Diclopal; Tablet, Med Manor Organics Pvt, Diclopal

DICLOPAL - Tablet, Med Manor Organics Pvt. Ltd.

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Dawabazar. in is a free content encyclopedia especially for pharmaceutical field. This website provides information about all manufacturing. marketing companies and their products, its compositions along with its dealers. retailers in India. This website also provides many findings on medicines, Pharma companies, Pharma dealers, Pharma retailers, active pharmaceutical ingredients, therapeutic index and pharmacological index which is useful for doctors. medical students and common person.

Buy Gastrointestinal - Tezosyn (Brand Name Hytrin) Online - Order Terazosin - Purchase Gastrointesti

Hytrin is used for treating high blood pressure and treating signs and symptoms of benign prostatic hyperplasia (BPH). Hytrin is an alpha-blocker. It works by relaxing muscles in the blood vessels, resulting in lowering of blood pressure. In BPH, alpha-blockers work by relaxing muscles around the urethra (tube that drains urine from the bladder), which improves urinary symptoms.

Use Hytrin as directed by your doctor.

Take Hytrin by mouth with or without food.

Hytrin may cause a sudden drop in blood pressure after the first dose. Take your first dose at bedtime. If you get up during the night, sit up slowly, then stand slowly.

If you miss a dose of Hytrin, 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. If more than one dose is missed, contact your doctor or pharmacist.

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

Store Hytrin 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 Hytrin out of the reach of children and away from pets.

Active Ingredient: Terazosin hydrochloride.

Do NOT use Hytrin if:

you are allergic to any ingredient in Hytrin or to similar medicines (eg, prazosin).

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

Some medical conditions may interact with Hytrin. 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 prostate cancer, angina pectoris, heart disease, or kidney or liver problems

if you will be having eye surgery.

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

Phosphodiesterase type 5 (PDE5) inhibitors (eg, sildenafil) or verapamil because severe dizziness, lightheadedness, or fainting may occur.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Hytrin 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:

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

Do not drink alcohol or use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are using Hytrin; it may add to their effects. Ask your pharmacist if you have questions about which medicines may cause drowsiness.

Hytrin may cause a sudden drop in blood pressure after the first dose. Take your first dose at bedtime. If you get up during the night, sit up slowly, then stand slowly. This will help to reduce your lightheadedness or dizziness. These effects are more likely to occur after the first few doses or if your dose has increased, but can occur at any time while you are taking the medicine. It can also occur if you stop taking the medicine and then restart treatment.

Hytrin 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.

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.

Do NOT take more than the recommended dose without checking with your doctor.

Hytrin may rarely cause a prolonged, painful erection. This could happen even when you are not having sex. If this is not treated right away, it could lead to permanent sexual problems such as impotence. Contact your doctor right away if this happens.

Tell your doctor or dentist that you take Hytrin before you receive any medical or dental care, emergency care, or surgery (including eye surgery).

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

Hytrin 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 Hytrin while you are pregnant. It is not known if Hytrin is found in breast milk. If you are or will be breast-feeding while you use Hytrin, 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:

Dizziness; drowsiness; lightheadedness; nasal congestion; nausea; weakness.

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); blurred vision or other vision changes; chest pain; decreased sexual desire or ability; fainting; fast, slow, or irregular heartbeat;painful, prolonged erection; severe or prolonged dizziness or headache; shortness of breath; swelling of the ankles, feet, or hands.

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.

Tamil Alphabet, Pronunciation And Language, Tomill

Tamil

The earliest known inscriptions in Tamil date back to 2,200 BC. Tamil literature emerged in around 300 BC, and the language used from then until the 700 AD is known as Old Tamil. From 700-1600 AD the language is known as Middle Tamil, and since 1600 the language has been known as Modern Tamil.

Tamil was originally written with a version of the Brahmi script known as Tamil Brahmi, and by the the 5th century AD this script had become more rounded and developed into the vaṭṭeḻuttu script. The modern Tamil script (தமிழ் அரிச்சுவடி tamiḻ ariccuvaṭi ), however, was created during the 7th century based on the Grantha script, as descendent of Brahmi. Over time the script has changed somewhat, and it was simplified in the 19th and 20th centuries.

The alphabet is well suited to writing literary Tamil, centamiḻ (செந்தமிழ்). However it is ill-suited to writing colloquial Tamil, koṭuntamiḻ (கொடுந்தமிழ்). During the 19th century, attempts were made to create a written version of the colloquial spoken language. Nowadays the colloquial written language appears mainly in school books and in passages of dialogue in fiction.

Notable features

Type of writing system: syllabic alphabet

Direction of writing: left to right in horizontal lines

When they appear the the beginning of a syllable, vowels are written as independent letters.

Some of the non-standard consonant-vowel combinations are not used in official documents.

The alphabet was originally written on palm leaves. As a result, the letters are made up mainly of curved strokes which didn't rip the leaves.

Used to write:

Tamil (தமிழ்), a Dravidian language spoken by around 52 million people in Indian, Sri Lanka, Malaysia, Vietnam, Singapore, Canada, the USA, UK and Australia. It is the first language of the Indian state of Tamil Nadu, and is spoken by a significant minority of people (2 million) in north-eastern Sri Lanka.

Tamil alphabet

Vowels and vowel diacritics

Non-standard consonant-vowel combinations

Dermesone, Dermesone

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Betnovate N

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DISCLAIMER: MediGuard is not intended to be a substitute for professional medical advice. MediGuard cannot and does not take into consideration every possible interaction or account for individual responses to medicine. Different individuals may respond to medication in different ways. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective, or appropriate for any given patient. Always seek the advice of a qualified health provider with any questions you may have before making any changes to your treatment. The use of the MediGuard site and its content is at your own risk. The MediGuard site and the information contained in it is intended for users in the United States and information in other countries may be different.

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Amopen Generic Name Amoxicillin Online, Amopen

Amopen General Information

Amopen - Pharmacology:

Amopen binds to penicillin-binding protein 1A (PBP-1A) located inside the bacterial cell well. Penicillins acylate the penicillin-sensitive transpeptidase C-terminal domain by opening the lactam ring. This inactivation of the enzyme prevents the formation of a cross-link of two linear peptidoglycan strands, inhibiting the third and last stage of bacterial cell wall synthesis. Cell lysis is then mediated by bacterial cell wall autolytic enzymes such as autolysins; it is possible that amoxicllin interferes with an autolysin inhibitor.

Amopen for patients

Amopen is an antibiotic for treatment of infection. Take at regular intervals, around the clock. Always finish course of therapy. Take with or without meals. May cause serious allergic reactions in those with penicillin allergy. May cause nausea, vomiting and diarrhea; notify your doctor or pharmacist if these occur.

This description is suitable for active ingredient Amoxicillin

Amopen Interactions

Probenecid decreases the renal tubular secretion of amoxicillin. Concurrent use of amoxicillin and probenecid may result in increased and prolonged blood levels of amoxicillin.

Chloramphenicol, macrolides, sulfonamides, and tetracy-clines may interfere with the bactericidal effects of penicillin. This has been demonstrated in vitro; however, the clinical significance of this interaction is not well documented.

Drug/Laboratory Test Interactions: High urine concentrations of ampicillin may result in false-positive reactions when testing for the presence of glucose in urine using CLINITEST ®. Benedictis Solution, or Fehlingis Solution. Since this effect may also occur with amoxicillin, it is recommended that glucose tests based on enzymatic glucose oxi-dase reactions (such as CLINISTIX ® ) be used.

Following administration of ampicillin to pregnant women, a transient decrease in plasma concentration of total conjugated estriol, estriol-glucuronide, conjugated estrone, and estradiol has been noted. This effect may also occur with amoxicillin.

Carcinogenesis, Mutagenesis, Impairment of Fertility:

Long-term studies in animals have not been performed to evaluate carcinogenic potential. Studies to detect mutagenic potential of amoxicillin alone have not been conducted; however, the following information is available from tests on a 4:1 mixture of amoxicillin and potassium clavulanate (AUGMENTIN). AUGMENTIN was non-mutagenic in the Ames bacterial mutation assay, and the yeast gene conversion assay. AUGMENTIN was weakly positive in the mouse lymphoma assay, but the trend toward increased mutation frequencies in this assay occurred at doses that were also associated with decreased cell survival. AUGMENTIN was negative in the mouse micronucleus test, and in the dominant lethal assay in mice. Potassium clavulanate alone was tested in the Ames bacterial mutation assay and in the mouse micronucleus test, and was negative in each of these assays. In a multi-generation reproduction study in rats, no impairment of fertility or other adverse reproductive effects were seen at doses up to 500 mg/kg (approximately 3 times the human dose in mg/m 2 ).

Pregnancy: Teratogenic Effects: Pregnancy Category B. Reproduction studies have been performed in mice and rats at doses up to 10 times the human dose and have revealed no evidence of impaired fertility or harm to the fetus due to amoxicillin. There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

Labor and Delivery: Oral ampicillin-class antibiotics are poorly absorbed during labor. Studies in guinea pigs showed that intravenous administration of ampicillin slightly decreased the uterine tone and frequency of contractions but moderately increased the height and duration of contractions. However, it is not known whether use of amoxicillin in humans during labor or delivery has immediate or delayed adverse effects on the fetus, prolongs the duration of labor, or increases the likelihood that forceps delivery or other obstetrical intervention or resuscitation of the newborn will be necessary.

Nursing Mothers: Penicillins have been shown to be excreted in human milk. Amopen use by nursing mothers may lead to sensitization of infants. Caution should be exercised when amoxicillin is administered to a nursing woman.

Pediatric Use: Because of incompletely developed renal function in neonates and young infants, the elimination of amoxicillin may be delayed. Dosing of AMOXIL should be modified in pediatric patients 12 weeks or younger (?3 months). ( See DOSAGE AND ADMINISTRATIONnNeonates and infants.)

Amorim Cork, Amoram

Synthetic closures are getting better all the time; isn’t it only a matter of time before existing problems are resolved?

It’s good that all closure manufacturers seek to improve their product. However, according to recent research, synthetic closures still have some way to go, especially in relation to oxidation and flavour ‘scalping’.

Cork on the other hand also continues to improve and retains all the benefits of a natural wine closure. So even if parallel advances are achieved by the plastic stoppers, we will be able to retain cork’s advantageous departing position.

Amorim launches world's first whole natural corks with proven non-detectable TCA guarantee

Amorim has achieved a major technological breakthrough to become the world’s first cork producer to deliver natural cork stoppers to winemakers in six countries with a non-detectable TCA guarantee*, using cutting-edge technology that has not only been successfully trialed, but which is also being independently validated on performance.

When it comes to wine closures, Amorim is worlds apart and our new video shows it

Amorim is the largest producer and supplier of cork stoppers worldwide and in whom the main wine producers trust.

Stefanie Costa and Paulo Castro students of Universidade de Aveiro won the first prize at the Glassberries Design Awards

A cerimonia de entrega de premios teve lugar pela primeira vez em Madrid, numa gala aberta ao publico no Medialab-Prado.

Brazil: Cork Stoppers mean quality wines

Consumers believe that cork best preserves the natural properties of wines.

Recycling of Cork Stoppers in France reverts to the fight against cancer

In the framework of the Ecobouchon recycling programme, Amorim Cork France collected 46 tons of cork stoppers.

Amorim Cork South Africa supports the Cape Winemakers Guild Protege Programme

Amorim Cork South Africa has associated itself to The Cape Winemakers Guild Protege Programme – a reputable training and mentoring initiative for future winemakers and vineyard owners.

A toast to cork!

High in the mountains of Portugal's Algarve region, correspondent Martha Teichner finds herself in “what feels like a misty, magic forest, where giant cork trees grow”.

The cork oak and natural cork play an instrumental role in the fight against climate changes

A well-managed cork oak forest can sequester 14.7 tons of CO 2 per hectare and per year

Natural cork closure adds value to the average price of a bottle and is a convincing sales pitch

A trend analysis using data from AC Nielsen on the TOP 100-selling premium wine brands in the USA shows that since 2010, the year when the study began, there has been a significant 30% increase in the market share of wines sealed with natural cork compared to a 9% increase in wines bottled with alternative wine closures.

Ervideira and Corticeira Amorim present Helix at El Corte Ingles

The first major wine packaging innovation of the 21st century was presented on the 24th of July by Ervideira (a wine producer in the region of Alentejo) and Corticeira Amorim at El Corte Ingles, in Lisbon.

Veuve Clicquot Cave Privee

350 bottles of Champagne were submerged into the sea at a depth of 43 m, in total darkness and a constant water temperature of around 4-6°C

Metamorphosis: Innovation and Creativity

The result of a process of research and development around the cork potential

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Cefalexin Uses, Side Effects, Interactions, Pictures, Warnings & Dosing, Axcel Cephalexin

Medicines & treatments centre

CEFALEXIN WARNINGS

Cefalexin should be used with caution by:

Patients who are penicillin-sensitive

Patients who have had allergic reactions to other drugs

Patients who have a severe kidney problem

Patients taking probenecid (treatment for gout )

Patients taking metformin (treatment for diabetes )

Patients taking other medicines for infections such as aminoglycosides and other cephalosporins

Patients taking furosemide (a water tablet - diuretic used to treat high blood pressure and /or heart failure )

Pregnancy and breast feeding

It should not be used by people who are allergic to cefalexin or have a known allergy to the cephalosporin group of antibiotics.

Also see list of precautions and interactions

STORAGE

Tablets or capsules: Do not store above 25?C. Keep containers tightly closed.

Oral suspensions: the dry powder should be stored below 25?C, whereas the suspension made up by the pharmacist should be stored in a refrigerator (2°C-8°C) and used within 14 days.

CEFALEXIN USES

What is it used for?

Cefalexin is used to treat certain types of bacterial infection.

It is a type of antibiotic known as a cephalosporin.

It is used to kill certain types of bacteria that cause infections.

In general this drug is used to treat a variety of bacterial infections, as it is a broad spectrum antibiotic. It is often used to treat urinary tract infections that have not responded to other drugs.

Benefits of being on this drug can include killing or stopping the bacterial growth of sensitive bacteria bringing relief from the symptoms of the infection.

Listed below are the typical uses of cefalexin.

Bacterial infections of the lungs and airways (respiratory tract), such as bronchitis and mild to moderate pneumonia

Bacterial infections of skin or soft tissue, such as wound infection

Bacterial infections of bones and joints

Bacterial infections of the urinary tract

Bacterial infections of the genitals

Bacterial infections of teeth or gums

Bacterial infections of middle ear (otitis media )

On occasion your doctor may prescribe this medicine to treat a condition not on the above list.

HOW TO USE/TAKE

How often do I take it?

This medication is available as tablets, capsules and as an oral suspension/syrup. The oral suspension is made up from cefalexin granules by adding water. The pharmacist normally does this at the time of dispensing.

Take this medication orally usually daily in divided doses, with or without food. Most infections require dosage every eight hours, but an appropriate frequency will be prescribed by doctor.

Use this medication for duration of prescription in order to get the most benefit from it.

Remember to use it at the same time each day - unless specifically told otherwise by your doctor.

It may take up to several days before the full benefit of this drug takes effect, depending on the type of infection.

Certain medical conditions may require different dosage instructions as directed by your doctor.

What dose?

Dosage is based on your age, gender, medical condition, response to therapy, and use of certain interacting medicines.

Do I need to avoid anything?

This medication is not known to affect driving or operating machinery. However, people should be aware of how they react to the medication before initiating these activities. Consult your doctor or pharmacist for more details.

When can I stop?

Always complete the full course as prescribed by your doctor.

CEFALEXIN SIDE EFFECTS

Diarrhoea

Indigestion

Abdominal pain

Changes in blood cell counts (some types of white blood cells, red blood cells and platelets)

Genital and anal itching

Genital infections, such as thrush

Vaginal inflammation

Vaginal discharge

Rash or itching

Skin wheals

Tiredness

Headaches

Dizziness

Hallucinations

Agitation

Confusion

Pain or inflammation of joints

Fever

Nausea and vomiting

Yellowing skin and eyes

Kidney inflammation

Other allergic reactions such as erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis or anaphylaxis

Slight increases in some liver enzymes

If any of these persist or you consider them severe then inform doctor or pharmacist.

Tell your doctor immediately if you develop any of the following symptoms:

Swelling of face. lips, tongue or throat

Rash or itching spots on arms and legs or severe, extensive, blistering skin rash

Fever, sore throat and joint pain with severe, extensive, blistering skin rash

Watery and/or bloody diarrhoea

Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.

A serious allergic reaction to this drug is unlikely, but seek immediate medical attention if it occurs. Symptoms of a serious allergic reaction include: rash, itching/swelling (especially of the face /tongue/throat), dizziness, trouble breathing.

This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.

The Yellow Card Scheme allows you to report suspected side effects from any type of medicine (which includes vaccines, herbals and over the counter medicines) that you are taking. It is run by the medicines safety watchdog called the Medicines and Healthcare products Regulatory agency (MHRA). Please report any suspected side effect on the Yellow Card Scheme website.

CEFALEXIN PRECAUTIONS

Before taking cefalexin, tell your doctor or pharmacist if you are allergic to it; or to other cephalosporins; or if you have any other allergies.

This medication should not be used if you have certain medical conditions. Before using this medicine, consult your doctor or pharmacist if you have:

Known allergy to the cephalosporin group of antibiotics

Before using this medication, tell your doctor or pharmacist your medical history, especially any of the following

Penicillin-sensitivity

Allergic reactions to other drugs

Severe kidney problem

Before having surgery, tell your doctor or dentist that you are taking this medication.

Does alcohol intake affect this drug?

Alcohol intake is not known to affect cefalexin.

The elderly. cefalexin should be used with caution in the elderly due to declining kidney function; therefore dosage adjustment may be necessary.

Pregnancy and breastfeeding - please ensure you read the detailed information below

PREGNANCY

Cefalexin is suitable to take during pregnancy, although caution should be exercised. Ask your doctor or pharmacist for advice before taking medication.

It is sensible to limit use of medication during pregnancy whenever possible. However, your doctor may decide that the benefits outweigh the risks in individual circumstances and after a careful assessment of your specific health situation.

If you have any doubts or concerns you are advised to discuss the medicine with your doctor or pharmacist.

BREAST FEEDING

Cefalexin is suitable to take if you are breastfeeding. However, caution should be taken when cefalexin is administered to breastfeeding women as cefalexin is excreted in breast milk. Ask your doctor or pharmacist for advice before taking medication.

It is sensible to limit use of medication during breastfeeding whenever possible. However, your doctor may decide that the benefits outweigh the risks in individual circumstances and after a careful assessment of your specific health situation.

If you have any doubts or concerns you are advised to discuss the medicine with your doctor or pharmacist.

CEFALEXIN INTERACTIONS

Before using this medicine, tell your prescriber of all the medicines you are taking including prescription medicines and medicines you have bought over the counter without a prescription. Tell your prescriber if you are taking vitamins or complementary remedies such as herbal products, as these can also interact with medicines.

If you are taking more than one medicine, these may interact with each other. Your prescriber may decide to use medicines which interact with each other if the benefit outweighs the risks. In these cases, the dose of your medicines may need to be adjusted or you may be monitored more closely.

The following medicines may interact with cefalexin:

Blood-thinning medicines, such as warfarin

Probenecid used to treat gout

Metformin used in the treatment for diabetes

Aminoglycosides and other cephalosporins (treatment for infections)

Diuretics (also known as water tablets) such as furosemide

This information does not contain all possible interactions. Therefore, tell your prescriber of all the products you are using before taking this medicine.

If you have a question or want to discuss anything about your medicine, speak to your local pharmacist.

CEFALEXIN OVERDOSE

Symptoms of overdose may include nausea, vomiting. epigastric distress (stomach pain), diarrhoea and haematuria (presence of blood in the urine ).

In the event of severe overdosage, general supportive care in hospital is recommended, including close clinical and laboratory monitoring of blood, kidney and liver functions, and blood clotting status until the patient is stable.

If you think you, or someone you care for, might have accidentally taken more than the recommended dose of cefalexin or intentional overdose is suspected, contact your local hospital, GP or if in England call 111. In Scotland call NHS 24. In Wales, call NHS Direct Wales. In the case of medical emergencies, always dial 999.

MISSED DOSE

If you miss a dose, take it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.

Provera - Woman S Health, Mepastat

Common use Provera contains medroxyprogesterone acetate, female hormone used to regulate ovulation and menstrual periods. The medication is used to treat secondary amenorrhea and abnormal uterine bleeding caused by hormonal imbalance (fibroids, uterine cancer), to reduce the incidence of endometrial hyperplasia in postmenopausal women.

Dosage and direction Take 5 or 10 mg of this medication daily for 5 -10 days. Take in strict accordance with recommendations of your doctor. Avoid taking larger amounts of the medication. Your doctor may administer to start taking the medication on a certain day of your menses. While you are on Provera, examine your breasts for lumps on a monthly basis. Provera may change results of certain medical tests. Inform your doctor that you are taking this drug.

Precautions Do not smoke while taking Provera, unless risk of blood clotting increases. Inform your doctor about conditions you may have as dose adjustment may be required: hypertension, heart disease, recent stroke or heart attack, congestive heart failure, hypercalcinemia, high cholesterol or triglycerides, recent miscarriage or abortion, severe pelvic pain, asthma, migraine headaches, epilepsy, a thyroid disorder, diabetes, kidney disease, lupus, depression.

Do not take this medication if you have hypersensitivity to its components, pregnant, suffer with a hormone-related cancer of genitals or mammary gland, abnormal vaginal bleeding that has not been diagnosed, have liver disease, a history of stroke or blood clot, or breastfeed.

Side effects The most frequent side effects of Provera are headache, dizziness, irritability, insomnia, drowsiness, fatigue, depression, nausea, abdominal pain, thrombophlebitis, cerebrovascular disorders, hypersensitivity nipple breast, galactorrhoea, erosion of the cervix, dysmenorrhea. High doses of the medication may produce acne, hirsutism, changes in body weight, moon face, hyperthermia, alopecia. Allergic reactions such as hives, rash, facial swelling and difficulty breathing are also possible.

Aminoglutethimide reduces plasma concentrations and reduces efficiency of Provera. Inform your doctor about all prescribed and over-the-counter medications, herbal products, vitamins and food supplements you use.

Missed dose Never take a double dose of this medication. If it is almost time of the next dose, just skip the missed portion and continue taking the medicine according to the schedule.

Overdose Overdose symptoms may be: dizziness, drowsiness, stomach pain, nausea, vomiting, breast tenderness, or vaginal bleeding. Seek immediate medical help if you experience the symptoms listed above.

Storage Store at room temperature between 20-25 C (68-77 F). Store away from moisture, heat, and sunlight. It is not recommended to store in a bathroom and places available for children.

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.

Common use Provera contains medroxyprogesterone acetate, female hormone used to regulate ovulation and menstrual periods. The medication is used to treat secondary amenorrhea and abnormal uterine bleeding caused by hormonal imbalance (fibroids, uterine cancer), to reduce the incidence of endometrial hyperplasia in postmenopausal women.

Dosage and direction Take 5 or 10 mg of this medication daily for 5 -10 days. Take in strict accordance with recommendations of your doctor. Avoid taking larger amounts of the medication. Your doctor may administer to start taking the medication on a certain day of your menses. While you are on Provera, examine your breasts for lumps on a monthly basis. Provera may change results of certain medical tests. Inform your doctor that you are taking this drug.

Precautions Do not smoke while taking Provera, unless risk of blood clotting increases. Inform your doctor about conditions you may have as dose adjustment may be required: hypertension, heart disease, recent stroke or heart attack, congestive heart failure, hypercalcinemia, high cholesterol or triglycerides, recent miscarriage or abortion, severe pelvic pain, asthma, migraine headaches, epilepsy, a thyroid disorder, diabetes, kidney disease, lupus, depression.

Do not take this medication if you have hypersensitivity to its components, pregnant, suffer with a hormone-related cancer of genitals or mammary gland, abnormal vaginal bleeding that has not been diagnosed, have liver disease, a history of stroke or blood clot, or breastfeed.

Side effects The most frequent side effects of Provera are headache, dizziness, irritability, insomnia, drowsiness, fatigue, depression, nausea, abdominal pain, thrombophlebitis, cerebrovascular disorders, hypersensitivity nipple breast, galactorrhoea, erosion of the cervix, dysmenorrhea. High doses of the medication may produce acne, hirsutism, changes in body weight, moon face, hyperthermia, alopecia. Allergic reactions such as hives, rash, facial swelling and difficulty breathing are also possible.

Aminoglutethimide reduces plasma concentrations and reduces efficiency of Provera. Inform your doctor about all prescribed and over-the-counter medications, herbal products, vitamins and food supplements you use.

Missed dose Never take a double dose of this medication. If it is almost time of the next dose, just skip the missed portion and continue taking the medicine according to the schedule.

Overdose Overdose symptoms may be: dizziness, drowsiness, stomach pain, nausea, vomiting, breast tenderness, or vaginal bleeding. Seek immediate medical help if you experience the symptoms listed above.

Storage Store at room temperature between 20-25 C (68-77 F). Store away from moisture, heat, and sunlight. It is not recommended to store in a bathroom and places available for children.

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.

Common use Provera contains medroxyprogesterone acetate, female hormone used to regulate ovulation and menstrual periods. The medication is used to treat secondary amenorrhea and abnormal uterine bleeding caused by hormonal imbalance (fibroids, uterine cancer), to reduce the incidence of endometrial hyperplasia in postmenopausal women.

Dosage and direction Take 5 or 10 mg of this medication daily for 5 -10 days. Take in strict accordance with recommendations of your doctor. Avoid taking larger amounts of the medication. Your doctor may administer to start taking the medication on a certain day of your menses. While you are on Provera, examine your breasts for lumps on a monthly basis. Provera may change results of certain medical tests. Inform your doctor that you are taking this drug.

Precautions Do not smoke while taking Provera, unless risk of blood clotting increases. Inform your doctor about conditions you may have as dose adjustment may be required: hypertension, heart disease, recent stroke or heart attack, congestive heart failure, hypercalcinemia, high cholesterol or triglycerides, recent miscarriage or abortion, severe pelvic pain, asthma, migraine headaches, epilepsy, a thyroid disorder, diabetes, kidney disease, lupus, depression.

Do not take this medication if you have hypersensitivity to its components, pregnant, suffer with a hormone-related cancer of genitals or mammary gland, abnormal vaginal bleeding that has not been diagnosed, have liver disease, a history of stroke or blood clot, or breastfeed.

Side effects The most frequent side effects of Provera are headache, dizziness, irritability, insomnia, drowsiness, fatigue, depression, nausea, abdominal pain, thrombophlebitis, cerebrovascular disorders, hypersensitivity nipple breast, galactorrhoea, erosion of the cervix, dysmenorrhea. High doses of the medication may produce acne, hirsutism, changes in body weight, moon face, hyperthermia, alopecia. Allergic reactions such as hives, rash, facial swelling and difficulty breathing are also possible.

Aminoglutethimide reduces plasma concentrations and reduces efficiency of Provera. Inform your doctor about all prescribed and over-the-counter medications, herbal products, vitamins and food supplements you use.

Missed dose Never take a double dose of this medication. If it is almost time of the next dose, just skip the missed portion and continue taking the medicine according to the schedule.

Overdose Overdose symptoms may be: dizziness, drowsiness, stomach pain, nausea, vomiting, breast tenderness, or vaginal bleeding. Seek immediate medical help if you experience the symptoms listed above.

Storage Store at room temperature between 20-25 C (68-77 F). Store away from moisture, heat, and sunlight. It is not recommended to store in a bathroom and places available for children.

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.

Ibugel Gel, Ibugel

IBUGEL GEL

Transcript

PACKAGE LEAFLET Information for the user

IBUGEL ibuprofen 5% w/w

Read all of this leaflet carefully before using this product. Keep this leaflet. You may need to read it again. Ask your doctor or pharmacist if you need more information or advice. You must contact a doctor if your symptoms worsen or do not improve after a few weeks. 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.

1. WHAT IBUGEL IS AND WHAT IT IS USED FOR

• Ibugel is an anti-inflammatory painkiller applied to, and absorbed through, the skin. • It is for the treatment of the following conditions involving the musculoskeletal system: • backache • rheumatic or muscular pain • sprains • strains • neuralgia. • It is also for pain relief in common arthritic conditions. • Ibugel is recommended for use by adults, the elderly and children over the age of 12 years. Children under the age of 12 may also use it if recommended by their doctor. • The active ingredient in this product is ibuprofen. This is one of a group of medicines known as non-steroidal anti-inflammatory drugs (NSAIDs). • Ibuprofen works by: • relieving pain • reducing swelling and inflammation.

2. BEFORE YOU USE IBUGEL

Do not use Ibugel: • if you are allergic (hypersensitive) to ibuprofen or any of the other ingredients of Ibugel listed in Section 6; • if you are asthmatic, or suffer from rhinitis (allergic runny nose) or urticaria (hives) and have ever had a bad reaction to aspirin, ibuprofen or other NSAIDs in the past; • if you are pregnant or breast-feeding; • on broken, damaged, infected or diseased skin. Before applying this product for the first time, make sure it is suitable for you to use: Because Ibugel is delivered through the skin, directly over the painful area, there is less risk of the complications that sometimes occur when ibuprofen (or a similar anti-inflammatory painkiller) is taken by mouth. However, in rare cases you may be at risk: • if you have a stomach ulcer (also called a peptic or gastric ulcer); • if you have ever had kidney problems; • if you have ever had asthma; • if you have ever had a bad reaction to aspirin or ibuprofen taken by mouth.

If any of the above apply to you, only use this product on advice from your doctor or pharmacist. Take special care when using this product: • Use it only on the skin. • Do not use it on children under 12 years old unless advised by a doctor. • Do not apply it to broken or irritated skin. • Keep the gel away from the eyes, nose and mouth. Using other medicines • Interaction between Ibugel and blood pressure lowering drugs and anticoagulants (medicines that stop blood clotting) is possible, in theory, although very unlikely. If you would like more advice about this, speak to your doctor or pharmacist. • If you are also taking aspirin or other NSAIDs by mouth, discuss this beforehand with your doctor or pharmacist because these may increase the risk of undesirable effects. • Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines including other medicines obtained without prescription. Pregnancy and breast-feeding You should not use Ibugel if you are pregnant or breast-feeding. Driving and using machinery Using this product is not known to affect your ability to drive or use machinery. Important information about one of the ingredients of Ibugel The product contains a small amount of propylene glycol. This ingredient may cause skin irritation in a small number of people who are intolerant to it. If your doctor has told you that you have an intolerance to propylene glycol, please talk to your doctor before using this product.

3. HOW TO USE IBUGEL

Before using this tube of gel for the first time, open it as follows: • U nscrew the cap, turn it upside down and then use the sharp point of the cap to pierce the membrane in the neck of the tube. The tube squeezer key: To make Ibugel easier and more economical to use, a blue tube squeezer key has been provided. Once fitted to the tube, simply turning the key will dispense the gel more easily for patients who experience difficulties in squeezing tubes. For economy, the key will also help expel the last few grams of Ibugel when the tube is nearly empty. continued…

In this leaflet: 1. What Ibugel is and what it is used for 2. Before you use Ibugel 3. How to use Ibugel 4. Possible side effects 5. How to store Ibugel 6. Further information

To use the gel (for adults, the elderly and children over 12 years old): • Use the gel up to three times a day, or as often as advised by your doctor. • Lightly apply the gel to intact skin over the painful area. • Apply only enough gel to thinly cover the affected area, then massage gently until absorbed. • Wash hands after use, unless treating them. • Carry on using the gel in this way until your condition gets better (you may find you need to use it for a few weeks, and your doctor may want you to continue using it for longer than this). • If your symptoms worsen or continue for more than a few weeks, discuss this with your doctor before continuing treatment. If the gel comes into contact with broken skin or gets into the eyes, nose or mouth • The product may cause irritation if it comes into contact with broken skin or gets into the eyes, nose or mouth. If this happens, rinse the affected areas with plenty of water. If rinsing one eye, take care to avoid washing product into the other eye. If irritation persists, tell your doctor or pharmacist. If the gel is accidentally swallowed • Symptoms may include headache, vomiting, drowsiness and low blood pressure. • If you experience any of these symptoms contact a doctor or hospital straight away. If you forget to use this product Do not worry if you occasionally forget to use this product, just carry on using it when you remember. If you have any further questions on the use of this product, ask your doctor or pharmacist.

4. POSSIBLE SIDE EFFECTS

Like all medicines, Ibugel can cause side effects, although not everybody gets them. Occasionally, mild skin rashes, itching or irritation can sometimes occur at the site of application. If this is unacceptable, or persists, stop using the product and tell your doctor or pharmacist. Very rarely, the following side effects can happen with ibuprofen, although these are extremely uncommon with products such as Ibugel that are applied to the skin. If you experience any of the following, stop using Ibugel immediately and tell your doctor: • Allergic reactions (particularly in people who have a history of asthma or allergic problems), such as:

• u nexplained runny nose and watery eyes, or, in more serious cases asthma or aggravated asthma involving breathing difficulties, wheezing or chest tightness; • generalised allergic skin reactions involving itch, swelling, inflammation, redness and perhaps blistering and light sensitivity; • other more serious generalised allergic reactions possibly involving unexplained nausea and vomiting, swollen eyes, face or tongue, difficulty swallowing, dizziness or light-headedness. Unconsciousness could perhaps occur in the most serious cases. • Kidney problems (particularly in people who have a history of kidney disease), such as: • decreased urine volume; • loss of appetite / weight loss; • swelling to abdomen. • Problems with the digestive system (particularly in people who have a history of stomach ulcers etc), such as: • stomach pain; • heartburn / indigestion. If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist. 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.

Keep it out of the reach and sight of children. Always replace the cap tightly after use. Do not store the product above 25°C. Do not use after the expiry date shown on the fold of the tube and the carton. The expiry date refers to the last day of that month. • Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.

6. FURTHER INFORMATION ABOUT IBUGEL

What Ibugel contains: The active ingredient is ibuprofen (5% w/w). The other ingredients are industrial methylated spirit, carbomers, propylene glycol, diethylamine and purified water. What Ibugel looks like and contents of the pack • The product is a clear, colourless gel that contains no fragrance. • The gel is available in tubes containing 100g. The packs also contain a tube key. The Marketing Authorisation holder is Dermal Laboratories, Tatmore Place, Gosmore, Hitchin, Herts, SG4 7QR, UK. The Manufacturer is Fleet Laboratories Ltd, 94 Rickmansworth Road, Watford, Herts, WD18 7JJ, UK. This leaflet was last revised in March 2015. To listen to or request a copy of this leaflet in Braille, large print or audio, please call free of charge: 0800 198 5000 (UK only). Please be ready to give the following information: Ibugel, 00173/0050. This is a service provided by the Royal National Institute of Blind People (RNIB).

To fit the tube squeezer key: • Ensure that the tube nozzle has been pierced using the point of the cap. • Slide the slit of the key over the folded end of the tube. • Carefully turn the key to roll up the tube until the required amount of gel has been expelled. • Always replace the cap after use, leaving the key in place on the end of the tube.

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.

Pain Relief For Headaches, Migraines & Minor Arthritis, Advilcaps

Advil ® temporarily reduces fever and relieves minor aches and pains due to: headache, the minor pain of arthritis, toothache, backache, menstrual cramps, the common cold and muscular aches.

If you are pregnant or nursing a baby, you should seek the advice of a health professional before using Advil ®. Do not use ibuprofen during the last three months of pregnancy unless directed by a physician.

Advil ® Liqui-Gels ®. Advil ® Migraine and Advil ® PM Liqui-Gels ® all contain a wheat derivative, and are not gluten-free. Check with your doctor if you have any concerns about taking this product.

When taken as directed, adverse effects on the liver are uncommon. Effects on the liver are rare but may include liver disorder, abnormal liver function, hepatitis and jaundice, and, they may occur at higher than recommended OTC doses. Consult your physician before taking Advil ® if you have liver cirrhosis, or any other concerns about taking this product.

One of the main classes of chemicals that the body produces as part of the inflammatory process is prostaglandins, which produce pain and fever. Advil ® temporarily blocks the body's production of prostaglandins, reducing pain and fever.

Form is a matter of preference, as each is effective as indicated by label. Tablets are the original round form of Advil ®. which has been trusted by millions for over 30 years. Oblong-shaped Advil ® are called caplets — which are available with a gel coating (gel caps) so they’re easier to swallow. Advil ® Liqui-Gels ® don’t just look different from the others, they are different as they contain solubilized ibuprofen. Consequently they’re absorbed into the body more quickly for faster pain relief. Fast acting Advil ® Film-Coated Tablets have a Rapid Release Formula with a core of ibuprofen sodium, a salt form of ibuprofen that is much more soluble in water than standard ibuprofen. Because they are more soluble, they dissolve fast, and can be absorbed into the body fast.

It is not necessary to take Advil ® with food, however, take it with food or milk if an upset stomach occurs. Consult your physician before taking any NSAID or if you have a history of stomach problems such as heartburn, upset stomach or stomach pain.

NSAIDs, nonsteroidal anti-inflammatory drugs, are a group of chemical compounds that often are chemically unrelated but share therapeutic actions such as analgesic (pain-relieving) and antipyretic (used reduce fever) effects.

Most retail grocery, pharmacy and convenience stores carry a variety of Advil ® products. Please check our "Buy Now" page on this website to locate a store near you that carries our products. You may also find online stores that carry the products on this page as well.

Yes! Advil ® Menstrual Pain treats menstrual cramps, as well as headaches, backaches, and muscle aches, which are all pains women commonly experience with their period (and Advil ® Menstrual Pain will treat these pains even if you don’t have your period!). Please refer to the product label for a full list of uses.

Advil ® Menstrual Pain is formulated with ibuprofen sodium, a salt form of ibuprofen that dissolves differently from standard ibuprofen (which is in Advil ® Tablets). While there is no difference in effectiveness between Advil ® Menstrual Pain and Advil ® Film-Coated, we saw an unmet need for a pain reliever targeted to women which provides powerful relief of all the pains associated with periods. Consequently we created Advil ® Menstrual Pain!

No. Unlike certain combination products, Advil ® Menstrual Pain is caffeine free and antihistamine free, so it won’t keep you up at night or make you sleepy during the day. Advil ® Menstrual Pain contains ibuprofen sodium, a powerful pain reliever which targets the cause of your menstrual pain for up to six hours of relief.

You can buy Advil ® Menstrual Pain at many national retailers including Target, CVS, Rite-Aid, and Walmart. Look for it with menstrual pain relievers in the OTC aisle, or in the Feminine Hygiene aisle. We do recommend contacting your local store to confirm they have it in stock though.

About Melo Kan, Melokan

Melo KAN

Biography

Fusing an eclectic blend of passion and insightful lyricism, Melo creates a sound that resonates universally. To put it simply, Melo is not an artist created in a demographic vacuum. His stories of struggle and triumph transcend age, race, and demographic barriers and serve as inspiration to a generation lacking any definitive leadership. His artistry stands out in an industry of sameness as he pushes the limits of creativity while balancing the needs of his listeners who crave much more than just a short sugar high. Melo says, “Nobody makes albums that people can still listen to years down the line anymore. I strive to make records so complete that ten years later when you listen, you’ll say damn I wish brotha’s still made records like this!” Similar to early rap pioneers such as Public Enemy, Ice Cube, and Grandmaster Flash; there is a message in Melo’s music. While he believes music should be fun, he also believes it should address socioeconomic issues of the time. Melo says “I was told when I get my turn to speak; I should have something important to say.” With songs like “So Cold” off 2007’s EPU album, where Melo addresses the despondent issues of homelessness and “H. A.T. E”, also off EPU, where he deliberates on the racial divisiveness in America; Melo definitely provides a voice that Hip Hop is in desperate need of.

Melo founded his own company in 2002; 4LB (four pound) Musik. Under this umbrella, Melo’s extensive catalog of music stretches over ten mixtapes, two underground releases and six officially released albums on Itunes. His songs have been featured on Inland Empire’s Wild 97 and his radio drops for Julio G and DJ Dense were getting spins on Los Angeles’s 93.5 KDAY. Melo more recently has had his song featured as the 1st track on both DJ Green Lantern's Overtime Grind Pt 2 and DJ Drama's 3rd Infantry Division Pt 2! Both songs were tracks off the Mama's Only Sun EP.

As far as live performances, Melo has shared stages with the likes of Little Brother, Dead Prez, and Nappy Roots. He recently toured with a soul artist K. D. Brosia in addition to running thru sets at SXSW and A3C festivals sponsored by the likes of ALLHIPHOP. COM. Whether his set is with resident DJ’s Swank or Mino from his 4LB camp, or with a live band, Melo leaves the crowd in a passionate daze, emotionally drawn in becoming literal parts of the performance itself.

Melo’s grind is a result of pure dedication and shear will at times. With no assistance from managers or investors, Melo continues to come up with innovative ways to push his music and brand to the public. Although Melo had the opportunity to collab with several heavy hitters Ric Rude, 1500 or Nothin' and Kendrick Lamar on the Mama's Only Sun EP, his full length follow up, The Heart of the City, will be solely produced by industry renowned THX. "Not only is it some of my best material, but the level of musicianship going into this project will definitely leave the listener feeling fullfilled”, Melo says. With all of Melo’s accomplishments, and intentions, the question still remains; are people really ready for an artist like Melo? Do people really want music that speaks to them directly and touches them emotionally? Every live performance proves that they are and Melo shows no signs of slowing down.

Other Info

Record Label: 4LB Records Record label website: http://melokan. com/ Cover band: No

Links

Lyrics

Love You

Written By . Melo KAN

Hook: Its somethin' that i wanted to say, but somethin' always got in the way, for everytime that you cried out lookin' for a shoulder to take, I was there for you givin' you strength, you know why because I. Love you (repeat)

Verse 1: I recall those times too, so no you don't have to remind me, I cried too, letting all the happiness blind me, i held you, in the highest regard, you couldn't see it, I would see you and just try to be hard, 'cause im a knucklehead, knowin' that i've missed you all week, you a freak, plus i love when you rub on my head, when i'm sleep, you're the closest thing that i've ever had to complete, but i still couldn't give you that title, why you gettin mad? Hate seeing tears in your eyes, i know you tried, and you stayed saying "tell me its mine" and i would lie and say it is, knowing that my heart was in the mix with a woman and her kid I just wasn't as prepared as I thought, thinkin' that you'd always be there, and I could break your little heart and repair it, but it got old to you, you don't even know do you? how much I know that I owe you, I just couldn't find the way to show you but.

hook: Its somethin' that i wanted to say, but somethin' always got in the way, for everytime that you cried out lookin' for a shoulder to take, I was there for you givin' you strength, you know why because I. Love you (repeat)

Verse 2: You ain't alone lady, you ain't the only one hurt, you ain't the only person goin' thru it, shyt cause I'm goin' through it, like yellow lights, crash and burn hello life, its been a while since I petaled this path, it's been a while since i felt the same thing that she had, i was a child when i felt the same thing that she had, was in denial for a minute 'bout how you were feelin' 'cause I knew about those demons you had off in your past, it didn't matter 'cause the fact was that we were just cool, people swore we were fukkn but we were just cool, i kept you close to me then i started gettin' possessive thats when i knew i had to find me an exit and so i took one, didn't wanna hurt you or desert you, but earth you gotta let the sun shine, patience is a virtue, later down the line it may be worth it, or it may be worthless, but right now is all we've got to work with

hook: Its somethin' that i wanted to say, but somethin' always got in the way, for everytime that you cried out lookin' for a shoulder to take, I was there for you givin' you strength, you know why because I. Love you (repeat)

Verse 3: Look I know it ain't right for me to be like, that this is my life, and you can just leave, then you tell me that you can't be with no one else, and got sick when I told you there was some one else, but i was torn, i didn't know these feelings had formed beneath the surface where i kept them deformed, 'cause whats love got to do with anything besides drama and stress, paranoid insecurities is heightened now we fightin' and its frieghtnin' how you tell me that you love me so much, and i could never say it back, a devastating fact, but I felt you, I still do now, you used to tell me when you're gone I'm a wish you were back and you was right, but i knew all along, the same way you know its you in this song, the hardest thing i've had to do was move on, but life happens and we learn through the madness to be strong, wish i had the nerve to say it before, but guess what.

hook:Its somethin' that i wanted to say, but somethin' always got in the way, for everytime that you cried out lookin' for a shoulder to take, I was there for you givin' you strength, you know why because I. Love you (repeat)

Discography

(2015) Sho Out - Single

(2014) Push Thru - Single

(2014) Bluez Man - Single

(2013) Smilez N Kriez Vol. II

(2012) Mama's Only Sun - EP

(2010) The Unkomfortable Silence - Street Album (2009)Bring Da Blues II-EP (2007)E. P.U - LP (2007)Nikka Pleez!-Mixtape (2006)Melokan. com-Mixtape (2006)How 2 Rap 101(2discs)-Mixtape (2006)Roc or Bust-Mixtape (2005)The Appetizer-Mixtape (2005)Blokk Movement The Streetqual 2.1-Mixtape (2005)Blokk Movement Part 2-Mixtape (2004)Blokk Movement-Mixtape (2001)Bring The Bluez-LP (2002)The Kantradikshun-LP

(2005) "My Hood" *single WILD96 in L. A.

Set List

Set list varies. Typical set can be from 15-30 minutes in length. Always uses original lyrics although he has been known to incorporate industry beats in his show.

Diet, Sehat, Dan Kaya Omeprazole, Ulpraz

Omeprazole, Obat apa sih?

Omeprazole termasuk dalam kelompok obat pompa proton inhibitor (PPi). Omeprazole digunakan untuk mengobati gejala penyakit gastroesophageal reflux (GERD ) dan kondisi lain yang disebabkan oleh asam lambung berlebih. Hal ini juga digunakan untuk mempercepat penyembuhan esofagitis erosif (kerusakan kerongkongan Anda yang disebabkan oleh asam lambung ).

Obat bekerja menghambat asam lambung dengan cara berikatan dengan H+/K+ ATP Ase (pompa proton) Omeprazole juga dapat diberikan bersamaan dengan antibiotik untuk mengobati ulkus lambung yang disebabkan infeksi Helicobacter pylori (H. pylori ). Omeprazole bukan untuk bantuan langsung dari gejala sakit maag.

Informasi penting tentang omeprazole Omeprazole bukan untuk bantuan langsung dari gejala sakit maag . Obat ini jangan dikunyah. Minum obat 30-60 menit sebelum makan, sebaiknya pagi hari. Efetivitas PPi dapat turun pada perokok. Walaupun gejala-gejala dapat segera membaik, terapi obat harus tetap diteruskan selama waktu tertentu.

Beberapa kondisi yang diobati dengan kombinasi dari omeprazole dan antibiotik. Gunakan semua obat seperti yang diarahkan oleh dokter Anda. Baca panduan pengobatan atau instruksi yang diberikan pasien dengan obat-obatan masing-masing. Jangan mengubah dosis atau jadwal pengobatan tanpa saran dokter Anda. Anda tidak harus minum obat ini jika Anda alergi terhadap omeprazol atau kepada obat benzimidazole lain seperti Albendazole. atau mebendazole . Obat ini diminum l hanya sekali setiap 24 jam selama 14 hari. Obat ini akan memberi efek penuh setelah pemakaian 4 hari. Jangan meminum lebih dari satu tablet setiap 24 jam. Cari bantuan medis darurat jika Anda memiliki nyeri dada atau rasa berat. nyeri menyebar ke lengan atau bahu. mual, berkeringat, dan perasaan sakit umum. Tanyakan dokter atau apoteker apakah aman bagi Anda untuk mengambil omeprazol jika Anda memiliki penyakit hati atau penyakit jantung, atau rendahnya tingkat magnesium dalam darah Anda.

Berdasarkan FDA ( Food Drug Asociation ) obat ini masuk kedalam kategori C pada wanita hamil. Tidak diketahui apakah omeprazol akan membahayakan bayi yang belum lahir.

Katakan kepada dokter Anda jika Anda sedang hamil atau merencanakan untuk hamil ketika menggunakan obat ini. Omeprazole dapat masuk ke dalam ASI dan dapat membahayakan bayi menyusui. Anda tidak harus menyusui saat Anda mengambil omeprazol. Jangan memberikan obat ini kepada seorang anak dibawah 1 tahun tanpa saran dari dokter.

Bagaimana saya harus meminum omeprazole ? Minum omeprazol seperti yang ditentukan oleh dokter Anda. Jangan minum dalam jumlah besar atau lebih kecil atau lebih lama dari yang direkomendasikan. Ikuti petunjuk pada label resep Anda. Omeprazole biasanya diminum sebelum makan pada hari. Ikuti petunjuk dokter . Jangan menghancurkan. mengunyah, atau menghancurkan tablet omeprazol. Telan pil dalam keadaan utuh. Omeprzole hanya diminum sekali setiap 24 jam selama 14 hari. Minum obat di pagi hari sebelum Anda makan sarapan. Simpan omeprazol pada suhu kamar jauh dari kelembaban dan panas.

Apa yang harus dilakukan jika llupa meminum obat ini ? Minum obat segera setelah Anda ingat. Lewati meminum obat ini jika waktu hampir untuk dosis berikutnya dijadwalkan. Jangan minum obat ini melebihi dosis yang dianjurkan. Apa yang terjadi jika saya bisa mengalami overdosis ? Cari bantuan medis darurat. Gejala overdosis mungkin termasuk pusing, penglihatan kabur. detak jantung cepat. mual, muntah, berkeringat, sakit kepala, atau mulut kering.

Apa yang harus saya hindari saat mengambil omeprazole ? Ikuti petunjuk dokter tentang pembatasan pada makanan. minuman, atau kegiatan.

Efek Samping Omeprazole Dapatkan bantuan medis darurat jika Anda memiliki salah satu tanda-tanda reaksi alergi terhadap omeprazol: gatal-gatal, kesulitan bernafas, pembengkakan wajah, bibir, lidah, atau tenggorokan. Hubungi dokter Anda sekaligus jika Anda memiliki gejala-gejala dari magnesium rendah: pusing, kebingungan; denyut jantung yang tidak menentu; merasa gelisah; otot kram, kelemahan otot atau perasaan lemas; batuk atau tersedak perasaan; atau kejang (konvulsi).

Efek samping ringan dari omeprazol : demam; dingin gejala seperti tersumbat, bersin hidung tenggorokan, sakit; sakit perut, gas; mual, muntah, diare, atau sakit kepala. Hubungi dokter atau Apoteker jika terjadi efek samping.

Informasi Dosis Omeprazole

Dosis dewasa untuk Ulkus duodenum: 20 mg oral sekali sehari sebelum makan. Kebanyakan pasien sembuh dalam 4 sampai 8 minggu.

Dosis dewasa untuk Helicobacter pylori Infeksi: Terapi Ganda dengan antibiotik. omeprazol 40 mg oral sekali sehari di pagi hari ditambah klaritromisin 500 mg secara oral 3 kali sehari pada hari 1 sampai 14. Dimulai pada hari ke 15, omeprazol 20 mg oral sekali sehari di pagi hari pada hari 15 sampai 28.

Terapi dengan tiga kombinasi: omeprazole 20 mg ditambah klaritromisin 500 mg ditambah amoksisilin 1000 mg semua diberikan secara oral dua kali sehari selama 10 hari. Jika maag hadir pada mulai terapi, terus omeprazol 20 mg oral sekali sehari selama 18 hari tambahan.

Dosis untuk Maag Lambung: 40 mg oral sekali sehari sebelum makan selama 4 sampai 8 minggu.

Dosis untuk esofagitis erosif: 20 mg oral sekali sehari sebelum makan. Dosis ini dapat ditingkatkan sampai 40 mg per hari berdasarkan respon klinis yang diinginkan dan toleransi pasien. Studi telah selesai hingga 12 bulan untuk terapi pemeliharaan esofagitis erosif.

Dosis untuk Sindrom Zollinger-Ellison: Awal: 60 mg oral sekali sehari. Dosis harus individual dengan kebutuhan pasien. Pemeliharaan: dosis hingga 120 mg 3 kali sehari telah diberikan. Dosis harian lebih besar dari 80 mg harus dibagi.

Dosis untuk Gastroesophageal Reflux Disease (GERD): Awal: 20 mg oral sekali sehari sebelum makan selama 4 sampai 8 minggu. Dosis ini dapat ditingkatkan sampai 40 mg per hari jika diperlukan. Pemeliharaan: pengobatan jangka panjang dengan dosis 10 sampai 20 mg per hari mungkin diperlukan untuk terapi pemeliharaan penyakit tahan api dan tampaknya aman.

Dosis untuk Adenoma Endokrin Beberapa: Awal: 60 mg oral sekali sehari sebelum makan. Dosis ini dapat dititrasi berdasarkan respon klinis yang diinginkan dan toleransi pasien. Pemeliharaan: dosis hingga 120 mg 3 kali sehari telah diberikan. Dosis harian lebih besar dari 80 mg harus dibagi.

Dosis untuk mastositosis sistemik: Awal: 60 mg oral sekali sehari sebelum makan. Dosis ini dapat dititrasi berdasarkan respon klinis yang diinginkan dan toleransi pasien. Pemeliharaan: dosis hingga 120 mg 3 kali sehari telah diberikan. Dosis harian lebih besar dari 80 mg harus dibagi.

Dosis untuk Dispepsia: Pencegahan mulas sering: 20 mg oral sekali sehari, sebelum makan, selama 14 hari. Dosis Pediatric Omeprazole untuk Gastroesophageal Reflux Disease: > 2 tahun < 20 kg: 10 mg sekali sehari > = 20 kg: 20 mg sekali sehari

Dosis Pediatric Omeprazole untuk esofagitis erosif: > 1 tahun: 0,7-3,5 mg / kg / hari (maksimum 80 mg / hari), selama 3 bulan. Dosis penambahan sebesar 0,7 mg / kg / hari untuk mencapai pH perut < 4.

Obat lain apa yang akan mempengaruhi omeprazol? Beritahu dokter tentang semua obat-obatan lain yang Anda gunakan, terutama: pengencer darah seperti warfarin; diuretik; cilostazol; clopidogrel; diazepam; digoxin; disulfiram; siklosporin; tacrolimus; fenitoin; ketoconazole, vorikonazol; ampisilin; HIV atau AIDS obat seperti atazanavir (atazanavir), nelfinavir, saquinavir, atau obat yang mengandung besi (Fe). Daftar ini tidak lengkap dan obat lain dapat berinteraksi dengan omeprazole. Beritahu dokter tentang semua obat yang Anda gunakan. Ini termasuk resep, produk over-the-counter, vitamin, dan herbal. Jangan memulai obat baru tanpa memberitahu dokter Anda.

Sanbe Farma, Amoxsan

AMOXSAN ®

Each tablet contains Amoxicillin Trihy - drate equivalent to 250 mg of Amoxicillin.

PHARMACOLOGY Amoxicillin is a derivative of semisynthetic penicillin which is acid stable. Its bactericidal activity is similar to that of ampicillin. Amoxicillin is rapidly and well absorbed from the gastrointestinal tract, irrespective of the presence of food, giving a high blood level after one hour. Its absorption is better than that of ampicillin. Amoxicillin is mainly excreted through the kidneys, in the urine Amoxicillin is recovered in active form. Amoxicillin is effective against Gram-positive and Gram-negative organisms. Among those bacteria which are sensitive to Amoxicillin are.

- Staphylococcus - Streptococcus - Diplococcus pneumoniae - Bacillus anthracis - Enterococcus - Corynebacterium diphtheriae - Salmonella sp

INDICATIONS

Respiratory tract infections : Tonsillitis, sinusitis, laryngitis, pharyngitis, otitis media, bronchitis, bronchiectasis, pneumonia.

Genitourinary tract infections : Pyelonephritis, cystitis, urethritis, gonorrhoea.

Skin and soft tissue infections : Wounds, cellulitis, furunculosis, pyoderma.

CONTRA-INDICATIONS

Hypersensitivity to betalactam antibiotics e. g. penicillins, cephalosporins.

Babies born of mothers hypersensitive to penicillin.

ADVERSE REACTIONS

Hypersensitivity reactions such as erythematous maculopapular rashes, urticaria, skin rashes, serum sickness.

Serious and fatal hypersensitivity reaction is anaphylaxis, especially in patient with hypersensitivity condition to penicillin.

Gastrointestinal disturbances, such as nausea, vomiting and diarrhoea.

Haematological reactions (usually reversible).

PRECAUTIONS

Before initiating therapy with Amoxicillin, careful inquiry should be made concerning previous hypersensitivity reactions to penicillin.

Amoxicillin must be used with caution in pregnant and lactating women.

Periodic assessment of renal, hepatic and hematopoietic functions should be made during prolonged therapy.

Patient with renal disorder must be monitored for its plasma and urine level.

As with other antibiotics, Amoxicillin administration may cause superinfection (the common causes are Pseudomonas, Enterobacterium, S. aureus and Candida). If it occurs, treatment should be discontinued and appropriate therapy should be instituted.

Not for meningitis or body joint treatment (since oral Amoxicillin does not penetrate the cerebrospinal or sinovial liquid).

Caution should be taken when this drug is administered to patients with lymphatic leukemia due to Amoxicillin-induced skin rash susceptibility.

Amoxicillin administration may cause severe colitis.

DRUG INTERACTIONS

Probenecid may increase and prolong blood level of Amoxicillin.

Concomitant use with allopurinol may result in increased skin reactions.

DOSAGES

Moderate infections

Adults and children ≥ 20 kg. 250 mg - 500 mg every 8 hours.

Children with body weight of < 20 kg. 20 - 40 mg/kg body weight/day in divided doses every 8 hours.

For more severe infections higher doses may be given.

For patients receiving peritoneal dialysis, recommended maximum dose is 500 mg/day.

For treatment of Gonococcus urethritis . 3000 mg as a single dose.

Dry syrup is recommended for children > 8 kg. 125 mg - 250 mg every 8 hours.

Pediatric drops are recommended for children under six months of age. Usually dosage for all indication except infections of the lower respiratory tract.

< 6 kg. 0.25 ml - 0.50 ml every 8 hours.

6 - 8 kg. 0.50 ml - 1.0 ml every 8 hours.

Infections of the lower respiratory tract.

< 6 kg. 0.50 ml - 1.0 ml every 8 hours.

6 - 8 kg. 1.0 ml - 1.5 ml every 8 hours.

Direction for suspension and dispersible tablet preparation Dry Syrup, for volume 60 ml. Pour drinking water until slightly below mark. Close bottle tightly. Hold bottle upside-down and shake until all gran-ules are dispersed. Add sufficient drinking water up to mark (60 ml) and shake well.

Pediatric Drops, for volume 15 ml. Pour 8 ml of drinking water. Close bottle tightly. Hold bottle upside-down and shake until all powder are dispersed. After reconstitution with drinking water, the suspension must be used within 7 days. Store in a refrigerator (2° - 8° C) or in a place away from light.

Dispersible Tablet Dissolve one dispersible tablet into a spoonful of drinking water (teaspoonful or spoonful) wait for about 30 - 40 seconds until the tablet is completely dispersed into small granules. The suspension may be directly given to patient, followed by drinking water.

SPECIAL DOSAGE RECOMMENDATIONS FOR SPECIFIC INFECTIONS

Renal function impairment condition

For patients with renal impairment monitoring of drug concentration in plasma and urine should be undertaken. Suggested dosages.

Moderate renal impairment with creatinine clearance 10 - 30 ml/min. 1 g followed by 500 mg every 12 hours.

Severe renal impairment with creatinine clearance ≤ 10 ml/min: 1 g followed by 500 mg every 24 hours.

SPECIFIC DOSAGE RECOMMENDATIONS

STORAGE Store at room temperature (25° - 30° C), away from light.

AMOXSAN ®

Amoxicillin

Sterile Powder for Injection i. m./i. v.

Each vial contains : Amoxicillin Sodium equivalent to 1 g of Amoxicillin.

PHARMACOLOGY Amoxicillin is a derivative of a semisynthetic penicillin which is acid stable. Its bactericidal activity is similar to that of ampicillin. Amoxicillin is rapidly and well absorbed in gastrointestinal tract, irrespective of the presence of food, giving a high blood level after one hour. It absorption is better than that of ampicillin. Amoxicillin is mainly excreted through the kidney, in urine amoxicillin is recovered into its active form. Amoxicillin is effective against Gram-positive and Gram-negative organisms. Among those bacteria which are sensitive to Amoxicillin are.

- Staphylococcus - Streptococcus - Diplococcus pneumoniae - Bacillus anthracis - Enterococcus - Corynebacterium diphtheriae - Salmonella sp

INDICATIONS

Respiratory tract infections : Tonsillitis, sinusitis, laryngitis, pharyngitis, otitis media, bronchitis, bronchiectasis, pneumonia.

Genitourinary tract infections : Pyelonephritis, cystitis, urethritis, gonorrhoea.

Skin and soft tissue infections : Wounds, cellulitis, furunculosis, pyoderma.

CONTRA-INDICATIONS

Hypersensitivity to betalactam antibiotics e. g. penicillins, cephalosporins.

Babies born of mothers hypersensitive to penicillin.

ADVERSE REACTIONS

Hypersensitivity reactions such as erythematous maculopapular rashes, urticaria, skin rashes, serum sickness.

Serious and fatal hypersensitivity reaction is anaphylaxis, especially in patient with hypersensitivity condition to penicillin.

Gastrointestinal disturbances, such as nausea, vomiting and diarrhoea.

i. m. administration. Pain at injection site.

i. v. administration. Phlebitis

PRECAUTIONS

Before initiating therapy with Amoxicillin, careful inquiry should be made concerning previous hypersensitivity reactions to penicillin.

Amoxicillin must be used with caution in pregnant and lactating women.

Periodic assessment of renal, hepatic and hematopoietic functions should be made during prolonged therapy.

Amoxicillin should not be mixed with blood products, protein liquids such as protein hydrolysate or intravenous lipid emulsions.

If Amoxicillin is to be given concomitantly with aminoglycosides, both antibiotics should not be mixed in the same syringe, infuse bottle or giving set because the aminoglycoside activity may decrease in such condition.

During therapy using high-dose Amoxicillin, especially in bolus injection, adequate intake of water and urine excretion should be maintained. Flow rate of catheter should be monitored periodically, because in room temperature, precipitation in urine may occur in high concentration of several drugs including Amoxicillin.

Amoxicillin is stable when mixed with common intravenous solutions at 23°C. This solution should be used up within 6 hours.

If amoxicillin is administered in solution that contains dextrose or other carbohydrate, solution must be replaced after 1 hour of usage, or after 3 hours of usage if mixed with sodium lactate contained solutions.

It may cause super infections (commonly cause by Enterobacterium, Pseudomonas, S. aureus . Candida) if it occurs, treatment should be discontinued and other alternative therapy should be given.

DRUG INTERACTIONS

Probenesid may increase and prolong concentration level of Amoxicillin.

The usages concomitant with allupurinol may increase possibility of skin reactions.

DOSAGES Patients with normal renal function :

Upper respiratory tract infections, urogenital tract infections, skin and soft tissues infections : Adult. 250 mg every 6 - 8 hours, depends on patients condition. Children (body weight < 20 kg). 20 mg/kg/day in divided dose every 6 - 8 hours. In severe infections, dose may increased up to 500 mg every 6 - 8 hours (adult) and 40 mg/kg/day in divided dose every 6 - 8 hours.

Lower respiratory tract infections : Adult. 500 mg every 6 - 8 hours. Children (body weight < 20 kg). 40 mg/kg/day in divided dose every 6 - 8 hours.

Septicemia : Adult. in severe infections. 1 g every 6 hours with slow intravenous injections or intravenous infusion for 30 minutes - 1 hours. Children (body weight < 20 kg). 20 - 40 mg/kg every 6 - 8 hours.

In patients with renal dysfunctions : For creatinine clearance up to 30 ml/minutes no need dose adjustment. Recommended i. v. dose for adult with renal dys-functions are.

Moderate dysfunction with creatinine clearance 10 - 30 ml/minutes. 1 gram continued with 500 mg every 12 hours.

Severe dysfunction with creatinine clearance < 10 ml/minutes. 1 gram continued by 500 mg every 24 hours.

Direction of Use i. m. Dissolve 1 g of sterile powder into 2.5 ml aqua pro injection and shake strongly. i. v./infusion. Dissolve 1 g of sterile powder into 20 ml of aqua pro injection, administered slowly (3 - 4 minutes) or 50 ml infusion in 20 - 30 minutes.

THE SOLUTION MUST BE INJECTED IMMEDIATELY AFTER RECONSTITUTED. If pain occurs at i. m. injection, aqua pro injection may be exchanged with lignocain HCl 1% or procain 0.5% solution. Adult total dose should not exceed 6 g daily or 100 mg/kg body weight/day.

ON MEDICAL PRESCRIPTION ONLY

PRESENTATIONS Box of 10 vials @ 1 g. Reg. No. DKL0832401844A1

STORAGE Store at room temperature (25° - 30° C) and dry place, away from light.

Dolocox, Dolocox

Dolocox

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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Fungicure Anti-Fungal Liquid, Fungicur

FungiCure Anti-Fungal Liquid 1.0fl oz

Flexible Spending Accounts (FSA)

What is a Flexible Spending Account (FSA)?

A Flexible Spending Account (FSA) allows consumers to deduct pre-tax dollars from their paychecks and deposit those funds in employer-sponsored accounts to pay for medical expenses. Consumers then submit expense receipts to healthcare administrators for reimbursement.

For more information about FSAs, contact your employer.

Find FSA-eligible products quickly: Shop our FSA Store

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Redeem online or in store Expires > (Puerto Rico: online only)

Description

Cures most athlete's foot & ringworm

Relieves itching, burning & cracking

Fast drying, no unpleasant odor

Contains an ingredient that kills 6 types of infection-causing fungus. This liquid works on exposed nail-bed surfaces where nails are missing, cracked open or otherwise breached, as well as around adjacent to and under nail-tips wherever reachable with its applicator brush.

The active ingredient in this liquid has been recognized to be safe and effective by an FDA expert advisory panel when used as directed.

Nothing stronger without a doctor's prescription

Broad spectrum anti-fungal

Fast drying

Crystal clear

No unpleasant odor

Maximum strength

Read all package directions and warnings before using

Use only as directed

Clean the affected area with soap and warm water and dry thoroughly

Apply a thin layer of liquid over the affected area twice daily (morning and night), or as directed by a doctor

This product is not effective on scalp or nails

For athlete's foot, pay special attention to spaces between toes; wear well fitting, ventilated shoes, and change shoes and socks at least once daily

For athlete's foot and ringworm, use daily for 4 weeks. IF condition persists longer, consult a doctor

Intended for use by normally healthy adults only

Persons under 18 years of age or those with highly sensitive or allergic skin should use only as directed by a doctor

Supervise children in the use of this product

Keep container tightly closed when not in use. Store away from excessive heat and cold. Other Information:

May be applied to cuticles, around nail edges and under nail tips where reachable with its applicator brush

This product is not intended to, nor will it, penetrate hard nail surfaces

While not all finger and toe fungal infections are curable with OTC topical medications, if you see improvement within 4 weeks of use, you may continue to use Fungicure until satisfactory results are obtained

You may report serious side effects to 1-800-792-2582

© 2005-2013 Alva

Shipping

This product cannot be shipped to the following state(s):

Warnings

Warnings For external use only. Ask a doctor before use on children under 2 years of age. When using this product avoid contact with the eyes. Stop use and ask a doctor if

Irritation occurs

There is no improvement within 4 weeks

Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

For the cure of most ringworm (tinea corporis) & athlete's foot (tinea pedis). For relief of itching, scaling, cracking, burning, redness, soreness, irritation & discomforts which may accompany these conditions.

Ingredients

Active Ingredients: Undecylenic Acid (25%)

Inactive Ingredients: Aloe Vera Gel, Fragrance, Hypromellose, Isopropyl Alcohol (70% v/v), Purified Water, Vitamin E

FungiCure Anti-Fungal Liquid 1.0fl oz

Flexible Spending Accounts (FSA)

What is a Flexible Spending Account (FSA)?

A Flexible Spending Account (FSA) allows consumers to deduct pre-tax dollars from their paychecks and deposit those funds in employer-sponsored accounts to pay for medical expenses. Consumers then submit expense receipts to healthcare administrators for reimbursement.

For more information about FSAs, contact your employer.

Find FSA-eligible products quickly: Shop our FSA Store

1 || (!offerValue &&!offerPercentage))"> 1 || (!offerValue &&!offerPercentage))" class="btn wag-btn-green-secondary-sm promotionelipses" title=" > Coupon available"> 1?couponLength +' coupons available':'Coupon available'>>

Redeem online or in store Expires > (Puerto Rico: online only)

Description

Cures most athlete's foot & ringworm

Relieves itching, burning & cracking

Fast drying, no unpleasant odor

Contains an ingredient that kills 6 types of infection-causing fungus. This liquid works on exposed nail-bed surfaces where nails are missing, cracked open or otherwise breached, as well as around adjacent to and under nail-tips wherever reachable with its applicator brush.

The active ingredient in this liquid has been recognized to be safe and effective by an FDA expert advisory panel when used as directed.

Nothing stronger without a doctor's prescription

Broad spectrum anti-fungal

Fast drying

Crystal clear

No unpleasant odor

Maximum strength

Read all package directions and warnings before using

Use only as directed

Clean the affected area with soap and warm water and dry thoroughly

Apply a thin layer of liquid over the affected area twice daily (morning and night), or as directed by a doctor

This product is not effective on scalp or nails

For athlete's foot, pay special attention to spaces between toes; wear well fitting, ventilated shoes, and change shoes and socks at least once daily

For athlete's foot and ringworm, use daily for 4 weeks. IF condition persists longer, consult a doctor

Intended for use by normally healthy adults only

Persons under 18 years of age or those with highly sensitive or allergic skin should use only as directed by a doctor

Supervise children in the use of this product

Keep container tightly closed when not in use. Store away from excessive heat and cold. Other Information:

May be applied to cuticles, around nail edges and under nail tips where reachable with its applicator brush

This product is not intended to, nor will it, penetrate hard nail surfaces

While not all finger and toe fungal infections are curable with OTC topical medications, if you see improvement within 4 weeks of use, you may continue to use Fungicure until satisfactory results are obtained

You may report serious side effects to 1-800-792-2582

© 2005-2013 Alva

Shipping

This product cannot be shipped to the following state(s):

Warnings

Warnings For external use only. Ask a doctor before use on children under 2 years of age. When using this product avoid contact with the eyes. Stop use and ask a doctor if

Irritation occurs

There is no improvement within 4 weeks

Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

For the cure of most ringworm (tinea corporis) & athlete's foot (tinea pedis). For relief of itching, scaling, cracking, burning, redness, soreness, irritation & discomforts which may accompany these conditions.

Ingredients

Active Ingredients: Undecylenic Acid (25%)

Inactive Ingredients: Aloe Vera Gel, Fragrance, Hypromellose, Isopropyl Alcohol (70% v/v), Purified Water, Vitamin E

Ifor - What Does Ifor Stand For The Free Dictionary, Ifor

References in periodicals archive ?

An English language proficiency at the 3-level proved inadequate for staff officers operating in the field; either at NORDPOL Brigade HQ at Doboj, Bosnia-Herzegovina--where 21 and 38 officers served during IFOR and SFOR respectively--or at the Nordic Support Group in Pecs, Hungary.

The Czech IFOR contingent totaled 920 (30 at HQ, a Mechanized Battalion of 872 troops, and 18 for helicopter operations); and a SFOR contingent of 644 (22 at HQ, a mechanized battalion troops of 600 troops, and 22 for helicopter operations--the only non-NATO air units in the field).

Initial problems resulted because the Czechs lacked experience in operating in multinational commands and a Czech representative was not present in the British IFOR sector command in Zagreb.

Hence, when the Czechs established their IFOR contingent they decided to staff one-half of it with reserve officers, who were either veterans of UNPROFOR, the Rapid Deployment Brigade, or the elite Prostejov Airborne Brigade.

Romania, as with Hungary, contributed the non-combat Engineering Battalion 96, with 200 troops, to IFOR and SFOR, which was subordinated to the ARRC command in Sarajevo.

That stance has angered many in the Bosnian government, who had hoped to see IFOR troops bring indicted war criminals, most of whom are Serbian, to trial.

Sacirbey said IFOR "has not been entirely consistent with what we agreed to in Dayton.

Three planning factors are pivotal to an IFOR follow-on force.

If an IFOR follow-on force is needed, options include:

Of these options, only a NATO-led force would be capable of enforcing peace by December 1996, when IFOR redeploys.

A post - IFOR force might be considered if some IFOR missions had to continue beyond 12 months.

Paul Newman, managing director of IFOR. said: "We're not just here to provide solutions to IT problems, our aim is to be pro-active in preventing them.

Biscor, Biscor

A Global Leader in Specialty Coated Performance Materials

Biscor, a PTFE Group Company, is a leading global provider of high performance specialty coated fabrics, belts and tapes used in an ever expanding range of industries and applications.

PTFE Group produces a wide variety of performance materials including specialty-coated fabrics, tapes, and belts.

PTFE Group of Companies (PTFE Group) is a leading manufacturer of specialty-coated performance fabrics, tapes and belts used in a wide range of manufacturing, packaging, maintenance and repair environments around the world. From the aviation industry to consumer products, we supply performance materials and technical expertise to 21 different industries for use in over 100 applications.

With 47 years of proven experience, demand for our products is driven by worldwide recognition of our high quality standards and technical support. PTFE Group performance materials stand up to extreme temperatures (high and low), moisture, abrasion, and chemical exposure that can easily degrade most materials.

Our core performance materials consist of fiberglass or aramid substrate coated with PTFE (polytetrafluoroethylene) or silicone in specifically engineered thicknesses, combinations, and grades, depending on the needs of the application.

Key attributes that make our PTFE and silicone coated materials suitable for a wide range of industry applications include but are not limited to:

Resistance to extreme temperatures (-73°C / -100°F to 287°C/550°F).

Excellent release properties (non-stick)

Chemically inert, non-toxic

Thermal stability, resistant to thermal shocking

Low co-friction surface texture

Good insulating properties (at thicker cross-sections)

Excellent heat transfer properties (at thinner cross-sections)

High strength (fiberglass and aramid based materials)

Excellent dimensional stability

FDA approved

Easy to clean

PTFE Group began producing high quality performance materials in 1966 as Green Belting Industries Limited. Today, PTFE Group of Companies includes Green Belting Industries Limited (Canada), Greenbelt Industries Inc. (US), Biscor Limited (UK) and Mapelli SRL (Italy) with plants and offices in each of these country locations.

An ISO 9001 Quality Registered company, PTFE Group strives for continuous improvement and is committed to producing products and providing service of the highest quality.

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Sulfasalazine Oral Uses, Side Effects, Interactions, Pictures, Warnings - Dosing, Salazopyrin

sulfasalazine

GENERIC NAME(S): SULFASALAZINE

Uses

Sulfasalazine is used to treat a certain type of bowel disease called ulcerative colitis. This medication does not cure this condition, but it helps decrease symptoms such as fever, stomach pain. diarrhea. and rectal bleeding. After an attack is treated, sulfasalazine is also used to increase the amount of time between attacks. This medication works by reducing irritation and swelling in the large intestines .

In addition, delayed-release tablets of sulfasalazine are used to treat rheumatoid arthritis. Sulfasalazine helps to reduce joint pain. swelling, and stiffness. Early treatment of rheumatoid arthritis with sulfasalazine helps to reduce/prevent further joint damage so you can do more of your normal daily activities. This medication is used with other drugs, rest, and physical therapy in patients who have not responded to other medications (salicylates. nonsteroidal anti-inflammatory drugs-NSAIDs ).

OTHER USES: This section contains uses of this drug that are not listed in the approved professional labeling for the drug but that may be prescribed by your health care professional. Use this drug for a condition that is listed in this section only if it has been so prescribed by your health care professional.

This medication may also be used to treat another type of bowel disease called Crohn's disease .

How to use sulfasalazine

Take this medication by mouth after meals with a full glass of water (8 ounces or 240 milliliters) or as directed by your doctor. To prevent stomach upset, your doctor may recommend a slow increase in your dosage when starting treatment. Dosage is based on your medical condition and response to therapy. In children, dosage is also based on weight .

If you are taking the delayed-release tablets, swallow them whole. Do not crush, chew, or break the tablets. Doing so may increase the chance of stomach upset.

Drink plenty of fluids during treatment with this medication unless otherwise directed by your doctor. This will help prevent kidney stones .

Take this medication regularly to get the most benefit from it. To help you remember, take it at the same times each day.

Inform your doctor if your condition does not improve or if it worsens. For the treatment of rheumatoid arthritis. it may take 1-3 months before you notice any improvement in your symptoms.

Side Effects

Stomach upset, nausea. vomiting. loss of appetite, headache. dizziness. or unusual tiredness may occur. If any of these effects persist or worsen, notify your doctor or pharmacist promptly.

This medication may cause your skin and urine to turn orange-yellow. This effect is harmless and will disappear when the medication is stopped.

Rarely, delayed-release tablets of sulfasalazine may appear whole or only partly dissolved in your stool. If this occurs, tell your doctor right away so your treatment can be changed.

Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.

This medication may cause temporary male infertility. This effect is reversible when the medication is stopped.

Tell your doctor right away if you have any serious side effects, including: sun sensitivity, hearing changes (e. g. ringing in the ears ), mental/mood changes, signs of kidney problems (such as change in the amount of urine, painful urination. blood in the urine ), new lump/growth in the neck (goiter ), numbness/tingling of the hands/feet, signs of low blood sugar (e. g. hunger. cold sweat, blurred vision. weakness. fast heartbeat), swollen glands .

This medication may rarely cause very serious allergic reactions (e. g. Stevens-Johnson syndrome), blood disorders (e. g. agranulocytosis. aplastic anemia ), liver damage, nerve/muscle problems and infections. Get medical help right away if you have any very serious side effects, including: skin rash /blisters/peeling, mouth sores, itching/swelling (especially of the face/tongue/throat), severe dizziness, trouble breathing. chest pain. signs of infection (such as fever, chills, persistent sore throat. cough), easy bruising/bleeding, severe tiredness, muscle pain /weakness (especially with fever and unusual tiredness), pale or blue skin/lips/nails, new/worsening joint pain, confusion, persistent/severe headache. unexplained neck stiffness, seizures. signs of liver problems (e. g. persistent nausea/vomiting, severe stomach/abdominal pain, yellowing eyes/skin, dark urine).

This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or at www. fda. gov/medwatch.

In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.

Precautions

Before taking sulfasalazine, tell your doctor or pharmacist if you are allergic to it; or to sulfa drugs; or to aspirin and related drugs (salicylates, NSAIDs such as ibuprofen); or to mesalamine; 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: intestinal blockage, urinary blockage, kidney disease, liver disease, blood disorders (such as aplastic anemia, porphyria), a certain genetic condition (G6PD deficiency), asthma, severe allergies, current/recent/returning infections.

This drug may make you dizzy. 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.

This medication may make you more sensitive to the sun. Avoid prolonged sun exposure, tanning booths, and sunlamps. Use a sunscreen and wear protective clothing when outdoors.

This medication is similar to aspirin. Children and teenagers should not take aspirin or aspirin-related medications (e. g. salicylates) if they have chickenpox, flu, or any undiagnosed illness, or if they have just been given a live virus vaccine (e. g. varicella vaccine), without first consulting a doctor about Reye's syndrome, a rare but serious illness.

During pregnancy, this medication should be used only when clearly needed. Caution is advised if this medication is used near the expected delivery date because similar drugs may cause harm to a newborn. Discuss the risks and benefits with your doctor. If you become pregnant while taking this drug, contact your doctor right away. This medication may lower your folic acid levels, increasing the risk of spinal cord defects. Therefore, check with your doctor to make sure you are taking enough folic acid. Prenatal care should include tests for spinal cord defects.

This drug passes into breast milk and could have undesirable effects on a nursing infant. Consult your doctor before breast-feeding.

Interactions

Drug interactions may change how your medications work or increase your risk for serious side effects. This document does not contain all possible drug interactions. Keep a list of all the products you use (including prescription/nonprescription drugs and herbal products) and share it with your doctor and pharmacist. Do not start, stop, or change the dosage of any medicines without your doctor's approval.

Some products that may interact with this drug include: cyclosporine, digoxin, folic acid, methenamine, PABA taken by mouth, phenytoin.

Sulfasalazine is very similar to mesalamine. Do not use mesalamine medications taken by mouth while using sulfasalazine.

This medication may interfere with certain laboratory tests (including urine normetanephrine levels), possibly causing false test results. Make sure laboratory personnel and all your doctors know you use this drug.

Overdose

If overdose is suspected, contact a poison control center or emergency room right away. US residents can call their local poison control center at 1-800-222-1222. Canada residents can call a provincial poison control center. Symptoms of overdose may include: severe stomach/abdominal pain, persistent vomiting, extreme drowsiness, seizures.

Notes

Do not share this medication with others.

Laboratory and/or medical tests (e. g. complete blood count, liver and kidney function tests) should be performed periodically to monitor your progress or check for side effects. Consult your doctor for more details.

Missed Dose

If you miss a dose, take it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.

Storage

Store at room temperature away from light and moisture. Do not store in the bathroom. Keep all medications away from children and pets.

Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company.

Information last revised May 2016. Copyright(c) 2016 First Databank, Inc.

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Itil Certification, Mitil

ITIL Portal

ITIL Certification Path

ITIL Practitioner

Wise Words

"Intellectuals try not to drown, while the whole purpose of love is drowning."

- The Illuminated Rumi

ITIL Overview

The ITIL abbreviation stands for IT Infrastructure Library . Originally, ITIL was developed by the Central Computer and Telecommunications Agency (CCTA) as a set of comprehensive and iter-related codes of practice. In IT community such code of good practice was / is very useful in terms of achieving the efficient support and delivery of high quality, cost effective IT services. CCTA, renamed the Office of Government Commerce (OGC) maintains the library and releases all updated related to ITIL.

The OGC is an office of HM Treasury (UK). It acts as an independent of any commercial intersts organization involved in ITIL (independent from software companies, software vendors, integrators, training protocols). This is why the ITIL is so widely used - its main asset is independency.

ITIL is accredited by Information Systems Examinations Board (ISEB). ISEB is an organization which prepares delegates for the ITIL Foundation Certificate in IT Service Management. The ISEB was formed in 1967 and currently functions under the auspieces of the British Computer Society (BCS). The ISEB aims to provide industry-recognized qualification thet measure comptence, ability and performance in many areas of information systems, whit the aim of raising industry standards, promoting career development and providing competitive edge for employrs.

Aother organization which provides ITIL examination is EXIN . The EXIN is an independent organization, Dutch-based IT examination provider. The EXIN esablishes educational requirements, develops and organize examinations in the field of Information Technology. The main goal of EXIN is to promote the quality of the Information Communication Technology (ICT) sector and the ICT professionals working in this sector by means of independent testing and certification.

Motrin - Pain Relief, Naprofidex

Motrin is used for treating rheumatoid arthritis, osteoarthritis, menstrual cramps, or mild to moderate pain. Motrin is an NSAID. NSAIDs treat the symptoms of pain and inflammation. They do not treat the disease that causes those symptoms.

Use Motrin as directed by your doctor.

Take Motrin by mouth with or without food. It may be taken with food if it upsets your stomach. Taking it with food may not lower the risk of stomach or bowel problems (eg, bleeding, ulcers). Talk with your doctor or pharmacist if you have persistent stomach upset.

Take Motrin with a full glass of water (8 oz/240 mL) as directed by your doctor.

If you miss a dose of Motrin 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. 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 the proper use of Motrin .

Store Motrin 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 Motrin out of the reach of children and away from pets.

Active Ingredient: Ibuprofen.

Do NOT use Motrin if:

you are allergic to any ingredient in Motrin

you have had a severe allergic reaction (eg, severe rash, hives, trouble breathing, growths in the nose, dizziness) to aspirin or an NSAID (eg, ibuprofen, celecoxib)

you have recently had or will be having bypass heart surgery

you are in the last 3 months of pregnancy.

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

Some medical conditions may interact with Motrin. 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 product, or dietary supplement

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

if you have a history of kidney or liver disease, diabetes, or stomach or bowel problems (eg, bleeding, perforation, ulcers)

if you have a history of swelling or fluid buildup, lupus, asthma, or growths in the nose (nasal polyps), or mouth inflammation

if you have high blood pressure, blood disorders, bleeding or clotting problems, heart problems (eg, heart failure), or blood vessel disease, or if you are at risk for any of these diseases

if you have poor health, dehydration or low fluid volume, or low blood sodium levels, you drink alcohol, or you have a history of alcohol abuse.

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

Anticoagulants (eg, warfarin), aspirin, corticosteroids (eg, prednisone), heparin, or selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because the risk of stomach bleeding may be increased

Probenecid because it may increase the risk of Motrin 's side effects

Cyclosporine, lithium, methotrexate, or quinolones (eg, ciprofloxacin) because the risk of their side effects may be increased by Motrin

Angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril) or diuretics (eg, furosemide, hydrochlorothiazide) because their effectiveness may be decreased by Motrin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Motrin 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:

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

Serious stomach ulcers or bleeding can occur with the use of Motrin. Taking it in high doses or for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Motrin 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.

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

Do not take aspirin while you are using Motrin unless your doctor tells you to.

Lab tests, including kidney function, complete blood cell counts, and blood pressure, may be done to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.

Use Motrin with caution in the elderly; they may be more sensitive to its effects, including stomach bleeding and kidney problems.

Motrin should be used with extreme caution in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: Motrin may cause harm to the fetus. Do not take it during the last 3 months of pregnancy. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Motrin while you are pregnant. It is not known if Motrin is found in breast milk. Do not breastfeed while taking Motrin .

All medicines can 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:

Constipation; diarrhea; dizziness; gas; headache; heartburn; nausea; stomach pain or upset.

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

Severe allergic reactions (rash; hives; itching; trouble breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody or black, tarry stools; change in the amount of urine produced; chest pain; confusion; dark urine; depression; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; mental or mood changes; numbness of an arm or leg; one-sided weakness; red, swollen, blistered, or peeling skin; ringing in the ears; seizures; severe headache or dizziness; severe or persistent stomach pain or nausea; severe vomiting; shortness of breath; stiff neck; sudden or unexplained weight gain; swelling of hands, legs, or feet; unusual bruising or bleeding; unusual joint or muscle pain; unusual tiredness or weakness; vision or speech changes; vomit that looks like coffee grounds; yellowing of the skin or eyes.

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.

Cell-Tech By Muscletech At - Best Prices On Cell-Tech, Celtec

MuscleTech: CELL-TECH

CELL-TECH Is The Ultimate Hardgainer Creatine Formula

Regular creatine was welcomed as the next generation of supplementation and was unleashed to help bodybuilders and other athletes get bigger than ever! For the most part, regular creatine delivers solid muscle size and strength gains. However, even as great as creatine is, there are clinically tested ways to make it better.

If you’ve been taking straight creatine monohydrate, it’s really just the tip of the iceberg. Researchers at MuscleTech® knew this and, after years of testing created CELL-TECH™ – a true third generation creatine formula that harnesses the anabolic power of insulin and is so powerful that it has not only stood the test of time, but has become legendary for its ability to pack on mass, size and strength like no other creatine formula before or since.*

7g

Creatine + Training + Insulin = THE PERFECT ANABOLIC STORM

Years of study by top human performance researchers has confirmed that insulin is one of the body’s most powerful musclebuilding hormones. In fact, research published in the Journal of Clinical Investigation found that insulin is so potent it could support protein synthesis in skeletal muscle1! Insulin is also very anti-catabolic and reduces protein degradation and stimulates cellular hydration – causing water retention within the muscle cells that translates into greater protein synthesis.

Early creatine researchers also knew the power of insulin, and in some of the first research published in the American Journal of Physiology, it was discovered that taking creatine along with a high dose of simple carbohydrates could trigger as much as 60% better creatine storage in the muscles2. Researchers reporting on their findings confirmed that insulin was the key to pushing more creatine through muscle cell membranes.*

The purpose of insulin in the body is to regulate blood glucose levels. When an elevation of blood glucose occurs, the beta cells of the pancreas secrete insulin into the portal vein (the “spike”). Ultimately, insulin works by triggering the movement of nutrients from the blood to the cells – fortifying your muscles with the ingredients they need to grow while at the same time normalizing your blood glucose levels.

Insulin needs to attach itself to receptors in order to have any effect. This is what determines how much of the glucose, amino acids and creatine in your blood are taken up by the cell transporters. In your muscle cells, there are two glucose transporters: GLUT-1 and GLUT-4. However, it’s the GLUT-4 receptors that are predominant in adult human muscles, and they play an important role.

GLUT-4 transporters migrate from the cytoplasm right to the cell surface in response to insulin and muscle contraction (lifting weights). Yes, training can actually increase the ability of your muscles to take in more nutrients because training increases the number of available receptors on the muscle membrane. The more available receptors there are, the more glucose, amino acids and creatine can be absorbed from the blood.*

This, in essence, creates the perfect anabolic storm – an optimal environment where insulin-sensitive muscle cells are able to quickly utilize anabolic nutrients like creatine, amino acids and glucose – priming them for incredible strength and massive muscular growth!*

Spiking Insulin to Drive GAINS

In order to maximize the absorption of creatine, insulin levels must be spiked. There’s no way around it. You need to have a high plasma glucose concentration and spiked serum insulin levels to drive maximum cellular creatine delivery.*

Higher glycemic carbs create a more powerful insulin spike and can increase the number of GLUT-4 transporters to the surface of your muscle cells to a greater degree. Taking creatine with fewer or no carbs elicits no significant insulin spike and ultimately fails to achieve your goal of getting the most creatine into your muscles as possible.*

The degree of insulin secretion is governed by the total amount of carbohydrates ingested and the glycemic index of the food consumed. MuscleTech researchers knew this when they began research on a third generation of creatine supplements. By harnessing the anabolic power of insulin and the muscle - and strength-building power of creatine, Team MuscleTech researchers engineered an absolute monster of a creatine supplement. One that hands-down is an uncontested breakthrough in creatine supplementation designed for nothing less than extreme musclebuilding!*

The Most Powerful Creatine Formula

CELL-TECH is a scientifically engineered hardcore creatine formula that is patent-protected and contains core ingredients supported by numerous clinical trials. Each two-scoop serving of CELL-TECH delivers 7g of HPLC-certified creatine monohydrate and 3 grams of creatine HCl. This dose of creatine is far higher than most creatine products, and yet those creatine products don’t utilize a delivery system! Ask yourself, how much creatine from these untested formulas is actually making its way into your muscles?

CELL-TECH delivers a multistage combination of carbohydrates, including glucose polymers, dextrose, ModCarb™ (oat bran, quinoa, buckwheat, millet), waxy maize and highly branched cyclic dextrin totaling 75g per two scoops. After each max serving of CELL-TECH, insulin levels rapidly peak in the bloodstream, priming muscles for maximum creatine hypersaturation and retention. This is the key to CELL-TECH’s unique ability to significantly increase insulin levels beyond what regular creatine supplements are capable of.*

The anabolic rush generated by this exclusive carb blend is engineered to force glucose, creatine and amino acids into the muscles at levels that are unmatched by any other creatine formula.*

In fact, based on available published research, CELL-TECH is the fastest acting, most powerful advanced musclebuilding creatine formula ever developed, and once you see how dramatically and rapidly CELL-TECH can help transform your physique, you won’t want to consider using anything else!*

How CELL-TECH Works

Forces Powerful Insulin Spike

CELL-TECH delivers a multistage combination of carbohydrates that forces a powerful insulin spike post-workout.*

Increases Glut-4 Transporters for Creatine Uptake

The powerful carbohydrates in CELL-TECH trigger insulin output, enabling insulin to shuttle the massive 10g dose of creatine and other nutrients straight into the muscle.*

With Added Alpha Lipoic Acid

CELL-TECH contains a full 200mg dose of alpha lipoic acid (ALA). Research suggests that ALA helps improve the absorption of creatine and glucose into the muscle cell through specialized transporters.*

Increases Cell Volumization - Priming Muscles for Growth

Improved GLUT-4 availability and increased muscle cell sensitivity allows insulin to rapidly replenish creatine and glycogen stores, facilitating glycogen super-compensation and an intense muscle-expanding effect. CELL-TECH also contains free-form amino acids that aid in this dramatic cell volumization!*

Clinically Tested - Faster Muscle Growth and More Strength*

CELL-TECH is more than just a supplement that works in theory. It’s actually been put to the test in a clinical setting – further cementing its effectiveness! In fact, subjects who consumed the amount of creatine and carbohydrates supplied during the CELL-TECH loading stage gained, on average, 3.4 lbs. of muscle in 7 days. Subjects taking creatine with juice gained only 0.8 lbs.3.*

In a second study performed at McMaster University, test subjects who used CELL-TECH for 8 weeks significantly increased their strength on the bench press by 17%, leg press by 29% and biceps curl by 28% respectively4.

Enhanced Nutrient Transport

Each serving of CELL-TECH includes 200mg of the powerful compound alpha lipoic acid (ALA). Research suggests that ALA helps improve the absorption of creatine and glucose into the muscle cell through specialized transporters. This powerful nutrient-partitioning agent supports the insulin sensitivity of active insulin receptors on the cells’ surface for greater nutrient uptake and creatine saturation.*

Branched-Chain and Cell-Volumizing Amino Acids

CELL-TECH also supplies the branched-chain amino acids L-leucine, L-valine and L-isoleucine in a 2:1:1 ratio. Branched-chain amino acids are free-form amino acids – singular molecules that are quickly digested and absorbed into the bloodstream. CELL-TECH also contains the amino acids taurine and alanine. These free-form amino acids are two of the most abundant amino acids in muscle and aid in cell volumization.*

No Cycling

A clinical study revealed that the use of CELL-TECH did not lead to the down regulation of creatine transporters. This allows athletes to continue to benefit from creatine use, instead of cycling on and off5. This means you can use it all year long – just like protein.*

Biolo et al. 1995. Journal of Clinical Investigation. 95:811-819.

Green et al. 1996. American Journal of Psychology. 271:E821-826.

Kalman et al. 2000. Medicine & Science in Sports & Exercise. 32(5):562(5136)[Abstract].

Tarnopolsky et al. 2001. Med Sci Sports Ecerc. 33(12):2044-52.

Parise et al. 2000. Canadian Journal of Applied Physiology. 25(5):396[Abstract].

TESTED FOR QUALITY AND PURITY

Team MuscleTech ensures only the highest - quality, pure HPLC-tested creatine manufactured by one of the world’s largest producers of creatine is used for CELL-TECH™. In fact, each batch of CELL-TECH™ undergoes strict quality control and is third-party tested and verified to ensure that each bottle of has the highest purity, quality and consistency.*

The CELL-TECH Advantage

Nitazoxanide Plus Lactulose Versus Lactulose Alone Treatment Of Hepatic Encephalopathy - Full Text V

Nitazoxanide Plus Lactulose Versus Lactulose Alone Treatment of Hepatic Encephalopathy

Other Name: Laxolac, Duphlac

Hepatic encephalopathy (HE) is a reversible neuropsychiatric syndrome associated with chronic and acute liver dysfunction. It is characterized by cognitive and motor deficits of varying severity.

Hepatic encephalopathy is caused by accumulation of nitrogenous substances, primarily ammonia, in the blood. In advanced stages it is referred to as hepatic coma which may be preceded by seizures. The treatment goal is to reduce nitrogen load from the GI tract and to improve central nervous system (CNS) status.

Treatment options include lactulose administered orally or by nasogastric tube or enema, non-absorbable antibiotics, and protein-restricted diets.

Lactulose is nonabsorbable disaccharides that are currently used as first line agents for the treatment of HE. Its action is thought to beconversion to lactic acid and acetic acid resulting in acidification of the gut lumen. This favors conversion of ammonia (NH3) to ammonium (NH4+), which is relatively membrane impermeable, and inhibits ammoniagenic coliform bacteria.

Nitazoxanide is an oral agent indicated for the treatment of infectious diarrhea caused by Crytpsporidiumparvum and Giardia lamblia. Basu and colleagues presented a pilot prospective study at the 2008 American Association for the Study of Liver Diseases meeting showing clinical improvement in HE among cirrhotic patients who received nitazoxanide and lactulose.

Mantry and colleagues showed that the number of hospitalizations and the duration of hospital stays were shortened for patients receiving combination therapy compared with those receiving lactulose monotherapy.

Cirrhosis, defined by a combination of any of the following:

Laboratory findings

Endoscopic results

Ultrasound

Histology Overt hepatic encephalopathy

• Creatinine>1.5 mg/dl

Alcohol use within prior 4 weeks

Non-hepatic metabolic encephalopathy

Hepatocellular carcinoma

Degenerative CNS disease

Any significant psychiatric illness or other medical comorbidity

Contacts and Locations

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials. gov identifier: NCT02464124

Comprar Barato Online Vulamox, Vulamox

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Buscar/Search/Chercher:

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Bendit, planchas de asar.

Mosen Cinto Verdaguer, 3 25100 Almacelles (Lleida) Tel. (34) 973 26 93 96 bendit@bendit. es www. bendit. es

Medi-Moses Clinic - Prostate Centre, Prostacure

Why Choose Us

Daily OPD consultation and treatment of all kinds of diseases using 100% pure herbal products and also orthodox medicines when appreciated. Choose us because we are the No. 1 point of call in;

Solving your prostate problems When you need it most.

Qualified Medical and health officers

State of the art Equipment

Certified Herbal Product

Well equipped state of the art Laboratory

State of the art Dispensary

Prostate Foundation

FACT SHEET ON PROSTACURE

PROSTACURE is a pure 100% Natural herbal food supplement use for improving urinary flow in men with Benign Prostate Hyperplasia (BPH) of Enlarged Prostate gland at Medi-Moses Prostate Centre. Prospective study carried out involving seven thousand patients aged between forty to seventy years with varying degrees of Enlarged Prostate gland over a period of four years showed complete improvement in their BHP Symptoms within two to eight weeks.

International Prostate Symptoms Score(IPSS) was used before treatment and after treatment as well as the Initial and Final Prostate weight was assessed using IPSS Standard questionnaire and Ultra sound scan respectively. Initial Prostate Specific Antigen (PSA) levels recorded include only those whose PSA level is below 10ng/ml to avoid or reduce possibility of including Prostate Cancer patients.

The herbal treatment using PROTACURE led to a remarkable improvement in symptoms of BPH such as straining or difficult urinary, incomplete emptying of the bladder, frequent urge to urinate, hesitancy, intermittency of interruption in urine flow, weak stream of urinary flow and frequent urination in the Night.

The most novel finding is the dramatic reduction in the size and weight of the Prostate gland to it normal weight of 40gram and below within a short period between two to eight weeks of treatment using PROSTACURE. There was also enhanced libido and sexual function after treatment. This is especially good news for men who have tried conventional therapies for BHP and experienced a decline in sex drive and performance.

Thus PROSTACURE is your reasonable first line Natural alternative for men with BPH.

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Hydrochlorothiazide - Blood Pressure, Cesplon Plus

Blood Pressure - Cesplon plus (Brand name: hydrochlorothiazide)

Hydrochlorothiazide is used for treating high blood pressure. It is also used to treat fluid buildup in the body caused by certain conditions (e. g. heart failure, liver cirrhosis, kidney problems) or medicines (e. g. corticosteroids, estrogen). It may be used alone or with other medicines. It may also be used for other conditions as determined by your doctor.

Use Hydrochlorothiazide as directed by your doctor.

Take Hydrochlorothiazide by mouth with or without food. Hydrochlorothiazide may increase the amount of urine or cause you to urinate more often when you first start taking it. To keep this from disturbing your sleep, try to take your dose before 6 pm. Ask your health care provider any questions you may have about how to use Hydrochlorothiazide. Drug Class and Mechanism

Hydrochlorothiazide is a thiazide diuretic. It helps the kidneys to remove fluid from the body.

If you miss a dose of Hydrochlorothiazide and are using 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.

Store Hydrochlorothiazide between 68 and 77 degrees F (20 and 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 Hydrochlorothiazide out of the reach of children and away from pets.

Do not use Hydrochlorothiazide if:

you are allergic to any ingredient in Hydrochlorothiazide; you are unable to urinate; you are taking dofetilide or ketanserin. Contact your doctor or health care provider right away if any of these apply to you.

Important : Hydrochlorothiazide may cause dizziness or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Hydrochlorothiazide with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it. Hydrochlorothiazide 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. Your doctor may also prescribe a potassium supplement for you. If so, take the potassium supplement exactly as prescribed. Do not start taking additional potassium on your own or change your diet to include more potassium without first checking with your doctor. Tell your doctor or dentist that you take Hydrochlorothiazide before you receive any medical or dental care, emergency care, or surgery. Tell your doctor if you will be exposed to high temperatures. The risk of certain side effects (eg, low blood sodium levels) may be increased in hot weather. Hydrochlorothiazide may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Hydrochlorothiazide. Use a sunscreen or wear protective clothing if you must be outside for more than a short time. Hydrochlorothiazide may raise your blood sugar. High blood sugar may make you feel confused, drowsy, or thirsty. It can also make you flush, breathe faster, or have a fruit-like breath odor. If these symptoms occur, tell your doctor right away. Diabetes patients - Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine. Lab tests, including kidney function, blood pressure, and electrolyte levels, may be performed while you use Hydrochlorothiazide. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments. Pregnancy and breast-feeding: Hydrochlorothiazide may cause harm to the fetus. If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Hydrochlorothiazide while you are pregnant. Hydrochlorothiazide is found in breast milk. If you are or will be breast-feeding while you use Hydrochlorothiazide, check with your doctor. Discuss any possible risks to your baby.

Possible Side Effects

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

Constipation; diarrhea; dizziness; lightheadedness (especially when sitting up or standing); loss of appetite; nausea; temporary blurred vision. 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); confusion; dark urine; decreased urination; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; increased thirst; joint pain, swelling, warmth, or redness (especially of the big toe joint); mental or mood changes; muscle pain or cramps; numbness or tingling; red, swollen, blistered, or peeling skin; seizures; severe or persistent dizziness; severe or persistent nausea or stomach pain; shortness of breath; unusual bruising or bleeding; unusual drowsiness, restlessness, tiredness, or weakness; unusually dry mouth; vomiting; yellowing of the eyes or skin.

If you have any questions about Hydrochlorothiazide, please talk with your doctor, pharmacist, or other health care provider. Hydrochlorothiazide is to be used only by the patient for whom it is prescribed. Do not share it with other people.

Blood Pressure - Cesplon plus (Brand name: hydrochlorothiazide)

Hydrochlorothiazide is used for treating high blood pressure. It is also used to treat fluid buildup in the body caused by certain conditions (e. g. heart failure, liver cirrhosis, kidney problems) or medicines (e. g. corticosteroids, estrogen). It may be used alone or with other medicines. It may also be used for other conditions as determined by your doctor.

Use Hydrochlorothiazide as directed by your doctor.

Take Hydrochlorothiazide by mouth with or without food. Hydrochlorothiazide may increase the amount of urine or cause you to urinate more often when you first start taking it. To keep this from disturbing your sleep, try to take your dose before 6 pm. Ask your health care provider any questions you may have about how to use Hydrochlorothiazide. Drug Class and Mechanism

Hydrochlorothiazide is a thiazide diuretic. It helps the kidneys to remove fluid from the body.

If you miss a dose of Hydrochlorothiazide and are using 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.

Store Hydrochlorothiazide between 68 and 77 degrees F (20 and 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 Hydrochlorothiazide out of the reach of children and away from pets.

Do not use Hydrochlorothiazide if:

you are allergic to any ingredient in Hydrochlorothiazide; you are unable to urinate; you are taking dofetilide or ketanserin. Contact your doctor or health care provider right away if any of these apply to you.

Important : Hydrochlorothiazide may cause dizziness or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Hydrochlorothiazide with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it. Hydrochlorothiazide 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. Your doctor may also prescribe a potassium supplement for you. If so, take the potassium supplement exactly as prescribed. Do not start taking additional potassium on your own or change your diet to include more potassium without first checking with your doctor. Tell your doctor or dentist that you take Hydrochlorothiazide before you receive any medical or dental care, emergency care, or surgery. Tell your doctor if you will be exposed to high temperatures. The risk of certain side effects (eg, low blood sodium levels) may be increased in hot weather. Hydrochlorothiazide may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Hydrochlorothiazide. Use a sunscreen or wear protective clothing if you must be outside for more than a short time. Hydrochlorothiazide may raise your blood sugar. High blood sugar may make you feel confused, drowsy, or thirsty. It can also make you flush, breathe faster, or have a fruit-like breath odor. If these symptoms occur, tell your doctor right away. Diabetes patients - Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine. Lab tests, including kidney function, blood pressure, and electrolyte levels, may be performed while you use Hydrochlorothiazide. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments. Pregnancy and breast-feeding: Hydrochlorothiazide may cause harm to the fetus. If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Hydrochlorothiazide while you are pregnant. Hydrochlorothiazide is found in breast milk. If you are or will be breast-feeding while you use Hydrochlorothiazide, check with your doctor. Discuss any possible risks to your baby.

Possible Side Effects

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

Constipation; diarrhea; dizziness; lightheadedness (especially when sitting up or standing); loss of appetite; nausea; temporary blurred vision. 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); confusion; dark urine; decreased urination; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; increased thirst; joint pain, swelling, warmth, or redness (especially of the big toe joint); mental or mood changes; muscle pain or cramps; numbness or tingling; red, swollen, blistered, or peeling skin; seizures; severe or persistent dizziness; severe or persistent nausea or stomach pain; shortness of breath; unusual bruising or bleeding; unusual drowsiness, restlessness, tiredness, or weakness; unusually dry mouth; vomiting; yellowing of the eyes or skin.

If you have any questions about Hydrochlorothiazide, please talk with your doctor, pharmacist, or other health care provider. Hydrochlorothiazide is to be used only by the patient for whom it is prescribed. Do not share it with other people.

List Of Anthelmintics, Anthelmin

Anthelmintics

Yosprala Yosprala (aspirin and omeprazole) is a platelet aggregation inhibitor and proton pump inhibitor.

Cuvitru Cuvitru immune globulin subcutaneous (human) is indicated as replacement therapy in the treatment.

Erelzi Erelzi (etanercept-szzs) is a tumor necrosis factor (TNF) blocker biosimilar to Enbrel indicated.

Troxyca ER Troxyca ER (oxycodone hydrochloride and naltrexone hydrochloride) is an extended-release.

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Tizanidine Uses, Dosage, Side Effects, Tizan

Tizanidine

Tizanidine is a short-acting muscle relaxer. It works by blocking nerve impulses (pain sensations) that are sent to your brain.

Tizanidine is used to treat spasticity by temporarily relaxing muscle tone.

Tizanidine may also be used for purposes other than those listed in this medication guide.

Important information

Tizanidine is a short-acting medication that should be taken only for daily activities that require relief from muscle spasticity.

Do not take tizanidine if you are also taking the antidepressant fluvoxamine (Luvox), or the antibiotic ciprofloxacin (Cipro). Do not use tizanidine at a time when muscle tone is needed to assure safe balance and movement for certain activities. In some situations, it may endanger your physical safety to be in a state of reduced muscle tone.

Switching between tizanidine tablets and capsules, or changing the way you take it with regard to eating, can cause an increase in side effects or a decrease in therapeutic effect. Follow your doctor's instructions carefully. After making any changes in how you take tizanidine, contact your doctor if you notice any change in how well the medicine works or if it causes increased side effects.

Do not take more than three doses (36 mg) of tizanidine in a 24-hour period. Too much of tizanidine can damage your liver. Cold or allergy medicine, narcotic pain medicine, sleeping pills, other muscle relaxers, and medicine for seizures, depression or anxiety can add to sleepiness caused by tizanidine. Tell your doctor if you need to use any of these other medicines together with tizanidine. Avoid drinking alcohol. It can increase some of the side effects of tizanidine.

What should I discuss with my healthcare provider before taking tizanidine?

Do not use this medication if you are allergic to tizanidine, or if you are also taking the antidepressant fluvoxamine (Luvox), or the antibiotic ciprofloxacin (Cipro).

Before using tizanidine, tell your doctor if you are allergic to any drugs, or if you have:

high or low blood pressure; or

a history of "Long QT syndrome."

If you have any of these conditions, you may not be able to use tizanidine, or you may need a dosage adjustment or special tests during treatment.

FDA pregnancy category C. This medication may be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. It is not known whether tizanidine passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. In older adults, tizanidine may take much longer to clear from the body. Follow your doctor's instructions about your specific dosage and medication schedule.

How should I take tizanidine?

Take tizanidine exactly as it was prescribed for you. Do not take the medication in larger amounts, or take it for longer than recommended by your doctor. Follow the directions on your prescription label.

Your doctor may occasionally change your dose to make sure you get the best results from tizanidine.

Take this medication with a full glass of water.

Tizanidine is a short-acting medication, and its effects will be most noticeable between 1 and 6 hours after you take it. This medication should be taken only for daily activities that require relief from muscle spasticity.

In most cases, you may take up to three doses in one day if needed. Allow 6 to 8 hours to pass between doses.

Carefully follow your doctor's instructions about taking this medication with or without food. Taking tizanidine tablets with food can increase the levels of tizanidine in your blood stream, but taking tizanidine capsules with food can decrease the levels.

Switching between tizanidine tablets and capsules, or changing the way you take it with regard to eating, can cause an increase in side effects or a decrease in therapeutic effect. Follow your doctor's instructions carefully. After making any changes in how you take tizanidine, contact your doctor if you notice any change in how well the medicine works or if it causes increased side effects.

Do not take more than three doses (36 mg) in a 24-hour period. Too much of this medication can damage your liver.

To be sure tizanidine is not causing harmful effects, your liver function will need to be tested on a regular basis. Do not miss any scheduled visits to your doctor.

You may have withdrawal symptoms such as dizziness, fast heart rate, tremors, anxiety, and increased spasticity when you stop using tizanidine after using it over a long period of time. Do not stop using this medication suddenly without first talking to your doctor. You may need to use less and less before you stop the medication completely.

Store tizanidine at room temperature away from moisture and heat.

What happens if I miss a dose?

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 at your next regularly scheduled time. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention if you think you have used too much of this medicine.

Overdose symptoms may include drowsiness, confusion, slow heart rate, shallow breathing, feeling light-headed, fainting, or coma.

What should I avoid?

Tizanidine can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert. Dizziness is most likely to occur when you rise from a sitting or lying position. Get up slowly to prevent dizziness and a possible fall. Do not use tizanidine at a time when muscle tone is needed to assure safe balance and movement for certain activities. In some situations, it may endanger your physical safety to be in a state of reduced muscle tone. Cold or allergy medicine, narcotic pain medicine, sleeping pills, other muscle relaxers, and medicine for seizures, depression or anxiety can add to sleepiness caused by tizanidine. Tell your doctor if you need to use any of these other medicines together with tizanidine. Avoid drinking alcohol. It can increase some of the side effects of tizanidine.

Tizanidine side effects

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 any of these serious side effects:

feeling light-headed, fainting, slow heart rate;

hallucinations, confusion, unusual thoughts or behavior;

nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes); or

burning or pain when you urinate.

Less serious tizanidine side effects may be more likely to occur, such as:

drowsiness or dizziness;

feeling anxious or nervous;

sweating or skin rash.

This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.

Tizanidine dosing information

Usual Adult Dose for Muscle Spasm:

The initial dosage of tizanidine recommended for this patient with increased muscle tone associated with spasticity related to multiple sclerosis or spinal cord injury is 4 mg orally once a day.

The dose of tizanidine may be repeated as needed at 6 to 8 hour intervals to a maximum dose 3 doses per 24 hours. The dose may be gradually increased (every 4 to 7 days) in increments of 1 to 2 mg until desired response is attained. The manufacturer recommends that total daily dose should not exceed 36 mg. Additionally. the use of single doses greater than 12 mg is not recommended.

Starting at a lower dose and titrating upward minimizes the risk for adverse effects. Experience with single doses greater than 8 mg and total daily dose greater than 24 mg is limited.

Effects appear to be dose related and gradually diminish within 3 to 6 hours after a dose. Use must be individualized and directed at times and activities where benefit is most important.

Usual Geriatric Dose for Muscle Spasm:

In geriatric patients, a starting dose of 2 mg orally once a day may be appropriate.

What other drugs will affect tizanidine?

Before taking tizanidine, tell your doctor if you are using any of the following drugs:

birth control pills;

antibiotics such as enoxacin (Penetrex), gatifloxacin (Tequin), levofloxacin (Levaquin), lomefloxacin (Maxaquin), moxifloxacin (Avelox), ofloxacin (Floxin), sparfloxacin (Zagam), trovafloxacin (Trovan), or norfloxacin (Noroxin);

blood pressure medications such as clonidine (Catapres), guanabenz (Wytensin), guanfacine (Tenex), or methyldopa (Aldomet); or

heart rhythm medications such as amiodarone (Cordarone, Pacerone), mexiletine (Mexitil), propafenone (Rhythmol), and verapamil (Calan, Covera, Isoptin).

This list is not complete and there may be other drugs that can interact with tizanidine. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.

More about tizanidine

Consumer resources

Professional resources

Related treatment guides

Where can I get more information?

Your pharmacist can provide more information about tizanidine.

Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use tizanidine only for the indication prescribed.

Disclaimer: Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

Copyright 1996-2016 Cerner Multum, Inc. Version: 2.05. Revision Date: 4/12/2009 4:42:37 PM.

Drug Status

Mobic - Pain Relief, Mepedo

Mobic is used to relieve the pain and stiffness of osteoarthritis and rheumatoid arthritis.

Take Mobic exactly as directed by your physician. It is recommended that you take it with a glass of water and a meal (to avoid an empty stomach).

If you miss a dose of Mobic, then skip it and continue with your regular schedule. However, do not take a double dose to make up for the missed dose.

Store Mobic at room temperature away from heat, light and moisture.

Some of the symptoms of a Mobic overdose include nausea, vomiting, stomach pain and bleeding. In extreme cases, it may lead to a heart attack or even coma. Seek medical attention immediately if you suspect an overdose.

Consult your doctor before starting treatment if you are allergic to aspirin, have asthma or experience difficulty breathing while using Mobic. Do not smoke, have alcohol or take steroidal medications while using this drug. Use only if prescribed.

Do not use Mobic if:

you are allergic to any ingredient in Mobic; you have had a severe allergic reaction (eg, severe rash, hives, trouble breathing, growths in the nose, dizziness) to aspirin or a nonsteroidal anti-inflammatory drug (NSAID) (eg, ibuprofen, celecoxib); you have recently had or will be having bypass heart surgery; you have a peptic ulcer; you are in the last 3 months of pregnancy. Contact your doctor or health care provider right away if any of these apply to you.

Important : Do not drive or perform other possibly 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. Mobic is an NSAID. Before you start any new medicine, check the label to see if it has an NSAID (eg, ibuprofen) in it too. If it does or if you are not sure, check with your doctor or pharmacist. Do not take aspirin while you are using Mobic unless your doctor tells you to. Lab tests, including kidney function, complete blood cell counts, and blood pressure, may be performed while you use Mobic. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments. Use Mobic with caution in the elderly; they may be more sensitive to its effects, especially stomach bleeding and kidney problems. Caution is advised when using Mobic in children; they may be more sensitive to its effects, especially diarrhea, fever, headache, stomach pain, and vomiting. Mobic should be used with extreme caution in children younger than 2 years old; safety and effectiveness in these children have not been determined. Pregnancy and breast-feeding: Mobic may cause harm to the fetus. Do not use it during the last 3 months of pregnancy. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of using Mobic while you are pregnant. It is not known if Mobic is found in breast milk. Do not breast-feed while taking Mobic.

Possible Side Effects

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

constipation; diarrhea; dizziness; gas; headache; heartburn; nausea; stomach upset; trouble sleeping. Seek medical attention right away if any of these severe side effects occur:

severe allergic reactions (rash; hives; itching; trouble breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody or black, tarry stools; change in the amount of urine produced; chest pain; confusion; dark urine; depression; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; mental or mood changes; numbness of an arm or leg; one-sided weakness; red, swollen, blistered, or peeling skin; ringing in the ears; seizures; severe headache or dizziness; severe or persistent stomach pain or nausea; severe vomiting; shortness of breath; sudden or unexplained weight gain; swelling of hands, legs, or feet; unusual bruising or bleeding; unusual joint or muscle pain; unusual tiredness or weakness; vision or speech changes; vomit that looks like coffee grounds; yellowing of the skin or eyes.

Mobic is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor.

Comprar Barato Online Herpevir, Herpevir

Comprar Herpevir

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Articulos de interes:

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Donde/Where/Ou

Bendit, planchas de asar.

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Retard - Definition Of Retard By The Free Dictionary, Metobeta

retard

retard

retard

to make slower or later. The country's economic progress was retarded by strikes; The baby's development was retarded by an accident he had shortly after birth. vertraag ?????? ????????? забавям retardar zpomalit verzogern sinke ????????? retrasar pidurdama ?? ????? ???????? ?? ????? ??????? ??? ?????? ???? ??? hidastaa retarder ??????? ?????? ????? usporiti, otegnuti kesleltet terlambat, terbelakang seinka, tefja ritardare ???? ??? ?? suletinti, sulaikyti []kavet; paleninat; kaveties; paleninaties membantutkan vertragen forsinke ; hefte ; hemme zahamowac. opozniac ??? ????? ?????? ? ????? ????? ???? ???? retardar a in­tarzia замедлять. задерживать spomalit zavirati usporiti forsena, bromsa, hamma ???????? geciktirmek ??,?? сповільнювати; гальмувати ????? ?? ???? lam ch?m l?i ??,??

?retar?dation ( ri?ta? - ) noun

vertraging ??????? ????? забавяне atraso zpomaleni die Verzogerung forsinkelse ??????????? retraso pidurdamine ??? ??????? ??? ???? hidastaminen retard ????? ??? usporenje, retardacija kesleltetes keterlambatan seinkun ritardo ?? ?? atsilikimas, suletinimas []kavesana; aizture pembantutan vertraging forsinkelse. hemming zahamowanie ??? ????? ??????? ? ?????? ? ?????? atraso intarziere замедление ; отставание spomalenie, omeskanie (vo vyvoji) zaostajanje usporenje forsening, hammande ???????????????????????????; ?????????????????? gecikme ?? сповільнення, затримка ????? s? ch?m l?i ??

a mentally retarded child. vertraagde ?????? ?????????? бавно развиващо се дете atrasado zaostaly zuruckgeblieben retarderet ??????????????. ?????????? ???????? retrasado alaarenenud, arengupeetusega ??? ?????? ?? ??? ???? jalkeenjaanyt arriere ???? ?????, ?????? dusevno zaostao, debilan (fig.) fogyatekos terbelakang sein?roska ritardato ????? ??? atsilikes atpalicis (attistiba) terbantut achterlijk psykisk utviklingshemmet opozniony ?? ???? ???? ???? ???? atrasado retardat замедленный; отсталый zaostaly vo vyvoji, retardovany zaostal retardiran utvecklingsstord ???????????????????????????? zeka ozurlu (??)????? відсталий ??? ch?m phat tri?n ?????

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References in classic literature ?

For some singular reason, an impression seemed to reign among the servants generally that Missis would not be particularly disobliged by delay; and it was wonderful what a number of counter accidents occurred constantly, to retard the course of things.

But when society is the name for such hollow gentlemen and ladies, Julia, and when its breeding is professed indifference to everything that can advance or can retard mankind, I think we must have lost ourselves in that same Desert of Sahara, and had better find the way out.

Let it be as thou wilt,'' said Rebecca, ``when eight days have passed away; but think not, and speak not now, of aught that may retard thy recovery.

As the figure moved like clockwork, however, and could neither hasten his enormous strides nor retard them, he arrived at the port when they were just beyond the reach of his club.

Struck by the circumstance, and not perceiving any new impediment to retard her footstep, the youth made a tender of his assistance.

These reflections were the only impediments which were able to retard the progress of D'Artagnan.

Hunt was obliged to retard his pace, that they might keep up with him.

Many circumstances combined to retard the wounded traveller in his way to the frontiers.

Aramis was astonished at that lightness of character which permitted this serious man to retard with advantage the moment for more important conversation, to which nobody made any allusion, although all three interlocutors felt its imminence.

He evidently believes that the man clinging to his mane is attempting to restrain him from overtaking his prey, and so he pays no attention to this enemy, who, of course, does not retard the mighty charge in the least.

Home - Arizona Business - Education Coalition, Az, Azbec

Arizona Business & Education Coalition

The Arizona Business & Education Coalition (ABEC) is the coalition of Arizona business and education leaders committed to help create public education policy essential to a vibrant, growing Arizona economy. The coalition is a 501(c)(3), non-partisan, statewide membership organization focused on K-12 public education, while recognizing the importance of early childhood development, post-secondary education and workforce development.

What we do.

Convene - ABEC pr ovides reliable information and insight on education and convenes regular forums to increase members' knowledge and ability to impact K-12 education's direction and quality.

Connect - ABEC offers ongoing opportunity for statewide networking between and among education and business leaders, and direct access to the people who are shaping Arizona education policy and practice.

Collaborate - Building on its strong reputation, ABEC collaborates with other major stakeholders in framing and advocating informed policy positions to key decision makers.

Create - ABEC leads the creation of a nonpartisan environment and platform for shaping long term education policy and financing, built on hard facts and practical experience.

Topster, Topster

Topster

For smooth and easy pouring, use a Topster! It is designed to fit broader thread supermarket plastic milk bottles and helps everyone to control pouring.

Choose from Blue, Red or Green to match your milk variety.

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STANDARD DELIVERY Orders should arrive within 5 days if items are in stock (UK mainland). NEXT DAY DELIVERY Choose Next Day Delivery for next working day delivery if orders are placed before 2pm Monday - Thursday. Orders placed on Friday before 2pm will be delivered the following Monday. This service is only available for UK mainland (excluding Scottish Highlands) and costs an additional ?5 to our normal postage rate but is not available for personalised items.

SATURDAY DELIVERY This service is only available for UK mainland (excluding Scottish Highlands - some AB, PH & PA postcodes). Place your order before 2pm Friday and we will despatch your parcel for delivery on Saturday. Orders placed on Friday after 2pm will be delivered a week on Saturday.

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Topster

For smooth and easy pouring, use a Topster! It is designed to fit broader thread supermarket plastic milk bottles and helps everyone to control pouring.

Choose from Blue, Red or Green to match your milk variety.

Multi-Buy Offer - Buy any 2 Topsters and save ?1.

We always aim to process orders as quickly as possible. You can select your preferred delivery method at checkout:

STANDARD DELIVERY Orders should arrive within 5 days if items are in stock (UK mainland). NEXT DAY DELIVERY Choose Next Day Delivery for next working day delivery if orders are placed before 2pm Monday - Thursday. Orders placed on Friday before 2pm will be delivered the following Monday. This service is only available for UK mainland (excluding Scottish Highlands) and costs an additional ?5 to our normal postage rate but is not available for personalised items.

SATURDAY DELIVERY This service is only available for UK mainland (excluding Scottish Highlands - some AB, PH & PA postcodes). Place your order before 2pm Friday and we will despatch your parcel for delivery on Saturday. Orders placed on Friday after 2pm will be delivered a week on Saturday.

Delivery charges can be found in the footer link 'Delivery & Returns' at the bottom of this product page.

Latest customer comments about our service level and delivery can be found in the footer link 'Customer Service Reviews' at the bottom of this page.

Here are 6 great reasons to shop with us today:

1) Over 26 years trading

2) Over 1 million satisfied customers

3) Over 2,500 quality products

4) Over ?265,000 given to charity

5) Exceptional customer service

6) No quibble returns policy*

Plus you can shop in confidence on our website using our online payment system. Our payments are handled by SagePay, a leading UK PCI DSS compliant payment provider. We do not store your credit card details on our systems.

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Mefloquine 250mg Tablets, Eloquine

MEFLOQUINE 250MG TABLETS

Transcript

PACKAGE LEAFLET: INFORMATION FOR THE PATIENT

Lariam® 250mg Tablets / Mefloquine 250mg Tablets (mefloquine hydrochloride) This medicine is available as either of the above names but will be referred to as Lariam throughout the following leaflet. 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, 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 side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. See section 4.

experienced a mild to serious potential life threatening allergic reaction to Lariam or any of its ingredients low blood glucose due to a pre-existing condition called congenital hyperinsulinemic hypoglycaemia

Some side effects may occur after you have stopped taking Lariam. In a small number of patients it has been shown that depression, dizziness or vertigo and loss of balance may persist for months or longer, even after you have stopped taking Lariam. Children Experience with Lariam in infants less than 3 months old or weighing less than 5 kg is limited. Other medicines and Lariam Before taking Lariam, make sure your doctor knows if you are taking other medicines (including those you have obtained without a prescription).

It occurs when small parasites are passed from one person to another by the bites of certain mosquitoes. Lariam is especially useful if you are travelling to countries where there is a type of malaria which is particularly difficult to treat. No single medicine is effective against all malaria parasites. The choice of a particular medicine depends on the sensitivity of the malaria parasites found in the area to be visited. Your doctor will advise you whether Lariam is suitable for the area to which you wish to go.

Tell your doctor, pharmacist or nurse if you are taking, have recently taken or might take any other medicines including: ? halofantrine, or you have been prescribed a course of halofantrine (see section 2 “Things you should know before taking Lariam”) ? medicines such as quinine, quinidine, or chloroquine, used to treat or to prevent malaria ? medicines for any heart trouble, or high blood pressure, such as ?-blocking agents, calcium channel blockers ? antihistamines for allergies ? medicines for some mental problems (psychiatric disorders). Anti-depressants such as tricyclic anti-depressants, selective serotonin reuptake inhibitors (SSRIs), bupropion or anti-psychotics such as phenothiazines ? medicines used to treat epilepsy, such as sodium valproate, carbamazepine, phenobarbital, phenytoin ? ketoconazole (used to treat fungal infections) – you should also ask your doctor for advice before taking ketoconazole within 15 weeks after taking Lariam ? antibiotics used to treat bacterial infections for example rifampicin, penicillins, cephalosporins ? efavirenz (used to treat HIV infections) ? tramadol (used to treat severe pain) ? medicines for blood clotting disorders or diabetes, as your doctor may wish to monitor you before you travel

To help minimise your chance of catching the disease and to protect you from possible serious side effects it is important that you read this leaflet carefully. Ask your doctor to explain anything you do not understand.

If you need an oral vaccine to help prevent you from catching typhoid, you should arrange to receive it at least 3 days before you need to start taking Lariam. Otherwise, Lariam may stop the vaccine from working properly.

2. What you need to know before you take Lariam

Pregnancy and breast-feeding Pregnant women should not normally take these tablets.

What is in this leaflet 1. What Lariam is and what it is used for 2. What you need to know before you take Lariam 3. How to take Lariam 4. Possible side effects 5. How to store Lariam 6. Contents of the pack and other information 1. What Lariam is and what it is used for Lariam contains the active ingredient mefloquine. Lariam is used to treat malaria and to help prevent you from catching malaria. Malaria is a life threatening disease and a major health risk for travellers visiting tropical countries.

Do not take Lariam if you have or have previously experienced: ? an allergy to mefloquine or any of the other ingredients of this medicine (see section 6 “Contents of the pack and other information”) or to similar medicines such as quinine or quinidine ? depression, thoughts about suicide and self-endangering behaviour ? any other mental problem, including anxiety disorder, schizophrenia or psychosis (losing touch with reality) ? fits (seizures or convulsions) ? severe liver problems ? blackwater fever (a complication of malaria that affects the blood and kidneys) If any of the above applies to you, make sure your doctor knows, so that your doctor can prescribe a different medicine for prevention or treatment of malaria. Also, consult your doctor immediately if you are already being treated with halofantrine, or you have been prescribed a course of halofantrine. Halofantrine (which is used to treat malaria) and Lariam taken at the same time can slow the heartbeat to a dangerous level. Therefore, to help avoid the possibility of a dangerous alteration in heart rhythm, you must not take halofantrine if you are already taking, or have taken Lariam within the last 15 weeks. Warnings and precautions Lariam may cause serious mental problems in some people. Tell your doctor immediately if you experience any of the following while taking Lariam: ? suicidal thoughts ? self-endangering behaviour ? severe anxiety ? feelings of mistrust towards others (paranoia) ? seeing or hearing things that are not there (hallucinations) ? nightmares / abnormal dreams ? depression ? feeling restless ? unusual behaviour ? feeling confused Please seek medical help immediately if you experience serious mental problems while taking Lariam. Lariam should be stopped immediately and replaced with another medicine to prevent malaria. Talk to your doctor, pharmacist, or nurse before taking Lariam if you have: ? epilepsy ? fits (seizures or convulsions) ? heart problems, especially changes in heart rhythm ? liver or kidney problems ? eye problems (e. g. loss of fine detail, colours seem faded, sudden loss of vision, poor vision at night) ? blood or lymphatic disorder (abnormal blood test showing a decrease or an increase in white blood cells, a decrease in red blood cells or platelets) ? neuropathy with signs of e. g. pins and needles, weakness, numbness, new or worsening clumsiness or unsteadiness on your feet, or shaking of the hands and fingers ? inflammation of the lungs, also known as pneumonitis. This is a serious, potentially lifethreatening allergic reaction in the lungs which may cause fever, chills, cough, shortness of breath or chest pain. ? previously contracted malaria even though you were taking Lariam for malaria prevention

Due to the seriousness of malaria during pregnancy, it is recommended that you should not travel to an area where you could become infected with malaria if you are pregnant, think that you may be pregnant, or if you are planning to have a baby. Lariam should be avoided by women who are breast-feeding. If you are pregnant or breast-feeding, think that you may be pregnant, or planning to have a baby, ask your doctor for advice before taking this medicine, as he or she may decide that you should not use this medicine. Driving and using machines Take special care if you perform activities requiring alertness and coordination (accurate small movements) and spatial awareness (being aware of distances) such as driving, piloting an aircraft, operating machinery, cycling and deep-sea diving as Lariam can cause dizziness, loss of balance and mental problems. If you are in any doubt about whether you can do a particular activity, talk to your doctor. In a small number of patients it has been shown that dizziness, vertigo and loss of balance may persist for months or longer after stopping Lariam. Lariam contains lactose If you have been told by your doctor that you have an intolerance to some sugars, such as lactose or galactose, you should not take Lariam. Contact your doctor before taking this medicinal product. 3. How to take Lariam Always take this medicine exactly as your doctor has told you. Check with your doctor if you are not sure. The advice you are given will depend on whether you are taking the tablets for prevention or treatment of malaria. Take the tablets with plenty of water, and preferably after a meal. Swallow the tablets whole, do not suck or chew them. Malaria prevention Please read the following section if you are taking the tablets to help prevent you from catching malaria. Important Take the tablets once a week, always on the same day. st Take the 1 dose 10 days before you leave: this is to make sure that Lariam is well nd tolerated. Take the 2 dose 3 days before you leave. • Continue taking the tablets on the same day of the week throughout your stay and for 4 weeks after your return. • The full course of tablets is at least 6 weeks, depending on your length of stay. • For effective prevention you must take the full course of tablets. • No anti-malarial tablets can be 100% guaranteed to work. There is a chance you could still get malaria during or after taking medicine to prevent it. If you develop a fever or flu-like symptoms during your travels or within 2 to 3 months after you leave the malarious area, check with a doctor immediately. • •

Adults and children over 45 kg body weight, dose: One tablet weekly (always on the same day). A pack of 8 tablets is enough to help prevent you from catching malaria if you are staying for 2 weeks in an area where malaria is present and you start taking the tablets at 10 days and 3 days before departure. Adults weighing less than 45 kg (99 lbs) should take the children’s dose (see below). Whether you are an adult or a child you should not take the tablets for more than 12 months.

Children's dose: The tablets are not recommended for children under 3 months of age, i. e. those who weigh less than 5 kg (11 lbs). For children over this weight, the dose is shown in the table below. The tablets can be divided by breaking along the score lines. As in adults, the dose should be taken once weekly on the same day, and continued for 4 weeks after return. Weight 5 – 19kg (approx. 11 – 43 lbs) 20 – 30kg (approx. 44 – 67 lbs) 31 – 45kg (approx. 68 – 99 lbs)

Age (approx.) 3 months – 5 years 6 – 8 years 9 – 14 years

Dose ? tablet ? tablet ? tablet

Malaria treatment Please read the following section if you are taking the tablets to treat malaria.

Your doctor will tell you how much medicine you need to take. This will depend on your weight and whether you have been living in a malarious area. Normally, you should not receive more than 6 tablets in total. You may be advised to split the total dose into 2 or 3 smaller doses, 6 - 8 hours apart, to reduce the likelihood or severity of side effects.

If you take more Lariam than you should, either for prevention or treatment If you take too many tablets the likelihood and severity of the side effects as described in section 4 may increase. There are no specific antidotes.

If you take too many tablets or someone else accidentally takes your medicine, contact your doctor, pharmacist or nearest hospital immediately. If you forget to take Lariam, either for prevention or treatment If you miss a dose, take it as soon as possible. If it is nearly time for your next dose, skip the missed dose and carry on as before. Do not take a double dose. 4. Possible side effects Like all medicines, this medicine can cause side effects although not everybody gets them. Lariam may cause serious mental problems in some people. Stop taking this medicine and contact your doctor immediately if you experience any of the following while taking Lariam: Common (may affect up to 1 in 10 people): ? depression ? anxiety Not known (frequency cannot be estimated from the available data): ? suicide ? attempted suicide ? suicidal thoughts ? self-endangering behaviour ? losing touch with reality (psychosis) ? feelings of mistrust towards others (paranoia) ? panic attacks ? unusual behaviour ? feeling confused ? seeing or hearing things that are not there (hallucinations) ? aggression ? agitation ? feeling restless ? unusual changes in your mood ? disturbance in attention Please seek medical help immediately if you experience serious mental problems while taking Lariam. Lariam should be stopped immediately and replaced with another medicine to prevent malaria. If you develop any of the following potentially serious symptoms, you should STOP taking this medicine and also consult a doctor immediately. Not known (frequency cannot be estimated from the available data): ? a mild to serious potential life-threatening allergic reaction (anaphylaxis) to Lariam or any of its ingredients with symptoms such as difficulty in breathing, swollen tongue, itching and severe rash ? severe changes in texture and appearance of the skin, especially serious blistering and peeling that affects the mouth eyes and genitals (Stevens Johnson syndrome) ? fits (seizures or convulsions) ? heart problems e. g. severe changes in heartbeat, including pounding, racing or skipped beats (palpitations) ? inflammation of the lungs, also known as pneumonitis. This is a serious, potentially lifethreatening allergic reaction in the lungs which may cause fever, chills, cough, shortness of breath or chest pain. ? severe liver problems which might be demonstrated by a transient increase in your liver enzymes shown by blood tests or other symptoms such as tender, firm or possibly enlarged liver, jaundice (yellowing of skin/ eyes), dark urine, light coloured stools and generalised itchiness Other possible side effects Very common (may affect more than 1 in 10 people): ? sleeping problems (sleepiness, unable to sleep, bad dreams) Common (may affect up to 1 in 10 people): ? dizziness ? headache ? problems with your vision ? loss of balance (vertigo) ? feeling sick (nausea), being sick (vomiting) ? diarrhoea ? stomach ache (abdominal pain) ? itching Not known (frequency cannot be estimated from the available data): ? abnormal blood test results showing a decrease or an increase in white blood cells, a decrease in red blood cells or platelets. Symptoms may include painful mouth or throat ulcers, fever, chills, bruises on the skin, nosebleeds, bleeding in the stomach or vaginal bleeding.

kidney problems, failure or infection, causing impairment, cessation. infection, or blood in the urine. Symptoms may include abnormal blood tests (increased blood creatinine), feeling dehydrated, fatigue, swelling (oedema), shortness of breath, feeling or being sick, loss of appetite, or headache decreased appetite fainting neuropathy with signs of e. g. “pins and needles”, weakness, new or worsening clumsiness or unsteadiness on your feet, or shaking of the hands and fingers forgetfulness (sometimes lasting for more than 3 months) difficulties in talking difficulties with sense of smell and taste, eye movement, facial sensation and expression, hearing, balance, tasting, tongue movement, head-turning, and raising your shoulders cataract, dazzled in the evenings or other vision disturbances, blurred vision changes to your hearing including ringing in the ears or difficulty in hearing (sometimes prolonged), everyday sounds seeming too loud changes to blood pressure or heart rate hot flushes breathlessness, cough pancreas problems; symptoms may include stomach pain, nausea, vomiting, changes to blood pressure or heart rates and breathlessness indigestion rash hair loss sweating muscle weakness muscle cramps joint pains muscle pains oedema chest pain tiredness fever or chills

Whilst taking this medicine, if you experience these or any other symptoms that concern you, tell your doctor. Some side effects may occur after you have stopped taking Lariam. In a small number of patients it has been shown that depression, dizziness or vertigo and loss of balance may persist for months or longer, even after you have stopped taking Lariam. 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 Lariam

Do not use after the expiry date printed on the carton label or blister strip. The expiry date refers to the last day of that month. Store in the original package to protect from moisture. Do not store above 35°C. Keep all medicines out of the sight and reach of children. If the tablets become discoloured or show signs of any deterioration, you should seek the advice of your pharmacist. Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.

6. Contents of the pack and other information Each tablet contains 250mg of the active ingredient mefloquine (as the hydrochloride) in a white round tablet, cross scored and marked ‘Roche’ and logo on one side and plain on the reverse. Lariam 250mg Tablets also contain the following inactive ingredients: Microcrystalline cellulose, lactose anhydrous, maize starch, ammonium-calcium alginate, polaxamer (polyoxyethylene-polyoxypropylene copolymer), talc and magnesium stearate. Lariam 250mg Tablets are available in blister packs of 8 tablets. POM

PL NO: 17805/0369

This product is manufactured by F. Hoffmann-La Roche A. G. Grenzacherstrasse 124, CH4070, Basle Switzerland and procured from within the EU by the Product Licence holder Delta Pharma (Europe) Ltd, 1 Colonial Way, P. O. Box 233, North Watford, Herts WD24 4EW and repackaged by O. P.D. Laboratories Ltd. Watford, Herts WD24 4PR. Leaflet revision and issue date (Ref.) 04.04.2016. Lariam is a registered Trade Mark of Roche Products Limited, UK You can get more information on Lariam from your doctor, pharmacist or nurse. It is essential that you follow the recommendations given for taking the tablets. Other preventative actions you should take If you are taking Lariam to prevent malaria, you should also take steps to avoid mosquito bites. Some information on how to avoid bites is given below. This is important as no medicine can be 100% guaranteed to protect you against malaria. ? Make sure you sleep in a room that is screened against mosquitoes or has full air conditioning, or that you use a mosquito net (preferably one that has been treated with an insect repellent) over the bed. ? Use insect repellents; ointments, lotions and sprays, to deter mosquitoes. ? In the evening, cover arms and legs with light-coloured, long-sleeved clothes and trousers, and use an insect repellent. Anklets are also available which have been treated with repellent. ? Vaporising electric “mats”, mosquito coils or tablets can be used at night-time around exposed areas of the body (ankles and feet). To request a copy of this leaflet in Braille, large print or audio please call 01923 332 796.

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.

Lithionit, Lithionit

Lithium

Therapeutic Category

Foreign Names

Lithium (Latin)

Lithium (German)

Lithium (French)

Litio (Spanish)

Generic Names

Lithium aceticum (IS)

DL-Asparaginsaure, Monolithiumsalz-1-Wasser (IS)

Lithium asparagicum (IS)

Lithium DL-asparaginat-1-Wasser (IS)

Lithium Carbonate (OS: JAN, USAN)

CP 15467-61 (IS)

Lithii carbonas (PH: Ph. Eur. 8, Ph. Int. 4)

Lithium (carbonate de) (PH: Ph. Eur. 8)

Lithium carbonate (PH: Ph. Eur. 8)

Lithium Carbonate (PH: BP 2016, JP XVI, Ph. Int. 4, USP 38)

Lithiumcarbonat (PH: Ph. Eur. 8)

CCRIS 5924 (IS)

NSC 327172 (IS)

Lithii citras (PH: Ph. Eur. 8)

Lithium (citrate de) (PH: Ph. Eur. 8)

Lithium Citrate (PH: BP 2016, USP 38)

Lithium citrate (PH: Ph. Eur. 8)

Lithiumcitrat (PH: Ph. Eur. 8)

D-Gluconsaure, Lithiumsalz (IS)

Lithium gluconicum (IS)

Lithium-D-gluconat (IS)

Brand Names

Depression - Lithionit (Brand name: lithium)

Lithium Carbonate is used to treat the manic episodes of manic-depressive illness, the condition when a person's mood swings from depression to excessive excitement. A manic episode may involve some or all of the following symptoms:

Aggressiveness; Elation; Fast, urgent talking; Frenetic physical activity; Grandiose, unrealistic ideas; Hostility; Little need for sleep; Poor judgment. Some doctors also prescribe Lithionit for premenstrual tension, eating disorders such as bulimia, certain movement disorders, and sexual addictions.

Use Lithium Carbonate as directed by your doctor.

To avoid stomach upset, take Lithium Carbonate immediately after meals or with food or milk. While taking Lithium Carbonate, you should drink 10 to 12 glasses of water or fluid a day. To minimize the risk of harmful side effects, eat a balanced diet that includes some salt and lots of liquids. If you have been sweating a great deal or have had diarrhea, make sure you get extra liquids and salt. Ask your health care provider any questions you may have about the usage of Lithium Carbonate.

Drug Class and Mechanism

Lithium Carbonate is an antimanic agent. The way Lithium works is not known exactly, but it may work by altering the balance of certain chemicals in the brain.

If you miss a dose of Lithium Carbonate and 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.

Store Lithium Carbonate 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 in a tight, light-resistant container. Keep Lithium Carbonate out of the reach of children and away from pets.

Do not use Lithium Carbonate if:

you are allergic to any ingredient in Lithium Carbonate; you have moderate to severe kidney, heart, or blood vessel problems; you have low blood sodium levels; you are severely dehydrated, ill, or weakened; you are taking an angiotensin-converting enzyme (ACE) inhibitor (e. g. enalapril) or a diuretic (e. g. furosemide, hydrochlorothiazide). Contact your doctor or health care provider right away if any of these apply to you.

Important: Lithium Carbonate may cause drowsiness or dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Lithium Carbonate with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it. Do not take more than the recommended dose without checking with your doctor. It may take 1 to 3 weeks for Lithium Carbonate to work. Do not stop using Lithium Carbonate without checking with your doctor. Tell your doctor or dentist that you take Lithium Carbonate before you receive any medical or dental care, emergency care, or surgery. Fever, infection, vomiting, diarrhea, or excessive sweating may affect the levels of Lithium Carbonate in your blood. If you experience any of these conditions, contact your doctor. Consult your doctor about the problem of salt loosing. Do not change the amount of salt in your diet unless instructed by your doctor. Check with your doctor before restricting your salt intake. Tell your doctor if you are on a low-salt diet. While you are taking Lithium Carbonate, lab tests - including blood Lithionit levels and kidney function tests - may be performed. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments. Use Lithium Carbonate with caution in the elderly; they may be more sensitive to its effects. Lithium Carbonate should not be used in children younger than 12 years old; safety and effectiveness in these children have not been confirmed. Pregnancy and breast-feeding: Lithium Carbonate 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 Lithium Carbonate while you are pregnant. Lithium Carbonate is found in breast milk. Do not breast-feed while taking Lithium Carbonate since it 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 Lithium Carbonate while you are pregnant. Lithium Carbonate is found in breast milk. Do not breast-feed while taking Lithium Carbonate.

Possible Side Effects

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

mild hand tremor; mild thirst; temporary, mild nausea and general discomfort at the beginning of treatment. 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); blurred vision; confusion; diarrhea; drowsiness; excessive weight gain; fainting; giddiness; inability to control the bladder or bowels; increased thirst; increased or decreased urination; involuntary twitching or muscle movements; loss of consciousness; loss of coordination; muscle weakness; persistent headache; persistent or severe nausea; ringing in the ears; seizures; slow or irregular heartbeat; slurred speech; swelling of the ankles or wrists; unsteadiness; vision changes; vomiting.

Lithium Carbonate is to be used only by the patient for whom it is prescribed. Do not share it with other people.

If your symptoms do not improve or if they become worse, check with your doctor.

Erythron - Definition Of Erythron By The Free Dictionary, Erythran

erythron

References in periodicals archive ?

Anaemia is promoted by erythropoietin deficiency, shortened existence of red blood cells, death of immature erythroblasts due to the Fas ligand and TRAIL, decreased responsiveness of the erythron to proliferative signals of erythropoietin, and the myelosuppressive effect of the chemotherapy (32), (33).

Iron is primarily transported to the developing red cell mass or erythron in the marrow.

Anemia management of patients with CKD on dialysis is a constant challenge, since a chronic disease state coexists with ongoing procedural blood loss, reduced marrow erythroid response, restricted availability of storage iron to reenter the erythron pool, shortened red cell survival, and possibly other factors.

Expression of the H-subunit and L-subunit of ferritin in bone marrow macrophages and cells of the erythron during cellular immune activation.

Evaluation of the erythron is a commonly used diagnostic technique to assess anemia in mammalian veterinary patients.

The second, collectively described as myeloid, generates red cells or the erythron. granulocytes and monocytes as well as megakaryocytes from which platelets will ultimately be derived (Fig.

erythron

References in periodicals archive ?

Anaemia is promoted by erythropoietin deficiency, shortened existence of red blood cells, death of immature erythroblasts due to the Fas ligand and TRAIL, decreased responsiveness of the erythron to proliferative signals of erythropoietin, and the myelosuppressive effect of the chemotherapy (32), (33).

Iron is primarily transported to the developing red cell mass or erythron in the marrow.

Anemia management of patients with CKD on dialysis is a constant challenge, since a chronic disease state coexists with ongoing procedural blood loss, reduced marrow erythroid response, restricted availability of storage iron to reenter the erythron pool, shortened red cell survival, and possibly other factors.

Expression of the H-subunit and L-subunit of ferritin in bone marrow macrophages and cells of the erythron during cellular immune activation.

Evaluation of the erythron is a commonly used diagnostic technique to assess anemia in mammalian veterinary patients.

The second, collectively described as myeloid, generates red cells or the erythron. granulocytes and monocytes as well as megakaryocytes from which platelets will ultimately be derived (Fig.

Tamoxifen Uses, Dosage, Side Effects, Tamoxifeni Citras

Tamoxifen

Tamoxifen blocks the actions of estrogen, a female hormone. Certain types of breast cancer require estrogen to grow.

Tamoxifen is used to treat some types of breast cancer in men and women. It is also used to lower a woman's chance of developing breast cancer if she has a high risk (such as a family history of breast cancer).

Tamoxifen may also be used for purposes not listed in this medication guide.

Important information

Do not use tamoxifen if you are pregnant. It could harm the unborn baby. Use a barrier form of birth control (such as a condom or diaphragm with spermicide) while you are using this medication and for at least 2 months after your treatment ends. You should not use tamoxifen if you are allergic to it, or if you have a history of blood clots in your veins or your lungs, or if you are also taking a blood thinner such as warfarin (Coumadin).

Before using this medicine, tell your doctor if you have liver disease, high triglycerides (a type of fat in the blood), a history of cataract, or a history of stroke or blood clot. Also tell your doctor if you if you are receiving chemotherapy or radiation treatment.

If you are taking tamoxifen to reduce your risk of breast cancer, you may need to take your first dose while you are having a menstrual period. You may also need to have a pregnancy test before you start taking this medicine, to make sure you are not pregnant. Follow your doctor's instructions.

Taking tamoxifen may increase your risk of uterine cancer, stroke, or a blood clot in the lung, which can be fatal. Talk with your doctor about your specific risks in taking this medication.

To make sure this medication is not causing harmful effects, your doctor may want you to have mammograms and to perform routine breast self exams on a regular basis. Your liver function may also need to be tested. Visit your doctor regularly.

Before taking this medicine

You should not use tamoxifen if you are allergic to it.

You should not use tamoxifen to reduce your risk of breast cancer if you are also taking a blood thinner such as warfarin (Coumadin, Jantoven).

Do not take tamoxifen if you are pregnant. It could harm the unborn baby. Avoid becoming pregnant while you are using this medicine, and for at least 2 months after your treatment ends.

Hormonal contraception (such as birth control pills, injections, implants, skin patches, and vaginal rings) may not be effective enough to prevent pregnancy while taking tamoxifen. Ask your doctor about using non hormonal birth control (condom, diaphragm with spermicide, or intrauterine device/IUD).

If you are taking tamoxifen to reduce your risk of breast cancer . you may need to take your first dose while you are having a menstrual period. You may also need to have a pregnancy test before you start taking tamoxifen, to make sure you are not pregnant. Follow your doctor's instructions.

Taking tamoxifen may increase your risk of uterine cancer, stroke, or a blood clot in the lung, which can be fatal. Talk with your doctor about your specific risks in taking this medicine.

To make sure tamoxifen is safe for you, tell your doctor if you have:

a history of stroke or blood clot;

high cholesterol or triglycerides (a type of fat in the blood);

a history of cataracts; or

if you are receiving chemotherapy or radiation.

It is not known whether tamoxifen passes into breast milk or if it could harm a nursing baby. This medicine may slow breast milk production. You should not breast-feed while taking tamoxifen.

How should I take tamoxifen?

Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Measure liquid medicine with the dosing syringe provided, or with a special dose-measuring spoon or medicine cup. If you do not have a dose-measuring device, ask your pharmacist for one.

Tamoxifen can be taken with or without food.

While using tamoxifen, you may need frequent blood tests.

If you need surgery or medical tests or if you will be on bed rest . you may need to stop using this medicine for a short time. Any doctor or surgeon who treats you should know that you are taking tamoxifen.

Have regular physical exams and mammograms, and self-examine your breasts for lumps on a monthly basis while using this medicine.

Use tamoxifen regularly to get the most benefit. Get your prescription refilled before you run out of medicine completely. You may need to keep using this medication for up to 5 years.

Store at room temperature away from moisture, heat, or cold. Do not freeze.

What happens if I miss 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.

What happens if I overdose?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

What should I avoid while taking tamoxifen?

This medicine can pass into body fluids (urine, feces, vomit). Caregivers should wear rubber gloves while cleaning up a patient's body fluids, handling contaminated trash or laundry or changing diapers. Wash hands before and after removing gloves. Wash soiled clothing and linens separately from other laundry.

Tamoxifen side effects

Get emergency medical help if you have signs of an allergic reaction to tamoxifen: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Tamoxifen can increase your risk of stroke or blood clots. Call your doctor at once if you have :

signs of a stroke - sudden numbness or weakness (especially on one side of the body), sudden severe headache, slurred speech, problems with vision or balance;

signs of a blood clot in the lung - chest pain, sudden cough, wheezing, rapid breathing, coughing up blood; or

signs of a blood clot in your leg - pain, swelling, warmth, or redness in one or both legs.

Also call your doctor at once if you have:

blurred vision, tunnel vision, eye pain, or seeing halos around lights;

unusual vaginal bleeding or discharge;

changes in your menstrual periods;

pain or pressure in your pelvic area;

a new breast lump;

liver problems - nausea, upper stomach pain, itching, tired feeling, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes); or

high levels of calcium in your blood - vomiting, constipation, increased thirst or urination, muscle weakness, bone pain, confusion, lack of energy, or tired feeling.

Common tamoxifen ide effects may include:

vaginal discharge; or

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

Tamoxifen dosing information

Usual Adult Dose for Breast Cancer:

For the treatment of metastatic breast cancer in women and men: 20 to 40 mg orally Dosages greater than 20 mg should be given in divided doses (morning and evening).

For the treatment of women with Ductal Carcinoma in Situ, following breast surgery and radiation: 20 mg orally daily for 5 years.

To reduce the incidence of breast cancer in women at high risk for breast cancer: 20 mg orally daily for 5 years.

Usual Adult Dose for Breast Cancer - Adjuvant:

For the treatment of node-positive breast cancer in postmenopausal women following total mastectomy or segmental mastectomy, axillary dissection, and breast irradiation: 10 mg orally 2 to 3 times a day for 5 years.

Usual Adult Dose for Breast Cancer - Palliative:

10 to 20 mg orally twice a day

A beneficial response may not be evident for several months after initiation of therapy.

Usual Pediatric Dose for McCune-Albright Syndrome:

For use in girls age 2 to 10 years with McCune-Albright Syndrome and precocious puberty: 20 mg once a day. The duration of treatment is up to 12 months.

Usual Pediatric Dose for Precocious Puberty:

For use in girls age 2 to 10 years with McCune-Albright Syndrome and precocious puberty: 20 mg once a day. The duration of treatment is up to 12 months.

What other drugs will affect tamoxifen?

Many drugs can interact with tamoxifen, and some drugs should not be used together. This includes prescription and over-the-counter medicines, vitamins, and herbal products. Not all possible interactions are listed in this medication guide. Tell your doctor about all medicines you use, and those you start or stop using during your treatment with tamoxifen. Give a list of all your medicines to any healthcare provider who treats you.

More about tamoxifen

Consumer resources

Professional resources

Related treatment guides

Where can I get more information?

Your pharmacist can provide more information about tamoxifen.

Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use tamoxifen only for the indication prescribed.

Disclaimer: Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

Copyright 1996-2016 Cerner Multum, Inc. Version: 8.04. Revision Date: 2015-08-04, 2:24:52 PM.

Drug Status

Availability Rx Prescription only

Pregnancy Category D Positive evidence of risk

CSA Schedule N Not a controlled drug

Approval History Calendar Drug history at FDA

Fusidic Acid - Brand Name List From, Fusindac

Fusidic acid

See also.

Disclaimer: The indications, uses and warnings for individual medications outside the USA are determined by local regulatory bodies in each country or region. The Drugs. com website is intended primarily for audiences in the United States and its territories. Indications, uses and warnings on Drugs. com patient information leaflets are derived from FDA product labels and may differ in countries outside the USA. Every effort has been made to ensure that the information provided on this page is accurate, up-to-date and complete, but no guarantee is made to that effect. Drugs. com does not endorse drugs, diagnose patients or recommend specific therapies. The information on this page is not a substitute for the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that a drug or drug combination is safe, effective or appropriate for any given patient. Drugs. com does not assume any responsibility for any aspect of healthcare administered with the aid of information provided here. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. Always consult your doctor or healthcare specialist for medical advice.

Chemical formula: C31H48O6 Drugbank ID: DB02703 ATC code(s): D06AX01, D09AA02, J01XC01, S01AA13

Listran Generic Name Nabumetone Online, Listran

Listran General Information

Listran - Pharmacology:

The parent compound is a prodrug, which undergoes hepatic biotransformation to the active component, 6-methoxy-2-naphthylacetic acid (6MNA), that is a potent inhibitor of prostaglandin synthesis, most likely through binding to the COX-1 and COX-2 receptors.

Listran for patients

Listran is a non-steroidal anti-inflammatory (NSAID) medication used to relieve pain, treat fever, and decrease inflammation and swelling. It is used commonly to treat osteoarthritis and rheumatoid arthritis. This medication should not be used by those with aspirin allergies producing symptoms of difficult breathing, red itching skin. This class of medications has been associated with ulcer and bleeding in the stomach. This is often relieved by taking the medication with food. Water retention may also occur and you should report any swelling of the feet or difficulty breathing to your physician immediately. This medication can be taken with or without food, however, food often alleviates stomach irritation.

This description is suitable for active ingredient Nabumetone

Listran Interactions

In vitro studies have shown that, because of its affinity for protein, 6MNA may displace other protein-bound drugs from their binding site. Caution should be exercised when administering nabumetone with warfarin since interactions have been seen with other NSAIDs.

Concomitant administration of an aluminum-containing antacid had no significant effect in the bioavailability of 6MNA. When administered with food or milk, there is more rapid absorption; however, the total amount of 6MNA in the plasma is unchanged .

Listran Contraindications

Listran is contraindicated in patients who have previously exhibited hypersensitivity to it.

Listran is contraindicated in patients in whom nabumetone, aspirin or other NSAIDs induce asthma, urticaria or other allergic-type reactions. Fatal asthmatic reactions have been reported in such patients receiving NSAIDs.

This description is suitable for active ingredient Nabumetone

Generic name, Overdose, Half Life Listran, Food Interactions, Chemical, etc..

Flagyl Er - Woman S Health, Kefavet

METRONIDAZOLE is an antiinfective. This medicine is used to treat many kinds of infections, like respiratory, skin, gastrointestinal, and bone and joint infections. It will not work for colds, flu, or other viral infections.

What should my health care professional know before I take this medicine?

They need to know if you have any of these conditions: anemia or other blood disorders disease of the nervous system fungal or yeast infection if you drink alcohol containing drinks liver disease seizures an unusual or allergic reaction to metronidazole, or other medicines, foods, dyes, or preservatives pregnant or trying to get pregnant breast-feeding

How should I take this medicine?

Take this medicine by mouth with a full 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 you are better. Do not skip doses or stop your medicine early.

Talk to your pediatrician regarding the use of this medicine in children. Special care may be needed.

If you think you have taken too much of this medicine contact a poison control center or emergency room at once.

NOTE: This medicine is only for you. Do not share this medicine with others.

What if I miss a dose?

If you miss a dose, take it as soon as you can. If it is almost time for your next dose, take only that dose. Do not take double or extra doses.

What may interact with this medicine?

Do not take this medicine with any of the following: alcohol or any product that contains alcohol amprenavir oral solution disulfiram paclitaxel injection ritonavir oral solution sertraline oral solution sulfamethoxazole-trimethoprim injection

This medicine may also interact with the following: cimetidine lithium phenobarbital phenytoin warfarin

This list may not describe all possible interactions. Give your health care providers a list of all the medicines, herbs, non-prescription drugs, or dietary supplements you use. Also tell them if you smoke, drink alcohol, or use illegal drugs. Some items may interact with your medicine.

What should I watch for while taking this medicine?

Tell your doctor or health care professional if your symptoms do not improve or if they get worse.

You may get drowsy or dizzy. Do not drive, use machinery, or do anything that needs mental alertness until you know how this medicine affects you. Do not stand or sit up quickly, especially if you are an older patient. This reduces the risk of dizzy or fainting spells.

Avoid alcoholic drinks while you are taking this medicine and for three days afterward. Alcohol may make you feel dizzy, sick, or flushed.

If you are being treated for a sexually transmitted disease, avoid sexual contact until you have finished your treatment. Your sexual partner may also need treatment.

What side effects may I notice from this medicine?

Side effects that you should report to your doctor or health care professional as soon as possible: allergic reactions like skin rash or hives, swelling of the face, lips, or tongue confusion, clumsiness dark or white patches in the mouth fever, infection numbness, tingling, pain or weakness in the hands or feet pain when passing urine seizures if you are unusually weak or tired vaginal irritation or discharge

Side effects that usually do not require medical attention (report to your doctor or health care professional if they continue or are bothersome): diarrhea headache metallic taste nausea stomach pain or cramps

This list may not describe all possible side effects.

Where can I keep my medicine?

Keep out of the reach of children.

Store at room temperature below 25 degrees C (77 degrees F). Protect from light. Keep the container tightly closed. Throw away any unused medicine after the expiration date.

Nobzol, Nobzol

Nobzol

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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