Froozer, in a statement emailed to CNBC, said, "We are delighted to have someone of Mr. Hague's caliber lead our organization."

"Our decision to engage Des was based on his experience, leadership qualities and prior business successes which speak for themselves," the company said. "Over a twenty-five-year period of leading global public and private companies, he has established himself as an innovative thinker in the international business world."

Froozer also cited the "significant amount of time and energy" Hague devotes to nonprofit charitable work and has helped raise more than $100 million over the past few years.

"This mirrors our corporate philosophy and was an important consideration for bringing Des on board, as opposed to an isolated, out-of-character incidence from the past," Froozer said. "In addition, we firmly believe that everyone deserves a second chance."

Hague's appointment as Froozer's top executive came a year after a Canadian judge fined him $5,000 and banned him from owning or controlling an animal for three years following his guilty plea to a single count of causing an animal to be in distress. The charge is the equivalent of a misdemeanor in the United States.

Hague had been charged by authorities after the emergence of an July 2014 surveillance video from a Vancouver hotel that showed him tormenting a 5-month-old Doberman pinscher named Sade in an elevator.

Hague is seen on the video repeatedly kicking the dog. He also pulled hard on her leash, to the extent that the pooch's paws left the floor of the elevator. Sade belonged to a friend of Hague's.

Disclosure of the video sparked a massive backlash against Hague and Stamford-based Centerplate, which provides food and beverage services to major sporting venues, arenas, convention centers and other locations across North America.

In addition to public outrage, Centerplate clients were concerned about the situation, including the San Francisco 49ers football team, which condemned Hague's conduct.

"I take full responsibility for my actions," Hague said in a statement at the time to the Canadian TV network Global News. "This incident is completely and utterly out of character and I am ashamed and deeply embarrassed."

On Friday, Hague told CNBC that before he got into the elevator with Sade, the dog had pulled on its leash so hard that it dislocated two of Hague's fingers."

"I wish I could have controlled the incident with the dog better," Hague said. "Jesus, I'm fallible. I'm human. I made a mistake. I lost my temper, and I regret that."

He also said, "I've replayed the incident time and time again." Hague said Sade's owner remains a friend of his.

Hague, who earned at least $4.7 million annually, originally agreed with Centerplate as a condition of his continued employment to undergo anger management counseling, donate $100,000 personally to an animal charity and do 1,000 hours of community service.

But the public relations furor continued unabated. Hague's resignation days later came after a change. org petition calling for his firing topped 150,000 signatures. His departure meant that he did not end up making the donation or performing the community service detailed by his agreement with Centerplate.

Hague pleaded guilty in February 2015 in the Canadian court to the charge of causing Sade distress.

At the sentencing two months later, the judge reportedly was told that Hague was taking prescription drugs for anxiety. and had alcohol in his system at the time he attacked the dog.

"Clearly, this is something I am very, very sorry about and I can assure the court these incidents will never happen ever again," Hague told the judge.

Within days of his sentencing, Hague joined the board of directors of the digital media solutions and signage company PING HD.

About a week later, Hague, whose web page identifies him as an "internationally renowned executive in the hospitality industry," launched a new investment and consulting company, Aegis.

Aegis since has made investments in The World of Beer, a beer specialist in Florida, as well as in William Caruso & Associates, a Denver-based design and consulting company, and in Froozer.

Last September, The Advocate reported that Hague, in an email to the newspaper. had said, "The past 12 months have been very difficult for me and my family. Due to the incident with Sade I have lost income, received hate mail and death threats to myself and my family. My son was actually attacked."

After the dog debacle, Hague joined the board of directors of the Stamford Youth Foundation, a charitable group that works with kids in his hometown.

Marc Lyons, founder and president emeritus of the foundation, said he was glad that the group was able to give Hague "a second chance in life."

"Everybody is entitled to make a mistake," Lyons said of Hague, who is corporate donations chairman for the group. Lyons said Hague has "done a great job" at raising money for the foundation.

"He's impressed me," Lyons said.

Hague's Twitter feed in recent months shows him enjoying a globe-trotting lifestyle.

Photos that he posted on Twitter show him in Italy, France and the Bahamas, going on winery tours, taking cooking classes, visiting museums and sight-seeing at the Colosseum and Sistine Chapel at the Vatican, and a site of the D-Day landings in Normandy. One photo from late April shows him dining with the U. S. speedskating team.

At the end of 2105, Hague wrote an essay on LinkedIn entitled "Slaying Dragons — Thrive in 2016," which referred vaguely to his professional and legal woes due to the puppy-kicking scandal, and offered some advice to others who also have had troubles of their own.

"As the year closes out, I wanted to take a moment and reflect on the lessons learned over the last year and work on improving myself. The last year, I have faced more adversity than in the last decade," Hague wrote. "So my focus is on how to keep moving forward and being positive inspite (sic) of difficult times."

"It goes without saying that we have all had our dark moments. We have done and said things we have wished we had not and most likely acted out inappropriately or even very inappropriately," Hague wrote. "If you have not then you are one of the very lucky or sheltered ones."

Elocom - Uses, Side Effects, Interactions, Elicasal

Elocom

How does this medication work? What will it do for me?

Mometasone belongs to the class of medications called topical corticosteroids . It is used to reduce the symptoms of skin rashes associated with conditions such as psoriasis and allergic eczema. It works by reducing inflammation, itching, and irritation of the skin.

This medication may be available under multiple brand names and/or in several different forms. Any specific brand name of this medication may not be available in all of the forms or approved for all of the conditions discussed here. As well, some forms of this medication may not be used for all of the conditions discussed here.

Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. If you have not discussed this with your doctor or are not sure why you are taking this medication, speak to your doctor. Do not stop taking this medication without consulting your doctor.

Do not give this medication to anyone else, even if they have the same symptoms as you do. It can be harmful for people to take this medication if their doctor has not prescribed it.

What form(s) does this medication come in?

Cream Each gram of white-to-off-white uniform cream contains mometasone furoate 1 mg. Nonmedicinal ingredients: aluminum starch octenylsuccinate, ceteareth-20, hexylene glycol, phosphoric acid to adjust the pH, propylene glycol stearate, purified water, stearyl alcohol, titanium dioxide, white petrolatum, and white wax.

Lotion Each gram of lotion contains mometasone furoate 1 mg. Nonmedicinal ingredients: hydroxypropyl cellulose, isopropyl alcohol, phosphoric acid to adjust the pH, propylene glycol, purified water, and sodium phosphate monobasic monohydrate.

Ointment Each gram of ointment contains mometasone furoate 1 mg. Nonmedicinal ingredients: hexylene glycol, phosphoric acid to adjust the pH, propylene glycol stearate, purified water, white petrolatum, and white wax.

How should I use this medication?

Cream/ointment: Apply a thin film to the affected skin areas once daily.

Lotion: Apply a few drops of the lotion to the affected skin areas (including scalp sites) once daily. Massage gently and thoroughly until the medication disappears.

Do not allow this product to get in your eyes. Severe irritation is possible if it contacts the eye. Should this occur, flush your eye immediately with a large amount of water.

Do not use an occlusive dressing (made of airtight material) to cover areas where this medication has been applied unless otherwise directed by your doctor.

Mometasone should be used for a maximum of 5 days on the face, scalp, skin-fold areas, and groin; it should be used for a maximum of 3 weeks on the body.

Many things can affect the dose of medication that a person needs, such as body weight, other medical conditions, and other medications. If your doctor has recommended a dose different from the ones listed here, do not change the way that you are using the medication without consulting your doctor.

It is important that this medication be used exactly as prescribed by your doctor. If you miss a dose, use it as soon as possible and continue with your regular schedule. If it is almost time for your next dose, skip the missed dose and continue with your regular dosing schedule. Do not apply a double dose to make up for a missed one. If you are not sure what to do after missing a dose, contact your doctor or pharmacist for advice.

Store this medication at room temperature and keep it out of the reach of children.

Do not dispose of medications in wastewater (e. g. down the sink or in the toilet) or in household garbage. Ask your pharmacist how to dispose of medications that are no longer needed or have expired.

Who should NOT take this medication?

Do not use mometasone if you:

are allergic to mometasone or any ingredients of this medication

are allergic to other corticosteroids

have untreated bacterial, tubercular, fungal, or viral infections involving the skin (including herpes simplex, skin rash resulting from vaccination, and chickenpox)

Mometasone should not be used to treat:

acne vulgaris

rosacea

itchy skin which is not inflamed

What side effects are possible with this medication?

Many medications can cause side effects. A side effect is an unwanted response to a medication when it is taken in normal doses. Side effects can be mild or severe, temporary or permanent.

The side effects listed below are not experienced by everyone who takes this medication. If you are concerned about side effects, discuss the risks and benefits of this medication with your doctor.

The following side effects have been reported by at least 1% of people taking this medication. Many of these side effects can be managed, and some may go away on their own over time.

Contact your doctor if you experience these side effects and they are severe or bothersome. Your pharmacist may be able to advise you on managing side effects.

burning and itching of skin (without other symptoms of a skin infection; see below)

inflammation of hair follicles

skin colour changes

thinning skin, with easy bruising

tingling and stinging of affected areas

Although most of the side effects listed below don't happen very often, they could lead to serious problems if you do not check with your doctor or seek medical attention.

Check with your doctor as soon as possible if any of the following side effects occur:

acne-like reaction

increased size of skin rash

infected, hard sores (furunculosis)

symptoms of a skin infection (such as warmth, redness, swelling, itching, or pus)

The following side effects may occur if this medication is used improperly or for a long time:

backache

blurring or loss of vision (occurs gradually if certain products have been used near the eye)

burning and itching of skin with pinhead-sized red blisters

filling or rounding out of the face

increased blood pressure

irregular heartbeat

irregular menstrual periods

irritability

irritation of skin around mouth

loss of appetite

depression

muscle cramps, pain, or weakness

nausea

rapid weight gain or loss

reddish-purple lines (stretch marks) on arms, face, legs, trunk, or groin

signs of high blood sugar (e. g. frequent urination, increased thirst, excessive eating, unexplained weight loss, poor wound healing, infections, fruity breath odour)

skin colour changes

stomach bloating, burning, cramping, or pain

swelling of feet or lower legs

unusual bruising

unusual decrease in sexual desire or ability (in men)

unusual tiredness or weakness

vomiting

weakness of the arms, legs, or trunk (severe)

worsening of infections

Stop taking the medication and seek immediate medical attention if any of the following occur:

blurred vision, eye pain, or increased eye pressure

symptoms of an allergic reaction (chills, fever, muscle aches, or flu-like symptoms that happen before or with a skin rash)

symptoms of high levels of corticosteroids in the blood stream (darkening of the skin, fatigue, low blood pressure, diarrhea, and digestive problems)

Some people may experience side effects other than those listed. Check with your doctor if you notice any symptom that worries you while you are taking this medication.

Are there any other precautions or warnings for this medication?

Before you begin using a medication, be sure to inform your doctor of any medical conditions or allergies you may have, any medications you are taking, whether you are pregnant or breast-feeding, and any other significant facts about your health. These factors may affect how you should use this medication.

Diabetes: When mometasone is used over large areas of the body for prolonged periods or under dressings that don't breathe it is possible that enough medication will absorb into the bloodstream to affect blood sugar levels. If you have diabetes, your doctor should closely monitor your condition while you are using mometasone, as it may affect blood sugar control.

Eyes: Use this medication with care on lesions close to the eye. Getting the medication in the eye can increase the risk of increased eye pressure, glaucoma, or cataracts. Report any changes in vision or eye pain to your doctor.

Infections: You may experience an infection in the treated area while using a topical (skin-applied) corticosteroid. If you notice symptoms of a skin infection such as redness, warmth, itching, pus, or swelling, contact your doctor.

Internal absorption: Absorption of topical corticosteroids will increase if large areas are treated or if you use dressings that don't breathe. If you need to use the medication in this way, speak to your doctor about what precautions you should take. This is especially important for infants and children.

Medical treatment: Inform all medical professionals that you see that you have been using topical (skin-applied) corticosteroids.

Poor circulation: If you have poor blood circulation, talk to your doctor about the risks and benefits of using this medication.

Prolonged use: Using topical corticosteroid medication for a long period of time can cause skin to thin or soften or cause stretch marks. Talk to your doctor about how long you should use this medication.

Thinning of skin: Prolonged use of topical corticosteroid products may produce thinning of the skin and tissues under it. If you notice this effect, contact your doctor

Pregnancy: This medication should not be used during pregnancy unless the benefits outweigh the risks. If you become pregnant while taking this medication, contact your doctor immediately.

Breast-feeding: It is not known if mometasone passes into breast milk. If you are a breast-feeding mother and are taking this medication, it may affect your baby. Talk to your doctor about whether you should continue breast-feeding.

Children: Children may be more likely to experience side effects from this medication. The risk of side effects increases when large body areas are treated, when treatment lasts for a long time, and when dressings that don't breathe are used. In these situations, side effects similar to those caused by oral corticosteroids (e. g. growth suppression) may occur. Mometasone is not recommended for use in children less than 18 years of age.

What other drugs could interact with this medication?

There may be an interaction between mometasone and any of the following:

aldesleukin

deferasirox

hyaluronidase

itraconazole

ritonavir

telaprevir

other topical medications that have irritating effects (e. g. retinoic acid, salicylic acid)

other topical (skin-applied) medications that contain corticosteroids (e. g. hydrocortisone)

If you are taking any of these medications, speak with your doctor or pharmacist. Depending on your specific circumstances, your doctor may want you to:

stop taking one of the medications,

change one of the medications to another,

change how you are taking one or both of the medications, or

leave everything as is.

An interaction between two medications does not always mean that you must stop taking one of them. Speak to your doctor about how any drug interactions are being managed or should be managed.

Medications other than those listed above may interact with this medication. Tell your doctor or prescriber about all prescription, over-the-counter (non-prescription), and herbal medications you are taking. Also tell them about any supplements you take. Since caffeine, alcohol, the nicotine from cigarettes, or street drugs can affect the action of many medications, you should let your prescriber know if you use them.

Indexon Indikasi - Kontraindikasi - Efek Samping - Dosis (Kerjanya), Indexon

Indexon

INDIKASI & KONTRAINDIKASI

Indexon adalah nama dagang dari deksametason. Obat ini termasuk ke dalam golongan kortikosteroid disamping prednison, hidrokortison, dll. Fungsi utama indexon adalah sebagai antiperadangan (antiinflamasi) dan antialergi. Oleh karena itu, obat ini digunakan secara luas untuk berbagai macam penyakit yang mempunyai gejala peradangan atau penyakit yang mekanisme dasarnya adalah alergi. Berikut contoh penyakit yang menjadi indikasi pemberian indexon:

1. Rheumatoid artritis

Penyakit rheumathoid arthritis terjadi akibat sistem kekebalan tubuh menyerang persendian. Akibatnya terjadi peradangan pada sendi yang terkena. Ciri-cirinya sendi nyeri, merah, bengkak. dan hangat. Pemberian indexon akan mengurangi gejala-gejala peradangan tersebut.

Pada asma bronkhial, terjadi peradangan saluran napas sehingga saluran napas membengkak, menyempit, dan mengeluarkan lebih banyak cairan. Ketiga keadaan ini menyebabkan penderita kesulitan bernapas. Pemberian indexon akan menghambat proses peradangan sehingga penyempitan saluran napas menghilang dan aliran udara keluar masuk paru-paru lancar kembali.

Salah satu contohnya adalah alergi telur. Pada alergi telur, tubuh salah mempersepsikan protein yang terdapat dalam telur. Normalnya, tubuh akan menganggap protein tersebut sebagai senyawa yang tidak berbahaya. Tapi pada orang yang alergi, tubuhnya menganggap protein telur sebagai benda asing yang harus dimusnahkan. Maka sistem pertahanan tubuh diaktifkan secara berlebihan, akibatnya muncul gejala alergi seperti gatal dan biduran seluruh badan, kadang-kadang disertai sesak napas. Pemberian indexon dapat menekan kekuatan reaksi pertahanan tubuh sehingga gejala alergi berkurang atau menghilang.

Indexon dapat mengiritasi lambung, sehingga perlu pertimbangan hati-hati pada penderita penyakit maag. Indexon juga dapat meningkatkan kadar gula darah sehingga dikontraindikasikan terhadap penderita penyakit gula atau diabetes mellitus. Kontraindikasi indexon lainnya adalah penyakit osteoporosis, tekanan darah tinggi. gagal jantung. infeksi bakteri, virus, atau jamur yang sedang sampai berat.

Efek samping indexon antara lain adalah luka lambung, tulang rapuh (osteoporosis), gemuk air, rentan infeksi, gangguan elektrolit darah, dan lain-lain.

Satu tablet indexon mengandung 0,5 mg deksametason. Umumnya pemakaian adalah 3 kali 1 tablet. Walaupun demikian, pada beberapa penyakit, dosis dapat diubah sesuai kebutuhan. Misalnya pada penyakit asma, hari pertama 6 mg, hari kedua 4,5 mg, hari ketiga 3 mg, dan hari keempat 1,5 mg. Dosis tersebut dibagi 3 dan diberikan 3 kali sehari.

Untuk menghindari iritasi lambung, indexon harus diberikan sesudah makan atau dalam keadaan perut terisi untuk menghindari iritasi lambung. Selain itu, sebaiknya tidak dikonsumsi bersama makanan atau minuman yang merangsang seperti buah asam, makanan pedas, kopi, minuman soda, dan lain-lain.

BACA JUGA

Qlimax 2009, Glimax

Это видео недоступно.

Qlimax 2009

Дата загрузки: 14 мар. 2011 г.

Isaac 01 Dustin Zahn - Stranger to Stability (Len Faki Podium Mix) 02 The Moon -- Shake It (CJ Bolland Big Bone Mix) 03 Rocket Base -- House-Bee 04 Unknown Analoq -- Go 05 Kernkraft 400 -- Zombie Nation 06 Isaac -- Thriller 07 Starsplash -- Daytona Beach 08 ollum & Yanny -- Shithead 09 Zenith & Avex -- I'm Your Deejay 10 The Real Booty Babes -- Derb LK 11 Geal -- Losing My Feelin' (The Beholder & Balistic Remix) 12 Cosmic Gate -- The Truth (Isaac Remix) 13 Tuneboy -- Demolition (Technoboy Remix) 14 Pep 'N Up -- Time & Space (Warp Brothers Remix) 15 Hocus Pocus -- Bow Chi Bow 16 DJ Isaac -- On The Edge A-Lusion 01 A-Lusion -- Drummer Beat 02 A-Lu sion -- Visual Perception 03 A-Lusion -- No Regrets 04 Second Idendity -- Identify 05 A-Lusion & Scope DJ -- Between Worlds 06 Josh & Wesz -- Rubdown 07 A-lusion -- The Voice 08 A-Lusion -- Too Close 09 A-Lusion -- Veritas 10 A-lusion -- In Every Place 11 Scope DJ -- Mashed Up Vol.1 12 A-Lusion -- Perfect Harmony 13 A-Lusion -- Reverse Order 14 Frontliner & B-Front -- Become The Sky 15 A-Lusion -- Perfect It Davide Sonar 01 Davide Sonar -- Don't Stop 02 Davide Sonar -- Temptation 03 Davide Sonar -- Be Quite 04 Davide Sonar -- Only One 05 Davide Sonar -- Believe 06 Davide Sonar -- All Of Me 07 Davide Sonar -- Spiritual Fire 08 Davide Sonar -- Natural 09 Davide Sonar -- My World

Brennan Heart 01 Brennan Heart -- Just As Easy (Wildstylez vs. SMD Remix) 02 Brennan Heart -- Musical Impressions 03 Brennan Heart feat. Shanokee -- Feel U Here 04 Brennan Heart -- Rockstar DJ 05 Showtek -- We Speak Music 06 Brennan Heart -- One Blade (Noisecontrollers Remix) 07 Wild Motherfuckers -- Fuck It Up 08 Clive King & Xzellar -- Evolution Leaps FWD 09 Showtek feat. MC Stretch -- Freak 10 G-Town Madness & The Viper -- Come As One (Brennan Heart Remix) 11 Noisecontrollers -- Venom (Wildstylez Remix Edit) 12 Headhunterz -- The Sacrifice (Brennan Heart Remix) 13 Brennan Heart -- Remember, remember 14 Frontliner -- The First Cut 15 Blademasterz -- Audiometric 16 Brennan Heart & Wildstylez -- Reputation Game Technoboy 01 Hunter -- TBA 02 Hardstyle Masterz ft. Max Enforcer -- Rambo Is A Pussy 03 Showtek -- Electronic Stereophonic 04. Tuneboy -- Re-Generate It 05 Bass Modulators -- NRGizer 06 Technoboy meets Ruffian -- The Undersound 07 Tuneboy -- Sexbusters (Scope DJ Remix) 10 Hardstyle Masterz Ft. Max Enforcer -- Respect 11 Technoboy -- Ti Sento 12 Headhunterz -- Rock Civilization (TBY Undersound Remix) 13 DJ Stephanie -- Black High Heels

D-Block & S-te-Fan 00 D-Block & S-Te-Fan -- The Nature Of Our Mind 01 D-Block & S-Te-Fan -- Music Made Addict 02 D-Block & S-Te-Fan & Wildstylez -- The Human Soul 03 DJ Isaac -- Tear The Club Up 04 D-Block & S-Te-Fan -- Dreamers Of Dreamz 05 D-Block & S-Te-Fan & Coone -- Crank 06 D-Block & S-Te-Fan -- Let'z Dance 07 D-Block & S-Te-Fan Feat. MC Villain -- Sound Of Thunder 08 Psyko Punkz -- The After MF 09 D-Block & S-Te-Fan -- Essence Of Sound 10 D-Block & S-Te-Fan -- Together 11 B-Front & Frontliner -- Magic 12 Tat & Zat -- Gangsta 13 D-Block & S-Te-Fan Feat. High Voltage -- Shiverz

Headhunterz 01 Headhunterz -- Psychedelic 02 Headhunterz & Wildstylez vs. Noisecontrollers -- Tonight 03 Builder -- Her Voice (Headhunterz Remix) 04 Wildstylez -- A Complex Situation 05 Headhunterz -- Subsonic (Live Edit) 06 The Prophet feat. Wildstylez -- Cold Rocking (Gostosa Remix) 07 Headhunterz -- Emptiness 08 Headhunterz -- The Muzikal Revolution 09 Smashing Guys -- Step Inside The Party (Technoboy Remix) 10 Chuckie -- Let The Bass Kick (Headhunterz Remix) 11 Project One -- Rate Reducer (Headhunterz Remix) 12 Gostosa -- Sutra 13 Headhunterz -- Hate It Or Love It 14 Project One -- The Story Unfolds 15 Headhunterz -- Woznotwoz 16 Headhunterz -- Dreamcatcher 17 Tuneboy -- Just A Detai 18 Headhunterz -- The Sacrifice (Evil Edit) 19 Headhunterz -- Fear Of Darkness 20 Alpha Twins & Wildstylez -- Atrocious 21 Tuneboy -- I Will Growl Noisecontrollers 01 JDX feat. Sarah Maria -- Live The Moment 02 Noisecontrollers & Zany -- Paranoid 03 Brennan Heart -- One Blade (Noisecontrollers Remix) 04 Showtek -- We Live For The Music (Noisecontrollers Remix) 05 Noisecontrollers -- Crump 06 Noisecontrollers -- Shreek 07 Brennan Heart -- Just As Easy (Wildstylez & SMD Remix) 08 Noisecontrollers -- Revolution Is Here 09 Headhunterz & Wildstylez vs. Noisecontrollers -- Tonight 10 Noisecontrollers -- CTRL. ALT. DELETE 11 Noisecontrollers -- Attack Again 12 Noisecontrollers -- Yellow Minute 13 Southstylers -- Pounding Senses (Zany & Noisecontrollers Edit) 14 Noisecontrollers -- Samara

Deepack 01 Deepack - The Prophecy 02 Ran-D -- Fanatics 03 D-Block & S-te-Fan -- Ride With Uz (Max Enforcer Remix) 04 Zany meets The Beholder -- Do You Want Heavy? 05 Josh & Wesz Ft. Low-E -- I've Lost You 06 Deepack feat. MC Lan -- Fire In Tha Place 07 The Vision & Pulse -- Pandorum

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Maxsoten, Maxsoten

Bisoprolol

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Lodoz (Bisoprolol Fumarate with Hydrochlorothiazide)

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Xeldrin

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Alderaan - Wookieepedia, Aldron

Alderaan

" The galaxy knows Alderaan as "the planet of beauty." Nature, poetry, philosophy, art, couture, cuisine—we freely share all with all. " ―Bail Organa [src]

Following the rise of Sheev Palpatine's Galactic Empire. Alderaan played a pivotal role in the establishment of the Rebel Alliance. a movement that sought to restore the Old Republic's values. Because of its ties with the Alliance, the planet was destroyed when Grand Moff Wilhuff Tarkin decided to test the superlaser of the Death Star. a moon - sized battle station developed by the Empire. Among the few survivors of that disaster was Princess Leia Organa. adopted daughter of Bail and Breha Organa and heiress to the royal house of Alderaan.

Contents

Description Edit

" Well, someday you'll come to Alderaan with me and see for yourself how wonderful it is. Not even you could be cynical about my world. " ―Nash Windrider. to Thane Kyrell [src]

Alderaan's snow-capped mountains.

From space. the planet of Alderaan, located in the star system of the same name. [2] appeared as a blue-green orb envelopped in a white web of clouds. [4] Its surface had vast bodies of water [2] and was covered in snow-capped mountains. [4] with patches of green grassy hills. [10] Alderaan was known to the galaxy as "the planet of beauty." [11] Famous natural landmarks of Alderaan included the Cloudshape Falls and the Isatabith rain forest. [5]

The cities on Alderaan were carefully designed to respect the natural beauty of their environment. For example, the palace of the royal family and the city around it blended into the local snow-capped peaks. Alderaanian architecture made use of white synthstone. which inspired the architecture of certain mining economies of the Outer Rim Territories. like the floating colony of Cloud City. and the planets Lothal and Garel. [1]

History Edit

The Old Republic Edit

The peaceful world of Alderaan was among the oldest members of the Galactic Republic. [13] the democratic union that governed most of the galaxy. [14] By the time of the Invasion of Naboo by the Trade Federation. it was represented in the Galactic Senate by Senator Bail Antilles. That year, the then-Supreme Chancellor of the Republic, Finis Valorum. was ousted from office, and Antilles was nominated for the position in the resulting election. However, the Alderaanian senator was defeated by Senator Sheev Palpatine. who represented the sovereign system of Naboo. [15]

The Clone Wars Edit

A city on Alderaan

Ten years later, Alderaan was represented in the Senate by Viceroy Bail Organa. [16] the prince consort of the planet's ruler, Queen Breha Organa. [4] At that time, the Republic was facing a secessionist crisis due to the existence of the Confederacy of Independent Systems led by Count Dooku. pushing the galaxy to the brink of war. Through Organa, Alderaan was a member of Chancellor Palpatine's Loyalist Committee. which concerned itself with the stability of the Republic during the Separatist crisis and which would later strive to limit Palpatine's increasing executive authority. That year, an army of clones was discovered on the planet Kamino. which would be appropriated by the Senate in order to combat the Separatists. To save the Republic from the impending threat, the Supreme Chancellor was granted emergency powers, a decision that was contrary to the pacifist values of Alderaan and its representative and which ultimately led to the outbreak of the Clone Wars. [16]

At some point during the Clone Wars, Alderaan hosted a conference concerned with aiding war refugees. Padme Amidala. then senator of Naboo, was nearly assassinated during the conference when the Hutt crime lord Ziro. whom Amidala had sent to prison. hired the bounty hunter Aurra Sing to take revenge. The plot, however, was thwarted by the Jedi apprentice Ahsoka Tano. [10] Around the time of the Battle of Kadavo. two Alderaanian tourists visiting Tatooine died in a speeder-bike accident. The Zygerrian News implied that the two had gotten intoxicated in the cantina of Mos Eisley. which caused the accident. [17]

The Galactic Empire Edit

With the Clone Wars coming to an end, Chancellor Palpatine revealed his true colors and abolished the Republic, establishing the Galactic Empire in its stead. [4] However, a small number of systems rebelled against this new regime, [2] and the Alliance to Restore the Republic was ultimately formed by Bail Organa and his former colleague in the Galactic Senate, Senator Mon Mothma of Chandrila. [18] During this time, Alderaan became the Alliance's main source of munitions. The planet's crown princess and representative in the Imperial Senate. Princess Leia Organa [2]. adoptive daughter of Bail and Breha Organa, began using her diplomatic immunity as an Imperial senator to carry out Rebel missions in restricted Imperial systems. [19]

About three years before the Battle of Yavin. Senator Bail Organa dispatched three Hammerhead corvettes to the Phoenix rebel cell. which has sustained losses while fleeing Garel. Since Alderaan could not be seen directly supporting the rebels, Senator Organa arranged for his adopted daughter Leia to deliver the vessels to Lothal. The Alderaanians risked losing their seat in the Imperial Senate among other Imperial sanctions. Senator Organa had arranged for the crew of the Ghost to "steal" the ships from an Imperial depot on Lothal so that Alderaan could not be blamed for the "theft." With the help of the crew of the Ghost and the former Governor Ryder Azadi. Leia managed to deliver the three Hammerhead corvettes to the Phoenix rebels following a skirmish at the Imperial depot. [19]

Destruction Edit

" Our position is correct, except…there's no Alderaan! " ―Han Solo [src]

The Death Star fires on Alderaan

Shortly before the Battle of Yavin, Princess Leia was captured by the Imperial Navy while on a mission to recruit the former Jedi Master Obi-Wan Kenobi into the Alliance's fight against the Death Star. a secret battle station built by the Empire. Leia had obtained the plans for the Death Star. a new Imperial superweapon. and hidden it in her astromech droid R2-D2. Organa was taken prisoner by the Sith Lord Darth Vader. the Emperor's second-in-command, and brought before the Death Star's commanding officer, Grand Moff Wilhuff Tarkin. The Imperials forced the princess to witness the obliteration of her home planet, an act that Tarkin hoped would instill fear among the secessionist systems in an effort to keep them in line. The planet's destruction left only an asteroid field behind, [2] which was blockaded by the Empire. [20]

Almost immediately after the Battle of Yavin. Leia Organa would embark on a mission to rescue the survivors of Alderaan from Imperial reprisals following the destruction of the First Death Star. [21]

On Coruscant. the Empire's planetary capital. the numerous Alderaanian residents of Level 3204 began to hold vigils for those who had perished in what they called "the Disaster ." However, as more information became available about the Empire's role in the destruction of Alderaan, the vigils soon turned into riots, which were quickly repressed by brute force. [22] Following the Battle of Yavin. Vader then took the remains of Alderaan to serve as reminders to worlds that attempted to resist the Emperor. Following an assassination attempt on himself at Shu-Torun. Vader then gave Trios. the newly Queen of that planet, one of these reminders. [23]

Legacy Edit

" What act of terror could be more horrible than what happened to Alderaan? Have you forgotten that? I was there. I saw it happen, stood there watching while they destroyed my world, my home, everyone I had ever loved— " ―Senator Leia Organa. to Senator Ransolm Casterfo [src]

By the time of the New Republic. Alderaan's destruction would become a stark reminder for future generations about the terrors of the Galactic Empire, and would often be an 'uncomfortable subject' for those that brought up the planet's destruction in conversation. As such, surviving Alderaanian's would be treated with great respect for their lost world and people. For collectors, rare bottles of the alcoholic beverage Toniray would become a highly-prized after commodity. [7]

Inhabitants Edit

" Soldiers are a thing of Alderaan's past, Leia. " ―Bail Organa, to his adopted daughter Leia [src]

Alderaan hosted a population of Humans. known as Alderaanians. who were known for their philosophy of paci?sm. Even in time of galactic conflicts, the Alderaanians shunned weapons. They were not, however, bereft of spirit, as many of them chose to join the rebellion against the Galactic Empire. Their society was ruled by the House of Organa. [9] in conjunction with an individual bearing the titles of Viceroy and First Chairman. [24] The female child of the royal couple was referred to as a princess. [2] For diplomatic missions, the Royal Family used streamlined cruisers. [25]

On Alderaan, its people were encouraged to learn and grow. All education was free, and people would volunteer to teach various skills or crafts just for fun. [5]

Behind the scenes Edit

" The Alderaan system actually consists of seven planets. Alderaan was the capital planet of that system. There was a Senate and my father was the president of that Senate. " ―George Lucas, assuming Leia Organa's character [src]

Alderaan first appeared in Star Wars . Episode IV A New Hope . the seminal movie of the Star Wars saga. In that movie, the planet was only seen from space during the scene depicting its destruction. [2] In the treatment. rough draft. second draft. and third draft of what would become A New Hope . the name of Alderaan was used for the capital of the "New Galactic Empire." At that time, it was described as a giant gas planet that resembled Bespin. with a city that resembled Cloud City on it. In the second draft of A New Hope . the home planet of Princess Leia was called Organa Major. Aquilae. Utapau and Ophuchi were also considered as names for worlds partially corresponding to Alderaan. [26]

Following the success of A New Hope . a full ancillary world was being built around the movie. In order to get everyone on the same page, George Lucas decided to create a few background stories and ideas. In those notes, Alderaan was described as a four or five million years old Earth-like planet, covered with high snowcapped mountains and green pastures. The same notes also described the planet as being the capital of its star system and possessing its own Senate. [27] In canon. the surface of Alderaan only made its first appearance in the 2005 movie Star Wars . Episode III Revenge of the Sith . [4] The planet's mountainous terrain was modelled after a location in the Swiss Alps. [28]

Appearances Edit

Anacin - Pain Relief, Zaramol

Anacin is used for treating pain including, headache, muscle aches, sprains, tooth extraction and toothache, menstrual cramps, arthritis and rheumatism, and pain and fever of the common cold. It may also be used for other conditions as determined by your doctor.

Use Anacin as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Take Anacin by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation. Taking it with food may not decrease the risk of stomach or bowel problems (eg, bleeding, ulcers) that may occur while taking Anacin.

Take Anacin with a full glass of water (8 oz/240 mL). Do not lie down for 30 minutes after taking Anacin.

Use Anacin exactly as directed on the package, unless instructed differently by your doctor. If you are taking Anacin without a prescription, follow any warnings and precautions on the label.

If you miss a dose of Anacin and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Anacin.

Store Anacin at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Anacin out of the reach of children and away from pets.

Anacin may cause dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Anacin with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

Avoid large amounts of food or drink that have caffeine (eg, coffee, tea, cocoa, cola, chocolate). This includes any medicines that contain caffeine.

Anacin has aspirin in it. Before you start any new medicine, check the label to see if it has aspirin in it too. If it does or if you are not sure, check with your doctor or pharmacist.

Talk to your doctor before you take Anacin or other pain relievers/fever reducers if you drink more than 3 drinks with alcohol per day. Serious stomach ulcers or bleeding can occur with the use of Anacin. Taking it in high doses or for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Anacin with food will NOT reduce the risk of these effects. Contact your doctor or emergency room at once if you develop severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling.

Do NOT take more than the recommended dose or use for longer than prescribed without checking with your doctor. Taking more than the recommended dose or taking Anacin regularly may be habit-forming.

Anacin may reduce the number of clot-forming cells (platelets) in your blood. To prevent bleeding, avoid situations in which bruising or injury may occur. Report any unusual bleeding, bruising, blood in stools, or dark, tarry stools to your doctor.

Aspirin has been linked to a serious illness called Reye syndrome. Do not give Anacin to a child or teenager who has the flu, chickenpox, or a viral infection. Contact your doctor with any questions or concerns.

Diabetes patients - Anacin may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

If Anacin has a strong vinegar-like smell upon opening, do not use. It means the medicine is breaking down. Throw the bottle away safely and out of the reach of children; contact your pharmacist and replace.

Tell your doctor or dentist that you take Anacin before you receive any medical or dental care, emergency care, or surgery.

Do not take Anacin for at least 7 days after any surgery unless directed by your health care provider.

Do not take Anacin for more than 10 days for pain or for more than 3 days for fever unless directed to do so by your health care provider.

Different brands of Anacin may have different dosing instructions for CHILDREN. Follow the dosing instructions on the package labeling. If your doctor has given you instructions, follow those. If you are unsure of the dose to give a child, check with your doctor or pharmacist.

Do NOT use Anacin if:

you are allergic to any ingredient in Anacin

you are a child or teenager with influenza (flu) or chickenpox

you have bleeding problems such as hemophilia, von Willebrand disease, or low blood platelets, or you have active severe bleeding

you have had a severe allergic reaction (eg, severe rash, hives, breathing difficulties, dizziness) to aspirin, tartrazine, or a nonsteroidal anti-inflammatory drug (NSAID) (eg, ibuprofen, naproxen, celecoxib)

you are taking anticoagulants (eg, heparin, warfarin) or methotrexate

Before using Anacin:

Some medical conditions may interact with Anacin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have alcoholism or if you consume 3 or more alcohol-containing drinks every day

if you have asthma, bleeding or clotting problems, growths in the nose (nasal polyps), kidney or liver problems, stomach or intestinal problems (eg, ulcer, inflammation), heart problems, heartburn, upset stomach, stomach pain, hives, influenza (flu) or chickenpox, or vitamin K deficiency

if you have anxiety, trouble sleeping, or heart problems

if you are a child with a stroke, a weakened blood vessel (cerebral aneurysm) or bleeding in the brain, rheumatic disease (eg, rheumatoid arthritis), or Kawasaki syndrome (a rare inflammation causing heart problems in children)

Some MEDICINES MAY INTERACT with Anacin. Tell your health care provider if you are taking any other medicines.

PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Anacin while you are pregnant. Anacin is not recommended during the last 3 months (third trimester) of pregnancy because it may cause harm to the fetus. Anacin is found in breast milk. If you are or will be breast-feeding while you use Anacin, check with your doctor. Discuss any possible risks to your baby.

All medicines may cause side effects, but many people have no, or minor, side effects. Anacin's side effects may include dizziness, heartburn, irritability, nausea, nervousness, rashes, hives, bloody stools, drowsiness, hearing loss, ringing in the ears, and trouble sleeping.

Check with your doctor if any of the listed above most COMMON side effects persist or become bothersome.

Seek medical attention right away if any of these SEVERE side effects occur: severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); black or bloody stools; confusion; diarrhea; drowsiness; hearing loss; ringing in the ears; severe or persistent dizziness; severe or persistent stomach pain or heartburn; shakiness; trouble sleeping; vomiting.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects.

Aciclovir - Anti Viral, Vacrax

Common use Aciclovir is an antiviral drug, it is a synthetic ingredient with a similar molecular structure to purine nucleoside. Aciclovir is used to treat viral infections such as cold sores, to stop the growth of Herpes simplex virus, Varicella zoster virus (caused by chickenpox and shingles), Epstein Barr Virus (caused by glandular fever), and to a lesser extent Cytomegalovirus (CMV). It is also useful in preventing genital herpes and in preventing viral infections occurring in those with a lowered immune system. This medication may also help reduce the time when pain remains after the sores heal. In addition, in people with a weakened immune system, Aciclovir can decrease the risk of the virus spreading to other parts of the body and causing serious infections.

Dosage and direction

Take this medication by mouth with or without food, usually 2 to 5 times a day as directed by your doctor. Take this medicine by mouth with a glass of water. Take your medicine at regular intervals. Do not take your medicine more often than directed. Take all of your medicine as directed even if you think your are better. If you are using the liquid form of this medication, shake the bottle well before each dose. Carefully measure the dose using a special measuring device/spoon. Do not use a household spoon because you may not get the correct dose. Dosage is based on your medical condition and response to treatment. In children, dosage is also based on weight.

You should talk with your healthcare provider prior to taking Aciclovir if you have kidney disease, including kidney failure (renal failure), any allergies, including allergies to food, dyes, or preservatives. Let your healthcare provider know if you are pregnant or thinking of becoming pregnant, breastfeeding. Make sure to tell your healthcare provider about all medicines you take, including prescription and non-prescription medicines, vitamins, and herbal supplements. The medication passes through breast milk. Therefore, if you are breastfeeding or plan to start, discuss this with your healthcare provider prior to taking the drug.

Aciclovir Injection is contraindicated for patients who develop hypersensitivity to Vacrax or valaciclovir.

Possible side effects Side effects are potentially serious and you should report to your doctor or health care professional as soon as possible. These include, but are not limited to: allergic reactions like skin rash, itching or hives, swelling of the face, lips, or tongue, chest pain, confusion, hallucinations, tremor, dark urine, increased sensitivity to the sun, redness, blistering, peeling or loosening of the skin (including inside the mouth), seizures, trouble passing urine or change in the amount of urine, unusual bleeding or bruising, or pinpoint red spots on the skin, unusually weak or tired, yellowing of the eyes or skin. Side effects that usually do not require medical attention: diarrhea, fever, headache, nausea, vomiting stomach upset. In this way report to your doctor or health care professional if they continue or are bothersome.

Drug interactions There are negative interactions that can occur when Aciclovir is combined with any of the drugs listed above. Phenytoin (Fosphenytoin) and Aciclovir: it may decrease the level of phenytoin in your blood, perhaps making it less effective. Your healthcare provider may need to measure the level of phenytoin in your blood (using a blood test) and adjust your dose as necessary. Probenecid can increase the level of Aciclovir in your blood, increasing your risk of acyclovir side effects. Your healthcare provider may need to decrease your acyclovir dosage to prevent this interaction from occurring. Acyclovir can increase the level of Tenofovir in your blood, potentially increasing your risk of side effects. Your healthcare provider may need to lower your tenofovir dosage to prevent drug interactions.

Take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine the next regularly scheduled time. Do not take extra medicine to make up the missed dose.

Seek emergency medical attention if you think you have used too much of this medicine. Overdose symptoms may include seizure (convulsions), hallucinations, and urinating less than usual or not at all.

Store at controlled room temperature of 15°C to 25°C (59°F to 77°F). Keep this medicine out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

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Prozac (Fluoxetine)

Myprox, Myprox

Myprox

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Norvasc - Blood Pressure, Amlokard

Common use This medication belongs to the group of calcium channel blockers. Norvasc selectively blocks channels of L-type (one of six types of channels in tissues) located in a vascular wall, myocard and in particular in cells of conducting and contractile systems of myocardium. By blocking Ca+ ions transfer through membrane Norvasc decreases tone of vessels, arterial pressure. The medication is used to treat hypertension, ischemic heart disease, angina.

Dosage and direction Do not take this drug if it was not administered to you. Follow all directions of your doctor. It is possible to take Norvasc with or without food. As it is metabolized in liver it should be administered cautiously in patients with liver failure.

Precautions Avoid drinking alcohol. Before taking Norvasc, inform your doctor if you have congestive heart failure or liver disease.

Contraindications Individual hypersensitivity, arterial hypotension, cardiogenic shock, pregnancy, breastfeeding. Cautiousness is important when Norvasc is administered in patients with chronic heart failure diabetes, lipid metabolism disorders, liver failure and to persons younger 18 y. o.

Possible side effect The most common side effects are edema of lower extremities and headache. Contact your doctor for medical attention if your feel them and also swelling in your hands, ankles, or feet, chest pain, slow, fast, or pounding heartbeats, easy bruising or bleeding, unusual weakness, numbness, burning, pain, or tingly feeling, jaundice.

Drug interaction Medications which contain Á2+ may decrease Norvasc effect. Non-steroid anti-inflammatory medications and estrogens may decrease effectiveness of Norvasc. Diuretics may increase Norvasc activity. Concomitant taking with medications containing lithium might aggravate their toxicity.

If you forgot to take a dose take it as soon as you remember unless it is almost time for the next intake. If so, do not take the missed dose and resume your regular schedule. Do not compensate the missed dose by taking an extra one.

Overdose If you experience tingly feeling, severe dizziness, and fainting, seek for immediate medical help.

Storage Keep at room temperature, 15-30 C (59-86 F), in a light-resistant container away from moisture.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information at the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Anacin - Pain Relief, Cotibin

Anacin is a pain reliever intended for the temporary relief of minor aches and pains. Anacin is a combination salicylate and stimulant. It works by blocking several different chemical processes within the body that cause pain, inflammation, and fever. It also reduces the tendency for blood to clot.

Availability: In Stock (17 packs)

Anacin is used for treating pain including, headache, muscle aches, sprains, tooth extraction and toothache, menstrual cramps, arthritis and rheumatism, and pain and fever of the common cold. It may also be used for other conditions as determined by your doctor.

Use Anacin as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Take Anacin by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation. Taking it with food may not decrease the risk of stomach or bowel problems (eg, bleeding, ulcers) that may occur while taking Anacin.

Take Anacin with a full glass of water (8 oz/240 mL). Do not lie down for 30 minutes after taking Anacin.

Use Anacin exactly as directed on the package, unless instructed differently by your doctor. If you are taking Anacin without a prescription, follow any warnings and precautions on the label.

If you miss a dose of Anacin and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Anacin.

Store Anacin at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Anacin out of the reach of children and away from pets.

Anacin may cause dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Anacin with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

Avoid large amounts of food or drink that have caffeine (eg, coffee, tea, cocoa, cola, chocolate). This includes any medicines that contain caffeine.

Anacin has aspirin in it. Before you start any new medicine, check the label to see if it has aspirin in it too. If it does or if you are not sure, check with your doctor or pharmacist.

Talk to your doctor before you take Anacin or other pain relievers/fever reducers if you drink more than 3 drinks with alcohol per day. Serious stomach ulcers or bleeding can occur with the use of Anacin. Taking it in high doses or for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Anacin with food will NOT reduce the risk of these effects. Contact your doctor or emergency room at once if you develop severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling.

Do NOT take more than the recommended dose or use for longer than prescribed without checking with your doctor. Taking more than the recommended dose or taking Anacin regularly may be habit-forming.

Anacin may reduce the number of clot-forming cells (platelets) in your blood. To prevent bleeding, avoid situations in which bruising or injury may occur. Report any unusual bleeding, bruising, blood in stools, or dark, tarry stools to your doctor.

Aspirin has been linked to a serious illness called Reye syndrome. Do not give Anacin to a child or teenager who has the flu, chickenpox, or a viral infection. Contact your doctor with any questions or concerns.

Diabetes patients - Anacin may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

If Anacin has a strong vinegar-like smell upon opening, do not use. It means the medicine is breaking down. Throw the bottle away safely and out of the reach of children; contact your pharmacist and replace.

Tell your doctor or dentist that you take Anacin before you receive any medical or dental care, emergency care, or surgery.

Do not take Anacin for at least 7 days after any surgery unless directed by your health care provider.

Do not take Anacin for more than 10 days for pain or for more than 3 days for fever unless directed to do so by your health care provider.

Different brands of Anacin may have different dosing instructions for CHILDREN. Follow the dosing instructions on the package labeling. If your doctor has given you instructions, follow those. If you are unsure of the dose to give a child, check with your doctor or pharmacist.

Do NOT use Anacin if:

you are allergic to any ingredient in Anacin

you are a child or teenager with influenza (flu) or chickenpox

you have bleeding problems such as hemophilia, von Willebrand disease, or low blood platelets, or you have active severe bleeding

you have had a severe allergic reaction (eg, severe rash, hives, breathing difficulties, dizziness) to aspirin, tartrazine, or a nonsteroidal anti-inflammatory drug (NSAID) (eg, ibuprofen, naproxen, celecoxib)

you are taking anticoagulants (eg, heparin, warfarin) or methotrexate

Before using Anacin:

Some medical conditions may interact with Anacin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have alcoholism or if you consume 3 or more alcohol-containing drinks every day

if you have asthma, bleeding or clotting problems, growths in the nose (nasal polyps), kidney or liver problems, stomach or intestinal problems (eg, ulcer, inflammation), heart problems, heartburn, upset stomach, stomach pain, hives, influenza (flu) or chickenpox, or vitamin K deficiency

if you have anxiety, trouble sleeping, or heart problems

if you are a child with a stroke, a weakened blood vessel (cerebral aneurysm) or bleeding in the brain, rheumatic disease (eg, rheumatoid arthritis), or Kawasaki syndrome (a rare inflammation causing heart problems in children)

Some MEDICINES MAY INTERACT with Anacin. Tell your health care provider if you are taking any other medicines.

PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Anacin while you are pregnant. Anacin is not recommended during the last 3 months (third trimester) of pregnancy because it may cause harm to the fetus. Anacin is found in breast milk. If you are or will be breast-feeding while you use Anacin, check with your doctor. Discuss any possible risks to your baby.

All medicines may cause side effects, but many people have no, or minor, side effects. Anacin's side effects may include dizziness, heartburn, irritability, nausea, nervousness, rashes, hives, bloody stools, drowsiness, hearing loss, ringing in the ears, and trouble sleeping.

Check with your doctor if any of the listed above most COMMON side effects persist or become bothersome.

Seek medical attention right away if any of these SEVERE side effects occur: severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); black or bloody stools; confusion; diarrhea; drowsiness; hearing loss; ringing in the ears; severe or persistent dizziness; severe or persistent stomach pain or heartburn; shakiness; trouble sleeping; vomiting.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects.

Solpadol, Solpadol

Solpadol

What is Solpadol?

Solpadol is a powerful painkiller. The active ingredients in this medicine are paracetamol and codeine. Paracetamol blocks the transmission of pain signals before they reach the brain and codeine suppresses pain signals. These two substances combined are a powerful painkiller which helps to relieve severe pain.

When is it used?

Solpadol is prescribed to treat severe pain from, for example, an operation, illness or injury, muscle and rheumatic pain, the flu (especially with dry coughing), headache and other pain symptoms. Solpadol is used when other painkillers are not effective or not effective enough.

How to use Solpadol

Solpadol is most effective when taken before meals. Dissolve the (effervescent) tablet in half a glass of water, stir well and drink immediately.

If you have forgotten to take a dose of Solpadol, take it as soon as you remember. Please note that the regular interval between the doses is at least four hours. Never take a double dose of Solpadol to make up for the missed one. See the package leaflet for more information on missed doses.

Dosage

Solpadol contains 500 mg paracetamol and 30 mg codeine per tablet. Solpadol is available as effervescent tablet in packs of 32, 100 and 232 tablets, and as regular tablet in pack size of 100 tablets.

The usual dose for an adult is one or two tablets every four hours, with a maximum of eight tablets a day. However, we advise that you follow your doctor’s orders when taking the medication.

Solpadol in the above strength is not suitable for children under the age of 12. The appropriate dosage for children aged 12 to 18 years should be determined by a doctor.

Side effects

Solpadol may cause side effects. Possible side effects include:

constipation (bowel obstruction). Be sure to drink plenty of liquids and eat fibre-rich foods

drowsiness, sleepiness, dizziness

nausea

See package leaflet for a complete list of possible contraindications, warnings and other side effects.

Pregnancy/alcohol/driving ability

Solpadol should only be used in consultation with a doctor if you are pregnant or breastfeeding.

Alcohol intensifies the effect of Solpadol. It is advisable to reduce or stop drinking alcohol while you are taking this medication.

Solpadol may cause you to feel dizzy, drowsy or sleepy. Please be aware of this and do not participate in traffic if you are experiencing these side effects.

Merdaten, Merdaten

Merdaten

Important Notice: The Drugs. com international database is in BETA release. This means it is still under development and may contain inaccuracies. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Consult with your healthcare professional before taking any medication.

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Remeron is used for treating depression. Remeron is a tetracyclic antidepressant. It is thought to increase the activity of certain chemicals in the brain (norepinephrine, serotonin), which help elevate mood.

Use Remeron as directed by your doctor.

Take Remeron by mouth with or without food.

Take Remeron in the evening before bedtime unless your doctor tells you otherwise.

Improvement should be noticed within 1 to 4 weeks of taking Remeron.

Continue to take Remeron even if you feel well. Do not miss any dose.

If you miss a dose of Remeron, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Remeron.

Store Remeron at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Remeron out of the reach of children and away from pets.

Active Ingredient: Mirtazapine.

Do NOT use Remeron if:

you are allergic to any ingredient in Remeron

you are taking furazolidone

you are taking or have taken a monoamine oxidase inhibitor (MAOI) (eg, phenelzine) within the last 14 days.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Remeron. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have liver or kidney disease or a low white blood cell count, or have attempted or thought about suicide.

Some medicines may interact with Remeron. Tell your health care provider if you are taking any other medicines, especially any of the following:

Hydantoins (eg, phenytoin) because they may decrease Remeron's effectiveness

Fluvoxamine, furazolidone, or MAOIs (eg, phenelzine) because side effects, such as nausea, dizziness, or seizures, may occur

Fluvoxamine because it may increase the risk of Remeron's side effects

Clonidine because it may decrease Remeron's effectiveness.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Remeron may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Remeron may cause drowsiness or dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Remeron with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Children, teenagers, and young adults who take Remeron may be at increased risk for suicidal thoughts or actions. Watch all patients who take Remeron closely. Contact the doctor at once if new, worsened, or sudden symptoms such as depressed mood; anxious, restless, or irritable behavior; panic attacks; or any unusual change in mood or behavior occur. Contact the doctor right away if any signs of suicidal thoughts or actions occur.

Lab tests, including liver function, kidney function, and complete blood cell counts, may be performed while you use Remeron. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Remeron should not be used in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Remeron while you are pregnant. It is not known if Remeron is found in breast milk. If you are or will be breast-feeding while you use Remeron, check with your doctor. Discuss any possible risks to your baby.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Abnormal dreams; abnormal thinking; constipation; dizziness; drowsiness; dry mouth; flu symptoms; increased appetite; weakness; weight gain.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); decreased ability to fight infection (fever, chills, sore throat); mental or mood changes; mouth sores; thoughts of hurting yourself; tremors; worsening of depression.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Remeron is used for treating depression. Remeron is a tetracyclic antidepressant. It is thought to increase the activity of certain chemicals in the brain (norepinephrine, serotonin), which help elevate mood.

Use Remeron as directed by your doctor.

Take Remeron by mouth with or without food.

Take Remeron in the evening before bedtime unless your doctor tells you otherwise.

Improvement should be noticed within 1 to 4 weeks of taking Remeron.

Continue to take Remeron even if you feel well. Do not miss any dose.

If you miss a dose of Remeron, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Remeron.

Store Remeron at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Remeron out of the reach of children and away from pets.

Active Ingredient: Mirtazapine.

Do NOT use Remeron if:

you are allergic to any ingredient in Remeron

you are taking furazolidone

you are taking or have taken a monoamine oxidase inhibitor (MAOI) (eg, phenelzine) within the last 14 days.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Remeron. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have liver or kidney disease or a low white blood cell count, or have attempted or thought about suicide.

Some medicines may interact with Remeron. Tell your health care provider if you are taking any other medicines, especially any of the following:

Hydantoins (eg, phenytoin) because they may decrease Remeron's effectiveness

Fluvoxamine, furazolidone, or MAOIs (eg, phenelzine) because side effects, such as nausea, dizziness, or seizures, may occur

Fluvoxamine because it may increase the risk of Remeron's side effects

Clonidine because it may decrease Remeron's effectiveness.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Remeron may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Remeron may cause drowsiness or dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Remeron with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Children, teenagers, and young adults who take Remeron may be at increased risk for suicidal thoughts or actions. Watch all patients who take Remeron closely. Contact the doctor at once if new, worsened, or sudden symptoms such as depressed mood; anxious, restless, or irritable behavior; panic attacks; or any unusual change in mood or behavior occur. Contact the doctor right away if any signs of suicidal thoughts or actions occur.

Lab tests, including liver function, kidney function, and complete blood cell counts, may be performed while you use Remeron. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Remeron should not be used in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Remeron while you are pregnant. It is not known if Remeron is found in breast milk. If you are or will be breast-feeding while you use Remeron, check with your doctor. Discuss any possible risks to your baby.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Abnormal dreams; abnormal thinking; constipation; dizziness; drowsiness; dry mouth; flu symptoms; increased appetite; weakness; weight gain.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); decreased ability to fight infection (fever, chills, sore throat); mental or mood changes; mouth sores; thoughts of hurting yourself; tremors; worsening of depression.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Remeron is used for treating depression. Remeron is a tetracyclic antidepressant. It is thought to increase the activity of certain chemicals in the brain (norepinephrine, serotonin), which help elevate mood.

Use Remeron as directed by your doctor.

Take Remeron by mouth with or without food.

Take Remeron in the evening before bedtime unless your doctor tells you otherwise.

Improvement should be noticed within 1 to 4 weeks of taking Remeron.

Continue to take Remeron even if you feel well. Do not miss any dose.

If you miss a dose of Remeron, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Remeron.

Store Remeron at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Remeron out of the reach of children and away from pets.

Active Ingredient: Mirtazapine.

Do NOT use Remeron if:

you are allergic to any ingredient in Remeron

you are taking furazolidone

you are taking or have taken a monoamine oxidase inhibitor (MAOI) (eg, phenelzine) within the last 14 days.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Remeron. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have liver or kidney disease or a low white blood cell count, or have attempted or thought about suicide.

Some medicines may interact with Remeron. Tell your health care provider if you are taking any other medicines, especially any of the following:

Hydantoins (eg, phenytoin) because they may decrease Remeron's effectiveness

Fluvoxamine, furazolidone, or MAOIs (eg, phenelzine) because side effects, such as nausea, dizziness, or seizures, may occur

Fluvoxamine because it may increase the risk of Remeron's side effects

Clonidine because it may decrease Remeron's effectiveness.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Remeron may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Remeron may cause drowsiness or dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Remeron with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Children, teenagers, and young adults who take Remeron may be at increased risk for suicidal thoughts or actions. Watch all patients who take Remeron closely. Contact the doctor at once if new, worsened, or sudden symptoms such as depressed mood; anxious, restless, or irritable behavior; panic attacks; or any unusual change in mood or behavior occur. Contact the doctor right away if any signs of suicidal thoughts or actions occur.

Lab tests, including liver function, kidney function, and complete blood cell counts, may be performed while you use Remeron. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Remeron should not be used in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Remeron while you are pregnant. It is not known if Remeron is found in breast milk. If you are or will be breast-feeding while you use Remeron, check with your doctor. Discuss any possible risks to your baby.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Abnormal dreams; abnormal thinking; constipation; dizziness; drowsiness; dry mouth; flu symptoms; increased appetite; weakness; weight gain.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); decreased ability to fight infection (fever, chills, sore throat); mental or mood changes; mouth sores; thoughts of hurting yourself; tremors; worsening of depression.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Emergency Surgery For Sifen - All God - S Children International, Sifen

Emergency Surgery for Sifen

9 Days Remaining

2-year-old Sifen needs emergency surgery! Sifen resides at our Hannah’s Hope partner home in Gambella Ethiopia. Sadly this little girl has no mobility in her legs due to a mistake made in surgery when she was just an infant. Despite her special needs, Sifen’s joy is infectious. We believe God has big things for her future!

This month AGCI learned that Sifen was diagnosed with hydrocephalus and is in need of urgent treatment. Her condition is deteriorating and the doctors in Addis Ababa are recommending a shunt surgery to be performed immediately in order to drain fluid around her brain. Sifen is currently very weak and dehydrated and remains on IV fluids at a local hospital in Addis Ababa. Our team in Ethiopia are fighting for her care, but we need a community of supporters to join us in providing the funds necessary for Sifen to have life-saving surgery.

Will you join us in providing Sifen with the emergency surgery she needs to reach her full potential?

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Headway Made In Solar Garden Disputes Between Xcel, Developers, Xcel

Headway made in solar garden disputes between Xcel, developers

Some headway was made Tuesday in settling long-running disputes between solar developers and Xcel Energy, a quarrel that has helped delay the rollout of one of the nation’s most ambitious solar garden projects.

Between regulators’ decisions made Tuesday and a recent Xcel policy change, a critical technical issue that has threatened the viability of some solar gardens appears to be partly resolved. “There’s been incremental progress,” said David Amster-Olszewski, CEO of SunShare Energy, one of the largest solar garden developers in Minnesota.

Community solar gardens are developed and operated by independent companies like Denver-based SunShare, which must connect into Xcel Energy’s grid. A solar garden’s customers are thus able to get solar power without the expense of building and operating their own rooftop systems.

Xcel was inundated with about 1,000 solar garden applications starting in late 2014 — causing delays. Numerous disputes between developers and Xcel have caused more delays, and so far only four small solar gardens are actually up and running. Those four together generate less than 1 megawatt — or a million watts — of power.

Projects totaling several hundred megawatts — at no more than 5 megawatts per site — are waiting to be built.

Xcel said in early July that it was “more than realistic” that 200 megawatts of solar garden power would be online by 2016’s end. But with September more than half over, “there’s no way that’s going to happen,” Amster-Olszewski said Tuesday.

In August 2015, the Minnesota Public Utilities Commission, which has limited staff, created a process to hire independent engineers to review complaints from solar garden developers. The first independent engineer’s report came out in April, blasting Xcel’s cost estimates and engineering standards for SunShare’s proposed solar garden near Becker, Minn.

Since then, about a dozen more independent engineers’ reports have been filed for other projects. Tuesday marked the first time the PUC directly took up some of the reports.

Commissioners waded into the highly technical subject of “flicker,” voltage fluctuation that could cause lights in homes near a power generation source — like a solar garden — to suddenly flicker. At least 28 solar garden projects are affected by potential flicker problems.

SunShare and other solar developers have argued that Xcel’s original flicker standard is too conservative and based on archaic engineering standards. Independent engineers have agreed.

However, Xcel recently loosened its flicker standard for some, but not all, solar gardens, from a 1.5 voltage variation to 2 percent, a level many developers can live with. A PUC decision Tuesday will allow for the 2 percent flicker standard at Becker and another SunShare site, Amster-Olszewski said. Without that change, the Becker project particularly wasn’t economical to build.

To better measure flicker, solar developers have urged the PUC to adopt a recent standard from the Institute of Electrical and Electronics Engineers (IEEE). The PUC Tuesday voted unanimously that Xcel and solar developers together assess using that IEEE standard.

“That is a really important step forward,” said Lynn Hinkle, policy director for the Minnesota Solar Energy Industry Association, a trade group.

The PUC weighed in on another important issue brought up in the independent engineers’ reports: cost estimates.

The engineers criticized Xcel for wide variations on cost estimates quoted to solar developers for grid interconnection. Xcel argued that the company’s cost estimation process was beyond the regulatory purview of the independent engineers.

The PUC didn’t set limits on Xcel’s cost variations, as the engineers had concluded should be done. Instead, the commission voted to better monitor the variations in Xcel’s cost estimates.

Cyprotel Cypria Maris (Paphos, Cyprus) - Hotel Reviews, Cyprotol

We had a sea view room on the 3rd floor, air con a bit noisy and walk in shower flooded each time we used it, but after refurb I am sure things will be corrected. The room otherwise was fine, a fridge at no cost was included, this was an added bonus. We found all the staff including cleaners very friendly and polite, always a smile. There was always a good choice at meal times, loved all the soups which I had most lunch times with some delicious bread. We used the sunbeds on the grass area facing the beach, there were ample sun beds for everyone to use. The entertainment team were hard working during the day and night, our sunbeds were next to the boules. so it was interesting to watch when the game was being played, the entertainment member, may have been called Victor was excellent teaching people the rules of the game and remembering all their name correctly. We had a lovely week at the hotel, maybe we will return one day.

“ Another wonderful holiday ”

Andrew O (13 reviews)

My wife and I have recently enjoyed our third holiday in successive years at this lovely hotel. We met up with and saw a number of other people who have been there at the same time as us in previous years and we know of some who have been returning for longer - recommendation in itself.

The hotel and grounds are beautiful and all the staff, without exception, are excellent. The animation team was, as usual, different from previous years and the two leaders, Andre and Emmi, were particularly good.

The hotel is to be closed until next summer for a full refurbishment programme to bring it up to five star standard. There is a danger that, by doing so, some of the charm of the place will disappear and it may become too expensive for many people. Whilst areas could do with upgrading, we would urge the new ownership not to spoil what is a beautiful hotel with a very loyal customer base. We would also hope that all the staff, many of whom have been there for a long time, are retained.

Questions & Answers

“ Please can you tell us if we need to take beach towels. ”

Hi, Thank you for your choice regarding your.

Traveller Room Tips

“Being refurbished for next year. ”

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Tarnasol, Tarnasol

Losartano kalio druska, 12,5mg, plevele dengtos tabletes

Vartojimas: vartoti per burna Registratorius: LABORATORIOS LICONSA S. A, Ispanija Receptinis: Receptinis Sudedamosios medziagos: Losartano kalio druska

1. Kas yra Tarnasol ir nuo ko jIs vartojamAs

Tarnasol priklauso vaistu, mazinanciu kraujospudi, grupei.

Gydytojas Jums skyre TARNASOL tabletes, nes Jums yra vienas ar keli is zemiau isvardintu sutrikimu: Sirdies nepakankamumas, t. y. sirdies funkcijos susilpnejimas (siekiant sustiprinti Jusu sirdies veikla). Didelio kraujospudzio liga. Sirdies skilvelio, kuris pagrindinai varineja krauja kunu, hipertrofija (siekiant sumazinti insulto rizika). 2-jo tipo diabetas ir slapime yra baltymo (siekiant apsaugoti Jusu inkstus).

2. Kas zinotina pries vartojant Tarnasol

Tarnasol plevele dengtu tableciu vartoti negalima: jeigu itariama, kad gali buti alergija (padidejes jautrumas) veikliajai ar bet kuriai pagalbinei preparato medziagai; jei esate nescia arba manote, kad galite buti nescia. Jei pastosite vartodama Tarnasol tableciu, nedelsdama kreipkites i gydytoja; jeigu zindote kudiki.

Losartano nerekomenduojama duoti vaikams ir paaugliams. Jei del TARNASOL vartojimo kyla abejioniu, kreipkites i gydanti gydytoja.

Specialiu atsargumo priemoniu reika Informuokite savo gydytoja, jei turite ar turejote kokiu nors problemu su sveikata.

Ypac svarbu pasakyti gydytojui:

jei sergate inkstu ar kepenu ligoma; jei sergate alergija. ypac jei buvote patyre angioneurozine edema (alergine reakcija, pasireiskiancia veido, lupu, kaklo ir/ ar liezuvio sutinimu); jei netekote daug vandens (pvz. jei neseniai labai gausiai vemete ir/ar viduriavote); jei turite sutrikima, vadinama aortos stenoze arba obstrukcija (sirdies aortos voztuvo susiaurejimas arba obstrukcija, neleidziantys jam reikiamai atsidaryti, todel blokuojamas kraujo istekejimas is kairiojo skilvelio i aorta); jei padidejes kalio kiekis kraujyje (hiperkalemija) arba jei laikotes dietos, kurioje mazai kalio; jei vartojate diuretikus arba AKF inhibitorius nuo sirdies nepakankamumo. jeigu mazas kraujospudis.

Jums reikes reguliariai atlikineti kraujo tyrimus, kad butu galima nustatyti kreatinino koncentracija kraujyje.

Kitu vaistu vartojimas Jeigu vartojate arba neseniai vartojote kitus vaistus, iskaitant isigytus be recepto, pasakykite gydytojui arba vaistininkui.

Ypac svarbu pasakyti gydytojui, jei vartojate kuriuos nors is zemiau isvardintu vaistu: - Kalio papildus, slapima varancius, sulaikancius kali preparatus arba druskos pakaitalus, turincius kalio. - Rifampicina (vaista nuo tuberkuliozes (TB). - Flukanozola (preparata nuo grybeliniu infekciju, pvz. nuo pienliges). - Indomentacina (nesteroidini preparata nuo griauciu ir raumenu sutrikimu, pvz. atrito) . - Priesuzdegiminius vaistus. - AKF inhibitorius nuo sirdies nepakankamumo. - Heparina - Liti

Priesuzdegiminiai vaistai gali susilpninti Tarnasol kraujospudi mazinanti poveiki.

TARNASOL vartojimas su maistu ir gerimais Paprastai Tarnasol nesaveikauja su maistu. Tabletes galima vartoti nepriklausomai nuo valgymo laiko.

Nestumas ir zindymo laikotarpis TARNASOL vartoti negalima: jei esate nescia arba manote, kad galite buti nescia; jei planuojate tapti nescia; jei zindote.

Jei pastosite vartodama Tarnasol tabletes, nedelsdama kreipkites i gydytoja. Pries vartojant bet koki vaista, butina pasitarti su gydytoju ar vaistininku.

Vairavimas ir mechanizmu valdymas Tarnasol retkarciais gali sukelti galvos svaigima. Reikia i tai atsizvelgti, atliekant darba, kai reikia labai sutelkti demesi (pvz. vairuojant transporto priemone arba atliekant kruopstumo reikalaujancias uzduotis).

Svarbi informacija apie kai kurias TARNASOL pagalbines medziagas Sio vaistinio preparato sudetyje yra laktozes monohidrato. Jei gydytojas Jums yra sakes, kad netoleruojate kokiu nors angliavandeniu, kreipkites i ji pries pradedami vartoti si vaista.

3. Kaip vartoti Tarnasol

Dozavimas TARNASOL visada vartokite tiksliai taip, kaip nurode gydytojas. Jeigu abejojate, kreipkites i gydytoja arba vaistininka. Priklausomai nuo Jusu bukles ir nuo to, ar vartojate kitus vaistus, gydytojas nuspres, kokia doze Jums reikalinga. Svarbu vartoti TARNASOL tiek laiko, kiek skiria gydytojas, kad galetumete tinkamai kontroliuoti savo kraujospudi. Neuzmirskite isgerti vaisto.

Vaikams ir paaugliams vartoti preparata nerekomenduojama, nes sio amziaus pacientu gydymo patirties nera.

Sirdies nepakankamumas: Rekomenduojama pradine TARNASOL doze yra 12,5 mg viena karta per para. Gydytojas sia doze Jums pamazu didins, kol bus pasiekta tinkamiausia. Iprasta palaikomoji doze yra 50 mg viena karta per para.

Didelio kraujospuzio liga ir kairiojo skilvelio hipertrofija (sustorejimas): Daugumai pacientu, kuriu kraujospudis padidejes, iprasta TARNASOL doze yra 50 mg viena karta per para, kuri kontroliuoja kraujospudi 24 valandas. Jei paaiskeja, kad si doze nepakankama, ja galima padidinti iki 100 mg viena karta per para. Maksimali doze yra 100 mg per para.

Iprasta TARNASOL doze pacientams, kuriems yra sirdies raumens hipertrofija, yra 50 mg viena karta per para. Si doze gali buti padidinta iki 100 mg viena karta per para.

II tipo diabetas: Iprasta TARNASOL doze daugumai pacientu yra 50 mg viena karta per para. Si doze gali buti padidinta iki 100 mg viena karta per para, atsizvelgiant i poveiki kraujospudziui. TARNASOL galima vartoti kartu su kitais antihipertenziniais vaistais. Stenkites isgerti tablete kasdien tuo paciu laiku. Esant butinybei, gydytojas padidins tableciu doze.

Pavartojus per didele TARNASOL doze Isgere per didele vaisto doze, nedelsdami kreipkites i gydytoja. Perdozavus gali sumazeti kraujospudis ir padazneti pulsas. Nukritus kraujospudziui, atsigulkite ir pakelkite auksciau kojas.

Pamirsus pavartoti Tarnasol Pamirsus isgerti tablete iprastiniu laiku, gerkite ja atejus kitos dozes vartojimo laikui. Negalima vartoti dvigubos dozes, norint kompensuoti praleista doze.

Jeigu kiltu daugiau klausimu del sio vaisto vartojimo, kreipkites i gydytoja arba vaistininka.

4.GALIMAS SALUTINIS POVEIKIS

TARNASOL, kaip ir kiti vaistai, gali sukelti salutini poveiki, nors jis pasireiskia ne visiems zmonems. Gali pasireiksti toliau isvardytas salutinis poveikis.

Daznas (nuo 1/100 iki 1/10 pacientu ) Mazas kraujospudis, galvos svaigimas.

Nedaznas (nuo 1/1000 iki 1/100 pacientu) Staigiai atsistojus, gali sumazeti kraujospudis, del to galite netekti samones.

Retas (nuo 1/10 000 iki 1/1000 pacientu ) Kepenu veiklos sutrikimas (jo simptomai gali buti akiu ir odos pageltimas ir i gripa panasus simptomai), dilgeline, niezulys, isberimas ir greitas kraujospudzio mazejimas (kurio simptomu gali buti galvos svaigimas, ypac atsistojant), migrena, viduriavimas, raumenu ir sanariu skausmas. angitas (kraujagysliu sieneliu uzdegimas. tarp ju ir smulkiuju venu uzdegimas. sukeliantis ryskiai violetines demes odoje, iskaitant tokius simptomus, kaip nuovargis, silpnumas ir pilvo skausmas ), angioneurozine edema (alergine reakcija, pasireiskianti veido, lupu, gerkles ir/arba liezuvio sutinimu), mazakraujyste (jos simptomais gali buti nuovargis arba dusulys, atsirandantis del mazesnio uz normalu raudonuju kraujo kuneliu ar hemoglobino kieki kraujyje), padidejusi kalio koncentracija kraujyje, kosulys ir trombocitopenija (trombocitu kiekio sumazejimas kraujyje, del kurio gali atsirasti neiprastu (nepaaiskinamu) kraujosruvu arba kraujavimas.

Jeigu pasireiske sunkus salutinis poveikis arba pastebejote siame lapelyje nenurodyta salutini poveiki, pasakykite gydytojui arba vaistininkui.

Kai kuriems pacientams, ypac tiems, kuriems yra II tipo diabetas ir baltymo slapime, gali padideti kalio koncentracija kraujyje, pasireiksti nuovargis, svaigimas, tapti mazas kraujospudis. Jei sergate inkstu liga ar 2-ojo tipo diabetu, susijusiu su baltymo atsiradimu slapime, arba vartojate kalio papildus, sulaikancius kali preparatus arba kalio turincius druskos pakaitalus, kreipkites i gydytoja.

Jei Jums pasireiske alergine reakcija (tinsta veidas, lupos, gerkle ir/arba liezuvis), del kurios sunku kvepuoti ar ryti, nutraukite TARNASOL vartojima ir nedelsiant kreipkites i gydytoja.

5. Kaip laikyti Tarnasol

Laikyti vaikams nepasiekiamoje ir nepastebimoje vietoje. Laikyti gamintojo pakuoteje. Ant dezutes nurodytam tinkamumo laikui pasibaigus, Tarnasol vartoti negalima. Vaistas tinkamas vartoti iki paskutines to menesio dienos.

Vaistu likuciu negalima mesti i kanalizacija arba kartu su buitinemis atliekomis. Kaip naikinti nereikalingus vaistus, klauskite vaistininko. Visa tai pades apsaugoti aplinka.

6. KITA INFORMACIJA

Tarnasol sudetis Veiklioji medziaga yra losartano kalio druska.

Vienoje Tarnasol 12,5 mg plevele dengtoje tableteje yra 12,5 mg losartano kalio druskos(1,06 mg kalio).

Vienoje Tarnasol 50 mg plevele dengtoje tableteje yra 50 mg losartano kalio druskos (4,24 mg kalio).

Vienoje Tarnasol 100 mg plevele dengtoje tableteje yra 100 mg losartano kalio druskos (8,48 mg kalio).

Pagalbines medziagos yra: Tabletes branduolys: laktozes monohidratas, pregelifikuotas kukuruzu krakmolas. mikrokristaline celiulioze ir magnio stereatas. Tabletes plevele: hidroksipropilceliulioze, hipromelioze, titano dioksidas ir briliantinis melynasis FCF (E 133) (tik 12,5 mg tabletese).

TARNASOL isvaizda ir kiekis pakuoteje Tarnasol 12,5 mg plevele dengtos tabletes yra apvalios, melynos. Tarnasol 50 mg ir 100 mg plevele dengtos tabletes yra apvalios, baltos.

Tarnasol 12,5 mg ir Tarnasol 50 mg: Vienoje pakuoteje yra 7, 10, 14, 15, 21, 28, 50, 56, 98, 100, 210, 280 plevele dengtu tableciu.

Tarnasol 100 mg: Vienoje pakuoteje yra 7, 10, 14, 15, 21, 28, 30, 50, 56, 98, 100, 210, 280 plevele dengtu tableciu.

Gali buti tiekiamos ne visu dydziu pakuotes.

Cozaar is used for treating high blood pressure alone or with other medicines. It is used in certain patients to decrease the risk of stroke. It is used in certain patients to treat kidney problems caused by diabetes (diabetic nephropathy). Cozaar is an angiotensin II receptor blocker (ARB). It works by relaxing blood vessels. This helps to lower blood pressure.

Use Cozaar as directed by your doctor.

Take Cozaar by mouth with or without food.

Take Cozaar on a regular schedule to get the most benefit from it. Taking Cozaar at the same time each day will help you remember to take it.

Continue to take Cozaar even if you feel well. Do not miss any dose.

If you miss a dose of Cozaar, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Cozaar.

Store Cozaar at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Cozaar out of the reach of children and away from pets.

Active Ingredient: Losartan potassium.

Do NOT use Cozaar if:

you are allergic to any ingredient in Cozaar

you are in your second or third trimester of pregnancy

the patient is a child with severe kidney problems.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Cozaar. Tell your health care provider if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you are able to become pregnant

if you have a history of angioedema (swelling of the hands, face, lips, eyes, throat, or tongue; difficulty swallowing or breathing; or hoarseness), including angioedema caused by treatment with an angiotensin-converting enzyme (ACE) inhibitor (eg, lisinopril)

if you have a history of heart problems (eg, heart failure), blood vessel problems, blood flow problems, liver or kidney problems, or diabetes

if you have a history of stroke or recent heart attack

if you are dehydrated or have low blood volume

if you have electrolyte problems (eg, high blood potassium levels, low blood sodium levels) or are on a low-salt (sodium) diet

if you are on dialysis or are scheduled to have major surgery.

Some medicines may interact with Cozaar. Tell your health care provider if you are taking any other medicines, especially any of the following:

Diuretics (eg, furosemide, hydrochlorothiazide) because the risk of low blood pressure may be increased

Potassium-sparing diuretics (eg, spironolactone, triamterene) or potassium supplements because the risk of high blood potassium levels may be increased

Nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, ibuprofen, indomethacin, celecoxib) or rifampin because they may decrease Cozaar's effectiveness

Lithium because the risk of its side effects may be increased by Cozaar.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Cozaar may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Cozaar may cause dizziness, lightheadedness, or fainting. These effects may be worse if you take it with alcohol or certain medicines. Use Cozaar with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Cozaar may cause dizziness, lightheadedness, or fainting; alcohol, hot weather, exercise, or fever may increase these effects. To prevent them, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of any of these effects.

Cozaar may cause a serious side effect called angioedema. Contact your doctor at once if you develop swelling of the hands, face, lips, eyes throat, or tongue; difficulty swallowing or breathing; or hoarseness.

Cozaar may not work as well to reduce the risk of stroke in black patients. Discuss any questions or concerns with your doctor.

Dehydration, excessive sweating, vomiting, or diarrhea may increase the risk of low blood pressure. Contact your health care provider at once if any of these occur.

Check with your doctor before you use a salt substitute or a product that has potassium in it.

Tell your doctor or dentist that you take Cozaar before you receive any medical or dental care, emergency care, or surgery.

Patients who take medicine for high blood pressure often feel tired or run down for a few weeks after starting treatment. Be sure to take your medicine even if you may not feel "normal." Tell your doctor if you develop any new symptoms.

If you have high blood pressure, do not use nonprescription products that contain stimulants. These products may include diet pills or cold medicines. Contact your doctor if you have any questions or concerns.

Diabetes patients - This may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

Lab tests, including blood pressure, blood electrolyte levels, and heart, kidney, or liver function, may be performed while you use Cozaar. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Cozaar should not be used in children younger 6 years; safety and effectiveness in these children have not been confirmed.

Pregnancy and breast-feeding: Cozaar may cause birth defects or fetal death if you take it while you are pregnant. If you think you may be pregnant, contact your doctor right away. It is not known if Cozaar is found in breast milk. Do not breastfeed while taking Cozaar.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Diarrhea; dizziness; tiredness.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; hoarseness); change in the amount of urine produced; chest pain; dark urine; difficulty swallowing; fast, slow, or irregular heartbeat; muscle pain or cramps; severe or persistent stomach pain (with or without nausea or vomiting); symptoms of low blood pressure (eg, fainting, severe dizziness, lightheadedness); unusual bruising or bleeding; vision changes; yellowing of the eyes or skin.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Diabetes - Tarnasol (Brand name: cozaar)

Cozaar is used for treating high blood pressure alone or with other medicines. It is used in certain patients to decrease the risk of stroke. It is used in certain patients to treat kidney problems caused by diabetes (diabetic nephropathy). Cozaar is an angiotensin II receptor blocker (ARB). It works by relaxing blood vessels. This helps to lower blood pressure.

Use Cozaar as directed by your doctor.

Take Cozaar by mouth with or without food.

Take Cozaar on a regular schedule to get the most benefit from it. Taking Cozaar at the same time each day will help you remember to take it.

Continue to take Cozaar even if you feel well. Do not miss any dose.

If you miss a dose of Cozaar, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Cozaar.

Store Cozaar at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Cozaar out of the reach of children and away from pets.

Active Ingredient: Losartan potassium.

Do NOT use Cozaar if:

you are allergic to any ingredient in Cozaar

you are in your second or third trimester of pregnancy

the patient is a child with severe kidney problems.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Cozaar. Tell your health care provider if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you are able to become pregnant

if you have a history of angioedema (swelling of the hands, face, lips, eyes, throat, or tongue; difficulty swallowing or breathing; or hoarseness), including angioedema caused by treatment with an angiotensin-converting enzyme (ACE) inhibitor (eg, lisinopril)

if you have a history of heart problems (eg, heart failure), blood vessel problems, blood flow problems, liver or kidney problems, or diabetes

if you have a history of stroke or recent heart attack

if you are dehydrated or have low blood volume

if you have electrolyte problems (eg, high blood potassium levels, low blood sodium levels) or are on a low-salt (sodium) diet

if you are on dialysis or are scheduled to have major surgery.

Some medicines may interact with Cozaar. Tell your health care provider if you are taking any other medicines, especially any of the following:

Diuretics (eg, furosemide, hydrochlorothiazide) because the risk of low blood pressure may be increased

Potassium-sparing diuretics (eg, spironolactone, triamterene) or potassium supplements because the risk of high blood potassium levels may be increased

Nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, ibuprofen, indomethacin, celecoxib) or rifampin because they may decrease Cozaar's effectiveness

Lithium because the risk of its side effects may be increased by Cozaar.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Cozaar may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Cozaar may cause dizziness, lightheadedness, or fainting. These effects may be worse if you take it with alcohol or certain medicines. Use Cozaar with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Cozaar may cause dizziness, lightheadedness, or fainting; alcohol, hot weather, exercise, or fever may increase these effects. To prevent them, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of any of these effects.

Cozaar may cause a serious side effect called angioedema. Contact your doctor at once if you develop swelling of the hands, face, lips, eyes throat, or tongue; difficulty swallowing or breathing; or hoarseness.

Cozaar may not work as well to reduce the risk of stroke in black patients. Discuss any questions or concerns with your doctor.

Dehydration, excessive sweating, vomiting, or diarrhea may increase the risk of low blood pressure. Contact your health care provider at once if any of these occur.

Check with your doctor before you use a salt substitute or a product that has potassium in it.

Tell your doctor or dentist that you take Cozaar before you receive any medical or dental care, emergency care, or surgery.

Patients who take medicine for high blood pressure often feel tired or run down for a few weeks after starting treatment. Be sure to take your medicine even if you may not feel "normal." Tell your doctor if you develop any new symptoms.

If you have high blood pressure, do not use nonprescription products that contain stimulants. These products may include diet pills or cold medicines. Contact your doctor if you have any questions or concerns.

Diabetes patients - This may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

Lab tests, including blood pressure, blood electrolyte levels, and heart, kidney, or liver function, may be performed while you use Cozaar. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Cozaar should not be used in children younger 6 years; safety and effectiveness in these children have not been confirmed.

Pregnancy and breast-feeding: Cozaar may cause birth defects or fetal death if you take it while you are pregnant. If you think you may be pregnant, contact your doctor right away. It is not known if Cozaar is found in breast milk. Do not breastfeed while taking Cozaar.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Diarrhea; dizziness; tiredness.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; hoarseness); change in the amount of urine produced; chest pain; dark urine; difficulty swallowing; fast, slow, or irregular heartbeat; muscle pain or cramps; severe or persistent stomach pain (with or without nausea or vomiting); symptoms of low blood pressure (eg, fainting, severe dizziness, lightheadedness); unusual bruising or bleeding; vision changes; yellowing of the eyes or skin.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Fexofenadine 24-Hour Tablet - Oral (Allegra) Side Effects, Medical Uses, And Drug Interactions, Alle

fexofenadine 24-hour tablet - oral, Allegra

The display and use of drug information on this site is subject to express terms of use. By continuing to view the drug information, you agree to abide by such terms of use.

GENERIC NAME: FEXOFENADINE 24-HOUR TABLET - ORAL (FEX-oh-FEN-a-deen)

BRAND NAME(S): Allegra

USES: Fexofenadine is an antihistamine used to relieve allergy symptoms such as watery eyes, runny nose. itching eyes/nose, sneezing. hives. and itching. It works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction .

HOW TO USE: If you are taking the over-the-counter product to self-treat, read all directions on the product package before taking this medication. If you have any questions, consult your pharmacist. If your doctor has prescribed this medication, take it as directed with or without food, usually once daily. Take this medication with water. Do not take with fruit juices (such as apple, grapefruit, or orange) since they may decrease the absorption of this drug. The dosage is based on your age, medical condition, and response to treatment. Do not increase your dose or take this medication more often than directed. Do not take antacids containing aluminum and magnesium within 2 hours of taking this medication. These antacids can decrease the absorption of fexofenadine. Tell your doctor if your condition does not improve or if it worsens.

Quick Guide Bad Bugs: Identify Bug Bites From Mosquitos, Spiders and More

Report Problems to the Food and Drug Administration

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

Selected from data included with permission and copyrighted by First Databank, Inc. This copyrighted material has been downloaded from a licensed data provider and is not for distribution, except as may be authorized by the applicable terms of use.

CONDITIONS OF USE: The information in this database is intended to supplement, not substitute for, the expertise and judgment of healthcare professionals. The information is not intended to cover all possible uses, directions, precautions, drug interactions or adverse effects, nor should it be construed to indicate that use of particular drug is safe, appropriate or effective for you or anyone else. A healthcare professional should be consulted before taking any drug, changing any diet or commencing or discontinuing any course of treatment.

Need help identifying pills and medications?

About Supernode, Supernide

About Supernode

Supernode is a student-run space, and all our equipment will always be free to use to anybody in the UC Berkeley community. The door is open whenever a member is inside (which is a lot of the time!).

Access and Membership

Where is Supernode? We’re located in 246 Cory Hall, the Chenming Hu Innovation Lab. Cory Hall is open from 7:30am–6:30pm on weekdays.

When is the lab open? The lab is open whenever a member is in the space. Members are expected to welcome members and non-members alike into the space whenever they are using it.

How do I become a member and get card key access? Membership gives you 24/7 cardkey access to Supernode. All you have to do is sign up for a training session and then be willing to take responsibility for the space while you are there. The training sessions themselves are an hour max and cover rules, safety, and basic equipment usage.

Student groups If your student group is interested in regularly using this space or requires storage please contact us.

Electronics

246 Cory contains two electronics workbenches with the same equipment as the downstairs introductory EE instructional laboratory.

We also have soldering equipment (including hot-air and a reflow oven), a stereo microscope, and a collection of breadboards, wire, and a wide assortment of components, all of which were either donated or purchased with grant money.

Fabrication

Our fabrication station currently consists of two FDM 3D printers, an Othermill, and a vinyl cutter.

These tools can be difficult to use! While anybody is free to use them, we highly suggest attending a training session, reading the documentation, and then getting in touch with us before using these.

Storage

If you are interested in getting a locker or a box, please email the list. Space is limited. Assignments are on a semesterly basis. The full policy is here .

Cory Student Workshop

The Cory Student Workshop is a 24/7-access basic machine shop associated with Supernode for working on mechanical projects. The Workshop has many power and hand tools available for your use. Separate training from the EECS department is required, see this bCourses page .

Once you have done that sign up on this form (CSW Training Signup Sheet).

Amateur Radio

Supernode is closely associated with both the W6BB and NU6XB UC Berkeley amateur radio clubs. Join the mailing list (supernode-ham@lists.berkeley.edu. there is also a channel on our Slack) and fill out this form to get access to 532 Cory, the fifth-floor NU6XB station (requires amateur radio license).

Antideprin, Antideprin

Antideprin

Antideprin - General Information

The prototypical tricyclic antidepressant. It has been used in major depression, dysthymia, bipolar depression, attention-deficit disorders, agoraphobia, and panic disorders. It has less sedative effect than some other members of this therapeutic group.

Pharmacology of Antideprin

Antideprin is a tricyclic antidepressant with general pharmacological properties similar to those of structurally related tricyclic antidepressant drugs such as amitriptyline and doxepin. A tertiary amine, imipramine inhibits the reuptake of serotonin more so than most secondary amine tricyclics, meaning that it blocks the reuptake of neurotransmitters serotonin and noradrenaline almost equally. It is also effective in migraine prophylaxis, but not in abortion of acute migraine attack .

Antideprin for patients

Patients should be warned that imipramine hydrochloride may enhance the CNS depressant effects of alcohol

Patients taking imipramine hydrochloride should avoid excessive exposure to sunlight, since there have been reports of photosensitization.

Antideprin Interactions

In occasional susceptible patients or in those receiving anticholinergic drugs (including antiparkinsonism agents) in addition, the atropine-like effects may become more pronounced (e. g. paralytic ileus).

Close supervision and careful adjustment of dosage is required when this drug is administered concomitantly with anticholinergic drugs.

Avoid the use of preparations such as decongestants and local anesthetics which contain any sympathomimetic amine (e. g. epinephrine, norepinephrine), since it has been reported that tricyclic antidepressants can potentiate the effects of catecholamines.

Caution should be exercised when imipramine hydrochloride is used with agents that lower blood pressure. Imipramine hydrochloride may potentiate the effects of CNS depressant drugs.

The plasma concentration of imipramine may increase when the drug is given concomitantly with hepatic enzyme inhibitors (e. g. cimetidine, fluoxetine) and decrease by concomitant administration of hepatic enzyme inducers (e. g. barbiturates, phenytoin), and adjustment of the dosage of imipramine may therefore be necessary.

Drugs Metabolized by P 450 2D 6

The biochemical activity of the drug metabolizing isozyme cytochrome P 450 2D 6 (debrisoquin hydroxylase) is reduced in a subset of the caucasian population (about 7 to 10% of caucasians are so called "poor metabolizers"); reliable estimates of the prevalence of reduced P 450 2D 6 isozyme activity among Asian, African and other populations are not yet available. Poor metabolizers have higher than expected plasma concentrations of tricyclic antidepressants (TCAs) when given usual doses. Depending on the fraction of drug metabolized by P 450 2D 6 . the increase in plasma concentration may be small, or quite large (8-fold increase in plasma AUC of the TCA).

In addition, certain drugs inhibit the activity of this isozyme and make normal metabolizers resemble p. o. metabolizers. An individual who is stable on a given dose of TCA may become abruptly toxic when given one of these inhibiting drugs as concomitant therapy. The drugs that inhibit cytochrome P 450 2D 6 include some that are not metabolized by the enzyme (quinidine; cimetidine) and many that are substrates for P 450 2D 6 (many other antidepressants, phenothiazines, and the Type 1C antiarrhythmics propafenone and flecainide). While all the selective serotonin reuptake inhibitors (SSRIs), e. g. fluoxetine, sertraline, and paroxetine, inhibit P 450 2D 6 . they may vary in the extent of inhibition. The extent to which SSRI-TCA interactions may pose clinical problems will depend on the degree of inhibition, and the pharmacokinetics of the SSRI involved. Nevertheless, caution is indicated in the co-administration of TCA 5 with any of the SSRIs and also in switching from one class to the other. Of particular importance, sufficient time must elapse before initiating TCA treatment in a patient being withdrawn from fluoxetine, given the long half-life of the parent and active metabolite (at least 5 weeks may be necessary).

Concomitant use of tricyclic antidepressants with drugs that can inhibit cytochrome P 450 2D 6 may require lower doses than usually prescribed for either the tricyclic antidepressant or the other drug. Furthermore, whenever one of these other drugs is withdrawn from cotherapy, an increased dose of tricyclic antidepressant may be required. It is desirable to monitor TCA plasma levels whenever a TCA is going to be co-administered with another drug known to be an inhibitor of P 450 2D 6 .

Antideprin Contraindications

The concomitant use of monoamine oxidase inhibiting compounds is contraindicated. Hyperpyretic crises or severe convulsive seizures may occur in patients receiving such combinations. The potentiation of adverse effects can be serious or even fatal. When it is desired to substitute imipramine hydrochloride in patients receiving a monoamine oxidase inhibitor, as long an interval should elapse as the clinical situation will allow, with a minimum of 14 days. Initial dosage should be low and increases should be gradual and cautiously prescribed.

The drug is contraindicated during the acute recovery period after a myocardial infarction. Patients with a known hypersensitivity to this compound should not be given the drug. The possibility of cross-sensitivity to other dibenzazepine compounds should be kept in mind.

Additional information about Antideprin

Antideprin Indication: For the relief of symptoms of depression and as temporary adjunctive therapy in reducing enuresis in children aged 6 years and older. Mechanism Of Action: Antideprin works by inhibiting the re-uptake of the neurotransmitters norepinephrine and serotonin by nerve cells. It binds the Sodium-dependent serotonin transporter and Sodium-dependent noradrenaline transporter, preventing or reducing the reuptake of norepinephrine and serotonin by nerve cells. As norepinephrine and serotonin are used to stimulate the synapse, and depression has been linked to a lack of stimulation of the recipient neuron at a synapse, slowing the reuptake of these neurotransmitters allows them to remain in the synaptic gap longer than it normal, increasing the stimulation of the recipient neuron and relieving the symptoms of depression. However, it does not act primarily by stimulation of the central nervous system. The clinical effect is also hypothesized as being due to potentiation of adrenergic synapses by blocking uptake of norepinephrine at nerve endings. Drug Interactions: Altretamine Risk of severe hypotension Atazanavir Atazanavir increases the effect and toxicity of tricyclics Carbamazepine The tricyclic increases the effect of carbamazepine Cimetidine Cimetidine increases the effect of tricyclic agent Cisapride Increased risk of cardiotoxicity and arrhythmias Grepafloxacin Increased risk of cardiotoxicity and arrhythmias Mesoridazine Increased risk of cardiotoxicity and arrhythmias Sparfloxacin Increased risk of cardiotoxicity and arrhythmias Terfenadine Increased risk of cardiotoxicity and arrhythmias Thioridazine Increased risk of cardiotoxicity and arrhythmias Tranylcypromine Possibility of severe adverse effects Rasagiline Possibility of severe adverse effects Phenelzine Possibility of severe adverse effects Isocarboxazid Possibility of severe adverse effects Clonidine The tricyclic decreases the effect of clonidine Dihydroquinidine barbiturate Quinidine increases the effect of tricyclic agent Quinidine Quinidine increases the effect of tricyclic agent Quinidine barbiturate Quinidine increases the effect of tricyclic agent Dobutamine The tricyclic increases the sympathomimetic effect Dopamine The tricyclic increases the sympathomimetic effect Ephedra The tricyclic increases the sympathomimetic effect Ephedrine The tricyclic increases the sympathomimetic effect Epinephrine The tricyclic increases the sympathomimetic effect Fenoterol The tricyclic increases the sympathomimetic effect Guanethidine The tricyclic decreases the effect of guanethidine Isoproterenol The tricyclic increases the sympathomimetic effect Mephentermine The tricyclic increases the sympathomimetic effect Terbutaline The tricyclic increases the sympathomimetic effect Terbinafine Terbinafine increases the effect and toxicity of the tricyclic Salbutamol The tricyclic increases the sympathomimetic effect Ritonavir Ritonavir increases the effect and toxicity of tricyclics Pseudoephedrine The tricyclic increases the sympathomimetic effect Procaterol The tricyclic increases the sympathomimetic effect Pirbuterol The tricyclic increases the sympathomimetic effect Phenylpropanolamine The tricyclic increases the sympathomimetic effect Phenylephrine The tricyclic increases the sympathomimetic effect Orciprenaline The tricyclic increases the sympathomimetic effect Norepinephrine The tricyclic increases the sympathomimetic effect Methoxamine The tricyclic increases the sympathomimetic effect Metaraminol The tricyclic increases the sympathomimetic effect Donepezil Possible antagonism of action Duloxetine Possible increase in the levels of this agent when used with duloxetine Galantamine Possible antagonism of action Fluoxetine Fluoxetine increases the effect and toxicity of tricyclics Fluvoxamine Fluvoxamine increases the effect and toxicity of tricyclics Rivastigmine Possible antagonism of action Fluconazole The imidazole increases the effect and toxicity of the tricyclic Ketoconazole The imidazole increases the effect and toxicity of the tricyclic Moclobemide Possible severe adverse reaction with this combination Rifabutin The rifamycin decreases the effect of tricyclics Rifampin The rifamycin decreases the effect of tricyclics Sibutramine Increased risk of CNS adverse effects Food Interactions: Avoid alcohol. Take with food. Avoid excessive quantities of coffee or tea (Caffeine). Avoid St. John's Wort. Do not take fibers at the same time. Generic Name: Imipramine Synonyms: Not Available Drug Category: Antidepressive Agents, Tricyclic; Norepinephrine-Reuptake Inhibitors; Adrenergic Uptake Inhibitors Drug Type: Small Molecule; Approved Other Brand Names containing Imipramine: Antideprin; Berkomine; Censtim; Censtin; DPID; Declomipramine; Dimipressin; Dyna-Zina; Dynaprin; Estraldine; Eupramin; IM; Imavate; Imidobenzyle; Imipramina; Imipramine Hcl; Imiprin; Imizin; Imizine; Imizinum; Impramine; Intalpram; Iramil; Irmin; Janimine; Melipramin; Melipramine; Nelipramin; Norfranil; Pramine; Prazepine; Presamine; Promiben; Psychoforin; Sk-Pramine; Surplix; Timolet; Tipramine; Tofranil, Base; Tofranil-Pm; Tofraniln A; Trimipramine Maleate; Absorption: Rapidly and well absorbed after oral administration Toxicity (Overdose): Oral, rat LD 50 . 355 to 682 mg/kg. Toxic signs proceed progressively from depression, irregular respiration and ataxia to convulsions and death. Protein Binding: 89–95% Biotransformation: Exclusively hepatic. Imipramine is converted in the liver to desipramine and 2-hydroxydesipramine, both active metabolites. Half Life: 11–25 hours Dosage Forms of Antideprin: Tablet Oral Chemical IUPAC Name: 3-(5,6-dihydrobenzo[b][1]benzazepin-11-yl)-N, N-dimethylpropan-1-amine Chemical Formula: C19H24N2 Imipramine on Wikipedia: http://en. wikipedia. org/wiki/Imipramine Organisms Affected: Humans and other mammals

Cabergoline - Side Effects, Dosage, Interactions, Caberlin

Cabergoline

Cabergoline is a medicine used to treat hyperprolactinemia, a condition characterized by high levels of prolactin — a natural substance in the body that helps breastfeeding women produce milk.

Too much prolactin can cause health problems in men, and in women who aren't breastfeeding.

Cabergoline can help treat symptoms associated with irregular menstruation, unwanted breast milk production, infertility, bone loss, and sexual problems.

People with pituitary gland tumors also produce too much prolactin. Cabergoline is often used to help treat this condition.

The drug is also occasionally used to help treat Parkinson's disease (a nervous system disorder that causes problems with movement, balance, and muscle control).

Cabergoline is in a class of medicines knowns as dopamine receptor agonists. It works by reducing levels of prolactin in the body.

The Food and Drug Administration (FDA) approved cabergoline in 1996. This generic medicine is manufactured by various pharmaceutical companies.

Cabergoline Warnings

Before taking cabergoline, tell your doctor if you have, or have ever had:

High blood pressure

Any condition that causes thickening or scarring of your heart, lungs, or abdomen

Heart valve disease

Liver disease

Allergies to medications

Cabergoline may cause dizziness or fainting if you get up too quickly from a lying position.

To avoid these issues, get out of bed slowly and rest your feet on the floor for a few minutes before standing up.

Some people who take cabergoline experience behavioral changes, such as compulsive gambling or feeling an increase in sexual urges.

These effects typically go away when treatment with the drug is stopped.

Call your doctor if you experience any unusual urges or behaviors.

Tell your healthcare provider that you're taking cabergoline before having any surgery, including a dental procedure.

Your doctor will probably want to perform frequent tests to check your body's response to cabergoline. Keep all appointments with your doctor and laboratory while taking this medicine.

Pregnancy and Cabergoline

Cabergoline isn't likely to harm an unborn baby, but be sure to tell your doctor if you're pregnant or might become pregnant while taking this medicine.

It's not known whether cabergoline can pass into breast milk.

Tell your doctor if you're breastfeeding or plan to breastfeed while taking this drug, as it may slow or stop the production of breast milk.

Cabergoline Side Effects

Common Side Effects of Cabergoline

Tell your doctor if any of the following side effects become severe or don't go away:

Nausea

Upset stomach

Vomiting

Constipation

Heartburn

Dizziness

Tiredness

Numbness, burning, or tingling in the hands, arms, legs, or feet

Serious Side Effects of Cabergoline

Tell your doctor right away if you experience any of the symptoms listed in the Cabergoline Warnings section above, or any of the following serious side effects:

Shortness of breath

Chest pain

Persistent cough

Difficulty breathing when lying down

Painful menstruation

Breast pain

Decrease in urination

Swelling of the hands, feet, ankles, or lower legs

Sudden, unexplained weight gain

Pain in the side, back, or groin

Vision problems

Pain or lumps in the stomach area

Unusual or extreme tiredness

Mood changes

Hallucinations

Signs of an allergic reaction (may include hives, rash, itching, chest tightness, or swelling of the face, lips, tongue, or throat)

Cabergoline Interactions

Tell your doctor about all prescription, non-prescription, illegal, recreational, herbal, nutritional, or dietary drugs you're taking, especially:

Cabergoline and Other Interactions

Cabergoline may cause dizziness or drowsiness.

Don't drive or perform activities that require alertness until you know how this medicine affects you.

Cabergoline and Alcohol

Alcohol may worsen certain side effects of cabergoline.

Talk to your doctor before drinking alcohol while taking this drug.

Cabergoline Dosage

Cabergoline comes as a tablet to take by mouth. It's typically taken with or without food twice a week.

Your doctor will most likely start you on a low dose of the drug and gradually increase it.

Follow the instructions on your prescription label carefully when taking this medicine.

Don't take more or less cabergoline than is recommended.

Don't stop taking this medicine without first talking to your doctor.

Cabergoline is usually stopped when prolactin levels are normal for six months, but your doctor will probably take you off the drug gradually.

Cabergoline Overdose

Symptoms of a cabergoline overdose may include:

Fainting

Hallucinations

Nasal congestion

If you suspect an overdose, contact a poison control center or emergency room immediately.

You can get in touch with a poison control center at 800-222-1222.

Missed Dose of Cabergoline

If you miss a dose of cabergoline, take it as soon as you remember.

But call your doctor for instructions if you've missed a dose and it's almost time for the next one.

Don't take an extra dose of cabergoline unless directed by your doctor to do so.

Ciproflav, Ciproflav

Ciprofloxacin

Antibacterial: Fluoroquinolone (gyrase inhibitor)

Chemical Name

3-Quinolinecarboxylic acid, 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-

Foreign Names

Generic Names

Ciprofloxacin (OS: BAN, USAN, JAN)

Ciprofloxacine (OS: DCF)

Bay q 3939 (IS)

Ciprofloxacin Betaine (IS)

Ciprofloxacin (PH: BP 2016, Ph. Eur. 8, Ph. Int. 4, USP 38)

Ciprofloxacine (PH: Ph. Eur. 8)

Ciprofloxacinum (PH: Ph. Eur. 8, Ph. Int. 4)

Ciprofloxacin Hydrochloride (OS: USAN, BANM, JAN)

Bay o 9867 monohydrate (IS: Bayer)

UNII-4BA73M5E37 (IS)

Ciprofloxacin Hydrochloride (PH: BP 2016, Ph. Int. 4, USP 38)

Ciprofloxacin hydrochloride (PH: Ph. Eur. 8)

Ciprofloxacine (chlorhydrate de) (PH: Ph. Eur. 8)

Ciprofloxacinhydrochlorid (PH: Ph. Eur. 8)

Ciprofloxacini hydrochloridum (PH: Ph. Eur. 8, Ph. Int. 4)

Ciprofloxacin sulfate (IS)

Ciprofloxacin Lactate (OS: BANM)

Brand Names

Click for further information on drug naming conventions and International Nonproprietary Names .

Important Notice: The Drugs. com international database is in BETA release. This means it is still under development and may contain inaccuracies. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Consult with your healthcare professional before taking any medication.

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Ciplox is used to treat different types of bacterial infections. It may also be used to prevent or slow anthrax after exposure.

Take Cipro exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.

Take Cipro with a full glass of water (8 ounces). Drink several extra glasses of fluid each day while you are taking this medicine. Cipro may be taken with or without food, but take it at the same time each day. Shake the oral suspension (liquid) for at least 15 seconds just before you measure a dose. To be sure you get the correct dose, measure the liquid with a marked measuring spoon or medicine cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.

When taking the Cipro oral liquid, swallow it without chewing the medicine beads you may notice in the liquid.

Do not crush, chew, or break an extended-release tablet. Swallow it whole. Breaking the pill may cause too much of the drug to be released at one time. Do not take Cipro with dairy products such as milk or yogurt, or with calcium-fortified juice. You may eat or drink these products as part of a regular meal, but do not use them alone when taking Cipro. They could make the medication less effective.

Take Cipro for the full prescribed length of time. Your symptoms may improve before the infection is completely cleared. Skipping doses may also increase your risk of further infection that is resistant to antibiotics. Cipro will not treat a viral infection such as the common cold or flu.

Store Cipro at room temperature away from moisture and heat. Do not allow the liquid medicine to freeze.

If you missed a dose - take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.

Take exactly as prescribed by your Health Provider.

Store this medicine at room temperature away from moisture and heat. Do not allow the liquid medicine to freeze.

You should not use Ciplox if you are taking tizanidine (Zanaflex), if you have a history of myasthenia gravis, or if you are allergic to ciprofloxacin or similar antibiotics such as gemifloxacin (Factive), levofloxacin (Levaquin), moxifloxacin (Avelox), norfloxacin (Noroxin), and others.

Before taking Ciplox, tell your doctor if you have a heart rhythm disorder, kidney or liver disease, joint problems, diabetes, muscle weakness or trouble breathing, a condition called pseudotumor cerebri, a history of seizures, a history of head injury or brain tumor, low levels of potassium in your blood, a personal or family history of Long QT syndrome, or if you have ever had an allergic reaction to an antibiotic.

Do not take Ciplox with dairy products such as milk or yogurt, or with calcium-fortified juice. Avoid taking antacids, vitamin or mineral supplements, sucralfate (Carafate), or didanosine (Videx) powder or chewable tablets within 6 hours before or 2 hours after you take Ciplox. Ciprofloxacin may cause swelling or tearing of a tendon (the fiber that connects bones to muscles in the body), especially in the Achilles' tendon of the heel. Stop taking Ciplox and call your doctor at once if you have sudden pain, swelling, tenderness, stiffness, or movement problems in any of your joints. Rest the joint until you receive medical care or instructions.

You should NOT take Ciplox if:

you are also taking tizanidine (Zanaflex);

you have a history of myasthenia gravis; or

you are allergic to ciprofloxacin or similar medications such as gemifloxacin (Factive), levofloxacin (Levaquin), moxifloxacin (Avelox), ofloxacin (Floxin), norfloxacin (Noroxin), and others.

To make sure you can safely take Ciplox, tell your doctor if you have any of these other conditions:

heart rhythm disorder, especially if you take quinidine (Quin-G), disopyramide (Norpace), bretylium (Bretylol), procainamide (Pronestyl, Procan SR), amiodarone (Cordarone, Pacerone), or sotalol (Betapace);

a history of head injury or brain tumor;

a condition called pseudotumor cerebri (high pressure inside the skull that may cause headaches, vision loss, or other symptoms);

a history of allergic reaction to an antibiotic;

joint problems;

kidney or liver disease;

epilepsy or seizures;

diabetes;

muscle weakness or trouble breathing;

low levels of potassium in your blood (hypokalemia); or

a personal or family history of Long QT syndrome.

FDA pregnancy category C. It is not known whether Ciplox will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using it. Ciprofloxacin passes into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. Ciplox may cause swelling or tearing of a tendon (the fiber that connects bones to muscles in the body), especially in the Achilles' tendon of the heel. These effects may be more likely to occur if you are over 60, if you take steroid medication, or if you have had a kidney, heart, or lung transplant. Stop taking Ciplox and call your doctor at once if you have sudden pain, swelling, tenderness, stiffness, or movement problems in any of your joints. Rest the joint until you receive medical care or instructions. Do not share Ciplox with another person (especially a child), even if they have the same symptoms you have.

Get emergency medical help if you have any of these signs of an allergic reaction to Ciplox: hives; difficult breathing; swelling of your face, lips, tongue, or throat. Stop using Ciplox and call your doctor at once if you have a serious side effect such as:

severe dizziness, fainting, fast or pounding heartbeats;

sudden pain, snapping or popping sound, bruising, swelling, tenderness, stiffness, or loss of movement in any of your joints;

diarrhea that is watery or bloody;

confusion, hallucinations, depression, unusual thoughts or behavior;

seizure (convulsions);

severe headache, ringing in your ears, dizziness, nausea, vision problems, pain behind your eyes;

pale or yellowed skin, dark colored urine, fever, weakness;

urinating less than usual or not at all;

easy bruising or bleeding;

numbness, tingling, or unusual pain anywhere in your body;

the first sign of any skin rash, no matter how mild; or

severe skin reaction -- fever, sore throat, swelling in your face or tongue, burning in your eyes, skin pain, followed by a red or purple skin rash that spreads (especially in the face or upper body) and causes blistering and peeling.

Less serious side effects:

nausea, vomiting;

dizziness or drowsiness;

blurred vision;

feeling nervous, anxious, or agitated; or

sleep problems (insomnia or nightmares).

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects.

Antibiotics - Ciproflav (Brand name: ciplox)

Ciplox is used to treat different types of bacterial infections. It may also be used to prevent or slow anthrax after exposure.

Take Cipro exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.

Take Cipro with a full glass of water (8 ounces). Drink several extra glasses of fluid each day while you are taking this medicine. Cipro may be taken with or without food, but take it at the same time each day. Shake the oral suspension (liquid) for at least 15 seconds just before you measure a dose. To be sure you get the correct dose, measure the liquid with a marked measuring spoon or medicine cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.

When taking the Cipro oral liquid, swallow it without chewing the medicine beads you may notice in the liquid.

Do not crush, chew, or break an extended-release tablet. Swallow it whole. Breaking the pill may cause too much of the drug to be released at one time. Do not take Cipro with dairy products such as milk or yogurt, or with calcium-fortified juice. You may eat or drink these products as part of a regular meal, but do not use them alone when taking Cipro. They could make the medication less effective.

Take Cipro for the full prescribed length of time. Your symptoms may improve before the infection is completely cleared. Skipping doses may also increase your risk of further infection that is resistant to antibiotics. Cipro will not treat a viral infection such as the common cold or flu.

Store Cipro at room temperature away from moisture and heat. Do not allow the liquid medicine to freeze.

If you missed a dose - take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.

Take exactly as prescribed by your Health Provider.

Store this medicine at room temperature away from moisture and heat. Do not allow the liquid medicine to freeze.

You should not use Ciplox if you are taking tizanidine (Zanaflex), if you have a history of myasthenia gravis, or if you are allergic to ciprofloxacin or similar antibiotics such as gemifloxacin (Factive), levofloxacin (Levaquin), moxifloxacin (Avelox), norfloxacin (Noroxin), and others.

Before taking Ciplox, tell your doctor if you have a heart rhythm disorder, kidney or liver disease, joint problems, diabetes, muscle weakness or trouble breathing, a condition called pseudotumor cerebri, a history of seizures, a history of head injury or brain tumor, low levels of potassium in your blood, a personal or family history of Long QT syndrome, or if you have ever had an allergic reaction to an antibiotic.

Do not take Ciplox with dairy products such as milk or yogurt, or with calcium-fortified juice. Avoid taking antacids, vitamin or mineral supplements, sucralfate (Carafate), or didanosine (Videx) powder or chewable tablets within 6 hours before or 2 hours after you take Ciplox. Ciprofloxacin may cause swelling or tearing of a tendon (the fiber that connects bones to muscles in the body), especially in the Achilles' tendon of the heel. Stop taking Ciplox and call your doctor at once if you have sudden pain, swelling, tenderness, stiffness, or movement problems in any of your joints. Rest the joint until you receive medical care or instructions.

You should NOT take Ciplox if:

you are also taking tizanidine (Zanaflex);

you have a history of myasthenia gravis; or

you are allergic to ciprofloxacin or similar medications such as gemifloxacin (Factive), levofloxacin (Levaquin), moxifloxacin (Avelox), ofloxacin (Floxin), norfloxacin (Noroxin), and others.

To make sure you can safely take Ciplox, tell your doctor if you have any of these other conditions:

heart rhythm disorder, especially if you take quinidine (Quin-G), disopyramide (Norpace), bretylium (Bretylol), procainamide (Pronestyl, Procan SR), amiodarone (Cordarone, Pacerone), or sotalol (Betapace);

a history of head injury or brain tumor;

a condition called pseudotumor cerebri (high pressure inside the skull that may cause headaches, vision loss, or other symptoms);

a history of allergic reaction to an antibiotic;

joint problems;

kidney or liver disease;

epilepsy or seizures;

diabetes;

muscle weakness or trouble breathing;

low levels of potassium in your blood (hypokalemia); or

a personal or family history of Long QT syndrome.

FDA pregnancy category C. It is not known whether Ciplox will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using it. Ciprofloxacin passes into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. Ciplox may cause swelling or tearing of a tendon (the fiber that connects bones to muscles in the body), especially in the Achilles' tendon of the heel. These effects may be more likely to occur if you are over 60, if you take steroid medication, or if you have had a kidney, heart, or lung transplant. Stop taking Ciplox and call your doctor at once if you have sudden pain, swelling, tenderness, stiffness, or movement problems in any of your joints. Rest the joint until you receive medical care or instructions. Do not share Ciplox with another person (especially a child), even if they have the same symptoms you have.

Get emergency medical help if you have any of these signs of an allergic reaction to Ciplox: hives; difficult breathing; swelling of your face, lips, tongue, or throat. Stop using Ciplox and call your doctor at once if you have a serious side effect such as:

severe dizziness, fainting, fast or pounding heartbeats;

sudden pain, snapping or popping sound, bruising, swelling, tenderness, stiffness, or loss of movement in any of your joints;

diarrhea that is watery or bloody;

confusion, hallucinations, depression, unusual thoughts or behavior;

seizure (convulsions);

severe headache, ringing in your ears, dizziness, nausea, vision problems, pain behind your eyes;

pale or yellowed skin, dark colored urine, fever, weakness;

urinating less than usual or not at all;

easy bruising or bleeding;

numbness, tingling, or unusual pain anywhere in your body;

the first sign of any skin rash, no matter how mild; or

severe skin reaction -- fever, sore throat, swelling in your face or tongue, burning in your eyes, skin pain, followed by a red or purple skin rash that spreads (especially in the face or upper body) and causes blistering and peeling.

Less serious side effects:

nausea, vomiting;

dizziness or drowsiness;

blurred vision;

feeling nervous, anxious, or agitated; or

sleep problems (insomnia or nightmares).

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects.

Ibuprofen 600 Mg Tablets, Ibucare

IBUPROFEN 600 MG TABLETS

Transcript

PACKAGE LEAFLET: INFORMATION FOR THE USER Ibuprofen 600 mg Film-coated Tablets (Ibuprofen) Read all of this leaflet carefully before you start taking this medicine because it contains important information for you. ? Keep this leaflet. You may need to read it again. ? If you have any further questions, ask your doctor, or pharmacist or nurse. ? This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours. ? If you get any of the side effects, talk to your doctor, or pharmacist or nurse. This includes any possible side effects not listed in this leaflet. See section 4.

What Ibuprofen Tablets are and what they are used for What you need to know before you take Ibuprofen How to take Ibuprofen Possible side effects How to store Ibuprofen Contents of the pack and other information

1. What Ibuprofen Tablets are and what they are used for Ibuprofen belongs to a group of medicines called Non Steroidal Anti-Inflammatory Drugs (known as NSAIDs), which relieve pain and reduce inflammation in joints and soft tissues such as muscles and ligaments. Ibuprofen tablets are used to: ? relieve mild to moderate pain e. g. post-operative pain, toothache, period pain and soft tissue injury (muscles and ligaments) ? relieve stiffness and pain in the back and other muscles ? reduce inflammation in different types of arthritis.

2. What you need to know before you take Ibuprofen Do NOT take Ibuprofen if you: ? are allergic to ibuprofen or any of the other ingredients of this medicine (listed in section 6). ? have or had an allergic reaction to aspirin or any other NSAID (you have ever had asthma, runny nose, itchy skin or swelling of the lips, face or throat after taking these medicines) ? have an increased tendency of bleeding ? are suffering from or have a history of repeated stomach ulcers or other gastric complaint ? are suffering from heart failure, which can cause shortness of breath or ankle swelling ? suffer from kidney or liver problems ? are in last 3 months of your pregnancy ? have systemic lupus erythematosus (SLE, sometimes known as lupus) or a connective tissue disease (autoimmune diseases affecting connective tissue). Do not take if you have a peptic ulcer (ulcer in your stomach or duodenum) or bleeding in your stomach, or have had two or more episodes of peptic ulcers, stomach bleeding or perforation. Warnings and precautions

Talk to your doctor, pharmacist or nurse before taking ibuprofen. If you: ? are elderly ? are suffering from or have a history of bronchial asthma ? have a history of stomach or bowel problems ? have problems with your kidneys, heart or liver ? have systemic lupus erythematosus (SLE, sometimes known as lupus) or a connective tissue disease (autoimmune diseases affecting connective tissue). ? have a history of gastrointestinal disease ? are severely dehydrated ? have problems conceiving or are in the first 6 months of pregnancy ? are taking any non-steroidal anti-inflammatory medicine, including aspirin as this may result into increased tendency of ulceration or bleeding ? have ulcerated colitis or Crohn’s disease If you suffer from any of the following at any time during your treatment STOP TAKING the medicine and seek immediate medical help: ? Pass blood in your faeces (stools/ motions) ? Pass black tarry stools ? Vomit any blood or dark particles that look like coffee grounds STOP TAKING the medicine and tell your doctor if your experience: ? Indigestion or heartburn ? Abdominal pain (pains in your stomach) or other abdominal stomach symptoms Anti-inflammatory/pain-killer medicines like ibuprofen may be associated with a small increased risk of heart attack or stroke, particularly when used at high doses. Do not exceed the recommended dose or duration of treatment. You should discuss your treatment with your doctor or pharmacist before taking Ibuprofen if you: - have heart problems including heart failure, angina (chest pain), or if you have had a heart attack, bypass surgery, peripheral artery disease (poor circulation in the legs of feet due to narrow or blocked arteries), or any kind of stroke (including ‘mini-stroke’ or transient ischaemic attack “TIA”). - have high blood pressure, diabetes, high cholesterol, have a family history of heart disease or stroke, or if you are a smoker. Other medicines and Ibuprofen Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines of the following: ? any other pain-relieving medication, including aspirin ?

medicines that are anti-coagulants (i. e. thin blood/prevent clotting e. g. aspirin/acetylsalicylic acid, warfarin, ticlopidine)

diuretics ('water tablets')

medicines that reduce high blood pressure (ACE-inhibitors such as captopril, beta-blockers such as atenolol medicines, angiotensin-II receptor antagonists such as losartan)

medicines for heart problems e. g. digoxin, digitoxin lithium, a drug used in the treatment of depression methotrexate, a treatment for leukaemia medicines known as immunosuppressants such as ciclosporin and tacrolimus (used to dampen down your immune response) mifepristone in the last 8 - 12 days, used to end a pregnancy corticosteroids (medicines to treat a variety of conditions such as allergies and hormone imbalances), e. g. aldosterone, hydrocortisone or prednisolone quinolone antibiotics, e. g. ciprofloxacin, norfloxacin or levofloxacin

zidovudine (an anti-viral drug) medicines known as selective serotonin reuptake inhibitors (SSRIs), used for the treatment of depression any other ibuprofen preparations, such as those you can buy without a prescription cholestyramine (a drug used to lower cholesterol) medicines known as sulphonylureas such as glibenclamide and glipizide (used to treat diabetes) voriconazole or fluconazole (types of anti-fungal drugs) Gingko biloba herbal medicine (there is a chance you may bleed more easily if you are taking this with ibuprofen) aminoglycosides (a type of antibiotic).

Some other medicines may also affect or be affected by the treatment of Ibuprofen You should therefore always seek the advice of your doctor or pharmacist before you take Ibuprofen with other medicines. Pregnancy, breast-feeding and fertility The use of Ibuprofen whilst pregnant or breast feeding should be avoided. Ibuprofen should not be used in the last 3 months of pregnancy and should only be taken in the first six months of pregnancy on the advice of your doctor. Driving and using machines Ibuprofen may make you feel dizzy or drowsy. If the tablets affect you in this way do not drive or operate machinery

3. How to take Ibuprofen Always take Ibuprofen exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure. If you suffer from heart, liver or kidney problems your doctor may lower your dose and carry out regular tests. If you see another doctor or go into hospital, let the doctor or the staff know what medicines you are taking. Ibuprofen with food and drink The tablets should be swallowed preferably with a drink of water. Take with or after food. The recommended dose is: ? Adults Initially 1200 mg per day in divided doses. Larger doses up to 1800 mg per day may be taken if necessary. The maintenance dose will be determined on an individual basis (between 600 - 1200 mg a day). Do not take more than 2400 mg in a 24-hour period. ?

Use in children and adolescents Ibuprofen 600 mg tablets are not recommended for use in children.

Elderly people To reduce the possibility of side effects if you are elderly, you should take the smallest dose for the shortest possible time. Your doctor may monitor you for bleeding in the stomach.

If you take more Ibuprofen than you should If you (or someone else) swallow a lot of the tablets all together, or if you think a child has swallowed any of the tablets, contact your nearest hospital casualty department or your doctor immediately. An overdose is likely to cause stomach pain, feeling sick, being sick, diarrhoea, ringing in the ears, headache, bleeding in the stomach or intestines. Please take this leaflet, any remaining tablets and the container with you to the hospital or doctor so that they know which tablets were consumed.

If you forget to take Ibuprofen If you forget to take a tablet, take one as soon as you remember, unless it is nearly time to take the next one. Do not take a double dose to make up for a forgotten dose. Take the remaining doses at the correct time. If you stop taking Ibuprofen Do not stop taking your medicine without talking to your doctor first even if you feel better. If you have any further questions on the use of this medicine, ask your doctor, pharmacist or nurse.

4. Possible side effects Like all medicines, Ibuprofen can cause side effects, although not everybody gets them. If any of the following happen, stop taking the tablets and tell your doctor immediately or go to the casualty department at your nearest hospital: ? an allergic reaction (swelling of the lips, face or neck leading to severe difficulty in breathing; skin rash or hives) ? Stevens-Johnson syndrome (severe blisters and bleeding in the mucous membranes of the lips, eyes, mouth, nasal passage, and genitals) or severe headache, high temperature, stiffness of the neck, a skin reaction causing blistering and flaking of the skin, intolerance to light ? you pass blood in your faeces (stools/motions) ? you pass black tarry stools ? you vomit any blood or dark particles that look like coffee grounds. ? blood disorders such as low numbers of red or white blood cells, reduction in blood platelets (which may increase the risk of bleeding and bruising), neutropenia (which may cause fever or chills, sore throat, ulcers in your mouth or throat) ? heart problems causing symptoms such as shortness of breath when exercising or lying flat, wheezing and a cough, weight gain. These are very serious but rare side effects. You may need urgent medical attention or hospitalisation. The following side effects have been reported at the approximate frequencies shown: Rare: may affect up to 1 in 1,000 people Stop taking the medicine and tell your doctor if you experience: ? abdominal pain (pains in your stomach) or other abnormal stomach symptoms, indigestion, heartburn, feeling sick and/or being sick ? unexplained wheezing, shortness of breath, skin rash, itching or bruising ? yellowing of the eyes and/or skin ? severe sore throat with high fever ? blurred or disturbed vision, or seeing/hearing strange things ? fluid retention (e. g. swollen ankles). Very rare: may affect up to 1 in 10,000 people Very rarely Ibuprofen Tablets may cause aseptic meningitis (inflammation of the protective membrane surrounding the brain) especially in patients with an auto-immune disease e. g. Systemic Lupus Erythematosus (SLE) or mixed connective tissue disease; symptoms may include stiff neck, headache, nausea, vomiting, fever, disorientation. Other side effects (Frequency unknown) Other side effects that have been reported while taking Ibuprofen: ? peptic ulcer (ulcer in your stomach or duodenum) or bleeding in your stomach ? pancreatitis (inflammation of the pancreas) ? diarrhoea REG0077715

constipation flatulence (wind) inflammation or ulceration of the mouth e. g. mouth ulcers and cold sores (ulcerative stomatitis) high blood pressure kidney problems such as inflammation of the kidneys, kidney damage or kidney failure liver problems such as abnormal liver function test results, inflammation of the liver (hepatitis) breathlessness and wheezing in patients suffering from or with a previous history of asthma or allergic disease e. g. allergy to house dust mites, cats or dogs runny nose problems with the senses such as vision problems, inflammation of the optic nerve, pins-and-needles or numbness, ringing in the ears or impaired hearing headaches, hallucinations, depression, confusion, dizziness and vertigo (a feeling of dizziness or “spinning”, drowsiness and a general feeling of being unwell, lethargy difficulty in sleeping, anxiety

Ibuprofen has also been shown to sometimes worsen the symptoms of Crohn’s disease or colitis Medicines such as ibuprofen may be associated with a small increased risk of heart attack (“myocardial infarction”) or stroke. If any of the side effects get serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist. You can minimise the risk of side effects by taking the least amount of tablets for the shortest amount of time necessary to control your symptoms. Reporting of side effects If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: www. mhra. gov. uk/yellowcard By reporting side effects you can help provide more information on the safety of this medicine.

5. How to store Ibuprofen Keep this medicine out of the sight and reach of children. These tablets should be stored in a dry place, at or below 25° C, protected from light in the package or container supplied. Do not transfer them to another container. Do not use Ibuprofen after the expiry date that is stated on the outer packaging. The expiry date refers to the last day of that month. Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help to protect the environment.

6. Contents of the pack and other information What Ibuprofen tablets contain: ? The active ingredient is ibuprofen. ? The other ingredients are pregelatinised maize starch, maize starch, colloidal silicon dioxide, sodium starch glycolate, and stearic acid. The tablet coating contains hydroxypropyl methylcellulose E464), talc, erythrosine (E127) and titanium dioxide (E171).

What Ibuprofen tablets look like and contents of the pack: ? The Ibuprofen 600 mg tablets are pink, capsule-shaped film coated tablets. They are coded 600 over 0531 and plain on the reverse. ?

The tablets are available in pack sizes of 7, 10, 14, 21, 28, 30, 50, 56, 60, 84, 90, 100, 110, 112, 120, 150, 160, 168, 250, 500, and 1000 tablets.

Not all pack sizes may be marketed. Marketing Authorisation Holder and Manufacturer The Marketing Authorisation holder and company responsible for manufacture is TEVA UK Limited, Eastbourne, BN22 9AG England. This leaflet was last revised: August 2015 PL 00289/0280

THIS IS A REPRESENTATION OF AN ELECTRONIC RECORD THAT WAS SIGNED ELECTRONICALLY AND THIS PAGE IS THE MANIFESTATION OF THE ELECTRONIC SIGNATURE

Teva Pharmaceuticals Europe B. V 1.3.1 pil-uk-pl-00289-0280-ibuprofen-600mg-film-coated-tablets

APPROVALS Signed by Darryl Hill

Meaning of Signature Regulatory Affairs Approval

Server Date 09-Sep-2015 09:57:42 AM

Source: Medicines and Healthcare Products Regulatory Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

Comprar Aprolac (Parlodel) Sin Receta, Aprolac

compra Aprolac (Parlodel) en linea sin receta

Aprolac (Parlodel) Explicacion

Aprolac se hace utilizando el metodo ideal que la asistencia sanitaria es una herramienta espectacular para towardsA ejemplo prolongada pechos de creacion de los productos lacteos, la infertilidad, amenorrea (ausencia de la menstruacion), junto con otros problemas provocados por la prolactina secretoras de crecimientos. Concentrese en asociado con Aprolac seria para disminuir el grado de prolactina que ayudan a crear senos lacteos, asi como la fertilidad masculina en las mujeres.

Aprolac puede pasar como atrapados tratamiento disminuyendo el grado de prolactina. Lanzado utilizado para remediar la enfermedad de Parkinson, las funciones a traves de la revitalizacion de dolor dopamina en ciertos componentes especificos de la mente.

Aprolac tambien puede ser referido como bromocriptina, Proctinal.

Aprolac es realmente una basura (agonista de la dopamina).

Aprolac no puede dar lugar a sangrado de la vagina, del utero o incluso el cancer de la mama, dolor de senos.

titulo general asociada con Aprolac es en realidad bromocriptina.

Marca asociada con Aprolac Aprolac es en realidad.

Aprolac (Parlodel) Dosis

Aprolac viene en:

segundo. Material de friccion dosis regular 5mg

Aprolac viene en son pildoras (2. cinco mg) que debe ser utilizado por via oral junto con los alimentos o incluso sin tener esto.

Get Aprolac cada dia al mismo tiempo por favor recuerde que la dosis depende de la condicion de bienestar de la persona.

Si usted desea lograr mejores resultados por lo general no dejar de usar Aprolac de repente.

Aprolac (Parlodel) Careciendo asocia con dosis

Por lo general, no reciben doble dosis. En caso de que salte la dosis que necesita para llevar una vez se tiene en cuenta en lo que respecta a su deficiente. Cuando es hora de la dosis que necesita para llevar a cabo su propia rutina de dosificacion normal.

Aprolac (Parlodel)

En el caso de que la sobredosis Aprolac y que tambien se evita gran usted necesita comprobar hacia fuera su medico o incluso el medico de inmediato.

Aprolac (Parlodel) Espacio de almacenamiento

La tienda debajo de veinticinco niveles D (77 niveles F) de la humedad, la iluminacion, asi como la temperatura. Mantener cuadro de texto firmemente cerrada. Fortalecer cualquier tipo de medicamento sin tocar a partir del dia de vencimiento. Mantener desde el lograr de los ninos.

Aprolac (Parlodel) Efectos negativos

Aprolac ofrece los efectos negativos. El mas tipico tienden a ser:

material de friccion congestion

material de friccion fatiga

nauseas o vomitos material de friccion

tapada nasal material de friccion area

material de friccion migrana

material de friccion arcadas

conciencia frio dentro de alcance de la mano, asi como material de friccion pies

seca material de superficie de friccion boca

material de friccion diarrea

vientre calambres material de friccion

sensacion de mareos material de friccion

material de friccion somnolencia

material de friccion hambre insuficiente

material de friccion de reflujo acido

material de friccion agotamiento

Mucho menos tipicos y graves efectos negativos en todo el uso de Aprolac:

respuestas reaccion alergica (urticaria, inhalando y exhalando, cuestiones de alergia, asi como la erupcion) material de friccion

material de friccion alucinaciones

unilateral un poco de material de friccion debilidad

material de friccion acciones inconscientes poco comun Material

modificaciones de vision friccion

malentendidos inesperados material de friccion

los trastornos depresivos material de friccion

hablar arrastrando las palabras o incluso problemas hablando material de friccion / li>

material de friccion desmayos

torrente sanguineo o tal vez un material como el material de friccion razones espresso

debilucho

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Mefloquine Dosage Guide With Precautions, Mefloquin

Mefloquine Dosage

Additional dosage information:

Usual Adult Dose for Malaria

1250 mg orally as a single dose

CDC recommendation for uncomplicated infections due to chloroquine-resistant Plasmodium vivax or P falciparum: 750 mg orally as initial dose, followed by 500 mg orally 6 to 12 hours after initial dose

Approved indication: For treatment of mild to moderate acute malaria due to mefloquine-susceptible P falciparum (both chloroquine-susceptible and - resistant strains) or P vivax

Usual Adult Dose for Malaria Prophylaxis

250 mg orally once a week

Comments : - Should be taken on the same day of each week, preferably after the main meal - Prophylaxis should begin 1 week (per manufacturer) to 2 or more weeks (per CDC) before arrival in an endemic area and should continue for 4 weeks after leaving such areas.

Approved indication: For prophylaxis of P falciparum and P vivax malaria infections, including prophylaxis of chloroquine-resistant strains of P falciparum

Usual Pediatric Dose for Malaria

6 months or older: 20 to 25 mg/kg orally as a single dose Maximum total dose: 1250 mg

CDC recommendation for uncomplicated infections due to chloroquine-resistant P vivax or P falciparum: 15 mg/kg orally as initial dose, followed by 10 mg/kg orally 6 to 12 hours after initial dose Maximum total dose: 1250 mg

Comments : - Manufacturer states splitting the total dose into 2 doses given 6 to 8 hours apart may reduce the occurrence or severity of side effects. - Pediatric dose should not exceed adult dose. - A second full dose should be given if the patient vomits less than 30 minutes after taking mefloquine. - An additional half-dose should be given if the patient vomits 30 to 60 minutes after taking mefloquine. - If vomiting recurs, the patient should be monitored closely and alternative malaria treatment should be considered if improvement is not observed within a reasonable period of time.

Approved indication: For treatment of mild to moderate acute malaria due to mefloquine-susceptible P falciparum (both chloroquine-susceptible and - resistant strains) or P vivax

Usual Pediatric Dose for Malaria Prophylaxis

20 to 30 kg: 125 mg (1/2 tablet) orally once a week 30 to 45 kg: 187.5 mg (3/4 tablet) orally once a week Greater than 45 kg: 250 mg (1 tablet) orally once a week

CDC recommendation : 9 kg or less: 5 mg/kg orally once a week Greater than 9 to 19 kg: 62.5 mg (1/4 tablet) orally once a week Greater than 19 to 30 kg: 125 mg (1/2 tablet) orally once a week Greater than 30 to 45 kg: 187.5 mg (3/4 tablet) orally once a week Greater than 45 kg: 250 mg (1 tablet) orally once a week

Comments : - Approximately 5 mg/kg (maximum: 250 mg/dose) orally once a week - Should be taken on the same day of each week, preferably after the main meal - Prophylaxis should begin 1 week (per manufacturer) to 2 or more weeks (per CDC) before arrival in an endemic area and should continue for 4 weeks after leaving such areas.

Approved indication: For prophylaxis of P falciparum and P vivax malaria infections, including prophylaxis of chloroquine-resistant strains of P falciparum

Renal Dose Adjustments

Data not available

Liver Dose Adjustments

Data not available

Precautions

Consult WARNINGS section for dosing related precautions.

Dialysis

Hemodialysis: No adjustment recommended. CAPD: Data not available

Other Comments

The dosage is expressed in terms of mefloquine hydrochloride (salt).

Administration advice : - Do not take mefloquine on an empty stomach; take with at least 8 ounces (240 mL) of water. - Tablets may be crushed and suspended in a small amount of water, milk, or other beverage for patients unable to swallow them whole.

General : - A Medication Guide and information wallet card (supplied by the manufacturer) must be given to patients when dispensing mefloquine. - Competent national expert centers should be consulted for current advice on geographical resistance patterns.

For malaria treatment : - Patients with life-threatening, serious, or overwhelming malaria infections due to P falciparum should be treated with IV antimalarials. Mefloquine may be used to complete the course of therapy after IV therapy is finished. - If a full treatment course with mefloquine does not lead to improvement within 48 to 72 hours, alternative treatment should be used for retreatment (not mefloquine). Similarly, if previous prophylaxis with mefloquine failed, it should not be used for curative therapy. - To avoid relapse, after initial treatment of acute P vivax malaria with mefloquine, patients should subsequently be treated with primaquine (to eliminate hepatic phase parasites).

For malaria prophylaxis : - Mefloquine prophylaxis should start at least 1 week before arrival in an endemic area, continue during the stay, and then continue for 4 weeks after leaving the area. - In certain cases (e. g. when traveler is taking other medications) it may be desirable to start prophylaxis 2 to 3 weeks prior to travel in order to ensure tolerance. - The CDC states that mefloquine can be started 3 to 4 weeks in advance to allow potential side effects to occur before travel. If unacceptable side effects develop, there would be time to change the drug before the traveler's departure.

Monitoring : - Hepatic: Hepatic function (periodically during prolonged use) - Nervous system: For neuropsychiatric symptoms (especially during prolonged use) - Ocular: Ophthalmic examinations (periodically during prolonged use) - Psychiatric: For neuropsychiatric symptoms (especially during prolonged use)

Patient advice : - Read the Medication Guide and carry the information wallet card during mefloquine use. - Additional precautions (e. g. protective clothing, insect repellents, bed nets) are important for malaria prophylaxis. - Seek medical attention for any febrile illness occurring after return from a malaria area. - Use caution during activities requiring alertness and fine motor coordination (e. g. driving, piloting aircraft, operating machinery, deep-sea diving) while neurologic symptoms persist.

Rifadin (Rifampin) Side Effects, Interactions, Warning, Dosage & Uses, Rotifamin

RIFADIN ® (rifampin) Capsules, USP

RIFADIN®IV (rifampin) Injection, USP

To reduce the development of drug-resistant bacteria and maintain the effectiveness of RIFADIN (rifampin capsules USP) and RIFADIN IV (rifampin for injection USP) and other antibacterial drugs, rifampin should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.

DRUG DESCRIPTION

RIFADIN (rifampin capsules USP) for oral administration contain 150 mg or 300 mg rifampin per capsule. The 150 mg and 300 mg capsules also contain, as inactive ingredients: corn starch, D&C Red No. 28, FD&C Blue No. 1, FD&C Red No. 40, gelatin, magnesium stearate, and titanium dioxide. RIFADIN IV (rifampin for injection USP) contains rifampin 600 mg, sodium formaldehyde sulfoxylate 10 mg, and sodium hydroxide to adjust pH.

Rifampin is a semisynthetic antibiotic derivative of rifamycin SV. Rifampin is a red-brown crystalline powder very slightly soluble in water at neutral pH, freely soluble in chloroform. soluble in ethyl acetate and in methanol. Its molecular weight is 822.95 and its chemical formula is C 43 H 58 N 4 O 12 . The chemical name for rifampin is either: 3-[[(4-Methyl-1-piperazinyl)imino]methyl]rifamycin

5,6,9,17,19,21-hexahydroxy-23-methoxy-2,4,12,16,20,22–heptamethyl-8-[N-(4-methyl-1-piperazinyl)formimidoyl]-2,7- (epoxypentadeca[1,11,13]trienimino)naphtho[2,1-b]furan-1,11(2H)-dione 21-acetate. Its structural formula is:

What are the possible side effects of rifampin (Rifadin)?

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if you have a serious side effect such as:

fever, chills, body aches, flu symptoms;

joint pain or swelling;

easy bruising or bleeding, weakness;

urinating less than usual or not at all; or

nausea, stomach pain, loss of appetite, itching, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes).

Less serious side effects may.

What are the precautions when taking rifampin (Rifadin)?

Before taking rifampin, tell your doctor or pharmacist if you are allergic to it; or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

Before using this medication, tell your doctor or pharmacist your medical history, especially of: diabetes, liver problems (e. g. hepatitis), HIV infection, history of alcohol use/abuse.

This drug may make you dizzy or drowsy. Do not drive, use machinery, or do any activity that requires alertness until you are sure you can perform such activities safely. Limit alcoholic beverages.

Before having surgery, tell your doctor or dentist that you are using this drug.

During pregnancy, this medication should.

Last reviewed on RxList: 12/14/2015 This monograph has been modified to include the generic and brand name in many instances.

Comprar Geriprost (Hytrin) Sin Receta, Geriprost

compra Geriprost (Hytrin) en linea sin receta

Geriprost (Hytrin) Explicacion

Geriprost es un tratamiento eficaz para la presion arterial alta. El enfoque en la puede ser la reparacion de la hiperplasia prostatica inofensivo.

Geriprost esta realmente operando a traves de endurecimiento de la clase especifica de la masa muscular dentro de la prostata con la puesta en marcha real de la vejiga.

Geriprost tambien puede ser referido como terazosina, Terapress.

titulo general asociada con Geriprost Terazosin es en realidad? ydrochloride.

Marca asociada con Geriprost Geriprost es en realidad.

Geriprost (Hytrin) Dosis

Geriprost viene en:

1mg Baja Dosis material de friccion

material de friccion dosis regular 2mg

5 mg Mejora Dosis material de friccion

Obtener pildoras Geriprost por via oral con o sin comidas.

Por lo general, no moler o incluso masticar esto.

Obtener Geriprost simultaneamente todos los dias junto con el agua potable.

Si usted desea lograr mejores resultados por lo general no dejar de usar Geriprost de repente.

Geriprost (Hytrin) Careciendo asocia con dosis

Por lo general, no reciben doble dosis. En caso de que salte la dosis que necesita para llevar una vez se tiene en cuenta en lo que respecta a su deficiente. Cuando es hora de la dosis que necesita para llevar a cabo su propia rutina de dosificacion normal.

Geriprost (Hytrin)

En el caso de una sobredosis Geriprost y que tambien se evita gran usted necesita comprobar hacia fuera su medico o incluso el medico de inmediato. Asociado con Geriprost sobredosis: desmayos, la sorpresa, la fatiga.

Geriprost (Hytrin) Espacio de almacenamiento

La tienda de las temperaturas del espacio entre los veinte, asi como veinticinco niveles D (68, asi como setenta y siete niveles F) de la humedad, la iluminacion, asi como la temperatura. Mayores temperaturas podrian causar que los comprimidos reales con el fin de hacer mas suave o incluso disolver. Fortalecer cualquier tipo de medicamento sin tocar a partir del dia de vencimiento. Mantener desde el lograr de los ninos.

Geriprost (Hytrin) Efectos negativos

Geriprost ofrece los efectos negativos. El mas tipico tienden a ser:

material de friccion migrana

palpitaciones cardiovasculares material de friccion

aturdimiento en material de friccion posicion

nauseas o vomitos material de friccion

material de friccion bloqueo

brazos inflamados, asi como material de friccion espinillas

un poco de material de friccion debilidad

aturdimiento material de friccion

material de friccion somnolencia

Mucho menos tipicos y graves efectos negativos en toda utilizando Geriprost: respuestas alergicas de reaccion (urticaria, inhalando y exhalando, cuestiones de alergia, asi como erupcion).

Los efectos negativos son indicaciones se basan en la medicacion que pueda estar utilizando, sino que ademas dependen de su estado de bienestar y otros aspectos.

Geriprost (Hytrin) Contraindicaciones

Por lo general no reciben Geriprost en caso de que son sensibles con el fin de elementos Geriprost.

Por lo general no reciben Geriprost si usted esta esperando otra manera tiene la intencion de tener un hijo, si no que realmente eres una mama medica.

Juega el papel de la utilizacion prudente Geriprost en caso de que usted esta utilizando analgesicos anti-inflamatorios no esteroideos, por ejemplo, Motrin y Naprosyn, algunos otros medicamentos de baja presion de la sangre, por ejemplo Dyazide, Vasotec, Verelan, Calan.

Si usted desea lograr mejores resultados, sin efectos negativos, es aconsejable evitar las bebidas alcoholicas.

Tenga cuidado en caso de dispositivo de viajar.

Por lo general, no dejar de fumar usando Geriprost de repente.

Geriprost (Hytrin) Preguntas comunes

Queen: ?Que es exactamente Geriprost?

El: Geriprost es realmente una excelente medicina que se consume en la reparacion de la presion arterial alta. Adicionalmente, se utiliza en el tratamiento de la hiperplasia prostatica inofensivo. Realmente esta funcionando a traves de endurecimiento de la clase especifica de la masa muscular dentro de la prostata con la puesta en marcha real de la bladder. A

Queen: Exactamente como debo conseguir Geriprost?

El: Geriprost viene en pastillas (1 miligramos, dos, cinco miligramos mg). Obten pildoras Geriprost por via oral con o sin comidas. Por lo general, no moler o incluso masticar esto. Obten Geriprost simultaneamente diaria junto con el agua potable. Si usted desea lograr mejores resultados por lo general no dejar de usar Geriprost todo de un sudden. A

Queen: Exactamente ?que debo FAG situacion asociada con sobredosis?

El: Por lo general no reciben pildoras Geriprost en grandes cantidades. En el caso de Geriprost mas de la dosis, usted tiene que comprobar hacia fuera medico o incluso medico instantly. A

Reina: ?Se puede realmente consumir alcohol?

El: Por supuesto que no, lo que realmente es inaceptable apreciar alcoholica beverages. A

Queen: ?Cuales son exactamente los efectos negativos Geriprost?

El: Geriprost ofrece los tipicos efectos negativos, por ejemplo, migrana, palpitaciones del corazon cardiovasculares, aturdimiento en posicion, nauseas o vomitos, obstruccion, inflamacion de los brazos, asi como las espinillas, alguna debilidad, mareo, somnolencia. Sin embargo en la situacion que se asocia con ser rechazado asociado con componentes Geriprost usted es capaz de encontrar efectos negativos mas graves: asociado con la reaccion alergica (dificultad junto con la inhalacion y la exhalacion, la inflamacion, los poros y la alergia de la piel o incluso colmenas). La probabilidad de efectos negativos a aparecer depende de la posicion de bienestar, asi como, naturalmente, en la receta Geriprost posterior correcta medications. A

Queen: ?Cuales son exactamente general, asi como las marcas asociadas con Geriprost?

El: Marca asociada con Geriprost Geriprost es en realidad. Titulo general asociada con Geriprost es en realidad Terazosina Hydrochloride. A

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Flavoxate Medlineplus Drug Information, Flavoxati

Flavoxate

Flavoxate is used to treat overactive bladder (a condition in which the bladder muscles contract uncontrollably and cause frequent urination, urgent need to urinate, and inability to control urination) relieve painful, frequent, or nighttime urination and urgency that may occur with infections of the prostate, bladder, or kidneys. Flavoxate is in a class of medications called antimuscarinics. It works by relaxing the bladder muscles. However, flavoxate is not an antibiotic; it does not cure infections.

How should this medicine be used?

Flavoxate comes as a tablet. Flavoxate usually is taken three or four times a day. This drug may be taken with or without food. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take flavoxate exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.

Other uses for this medicine

This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

What special precautions should I follow?

Before taking flavoxate,

tell your doctor and pharmacist what prescription and nonprescription medications you are taking, including vitamins.

tell your doctor if you have or have ever had glaucoma, ulcers, paralytic ileus, or obstructive disease (blockage) of the stomach, kidneys, or intestines.

tell your doctor and pharmacist if you are allergic to flavoxate or any other drugs.

tell your doctor if you are pregnant, plan to become pregnant, or are breast-feeding. If you become pregnant while taking flavoxate, call your doctor.

if you are having surgery, including dental surgery, tell the doctor or dentist that you are taking flavoxate.

you should know that this drug may make you drowsy. Do not drive a car or operate machinery until you know how this drug affects you.

remember that alcohol can add to the drowsiness caused by this drug.

What should I do if I forget a dose?

Take the missed dose as soon as you remember it. However, if it is almost time for the next dose, skip the missed dose and continue your regular dosing schedule. Do not take a double dose to make up for a missed one.

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Lamodex, Lamodex

Lamictal is used for treating certain types of seizures. It may be used alone or with other medicines. It may also be used to delay the occurrence of mood problems in certain patients with bipolar disorder. Lamictal is an anticonvulsant.

Use Lamictal as directed by your doctor.

Take Lamictal by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

Lamictal has a bitter taste. Do not crush or chew before swallowing. The tablet may be broken in half if your doctor tells you to do so.

Continue to take Lamictal even if you feel well. Do not miss any dose.

If you miss a dose of Lamictal, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Lamictal.

Store Lamictal at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Lamictal out of the reach of children and away from pets.

Active Ingredient: Lamotrigine.

Do NOT use Lamictal if:

you are allergic to any ingredient in Lamictal.

Some medical conditions may interact with Lamictal. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have liver, kidney, or heart problems; certain blood problems (eg, thalassemia); or if you receive dialysis treatment

if you have a skin rash or have ever developed a skin rash from taking Lamictal or any other medicines to treat seizures

if you have a history of mental or mood problems (eg, depression, suicidal thoughts or attempts).

Some medicines may interact with Lamictal. Tell your health care provider if you are taking any other medicines, especially any of the following:

Carbamazepine because it may decrease Lamictal's effectiveness, and the risk of side effects, such as dizziness, double vision, blurred vision, and decreased coordination, may be increased

Valproate (eg, valproic acid, divalproex sodium) because it may increase the risk of Lamictal's side effects

Estrogens, phenobarbital, phenytoin, primidone, rifampin, or succinimides (eg, methsuximide) because they may decrease Lamictal's effectiveness

Hormonal contraceptives (eg, birth control pills) because the effectiveness of both medicines may be decreased.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Lamictal may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Lamictal may cause drowsiness, dizziness, or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Lamictal with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Do not take more than the recommended dose or use for longer than prescribed without checking with your doctor.

Do not suddenly stop taking Lamictal or change your dose without checking with your doctor. Doing so may increase seizure frequency. If you need to stop taking Lamictal, your dose should be gradually reduced over a period of at least 2 weeks.

If you stop taking Lamictal for any reason, contact your doctor right away. Do not start taking it again unless your doctor tells you to. Discuss any questions or concerns with your doctor.

If you develop new or worsening seizures, contact your doctor right away.

Patients who take Lamictal may be at increased risk of suicidal thoughts or actions. The risk may be greater in patients who have had suicidal thoughts or actions in the past. Patients who have bipolar (manic-depressive) illness may also have an increased risk of suicidal thoughts or actions. Watch patients who take Lamictal closely. Contact the doctor at once if new, worsened, or sudden symptoms such as depressed mood; anxious, restless, or irritable behavior; panic attacks; or any unusual change in mood or behavior occur. Contact the doctor right away if any signs of suicidal thoughts or actions occur.

Hormonal birth control (eg, birth control pills) may change the amount of Lamictal in your blood. Talk to your doctor before you start or stop taking hormonal birth control while you are taking Lamictal. Women who take hormonal birth control may be at greater risk of side effects during the week of inactive pills in their pack. Contact your doctor if side effects, such as dizziness, decreased coordination, or double vision, occur.

Hormonal birth control (eg, birth control pills) may not work as well while you are using Lamictal. Check with your doctor if you have questions about how Lamictal might affect your hormonal birth control. Contact your doctor right away if you notice any unusual vaginal bleeding or spotting. If you wish to avoid pregnancy, talk with your doctor about the use of effective birth control methods.

Tell your doctor or dentist that you take Lamictal before you receive any medical or dental care, emergency care, or surgery.

Lab tests, including complete blood cell counts, may be performed while you use Lamictal. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Different medicines may look like or have names similar to Lamictal. Always check your medicine to make sure it is correct. If you notice any change in the appearance of your medicine (eg, shape, color, size, wording), check with your pharmacist.

Caution is advised when using Lamictal in children; they may be more sensitive to its effects, especially the risk of serious rash.

Increased sensitivity to the sun has been reported in some children taking Lamictal. Use a sunscreen or protective clothing if your child will be exposed to the sun. Discuss any questions or concerns with your doctor.

Lamictal should be used with extreme caution in children younger 18 years with bipolar disorder; safety and effectiveness in these children have not been confirmed.

Lamictal should be used with extreme caution in children younger than 2 years old; safety and effectiveness in these children have not been confirmed.

Pregnancy and breast-feeding: Lamictal may cause harm to the fetus. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of using Lamictal while you are pregnant. Lamictal is found in breast milk. Do not breastfeed while taking Lamictal.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Blurred or double vision; constipation; decreased coordination; diarrhea; dizziness; drowsiness; headache; nausea; painful menstrual periods; runny or stuffy nose; stomach upset or pain; tiredness; trouble sleeping; vomiting; weakness; weight loss.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); absent menstrual period or other menstrual changes; calf pain or tenderness; chest pain; dark urine; difficult or painful urination; fast or irregular heartbeat; fever, chills, or persistent sore throat; new or worsening mental or mood changes (eg, anxiety, depression, restlessness, irritability, panic attacks, behavior changes, suicidal thoughts or attempts); new or worsening seizures; pale stools; reddened, blistered, swollen, or peeling skin; severe muscle pain or tenderness; severe or persistent stomach pain; shortness of breath; sores in the mouth or around the eyes; swelling of the hands, ankles, or feet; swollen lymph glands; tremor; unusual bruising or bleeding; unusual weakness or tiredness; vaginal itching or discharge; vision changes; yellowing of the eyes or skin.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Lamictal is used for treating certain types of seizures. It may be used alone or with other medicines. It may also be used to delay the occurrence of mood problems in certain patients with bipolar disorder. Lamictal is an anticonvulsant.

Use Lamictal as directed by your doctor.

Take Lamictal by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

Lamictal has a bitter taste. Do not crush or chew before swallowing. The tablet may be broken in half if your doctor tells you to do so.

Continue to take Lamictal even if you feel well. Do not miss any dose.

If you miss a dose of Lamictal, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Lamictal.

Store Lamictal at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Lamictal out of the reach of children and away from pets.

Active Ingredient: Lamotrigine.

Do NOT use Lamictal if:

you are allergic to any ingredient in Lamictal.

Some medical conditions may interact with Lamictal. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have liver, kidney, or heart problems; certain blood problems (eg, thalassemia); or if you receive dialysis treatment

if you have a skin rash or have ever developed a skin rash from taking Lamictal or any other medicines to treat seizures

if you have a history of mental or mood problems (eg, depression, suicidal thoughts or attempts).

Some medicines may interact with Lamictal. Tell your health care provider if you are taking any other medicines, especially any of the following:

Carbamazepine because it may decrease Lamictal's effectiveness, and the risk of side effects, such as dizziness, double vision, blurred vision, and decreased coordination, may be increased

Valproate (eg, valproic acid, divalproex sodium) because it may increase the risk of Lamictal's side effects

Estrogens, phenobarbital, phenytoin, primidone, rifampin, or succinimides (eg, methsuximide) because they may decrease Lamictal's effectiveness

Hormonal contraceptives (eg, birth control pills) because the effectiveness of both medicines may be decreased.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Lamictal may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Lamictal may cause drowsiness, dizziness, or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Lamictal with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Do not take more than the recommended dose or use for longer than prescribed without checking with your doctor.

Do not suddenly stop taking Lamictal or change your dose without checking with your doctor. Doing so may increase seizure frequency. If you need to stop taking Lamictal, your dose should be gradually reduced over a period of at least 2 weeks.

If you stop taking Lamictal for any reason, contact your doctor right away. Do not start taking it again unless your doctor tells you to. Discuss any questions or concerns with your doctor.

If you develop new or worsening seizures, contact your doctor right away.

Patients who take Lamictal may be at increased risk of suicidal thoughts or actions. The risk may be greater in patients who have had suicidal thoughts or actions in the past. Patients who have bipolar (manic-depressive) illness may also have an increased risk of suicidal thoughts or actions. Watch patients who take Lamictal closely. Contact the doctor at once if new, worsened, or sudden symptoms such as depressed mood; anxious, restless, or irritable behavior; panic attacks; or any unusual change in mood or behavior occur. Contact the doctor right away if any signs of suicidal thoughts or actions occur.

Hormonal birth control (eg, birth control pills) may change the amount of Lamictal in your blood. Talk to your doctor before you start or stop taking hormonal birth control while you are taking Lamictal. Women who take hormonal birth control may be at greater risk of side effects during the week of inactive pills in their pack. Contact your doctor if side effects, such as dizziness, decreased coordination, or double vision, occur.

Hormonal birth control (eg, birth control pills) may not work as well while you are using Lamictal. Check with your doctor if you have questions about how Lamictal might affect your hormonal birth control. Contact your doctor right away if you notice any unusual vaginal bleeding or spotting. If you wish to avoid pregnancy, talk with your doctor about the use of effective birth control methods.

Tell your doctor or dentist that you take Lamictal before you receive any medical or dental care, emergency care, or surgery.

Lab tests, including complete blood cell counts, may be performed while you use Lamictal. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Different medicines may look like or have names similar to Lamictal. Always check your medicine to make sure it is correct. If you notice any change in the appearance of your medicine (eg, shape, color, size, wording), check with your pharmacist.

Caution is advised when using Lamictal in children; they may be more sensitive to its effects, especially the risk of serious rash.

Increased sensitivity to the sun has been reported in some children taking Lamictal. Use a sunscreen or protective clothing if your child will be exposed to the sun. Discuss any questions or concerns with your doctor.

Lamictal should be used with extreme caution in children younger 18 years with bipolar disorder; safety and effectiveness in these children have not been confirmed.

Lamictal should be used with extreme caution in children younger than 2 years old; safety and effectiveness in these children have not been confirmed.

Pregnancy and breast-feeding: Lamictal may cause harm to the fetus. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of using Lamictal while you are pregnant. Lamictal is found in breast milk. Do not breastfeed while taking Lamictal.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Blurred or double vision; constipation; decreased coordination; diarrhea; dizziness; drowsiness; headache; nausea; painful menstrual periods; runny or stuffy nose; stomach upset or pain; tiredness; trouble sleeping; vomiting; weakness; weight loss.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); absent menstrual period or other menstrual changes; calf pain or tenderness; chest pain; dark urine; difficult or painful urination; fast or irregular heartbeat; fever, chills, or persistent sore throat; new or worsening mental or mood changes (eg, anxiety, depression, restlessness, irritability, panic attacks, behavior changes, suicidal thoughts or attempts); new or worsening seizures; pale stools; reddened, blistered, swollen, or peeling skin; severe muscle pain or tenderness; severe or persistent stomach pain; shortness of breath; sores in the mouth or around the eyes; swelling of the hands, ankles, or feet; swollen lymph glands; tremor; unusual bruising or bleeding; unusual weakness or tiredness; vaginal itching or discharge; vision changes; yellowing of the eyes or skin.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Lisinopril Medlineplus Drug Information, Linopril

Lisinopril

Lisinopril is used alone or in combination with other medications to treat high blood pressure. It is used in combination with other medications to treat heart failure. Lisinopril is also used to improve survival after a heart attack. Lisinopril is in a class of medications called angiotensin-converting enzyme (ACE) inhibitors. It works by decreasing certain chemicals that tighten the blood vessels, so blood flows more smoothly and the heart can pump blood more efficiently.

High blood pressure is a common condition and when not treated, can cause damage to the brain, heart, blood vessels, kidneys, and other parts of the body. Damage to these organs may cause heart disease, a heart attack, heart failure, stroke, kidney failure, loss of vision, and other problems. In addition to taking medication, making lifestyle changes will also help to control your blood pressure. These changes include eating a diet that is low in fat and salt, maintaining a healthy weight, exercising at least 30 minutes most days, not smoking, and using alcohol in moderation.

How should this medicine be used?

Lisinopril comes as a tablet to take by mouth. It is usually taken once a day. To help you remember to take lisinopril, take it around the same time every day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take lisinopril exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.

Your doctor will probably start you on a low dose of lisinopril and gradually increase your dose.

Lisinopril controls high blood pressure and heart failure but does not cure them. Continue to take lisinopril even if you feel well. Do not stop taking lisinopril without talking to your doctor.

Other uses for this medicine

This medication may be prescribed for other uses; ask your doctor or pharmacist for more information.

What special precautions should I follow?

Before taking lisinopril,

tell your doctor and pharmacist if you are allergic to lisinopril; other ACE inhibitors such as enalapril (Vasotec, in Vaseretic), benazepril (Lotensin, in Lotrel), captopril (Capoten), fosinopril (Monopril), moexipril (Univasc, in Uniretic), perindopril (Aceon), quinapril (Accupril, in Accuretic, in Quinaretic), ramipril (Altace), and trandolapril (Mavik, in Tarka); any other medications; or any ingredients in lisinopril tablets. Ask your pharmacist for a list of the ingredients.

tell your doctor if you have diabetes and you are taking aliskiren (Tekturna, in Amturnide, Tekamlo, Tekturna HCT). Your doctor will probably tell you not to take lisinopril if you have diabetes and you are also taking aliskiren.

tell your doctor and pharmacist what prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking. Be sure to mention any of the following: aspirin and other nonsteroidal anti-inflammatory drugs (NSAIDs) such as indomethacin (Indocin, Tivorbex); diuretics ('water pills'); lithium (Lithobid); and potassium supplements. Your doctor may need to change the doses of your medications or monitor you carefully for side effects.

tell your doctor if you have or have ever had heart or kidney disease; diabetes; lupus; scleroderma (a condition in which extra tissue grows on the skin and some organs); or angioedema (a condition that causes difficulty swallowing or breathing and painful swelling of the face, throat, tongue, lips, eyes, hands, feet, ankles, or lower legs).

tell your doctor if you are breastfeeding.

if you are having surgery, including dental surgery, tell the doctor or dentist that you are taking lisinopril.

you should know that diarrhea, vomiting, not drinking enough fluids, and sweating a lot can cause a drop in blood pressure, which may cause lightheadedness and fainting.

What special dietary instructions should I follow?

Talk to your doctor before using salt substitutes containing potassium. If your doctor prescribes a low-salt or low-sodium diet, follow these directions carefully.

What should I do if I forget a dose?

Take the missed dose as soon as you remember it. However, if it is almost time for the next dose, skip the missed dose and continue your regular dosing schedule. Do not take a double dose to make up for a missed one.

What side effects can this medication cause?

Lisinopril may cause side effects. Tell your doctor if any of these symptoms are severe or do not go away:

cough

dizziness

headache

excessive tiredness

nausea

diarrhea

weakness

sneezing

runny nose

decrease in sexual ability

rash

Some side effects can be serious. If you experience any of these symptoms, call your doctor immediately:

swelling of the face, throat, tongue, lips, eyes, hands, feet, ankles, or lower legs

hoarseness

difficulty breathing or swallowing

fever, sore throat, chills, and other signs of infection

yellowing of the skin or eyes

lightheadedness

fainting

chest pain

Lisinopril may cause other side effects. Call your doctor if you have any unusual problems while taking this medication.

If you experience a serious side effect, you or your doctor may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online (http://www. fda. gov/Safety/MedWatch ) or by phone (1-800-332-1088).

What should I know about storage and disposal of this medication?

Keep this medication in the container it came in, tightly closed, and out of reach of children. Store it at room temperature and away from excess heat and moisture (not in the bathroom). Throw away any medication that is outdated or no longer needed. Talk to your pharmacist about the proper disposal of your medication.

In case of emergency/overdose

In case of overdose, call your local poison control center at 1-800-222-1222. If the victim has collapsed or is not breathing, call local emergency services at 911.

Symptoms of overdose may include the following:

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