Tetrafen, Tetrafen

Sumycin is used for treating infections caused by certain bacteria. Sumycin is a tetracycline antibiotic. It works by slowing the growth of sensitive bacteria by interfering with the production of proteins needed by the bacteria to grow. Slowing the bacteria's growth allows the body's defense mechanisms to destroy them.

Use Sumycin as directed by your doctor.

Take Sumycin by mouth on an empty stomach at least 1 hour before or 2 hours after eating.

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

If you also take antacids containing aluminum, calcium, or magnesium; preparations containing bismuth, iron, zinc, or sodium bicarbonate; or calcium rich foods (eg, milk, dairy products, calcium-enriched juices), do not take them within 2 to 3 hours before or after taking Sumycin. Check with your doctor if you have questions.

To clear up your infection completely, take Sumycin for the full course of treatment. Keep taking it even if you feel better in a few days.

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

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

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

Active Ingredient: Tetracycline hydrochloride.

Do NOT use Sumycin if:

you are allergic to any ingredient in Sumycin or other tetracycline antibiotics (eg, doxycycline)

you are taking acitretin or methoxyflurane.

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

Some medical conditions may interact with Sumycin. 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 diarrhea, a stomach infection, or kidney problems.

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

Acitretin or isotretinoin because side effects, such as increased pressure in the fluid surrounding the brain, may occur

Digoxin, methotrexate, methoxyflurane, or oral anticoagulants (eg, warfarin) because the risk of their side effects may be increased by Sumycin

Atovaquone, lithium, oral contraceptives (birth control pills), or penicillins (eg, amoxicillin) because their effectiveness may be decreased by Sumycin.

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

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

Contact your doctor right away if stomach pain or cramps, severe diarrhea, or bloody stools occur. Do not treat diarrhea without first checking with your doctor.

Be sure to use Sumycin for the full course of treatment. If you do not, the medicine may not clear up your infection completely. The bacteria could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future.

Sumycin may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Sumycin. Use a sunscreen or wear protective clothing if you must be outside for more than a short time.

Do not use after expiration date. Outdated medicine is highly toxic to the kidneys.

Long-term or repeated use of Sumycin may cause a second infection. Tell your doctor if signs of a second infection occur. Your medicine may need to be changed to treat this.

Hormonal birth control (eg, birth control pills) may not work as well while you are using Sumycin. To prevent pregnancy, use an extra form of birth control (eg, condoms).

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

Use of Sumycin in children may cause permanent discoloring of the teeth.

Sumycin should be used with extreme caution in children younger 8 years; safety and effectiveness in these children have not been confirmed.

Pregnancy and beast-feeding: Sumycin has been shown to 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 Sumycin while you are pregnant. Sumycin is found in breast milk. Do not breast-feed while taking Sumycin.

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:

Black hairy tongue; blurred vision; bulky loose stools; diarrhea; difficulty swallowing; fever; headache; hives; hoarseness; indigestion; inflammation or redness of tongue; joint pain; loss of appetite; mouth sores; nausea; rash; sensitivity to sunlight; sore throat; stomach pain; swelling and itching of the rectum.

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); infection (fever, chills, sore throat); itching; nausea; severe skin reaction to the sun; vaginal irritation or discharge; vomiting.

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

Sumycin is used for treating infections caused by certain bacteria. Sumycin is a tetracycline antibiotic. It works by slowing the growth of sensitive bacteria by interfering with the production of proteins needed by the bacteria to grow. Slowing the bacteria's growth allows the body's defense mechanisms to destroy them.

Use Sumycin as directed by your doctor.

Take Sumycin by mouth on an empty stomach at least 1 hour before or 2 hours after eating.

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

If you also take antacids containing aluminum, calcium, or magnesium; preparations containing bismuth, iron, zinc, or sodium bicarbonate; or calcium rich foods (eg, milk, dairy products, calcium-enriched juices), do not take them within 2 to 3 hours before or after taking Sumycin. Check with your doctor if you have questions.

To clear up your infection completely, take Sumycin for the full course of treatment. Keep taking it even if you feel better in a few days.

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

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

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

Active Ingredient: Tetracycline hydrochloride.

Do NOT use Sumycin if:

you are allergic to any ingredient in Sumycin or other tetracycline antibiotics (eg, doxycycline)

you are taking acitretin or methoxyflurane.

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

Some medical conditions may interact with Sumycin. 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 diarrhea, a stomach infection, or kidney problems.

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

Acitretin or isotretinoin because side effects, such as increased pressure in the fluid surrounding the brain, may occur

Digoxin, methotrexate, methoxyflurane, or oral anticoagulants (eg, warfarin) because the risk of their side effects may be increased by Sumycin

Atovaquone, lithium, oral contraceptives (birth control pills), or penicillins (eg, amoxicillin) because their effectiveness may be decreased by Sumycin.

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

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

Contact your doctor right away if stomach pain or cramps, severe diarrhea, or bloody stools occur. Do not treat diarrhea without first checking with your doctor.

Be sure to use Sumycin for the full course of treatment. If you do not, the medicine may not clear up your infection completely. The bacteria could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future.

Sumycin may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Sumycin. Use a sunscreen or wear protective clothing if you must be outside for more than a short time.

Do not use after expiration date. Outdated medicine is highly toxic to the kidneys.

Long-term or repeated use of Sumycin may cause a second infection. Tell your doctor if signs of a second infection occur. Your medicine may need to be changed to treat this.

Hormonal birth control (eg, birth control pills) may not work as well while you are using Sumycin. To prevent pregnancy, use an extra form of birth control (eg, condoms).

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

Use of Sumycin in children may cause permanent discoloring of the teeth.

Sumycin should be used with extreme caution in children younger 8 years; safety and effectiveness in these children have not been confirmed.

Pregnancy and beast-feeding: Sumycin has been shown to 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 Sumycin while you are pregnant. Sumycin is found in breast milk. Do not breast-feed while taking Sumycin.

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:

Black hairy tongue; blurred vision; bulky loose stools; diarrhea; difficulty swallowing; fever; headache; hives; hoarseness; indigestion; inflammation or redness of tongue; joint pain; loss of appetite; mouth sores; nausea; rash; sensitivity to sunlight; sore throat; stomach pain; swelling and itching of the rectum.

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); infection (fever, chills, sore throat); itching; nausea; severe skin reaction to the sun; vaginal irritation or discharge; vomiting.

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

Sumycin is used for treating infections caused by certain bacteria. Sumycin is a tetracycline antibiotic. It works by slowing the growth of sensitive bacteria by interfering with the production of proteins needed by the bacteria to grow. Slowing the bacteria's growth allows the body's defense mechanisms to destroy them.

Use Sumycin as directed by your doctor.

Take Sumycin by mouth on an empty stomach at least 1 hour before or 2 hours after eating.

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

If you also take antacids containing aluminum, calcium, or magnesium; preparations containing bismuth, iron, zinc, or sodium bicarbonate; or calcium rich foods (eg, milk, dairy products, calcium-enriched juices), do not take them within 2 to 3 hours before or after taking Sumycin. Check with your doctor if you have questions.

To clear up your infection completely, take Sumycin for the full course of treatment. Keep taking it even if you feel better in a few days.

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

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

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

Active Ingredient: Tetracycline hydrochloride.

Do NOT use Sumycin if:

you are allergic to any ingredient in Sumycin or other tetracycline antibiotics (eg, doxycycline)

you are taking acitretin or methoxyflurane.

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

Some medical conditions may interact with Sumycin. 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 diarrhea, a stomach infection, or kidney problems.

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

Acitretin or isotretinoin because side effects, such as increased pressure in the fluid surrounding the brain, may occur

Digoxin, methotrexate, methoxyflurane, or oral anticoagulants (eg, warfarin) because the risk of their side effects may be increased by Sumycin

Atovaquone, lithium, oral contraceptives (birth control pills), or penicillins (eg, amoxicillin) because their effectiveness may be decreased by Sumycin.

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

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

Contact your doctor right away if stomach pain or cramps, severe diarrhea, or bloody stools occur. Do not treat diarrhea without first checking with your doctor.

Be sure to use Sumycin for the full course of treatment. If you do not, the medicine may not clear up your infection completely. The bacteria could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future.

Sumycin may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Sumycin. Use a sunscreen or wear protective clothing if you must be outside for more than a short time.

Do not use after expiration date. Outdated medicine is highly toxic to the kidneys.

Long-term or repeated use of Sumycin may cause a second infection. Tell your doctor if signs of a second infection occur. Your medicine may need to be changed to treat this.

Hormonal birth control (eg, birth control pills) may not work as well while you are using Sumycin. To prevent pregnancy, use an extra form of birth control (eg, condoms).

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

Use of Sumycin in children may cause permanent discoloring of the teeth.

Sumycin should be used with extreme caution in children younger 8 years; safety and effectiveness in these children have not been confirmed.

Pregnancy and beast-feeding: Sumycin has been shown to 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 Sumycin while you are pregnant. Sumycin is found in breast milk. Do not breast-feed while taking Sumycin.

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:

Black hairy tongue; blurred vision; bulky loose stools; diarrhea; difficulty swallowing; fever; headache; hives; hoarseness; indigestion; inflammation or redness of tongue; joint pain; loss of appetite; mouth sores; nausea; rash; sensitivity to sunlight; sore throat; stomach pain; swelling and itching of the rectum.

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); infection (fever, chills, sore throat); itching; nausea; severe skin reaction to the sun; vaginal irritation or discharge; vomiting.

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

Alfatil - Drug Review Dosage, Side Effects, Action, Buy Alfatil, Alfatil

Alfatil

Alfatil is the generic name for a second-generation broad-spectrum antibiotic from the antibacterial medications known as cephalosporins. It is available as the brand names Ceclor. Ceclor CD. Ceclor Pulvules, and Raniclor.

Alfatil is used for the treatment of bacterial infections like inflammatory illness of the lung. and infections of the ear. lung, skin, throat, and urinary tract. It works by penetrating the body's tissues and fluids, and obstructing the growth of the bacteria that is causing the infection.

Patients should not take Alfatil if they are allergic to cephalosporin, penicillin or other antibiotics, or if they have a kidney disorder or any digestive illness like colitis. They should inform their doctor of these diseases and get a prescription for a different dosage and constant monitoring during the course of treatment.

In the suspension form, Alfatil contains sucrose, which is not advisable for diabetics. Pregnant women or those planning to become pregnant should talk with their doctor about their situation before treatment. Since Alfatil can be passed on through breast milk, nursing mothers need to tell their doctor if they are breastfeeding before taking any dosage of the medication, so as not to affect nursing infants.

Patients should not take antacids that contain magnesium or aluminum while under Alfatil treatment as these can lower the efficacy of the antibiotic. Some of these antacids are Rolaids, Maalox, Mylanta, and Milk of Magnesia. Other medications known to affect Alfatil include Warfarin (an anticoagulant), Probenecid (an arthritis and gout medication), loop diuretics or water pills, and other antibiotics. Patients should inform their doctor of any other medications, vitamins or herbal supplements they are taking prior to starting their Alfatil treatment.

Some known side effects include allergic reactions in the form of rashes, itching. uticaria (hives), fever. serum sickness-like reactions (hypersensitivity), arthralgia (joint pain), and anaphylaxis (whole body atopy). Patients may experience diarrhoea, nausea. vomiting. stomach upset, transient hepatitis, jaundice, headaches and Stevens-Johnson syndrome (a deadly allergic skin illness). In rare cases, blood disorders. nephritis (kidney inflammation), hyperactivity. nervousness, disrupted sleep, hallucinations. confusion and dizziness may occur.

Patients should immediately stop taking Alfatil and seek emergency medical attention if they experience severe allergic reactions which include breathing difficulties, swelling of the facial tissue, rashes, redness or itching, nausea, vomiting or diarrhoea, blood or mucus in their stools, or unexplained bleeding and bruising. All side effects should be reported to your doctor for evaluation, particularly if they interfere with day-to-day activities.

Alfatil is available in purple and white 250 mg. capsules, purple and gray 500 mg. capsules, and as a suspension (liquid) in strawberry flavor. Ceclor CD is manufactured in blue tables of 375 and 500 mgs. When taking Alfatil in liquid form, the bottle needs to be shaken and the correct dosage accurately measured using a measuring spoon or cup.

Alfatil can be taken with a full glass of water on a full or empty stomach. Ceclor CD, in extended release capsules, needs to be taken with food or milk to prevent stomach upset. Ceclor CD tablets are specially created to be released slowly in the body, so it is advisable not to cut, grind or chew them.

While symptoms of an infection usually disappear early on, the bacteria causing the infection may still remain in the body. Cutting the medication process short may cause the body to develop a resistance to antibiotics.

Alfatil needs to be taken regularly during the prescribed period to make sure the body maintains a consistent level of the medication, and to obtain the best effect from it. Any unused medication should be disposed of after 14 days.

Alfatil has the following structural formula:

• Molecular formula of alfatil is C15H14ClN3O4S • Chemical IUPAC Name is (6R,7R)-7-[(2-amino-2-phenylacetyl)amino]-3-chloro-8-oxo - 5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid • Molecular weight is 367.8074 g/mol • Alfatil available. 250mg capsules, 500mg capsules, 187mg/5ml suspension 100ml bottle, 375mg/5ml suspension 100ml bottle, 125mg/5ml suspension 150ml bottle, 250mg/5ml suspension 150ml bottle, 187mg/5ml suspension 50ml bottle, 375mg/5ml suspension 50ml bottle, 125mg/5ml suspension 75ml bottle, 250mg/5ml suspension 75ml bottle

Generic name: Cefaclor

Exter, Exter

Tastes you want to savour

Welcome to Exter

We specialise in creating authentic savoury tastes. Bouillon, meat, fish, chicken, vegetables, umami: we can make absolutely anything. Prepared naturally and according to our own authentic cooking process like reducing slowly and roasting in the oven.

And we have been doing this since 1928!

With customers in all continents, we really are a global player. Our secret? Our authentic preparation methods, knowledge ranging from raw materials to drying techniques as well as our personal approach. Because we can only create the taste consumers want to savour by working with you. Welcome to Exter!

More about the Exter taste portfolio

News

Plenty of choice between authentic tastes

20 October 2015

The latest Exter taste: Dark Mild Roast

5th of April - Exter present at 2016 NYIFT Suppliers’ Day

Synocrom By Croma 1% Hyaluronic Acid Prefilled 20 Mg, Synocrom

Synocrom by Croma 1% hyaluronic acid prefilled 20 mg/2ml viscosupplementation joint arthritis

SYNOCROM® is a high purity, biofermentativ produced hyaluronic acid, which resembles the body’s own hyaluronic acid. SYNOCROM® is free of preservatives and is tolerated extremely well. The shock-absorbing properties of SYNOCROM® relieve pain and increase mobility. The advantages at a glance:

1% HA biofermentative

Long-lasting therapeutic effect

1.6 million daltons

2 ml capacity (20 mg)

For all synovial joints

Viscosupplementation means the intraarticular administration of hyaluronic acid. Primary treatment goals are pain relief and the improvement of mobility by increasing the viscoelasticity of the synovial fluid in the joint. Numerous studies attest to the viscosupplementation a significant pain relief, improved joint function and disease modifying effect. 1), 2) The viscosupplementation treatment is extremely compatible and without side effects. The maximum therapeutic effect with early application can be achieved even at mild to moderate osteoarthritis. By intra-articular hyaluronic acid therapy, the need for analgesics and non-steroidal anti-inflammatory drugs can be significantly reduced. The hyaluronic acid therapy causes setting creates a general increase in the quality of life. 3)

A post-market study with 313 gonarthritis patients tested the satisfaction with the SYNOCROM® therapy and the assessment of SYNOCROM® therapy was collected by specialists. 4) • 87% of the certified specialists attested SYNOCROM® a very good or good effect. • 95% patients were convinced from a very good or good therapeutic response. The VAS pain score increases before and 6 months after the treatment confirmed the excellent pain-relieving effect of SYNOCROM ® in the treatment of hip osteoarthritis 5) .

Furthermore, it was shown in this study that over 50% of the patients which were destined for a hip prosthesis even 3 years after the viscosupplementation therapy did not need the prosthesis 5). The viscosupplementation, especially the SYNOCROM® therapy may alleviate also the long-term pain for these patients. 4)

Concentration: 10 mg / ml (1%) sodium hyaluronate Production process: Biofermentativ Molecular weight: 1.6 million daltons Dynamic viscosity: 6.000 Pa • s (at 2Hz) Composition: sodium hyaluronate, sodium dihydrogen phosphate, sodium chloride, citric acid and water for injection Pack sizes: 3, 5, 25, 50 Filling volume: 2.0 ml

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Co-Trimoxazole Uses, Side Effects, Interactions, Pictures, Warnings & Dosing, Trimoxal

Medicines & treatments centre

CO-TRIMOXAZOLE WARNINGS

Co-trimoxazole should be used with caution in: the elderly. infants under 6 weeks of age, pregnant women and women who are breastfeeding. those with asthma. severe allergy. kidney or liver problems, blood disorders, or those who are deficient in the enzyme called glucose-6-phosphate dehydrogenase (common in peoples from Africa, Asia, Oceania and Southern Europe).

It should not be used in: people with severe liver problems or severe kidney problems, or those with a blood disorder called acute porphyria.

Also see list of precautions and interactions.

STORAGE

Protect from light and do not store above 25°C.

CO-TRIMOXAZOLE USES

What is it used for?

Co-trimoxazole is used to treat a number of problems.

It is a mixture of two drugs: trimethoprim and sulfamethoxazole, and is sometimes known as an antibiotic .

It is used to treat infections caused by bacteria in many different parts of the body.

In general this drug is used to treat infections of the respiratory tract, middle ear. urinary tract, and conditions such as toxoplasmosis (a parasitic disease caused by the protozoan Toxoplasma gondii) and nocardiosis (a serious infectious disease affecting either the lungs or the whole body owing to infection by the Nocardia bacterium).

Benefits of being on this drug can include eradication and resolution of bacterial infections, allowing recovery and relief of symptoms such as pain or cough caused by the infection.

Listed below are the typical uses of co-trimoxazole.

To treat or prevent lung infections (pneumonia ) caused by a bacterium called Pneumocystis jiroveci

To treat or prevent infections caused by toxoplasma (toxoplasmosis)

To treat bladder or urinary tract infections

To treat lung infections such as worsening of long-term bronchitis

To treat ear infections such as acute otitis media

To treat an infection called nocardiosis, which can affect the lungs, skin and brain .

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?

Take this medication by mouth. usually twice daily, preferably with food. Tablets should be taken with a glass of water. It is also available as an oral suspension to be taken by mouth and as a liquid for intravenous infusion (when given by a doctor or other healthcare worker).

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

Remember to use it at the same time each day - unless specifically told not to by your doctor.

It may take some time before the full benefit of this drug takes effect.

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?

None known. Consult your doctor or pharmacist for more details.

When can I stop?

Always complete the full course as prescribed by your doctor.

CO-TRIMOXAZOLE SIDE EFFECTS

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

Tell your doctor immediately if you develop any of the following symptoms: heart problems. yellowing of the skin or eyes (jaundice ), increased sensitivity to light (photosensitivity).

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.

CO-TRIMOXAZOLE PRECAUTIONS

Before taking co-trimoxazole, tell your doctor or pharmacist if you are allergic to it; or to other antibiotics; 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 in case of: a blood disorder called acute porphyria.

Before using this medication tell your doctor or pharmacist your medical history, especially any of the following: a history of asthma. severe allergy. any kidney or liver problems, blood disorders, or if deficient in the enzyme called glucose-6-phosphate dehydrogenase (common in peoples from Africa, Asia, Oceania and Southern Europe).

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

Does alcohol intake affect this drug?

It is not known whether drinking alcohol affects this drug's action.

The elderly. co-trimoxazole should be used with caution in the elderly as it may cause worse side-effects than in younger patients.

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

PREGNANCY

Co-trimoxazole is not safe to take if you are, or are planning to become, pregnant.

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

Co-trimoxazole is not safe to take if you are breastfeeding.

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.

CO-TRIMOXAZOLE INTERACTIONS

Your doctor or pharmacist may already be aware of any possible drug interactions and may be monitoring you for them. Do not start, stop, or change the dosage of any medicine before checking with them first.

This drug should not be used with the following medications because very serious, possibly fatal interactions may occur:

Drugs to control abnormal heart rhythms (anti-arrhythmics), e. g. amiodarone .

If you are currently using any such medicine, tell your doctor or pharmacist before starting co-trimoxazole.

Before using this medication, tell your doctor or pharmacist of all prescription and non-prescription/herbal products you may use, especially of:

Other antibacterials (e. g. rifampicin, methenamine)

Immunosuppressants (e. g. ciclosporin )

Blood-thinning drugs (e. g. warfarin )

Anti-epileptics (e. g. phenytoin)

Anti-arrhythmics (e. g. digoxin or procainamide)

Antidiabetics (e. g. glibenclamide. glipizide or tolbutamide )

Anti-cancer drugs (e. g. methotrexate. azathioprine or mercaptopurine)

Anti-malarials (e. g. pyrimethamine)

Anti-psychotics (e. g. clozapine )

Antivirals (e. g. marviroc, ritonavir, tipranavir or zidovudine)

This information does not contain all possible interactions. Therefore, before using co-trimoxazole, tell your doctor or pharmacist of all the products you use.

CO-TRIMOXAZOLE OVERDOSE

Taking too much co-trimoxazole may cause the following: feeling sick (nausea), vomiting, dizziness and confusion.

People who have taken too much co-trimoxazole should be encouraged to vomit (if this has not already happened) and to seek assistance from a healthcare professional immediately.

If you think you, or someone you care for, might have accidentally taken more than the recommended dose of co-trimoxazole 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.

Larotid Oral Uses, Side Effects, Interactions, Pictures, Warnings - Dosing, Larotid

Larotid

Uses

Amoxicillin is used to treat a wide variety of bacterial infections. This medication is a penicillin - type antibiotic. It works by stopping the growth of bacteria.

This antibiotic treats only bacterial infections. It will not work for viral infections (such as common cold. flu ). Unnecessary use or misuse of any antibiotic can lead to its decreased effectiveness.

Amoxicillin is also used with other medications to treat stomach /intestinal ulcers caused by the bacteria H. pylori and to prevent the ulcers from returning.

OTHER USES: This section contains uses of this drug that are not listed in the approved US 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 drug may also be used by people with certain heart problems (such as heart valve disease) before medical/dental procedures (such as tooth /gum procedures) to prevent heart infection.

How to use Larotid

Take this medication by mouth with or without food as directed by your doctor, usually every 8 or 12 hours. The dosage is based on your medical condition and response to treatment.

Drink plenty of fluids while using this medication unless your doctor tells you otherwise.

Antibiotics work best when the amount of medicine in your body is kept at a constant level. Therefore, take this drug at evenly spaced intervals. To help you remember, take it at the same times each day.

Continue to take this medication until the full prescribed amount is finished, even if symptoms disappear after a few days. Stopping the medication too early may allow bacteria to continue to grow, which may result in a return of the infection.

Tell your doctor if your condition persists or worsens.

Side Effects

Nausea. vomiting. or diarrhea may occur. If any of these effects persist or worsen, tell your doctor or pharmacist promptly.

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.

Use of this medication for prolonged or repeated periods may result in oral thrush or a new vaginal yeast infection (oral or vaginal fungal infection). Contact your doctor if you notice white patches in your mouth. a change in vaginal discharge or other new symptoms.

Tell your doctor right away if any of these rare but serious side effects occur: dark urine, persistent nausea or vomiting, stomach /abdominal pain. yellowing eyes or skin. easy bruising or bleeding, persistent sore throat or fever.

This medication may rarely cause a severe intestinal condition (Clostridium difficile - associated diarrhea) due to a type of resistant bacteria. This condition may occur during treatment or weeks to months after treatment has stopped. Do not use anti-diarrhea products or narcotic pain medications if you have the following symptoms because these products may make them worse. Tell your doctor right away if you develop: persistent diarrhea, abdominal or stomach pain/cramping, blood /mucus in your stool.

A very serious allergic reaction to this drug is rare. However, get medical help right away if you notice any symptoms of a serious allergic reaction. including: rash. itching /swelling (especially of the face/tongue /throat), severe dizziness. trouble breathing .

Amoxicillin can commonly cause a mild rash that is usually not serious. However, you may not be able to tell it apart from a rare rash that could be a sign of a severe allergic reaction. Therefore, get medical help right away if you develop any rash.

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 amoxicillin, tell your doctor or pharmacist if you are allergic to it; or to penicillin or cephalosporin antibiotics ; 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: kidney disease. a certain type of viral infection (infectious mononucleosis ).

Before having surgery, tell your doctor or dentist about all the products you use (including prescription drugs, nonprescription drugs, and herbal products).

During pregnancy. this medication should be used only when clearly needed. Discuss the risks and benefits with your doctor.

Amoxicillin passes into breast milk. Consult your doctor before breast - feeding.

Interactions

The effects of some drugs can change if you take other drugs or herbal products at the same time. This can increase your risk for serious side effects or may cause your medications not to work correctly. These drug interactions are possible, but do not always occur. Your doctor or pharmacist can often prevent or manage interactions by changing how you use your medications or by close monitoring.

To help your doctor and pharmacist give you the best care, be sure to tell your doctor and pharmacist about all the products you use (including prescription drugs, nonprescription drugs, and herbal products) before starting treatment with this product. While using this product, do not start, stop, or change the dosage of any other medicines you are using without your doctor's approval.

Some products that may interact with this drug include: live bacterial vaccines. methotrexate .

Although most antibiotics are unlikely to affect hormonal birth control such as pills, patch, or ring, a few antibiotics (such as rifampin, rifabutin ) can decrease their effectiveness. This could result in pregnancy. If you use hormonal birth control. ask your doctor or pharmacist for more details.

Amoxicillin may cause false positive results with certain diabetic urine testing products (cupric sulfate-type). This drug may also affect the results of certain lab tests. Make sure laboratory personnel and your doctors know you use this drug.

This document does not contain all possible drug interactions. Keep a list of all the products you use. Share this list with your doctor and pharmacist to lessen your risk for serious medication problems.

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 vomiting, persistent diarrhea, a severe decrease in the amount of urine, or seizures.

Notes

Do not share this medication with others.

This medication has been prescribed for your current condition only. Do not use it later for another infection unless your doctor directs you to do so. A different medication may be necessary in that case.

With prolonged treatment, laboratory and/or medical tests (such as kidney and liver function, complete blood counts) may 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, use 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 according to the product labeling, away from light and moisture. Different brands of this medication have different storage needs. Check the product package for instructions on how to store your brand, or ask your pharmacist. 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 for more details about how to safely discard your product.

Information last revised October 2015. Copyright(c) 2015 First Databank, Inc.

Images

No data available at this time.

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

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

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Hydrochlorothiazide is used for treating high blood pressure. It is also used to treat fluid buildup in the body caused by certain conditions (eg, heart failure, liver cirrhosis, kidney problems) or medicines (eg, corticosteroids, estrogen). It may be used alone or with other medicines. Hydrochlorothiazide is a thiazide diuretic. It helps the kidneys to remove fluid from the body.

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.

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

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

Store Hydrochlorothiazide 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 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.

Some medical conditions may interact with Hydrochlorothiazide. 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 had a severe allergic reaction (eg, rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue) to a sulfonamide medicine (eg, sulfamethoxazole)

if you have gout, liver problems, (eg, cirrhosis), lupus, kidney problems, diabetes, asthma, parathyroid gland problems, or high blood cholesterol or lipid levels

if you have high or low blood electrolyte levels (eg, sodium, potassium, magnesium, calcium)

if you are taking another medicine for high blood pressure.

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

Digoxin, dofetilide, or ketanserin because the risk of irregular heartbeat may be increased

Barbiturates (eg, phenobarbital), corticotropin, corticosteroids (eg, prednisone), or narcotic pain medicines (eg, codeine) because they may increase the risk of Hydrochlorothiazide's side effects

Cholestyramine, colestipol, or nonsteroidal anti-inflammatory medicines (NSAIDs) (eg, ibuprofen) because they may decrease Hydrochlorothiazide's effectiveness

Diazoxide or lithium because the risk of their side effects may be increased by Hydrochlorothiazide

Diabetes medicines (eg, glipizide, metformin) or insulin because their effectiveness may be decreased by Hydrochlorothiazide.

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

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 possible 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.

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.

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.

Hydrochlorothiazide may interfere with certain lab tests, including parathyroid function tests. Be sure your doctor and lab personnel know you are taking Hydrochlorothiazide.

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.

Use Hydrochlorothiazide with caution in the elderly; they may be more sensitive to its effects, especially dizziness.

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.

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:

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.

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.

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Fucidin (Fusitop)

Fucidin cream is used to treat skin infections such as impetigo, infected eczema or infected wounds or cuts. It works by killing the organisms that have caused the infection.

Use Fucidin cream as directed by your doctor.

Fucidin cream is for use on the skin only. Do not get it in your eyes.

Wash your hands with soap and water before and after using this medicine.

Apply a thin layer of this medicine to the affected area of the skin 3 or 4 times daily until the infection has cleared. Rub it in gently.

Do not use cosmetics or other skin care products on the treated areas.

Do not bandage or otherwise wrap the skin being treated unless directed to do so by your doctor.

If the medicine is applied to the diaper area of an infant, do not use tight-fitting diapers or plastic pants unless directed to do so by your doctor.

If your doctor ordered an occlusive dressing or airtight covering to be applied over the medicine, make sure you know how to apply it. Occlusive dressings increase the amount of medicine absorbed through your skin, so use them only as directed. If you have any questions about this, check with your doctor.

If you miss a dose of Fucidin cream, skip the missed dose and go back to your regular dosing schedule. Do not apply a double dose to make up for a missed one.

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

Store Fucidin cream at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Keep Fucidin cream out of the reach of children and away from pets.

Active Ingredient: Fusidic acid.

Other Ingredients: White soft paraffin, Liquid paraffin, Butylated hydroxyanisole, Cetanol, Glycerol, Potassium sorbate, Purified water, Polysorbate 60.

Fusidic acid belongs to a class of medications known as antibiotics.

you are allergic to any ingredient in Fucidin cream.

Some medical conditions may interact with Fucidin cream. 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.

Some medicines may interact with Fucidin cream. There are no known important interactions between Fucidin cream and other medicines. If you experience any unusual symptoms while using Fucidin cream and other medicines you should tell your health care provider.

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

Breast-feeding: This medication may pass into breast milk. If you are a breast-feeding mother and are using fusidic acid, it may affect your baby. Talk to your doctor about whether you should continue breast-feeding.

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

Everyone's reaction to a medicine is different. It is difficult to predict which side effects

you will have from taking a particular medicine, or whether you will have any side effects

at all. The important thing is to tell your prescriber or pharmacist if you are having problems with your medicine.

Uncommon: More than 1 in 1000 people who use Fucidin cream:

Dermatitis (skin sensitivity reactions may occur if Fucidin cream is used for long

periods of time), irritation at the site of application (reactions include pain, redness of the skin, stinging, and burning sensations), itching, skin rash or rashes.

Rare: More than 1 in 10,000 people who use Fucidin cream:

Eye or eyesight problems, hypersensitivity reactions.

The frequency of these sideeffects is unknown:

Angioedema, antibiotic resistance to fusidic acid (this may happen if Fucidin cream is used for long periods of time), eczema, oedema around the eyes, urticaria.

If you feel unwell or if you have concerns about a side effect, you will need to seek advice. If you feel very ill, get medical help straight away.

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Metoprolol es un betabloqueante que afecta el corazón y el sistema circulatorio (las arterias y las venas).

Metoprolol se usa para el tratamiento de la angina de pecho (dolor de pecho) y la hipertensión (presión arterial elevada). También se usa par el tratamiento y la prevención del ataque cardíaco.

Metoprolol puede también usarse para fines no mencionados en esta guía del medicamento.

¿Cuál es la información más importante que debo saber sobre metoprolol?

Usted no debe usar este medicamento si tiene una un problema serio en el corazón (bloqueo cardíaco, síndrome de disfunción sinusal, latido cardíaco lento), problemas de la circulación severos, fallo cardíaco severo, o un historial de latidos cardíacos lentos que le han causado desmayos.

¿Qué debería discutir con el profesional de la salud antes de tomar metoprolol?

Usted no debe usar este medicamento si es alérgico a metoprolol u otros betabloqueantes (atenolol, carvedilol, labetalol, metoprolol, nadolol, nebivolol, propranolol, sotalol, y otras), o si usted tiene:

una condición cardíaca seria como bloqueo cardíaco, síndrome de disfunción sinusal. o latido cardíaco lento;

problemas de la circulación severos;

fallo cardíaco severo (que le haya requerido estar en el hospital); o

un historial de latidos del corazón lentos que le han causado desmayo.

Para asegurarse que metoprolol es seguro para usted, dígale a su médico si usted tiene:

asma, enfermedad pulmonar obstructiva crónica (EPOC; COPD, por sus siglas en Inglés), apnea al dormir, u otro trastorno de la respiración;

diabetes (tomar metoprolol puede hacer más difícil reconocer cuando su nivel de azúcar en la sangre baje);

enfermedad del hígado;

fallo cardíaco congestivo;

problemas de la circulación (como el síndrome de Raynaud);

trastorno de la glándula tiroidea; o

feocromocitoma (tumor de la glándula suprarrenal).

No se conoce si metoprolol causará daño al bebé nonato. Dígale de inmediato a su médico si queda embarazada mientras está usando esta medicina.

Metoprolol puede pasar a la leche materna y causarle daño al bebé lactante. Dígale a su médico si está dando de amamantar a un bebé.

Metoprolol no está aprobada para usarse en cualquier persona menor de 18 años de edad.

¿Cómo debo tomar metoprolol?

Siga todas las instrucciones en la etiqueta de su prescripción. Tal vez su médico en ocasiones cambie su dosis para asegurarse de que está obteniendo los mejores resultados. No tome esta medicina en cantidades mayores o menores, o por más tiempo de lo recomendado.

Tome la medicina a la misma hora cada día.

Metoprolol debe tomarse con una comida o después de terminar una comida.

La tableta Toprol XL puede dividirse por la mitad si su médico se lo ha indicado. La media tableta debe tragarse entera, sin masticar o triturarla.

Mientras usa metoprolol, usted puede necesitar exámenes de sangre con frecuencia en la oficina de su médico. Su presión arterial será medida con frecuencia.

Si necesita cirugía, dígale al cirujano por adelantado que usted está usando metoprolol.

Usted no debe dejar de usar metoprolol de forma repentina. Dejar de tomarlo de forma súbita puede empeorar su condición.

Si usted está recibiendo tratamiento para la presión arterial alta, siga usando esta medicina aunque se sienta bien. La presión arterial alta frecuentemente no tiene síntomas. Usted tal vez necesite tomar medicamento para la presión arterial el resto de su vida.

Guarde a temperatura ambiente, lejos de la humedad y el calor.

¿Qué sucede si me salto una dosis?

Tome la dosis que dejó de tomar tan pronto se acuerde. Sáltese la dosis que dejó de tomar si ya casi es hora para la siguiente dosis. No use más medicina para alcanzar la dosis que dejó de tomar.

¿Qué sucedería en una sobredosis?

Busque atención médica de emergencia o llame a la línea de Poison Help al 1-800-222-1222.

¿Qué debo evitar mientras tomo metoprolol?

Metoprolol puede perjudicar su pensamiento o reacciones. Tenga cuidado si usted conduce un vehículo o tiene que hacer algo que demande que se mantenga alerta.

Beber alcohol puede aumentar ciertos efectos secundarios de metoprolol.

¿Cuáles son los efectos secundarios posibles de metoprolol?

Busque atención medica de emergencia si usted tiene síntomas de una reacción alérgica: ronchas; dificultad para respirar; hinchazón de la cara, labios, lengua, o garganta.

Llame a su médico de inmediato si usted tiene:

latidos cardíacos muy lentos;

sensación de desvanecimiento, como que se va a desmayar;

falta de aire al respirar (aún cuando la actividad es leve), hinchazón o ganancia de peso rápida; o

sensación de frío en las manos y los pies.

Efectos secundarios comunes pueden incluir:

mareo, sensación de cansancio;

confusión, problemas de la memoria;

pesadillas, dificultad para dormir;

picazón o sarpullido leves.

Esta lista no menciona todos los efectos secundarios y puede ser que ocurran otros. Llame a su médico para consejos médicos relacionados a efectos secundarios. Usted puede reportar efectos secundarios llamando al FDA al 1-800-FDA-1088.

¿Qué otras drogas afectarán a metoprolol?

Dígale a su médico acerca de todas las medicinas que usted esté usando, comience a usar, o deje de usar durante su tratamiento con metoprolol, especialmente:

un antidepresivo--bupropion, clomipramine, desipramine, duloxetine, fluoxetine, fluvoxamine, paroxetine, sertraline;

una medicina derivada de cornezuelo del centeno (ergot)--dihydroergotamine, ergonovine, ergotamine, methylergonovine;

medicamentos para el corazón o la presión arterial--amlodipine, clonidine, digoxin, diltiazem, dipyridamole, hydralazine, methyldopa, nifedipine, quinidine, reserpine, verapamil, y otras;

un inhibidor de MAO--isocarboxazid, linezolid, phenelzine, rasagiline, selegiline, tranylcypromine; o

medicinas para el tratamiento de enfermedades mentales--chlorpromazine, fluphenazine haloperidol, thioridazine.

Esta lista no está completa. Otras drogas pueden interactuar con metoprolol, incluyendo medicinas que se obtienen con o sin receta, vitaminas, y productos herbarios. No todas las interacciones posibles aparecen en esta guía del medicamento.

¿Dónde puedo obtener más información?

Su farmacéutico le puede dar más información acerca de metoprolol.

Recuerde, mantenga ésta y todas las otras medicinas fuera del alcance de los niños, no comparta nunca sus medicinas con otros, y use este medicamento sólo para la condición por la que fue recetada.

Se ha hecho todo lo posible para que la información que proviene de Cerner Multum, Inc. ('Multum') sea precisa, actual, y completa, pero no se hace garantía de tal. La información sobre el medicamento incluida aquí puede tener nuevas recomendaciones. La información preparada por Multum se ha creado para uso del profesional de la salud y para el consumidor en los Estados Unidos de Norteamérica (EE. UU.) y por lo cual Multum no certifica que el uso fuera de los EE. UU. sea apropiado, a menos que se mencione específicamente lo cual. La información de Multum sobre drogas no sanciona drogas, ni diagnóstica al paciente o recomienda terapia. La información de Multum sobre drogas sirve como una fuente de información diseñada para la ayuda del profesional de la salud licenciado en el cuidado de sus pacientes y/o para servir al consumidor que reciba este servicio como un suplemento a, y no como sustituto de la competencia, experiencia, conocimiento y opinión del profesional de la salud. La ausencia en éste de una advertencia para una droga o combinación de drogas no debe, de ninguna forma, interpretarse como que la droga o la combinación de drogas sean seguras, efectivas, o apropiadas para cualquier paciente. Multum no se responsabiliza por ningún aspecto del cuidado médico que reciba con la ayuda de la información que proviene de Multum. La información incluida aquí no se ha creado con la intención de cubrir todos los usos posibles, instrucciones, precauciones, advertencias, interacciones con otras drogas, reacciones alérgicas, o efectos secundarios. Si usted tiene alguna pregunta acerca de las drogas que está tomando, consulte con su médico, enfermera, o farmacéutico.

Copyright 1996-2012 Cerner Multum, Inc. Version: 16.04. Revision Date: 8/22/2016 10:16:48 AM.

Tenormin - Heart Disease, Mirobect

Common use Tenormin is a beta-adrenergic blocking agent. Its role is to block the effects of adrenergic drugs, such as adrenaline or epinephrine, on nerves of the sympathetic nervous system. Tenormin reduces the heart rate and is used for treatment of abnormally rapid heart rhythms, arterial hypertension, angina, acute myocardial infraction, tachycardia (different types), ventricular fibrillation and others.

Dosage and direction Take Tenormin before meals or at bedtime. Your dose depends on your condition and should be administered by your doctor. Take the medication exactly as prescribed. Do not change the dose and do not stop suddenly treatment even if you feel better as hypertension often has no symptoms. Avoid drinking alcohol. Let your surgeon know if you are taking Tenormin if you plan to be operated.

Precautions Do not take Tenormin if it was not Tenormin should be taken with a glass of water once a day at the same time. Do not stop taking the medication suddenly as it may worsen your condition. Continue taking the medication even if you feel fine as hypertension and diseases of a heart maybe a life long illness. Inform your surgeon if you take Tenormin, if you need to be operated.

Hypersensitivity, sick sinus syndrome, sinus bradycardia (rate slower than 50 per minute), atrioventricular block (degree II and III), arterial hypotension, acute or chronic heart failure, peripheral blood flow disorders, breastfeeding. Cautiousness should be exercised in patients with diabetes, hypopotassemia, pulmonary emphysema, asthma, liver and kidney diseases pregnancy and with other conditions.

Possible side effect Side effects are rare and transient if occur. They may include weakness, fatigue, dizziness, headache, depression, dreaming, insomnia, memory loss, abdominal cramps, diarrhea, constipation, nausea, fever, impotence, lightheadedness, slow heart rate, low blood pressure, numbness, tingling, cold extremities, and sore throat and also allergy.

Drug interaction Tenormin can aggravate conditions of patients with asthma, chronic bronchitis, or emphysema. In patients with slow heart rates and heart blocks, Tenormin can slow up heart rates considerably. Tenormin reduces the force of heart muscle contraction and worsens conditions of patients with heart failure. Non-steroidal anti-inflammatory drugs, estrogens, sympathomimetics, xanthines weaken hypotensive effect of Tenormin.

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 Symptoms of an overdose are uneven heartbeats, shortness of breath, dizziness, weakness, fainting, bluish-colored fingernails, convulsions. If you experience this, call your doctor immediately.

Storage Tablets should be stored at room temperature between 25-25 C (68-70 F) away from light and moisture.

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

Common use Tenormin is a beta-adrenergic blocking agent. Its role is to block the effects of adrenergic drugs, such as adrenaline or epinephrine, on nerves of the sympathetic nervous system. Tenormin reduces the heart rate and is used for treatment of abnormally rapid heart rhythms, arterial hypertension, angina, acute myocardial infraction, tachycardia (different types), ventricular fibrillation and others.

Dosage and direction Take Tenormin before meals or at bedtime. Your dose depends on your condition and should be administered by your doctor. Take the medication exactly as prescribed. Do not change the dose and do not stop suddenly treatment even if you feel better as hypertension often has no symptoms. Avoid drinking alcohol. Let your surgeon know if you are taking Tenormin if you plan to be operated.

Precautions Do not take Tenormin if it was not Tenormin should be taken with a glass of water once a day at the same time. Do not stop taking the medication suddenly as it may worsen your condition. Continue taking the medication even if you feel fine as hypertension and diseases of a heart maybe a life long illness. Inform your surgeon if you take Tenormin, if you need to be operated.

Hypersensitivity, sick sinus syndrome, sinus bradycardia (rate slower than 50 per minute), atrioventricular block (degree II and III), arterial hypotension, acute or chronic heart failure, peripheral blood flow disorders, breastfeeding. Cautiousness should be exercised in patients with diabetes, hypopotassemia, pulmonary emphysema, asthma, liver and kidney diseases pregnancy and with other conditions.

Possible side effect Side effects are rare and transient if occur. They may include weakness, fatigue, dizziness, headache, depression, dreaming, insomnia, memory loss, abdominal cramps, diarrhea, constipation, nausea, fever, impotence, lightheadedness, slow heart rate, low blood pressure, numbness, tingling, cold extremities, and sore throat and also allergy.

Drug interaction Tenormin can aggravate conditions of patients with asthma, chronic bronchitis, or emphysema. In patients with slow heart rates and heart blocks, Tenormin can slow up heart rates considerably. Tenormin reduces the force of heart muscle contraction and worsens conditions of patients with heart failure. Non-steroidal anti-inflammatory drugs, estrogens, sympathomimetics, xanthines weaken hypotensive effect of Tenormin.

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 Symptoms of an overdose are uneven heartbeats, shortness of breath, dizziness, weakness, fainting, bluish-colored fingernails, convulsions. If you experience this, call your doctor immediately.

Storage Tablets should be stored at room temperature between 25-25 C (68-70 F) away from light and moisture.

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

Common use Tenormin is a beta-adrenergic blocking agent. Its role is to block the effects of adrenergic drugs, such as adrenaline or epinephrine, on nerves of the sympathetic nervous system. Tenormin reduces the heart rate and is used for treatment of abnormally rapid heart rhythms, arterial hypertension, angina, acute myocardial infraction, tachycardia (different types), ventricular fibrillation and others.

Dosage and direction Take Tenormin before meals or at bedtime. Your dose depends on your condition and should be administered by your doctor. Take the medication exactly as prescribed. Do not change the dose and do not stop suddenly treatment even if you feel better as hypertension often has no symptoms. Avoid drinking alcohol. Let your surgeon know if you are taking Tenormin if you plan to be operated.

Precautions Do not take Tenormin if it was not Tenormin should be taken with a glass of water once a day at the same time. Do not stop taking the medication suddenly as it may worsen your condition. Continue taking the medication even if you feel fine as hypertension and diseases of a heart maybe a life long illness. Inform your surgeon if you take Tenormin, if you need to be operated.

Hypersensitivity, sick sinus syndrome, sinus bradycardia (rate slower than 50 per minute), atrioventricular block (degree II and III), arterial hypotension, acute or chronic heart failure, peripheral blood flow disorders, breastfeeding. Cautiousness should be exercised in patients with diabetes, hypopotassemia, pulmonary emphysema, asthma, liver and kidney diseases pregnancy and with other conditions.

Possible side effect Side effects are rare and transient if occur. They may include weakness, fatigue, dizziness, headache, depression, dreaming, insomnia, memory loss, abdominal cramps, diarrhea, constipation, nausea, fever, impotence, lightheadedness, slow heart rate, low blood pressure, numbness, tingling, cold extremities, and sore throat and also allergy.

Drug interaction Tenormin can aggravate conditions of patients with asthma, chronic bronchitis, or emphysema. In patients with slow heart rates and heart blocks, Tenormin can slow up heart rates considerably. Tenormin reduces the force of heart muscle contraction and worsens conditions of patients with heart failure. Non-steroidal anti-inflammatory drugs, estrogens, sympathomimetics, xanthines weaken hypotensive effect of Tenormin.

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 Symptoms of an overdose are uneven heartbeats, shortness of breath, dizziness, weakness, fainting, bluish-colored fingernails, convulsions. If you experience this, call your doctor immediately.

Storage Tablets should be stored at room temperature between 25-25 C (68-70 F) away from light and moisture.

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

Figalol, Figalol

Figalol

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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Hidrazida

Hidrazida

neuropatie periferica dupa tratament cu hidrazida

Sec?iunea: Forum medical

tratament milgama. eu am luat in timpul tratamentului ci hidrazida vit. b6 zilnic. totul a inceput dupa terminarea tratamentului. boala s-a manifestat peritoneal si sunt operata.

Comele toxice la copil

Sec?iunea: Boli ?i afec?iuni

cloralhidrat), alcooli (alcool etilic, metilic, etilenglicol), digoxin, ciclofosfamida, methotrexat, hidrazida . paracetamol, teofilina, amanita faloides, hexaclorura de benzen, antidepresive triciclice, toxice halogene (bromuri, cloruri, ioduri), toxice.

Sec?iunea: Boli ?i afec?iuni

koch – streptomicina, rifampicina, fie chimioterpice anti-tuberculoase precum hin ( hidrazida acidului izonicotinic), etambutolul, pirazinamida. exista tuberculostatice majore - rifampicina, hin, care au rol.

Sec?iunea: Boli ?i afec?iuni

grupate in doua categorii: - medicamente de prima linie hidrazida acidului izonicotinic (izoniazida). rifampicina (sinerdol), etambutol (etb), streptomicina si pirazinamida;- medicamentele de a doua.

reactii adverse de la medicatie TBC?

Sec?iunea: Forum medical

nu am avut nervul optic afectat. acum iau numai hidrazida si sinerdol. sa fie o alergie la medicamente?

dureri scurte si foarte puternice intre stomac si anus

Sec?iunea: Forum medical

ani) si acolo imi dadeau 10 pastile deodata(prednison si hidrazida . cu toate ca nu aveam tbc plus vitamine). cred ca pastilele sunt una din cauzele.

Recidiva TBC-va rog din suflet sa-mi raspundeti.

Sec?iunea: Forum medical

am urmat tratamentul injectabil si medicamentos specific acestei boli(etambutol, hidrazida . etc). dupa care am urmat alte 6 luni de tratament cu medicamente pe care le luam.

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Sufil, Sufil

Sufil

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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Angi Sullins, Angicard

YOU WERE BORN TO THRIVE

Known as “The Muse” by her fans, Angi ignites inspiration wherever she goes. Playful, poetic, bright, deeply expressive and armed with a standup comic’s sense of humor, Angi is an engaging writer and an electric speaker, creating a one-woman performance like no other. Described by one reviewer as a curious mix of Dr. King and Dr. Seuss, Angi delivers deeply soul-stirring messages with humorous, whimsical wit. Audiences leave her performances enchanted, dipped in remembered magic, ready to create new and visionary works on the canvas of their lives.

Before the era of youtube, Angi created the short inspirational film “A Knock at the Door” that went viral, garnering over four million fans. She is the author of “Doorways and Dreamfields: A True Fairy Tale”, “A Knock at the Door,” “Digital Art Wonderland,” and highlights from her popular Message from the Muse blog were collected into her first audio book “Flaming Muse: Matchstick Tales that Ignite the Soul.”

As the founder and president of Duirwaigh Studios, a transmedia design studio creating products and services that inspire soulful imagination, she has helped artists and aspiring creatives find their unique voice, while molding a space in today’s market for creative consciousness. Her words and original works of art with partner Silas Toball can be found on hundreds of greeting cards, calendars, journals and collectibles worldwide.

Angi lives in the Land of Enchantment. Literally. "Land of Enchantment" is on all the license plates in Taos, New Mexico where she lives with her husband Silas and their menagerie of wonder. That pretty much says it all. Mostly.

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Supraproct-S, Betamethasone Valerate, Cinchocaine Hcl, Supraproct

Supraproct-s

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For the symptomatic relief of external and internal haemorrhoids and other inflammatory and pruritic manifestations of corticosteroid responsive dermatoses of the anal region.

Not to be used in * Acne vulgaris * Allergy to this medicine or similar medicines * Bacterial skin infections * Children under 12 years of age * Chronic inflammatory disorder of the facial skin (acne rosacea) * Inflammatory rash around the mouth (perioral dermatitis) * Nappy rash * Viral skin infections such as chickenpox or herpes simplex

* Rash * Skin darkening * Stinging and redness * Blistering * Excessive fluid retention in the body tissues, resulting in swelling (oedema) * Burning sensation * Excessive hair growth (hypertrichosis) * Skin thinning * Secondary infection * Inflammation of the hair follicles (folliculitis)

* You should not cover the area being treated with airtight dressings such as bandages or other dressings, including nappies, as these will enhance the absorption of the medicine into the body and may increase the risk of adverse effects. * Avoid contact of this medicine with the eyes. * In pregnancy, this medicine should not be applied extensively in large amounts, or for prolonged periods. * Continuous, long term use of this medicine should be avoided in children. * If skin irritation occurs, or an infection is not resolved, seek medical advice. * Long term use of this medicine on large areas of skin, particularly in skin folds or if the skin is damaged, may result in increased absorption of the medicine into the bloodstream, with an increased risk of side effects. * This medicine should not be used for longer than five days on the face or in children.

SOLUTION FOR INJECTION

Interactions Between Theostat Oral And Theophylline-Febuxostat, Theostat

Interactions

Theophylline/Febuxostat

This information is generalized and not intended as specific medical advice. Consult your healthcare professional before taking or discontinuing any drug or commencing any course of treatment.

Medical warning:

Moderate. These medicines may cause some risk when taken together. Contact your healthcare professional (e. g. doctor or pharmacist) for more information.

How the interaction occurs:

Febuxostat may slow down how quickly your body processes theophylline.

What might happen:

The amount of theophylline in your blood may increase and cause toxic side effects, which may include loss of appetite, nausea, vomiting, nervousness, agitation, headache, fast and/or irregular heartbeat, or seizures.

What you should do about this interaction:

Let your healthcare professionals (e. g. doctor or pharmacist) know that you are taking these medicines together. Let your doctor know right away if you develop loss of appetite, nausea, vomiting, nervousness, agitation, headache, fast and/or irregular heartbeat, or seizures. Your healthcare professionals may already be aware of this interaction and may be monitoring you for it. Do not start, stop, or change the dosage of any medicine before checking with them first. Reference:1.Uloric (febuxostat) US prescribing information. Takeda Pharmaceuticals America, Inc. November, 2011.

References:

Skincare - Gyno Dexacort (Brand Name Decadron) (Dexamethasone), Gyno Dexacort

Skincare - Gyno dexacort (Brand name: decadron)

Product Description Common use Decadron is used to treat conditions such as arthritis, blood/hormone/immune system disorders, allergic reactions, certain skin and eye conditions, breathing problems, certain bowel disorders. Also it is used in the treatment of cancers of the white blood cells (leukemias), and lymph gland cancers (lymphomas). Finally, Decadron is used as replacement therapy in patients whose adrenal glands are unable to produce sufficient amounts of corticosteroids.

Dosage and direction Take this medication by mouth as directed by your doctor. The initial oral dose is 0.75 to 9 mg daily depending on the disease. The initial dose should be adjusted according to the response to therapy. Take with food or milk to prevent stomach upset. Take this medication by mouth with food or a full glass of water or milk unless your doctor directs you otherwise. If you take this medication once daily, take it in the morning before 9 AM. Use this medication regularly in order to get the most benefit from it. Take it at the same time(s) each day. It is important to continue taking this medication even if you feel well. Follow the dosing schedule carefully, and take this medication exactly as prescribed. Do not stop taking this medication without consulting your doctor. Inform your doctor if your condition does not improve or worsens.

Precautions Do not get immunizations, vaccinations, or skin tests unless specifically directed by your doctor. Before taking Decadron, tell your doctor or pharmacist if you have any allergies, your medical history: active fungal infections, kidney or liver disease, mental/mood conditions, low blood minerals, thyroid disease, stomach/intestinal problems, high blood pressure, heart problems, diabetes, eye diseases, brittle bones, history of blood clots. If you have been taking this medication for a long time, your body may not make enough natural hormones while you are under physical stress. Your dose may need to be adjusted. If you have stopped taking this drug within the past 12 months, you may need to start taking it again if your body is under physical stress. Before having surgery, tell your doctor or dentist that you are using this medication or have taken it within the last 12 months. If you have a history of ulcers or take large doses of aspirin or other arthritis medication. Limit alcoholic beverages while taking this medication to decrease the risk of stomach/intestinal bleeding. If you have diabetes, this drug may make it harder to control your blood sugar levels. Monitor your blood sugar levels regularly and inform your doctor of the results. During pregnancy, this medication should be used only when clearly needed. Discuss the risks and benefits with your doctor. This drug may pass into breast milk and could have undesirable effects on a nursing infant. Therefore, breast-feeding is not recommended while using this medication. Avoid contact with people who have recently received oral polio vaccine or flu vaccine inhaled through the nose, chickenpox or measles unless you have previously had these diseases (in childhood). If you are exposed to one of these infections and you have not previously had it, seek immediate medical attention.

Contraindications Do NOT use Decadron if you are allergic to any ingredient in Decadron, you have a systemic fungal infection, you are taking mifepristone. Contact your doctor or health care provider immediately if any of these apply to you.

Possible side effects

Side effects of Decadron depend on the dose, the duration and the frequency of administration. Short courses of dexamethasone usually are well tolerated with few and mild side effects. Long term, high dose dexamethasone usually will produce predictable and potentially serious side effects. Whenever possible, the lowest effective dose of dexamethasone should be used for the shortest possible length of time to minimize side effects. Alternate day dosing also can help reduce side effects. Side effects include fluid retention, weight gain, high blood pressure, loss of potassium, headache, muscle weakness, puffiness, and hair growth on the face, thinning and easy bruising of skin, glaucoma, cataracts, peptic ulceration, worsening of diabetes, irregular menses, growth retardation in children, convulsions, stomach upset, headache, dizziness, menstrual changes, trouble sleeping, increased appetite, or weight gain may occur, depression, euphoria, insomnia, mood swings, personality changes, and even psychotic behavior. A very serious allergic reaction to this drug is rare. If any of these effects persist or worsen, notify your doctor or pharmacist promptly.

Drug interactions Drugs such as phenobarbital, ephedrine, phenytoin (Dilantin), and rifampin (Rifadin, Rimactane) may increase the breakdown of corticosteroids by the liver. As a result it may be lower blood levels and reduced effects. Therefore, the dose of corticosteroid may need to be increased if treatment with any of these agents is begun.

Missed dose If you are taking this medication daily and on a regular schedule, and 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.

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

Storage Decadron should be stored at 68-77 F (20-25 C) and not frozen

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

Asumalife, Asumalife

Ketotifen

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

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

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Curyken

Cada tableta contiene:

Loratadina. 10 mg

Excipiente c. b.p. 1 tableta.

AntihistamпїЅnico. CURYKEN* estпїЅ indicado para aliviar los sпїЅntomas de la rinitis alпїЅrgica estacional. TambiпїЅn estпїЅ indicado en el manejo del prurito eritema y otros sпїЅntomas que acompaпїЅan a la urticaria crпїЅnica y a otras afecciones alпїЅrgicas dermatolпїЅgicas.

FARMACOCINпїЅTICA Y FARMACODINAMIA:

La loratadina es un antihistamпїЅnico antagonista selectivo de los receptores perifпїЅricos H 1 con una actividad mпїЅnima a nivel del sistema nervioso central por lo que no presenta una acciпїЅn sedante.

AbsorciпїЅn: La loratadina es rпїЅpidamente absorbida en el tracto gastrointestinal. DespuпїЅs de administrar una dosis пїЅnica o dosis mпїЅltiples de loratadina los efectos antihistamпїЅnicos se inician en los primeros 30 minutos alcanzando su mпїЅximo efecto a las 8-10 horas con una duraciпїЅn de hasta 24 horas.

DistribuciпїЅn: La loratadina se encuentra unida a las proteпїЅnas plasmпїЅticas en 97% despuпїЅs de administrar una dosis terapпїЅutica. DespuпїЅs de una administraciпїЅn de loratadina concomitantemente con alimentos la biodisponibilidad oral de la loratadina y su metabolito activo la descarboetoxiloratadina se incrementan en 40 y 15% respectivamente y las concentraciones plasmпїЅticas del fпїЅrmaco y su metabolito se retardan aproximadamente una hora. PequeпїЅas cantidades del fпїЅrmaco se han encontrado presentes en la leche.

Al administrarse dosis terapпїЅuticas del fпїЅrmaco пїЅste se distribuye escasamente en el SNC y al parecer esta pobre distribuciпїЅn es debida a la incapacidad del fпїЅrmaco para cruzar las membranas de las cпїЅlulas endoteliales que envuelven los capilares en el cerebro. En pacientes con daпїЅo renal crпїЅnico (depuraciпїЅn de creatinina igual o menor a 30 ml/min) tanto la biodisponibilidad oral como el pico en la concentraciпїЅn plasmпїЅtica presentaron incrementos de alrededor de 75% de loratadina y 120% de descarboetoxiloratadina comparados con individuos con funciпїЅn renal normal.

Sin embargo la vida media de eliminaciпїЅn del fпїЅrmaco y su metabolito activo parecen ser similares a las de individuos con funciпїЅn renal normal. En pacientes con enfermedad crпїЅnica del hпїЅgado la biodisponibilidad y el pico en las concentraciones plasmпїЅticas de loratadina se reportaron al doble no asпїЅ la descarboetoxiloratadina. La vida media de eliminaciпїЅn del fпїЅrmaco y su metabolito activo se incrementaron conforme la severidad del daпїЅo hepпїЅtico.

EliminaciпїЅn: No se ha establecido claramente la vпїЅa metabпїЅlica del fпїЅrmaco al parecer пїЅste se metaboliza principalmente en el hпїЅgado.

El 27% de la dosis administrada se elimina por la orina en las primeras 24 horas. Aproximadamente 80% de la dosis total administrada se encuentra distribuida en la orina y las heces en forma de metabolitos despuпїЅs de 10 dпїЅas.

La vida media de eliminaciпїЅn reportada en individuos sanos fue de 8.4 horas (variando de 3 a 20 horas) para la loratadina y de 28 horas (variando de 8.8 a 92 horas) para el metabolito principal descarboetoxiloratadina. La hemodiпїЅlisis no parece afectar la farmacocinпїЅtica de la loratadina ni de la descarboetoxiloratadina.

El uso de CURYKEN* estпїЅ contraindicado en pacientes con hipersensibilidad o idiosincrasia al fпїЅrmaco o a cualquiera de los componentes de la fпїЅrmula durante el embarazo la lactancia en niпїЅos menores de 12 aпїЅos.

A los pacientes con insuficiencia hepпїЅtica grave debe administrarse una dosis inicial menor ya que pueden tener una depuraciпїЅn mпїЅs lenta del medicamento siendo la dosis inicial recomendada de 5 mg una vez al dпїЅa o 10 mg en dпїЅas alternos.

Este medicamento tambiпїЅn debe usarse con precauciпїЅn en pacientes con daпїЅo renal.

RESTRICCIONES DE USO DURANTE EL EMBARAZO Y LA LACTANCIA:

Debido a que se han reportado varios casos de hipospadias en niпїЅos cuyas madres estuvieron en tratamiento con loratadina antes o durante el embarazo no debe usarse el producto durante la gestaciпїЅn.

No debe administrarse el medicamento a mujeres lactando ya que el fпїЅrmaco y su metabolito pasan rпїЅpidamente a la leche materna logrando concentraciones equivalentes a las concentraciones plasmпїЅticas por lo que se debe decidir respecto a descontinuar la lactancia o el medicamento tomando en cuenta la importancia de пїЅste para la madre.

REACCIONES SECUNDARIAS Y ADVERSAS:

Los efectos secundarios comпїЅnmente reportados incluyen cefalea nerviosismo resequedad de las mucosas en boca nariz y garganta nпїЅusea vпїЅmito retenciпїЅn urinaria impotencia visiпїЅn borrosa y erupciпїЅn cutпїЅnea.

En raras ocasiones alopecia anafilaxia alteraciones hepпїЅticas.

INTERACCIONES MEDICAMENTOSAS Y DE OTRO GпїЅNERO:

Debido a que loratadina es metabolizada por las isoenzimas CYP3A4 y CYP2D6 del citocromo P-450 la administraciпїЅn con otros medicamentos que inhiban o sean metabolizados por estas enzimas hepпїЅticas puede dar como resultado cambios en las concentraciones plasmпїЅticas y posibles eventos adversos.

AsпїЅ se han reportado incrementos en las concentraciones plasmпїЅticas de loratadina y descarboetoxiloratadina en estudios clпїЅnicamente controlados en adultos sanos que recibieron 10 mg diarios de loratadina concomitantemente con dosis de 200 mg de ketoconazol cada 12 horas 500 mg de eritromicina cada 8 horas o 300 mg de cimetidina 4 veces al dпїЅa durante 10 dпїЅas.

En estos estudios el пїЅrea bajo la curva de la concentraciпїЅn plasmпїЅtica vs. tiempo (ABC) de la loratadina se incrementпїЅ a 307 40 пїЅ 103% con la administraciпїЅn concomitante de ketoconazol eritromicina o cimetidina respectivamente; sin embargo no se detectaron cambios clпїЅnicamente importantes en el ECG en evaluaciones de laboratorio en signos vitales o en la apariciпїЅn de efectos adversos. Adicionalmente en estos individuos no se presentaron cambios en el intervalo QTc sedaciпїЅn o sпїЅncope.

ALTERACIONES EN LOS RESULTADOS DE PRUEBAS DE LABORATORIO:

La loratadina puede alterar los resultados de las pruebas cutпїЅneas que emplean histamina o antпїЅgenos.

Se recomienda descontinuar el tratamiento con loratadina al menos 7 dпїЅas antes de realizar estas pruebas.

PRECAUCIONES EN RELACIпїЅN CON EFECTOS DE CARCINOGпїЅNESIS MUTAGпїЅNESIS TERATOGпїЅNESIS Y SOBRE LA FERTILIDAD:

A dosis terapпїЅuticas la loratadina no presenta potencial carcinogпїЅnico teratogпїЅnico ni mutagпїЅnico; asimismo no se han realizado a la fecha estudios controlados en mujeres embarazadas a fin de detectar alteraciones sobre la fertilidad.

DOSIS Y VпїЅA DE ADMINISTRACIпїЅN:

La dosis para adultos y niпїЅos mayores de 12 aпїЅos es de una tableta de 10 mg cada 24 horas antes de los alimentos.

La dosis inicial recomendada para adultos con daпїЅo hepпїЅtico o renal con filtraciпїЅn glomerular menor a 30 ml/min es de una tableta cada tercer dпїЅa.

MANIFESTACIONES Y MANEJO DE LA SOBREDOSIFICACIпїЅN O INGESTA ACCIDENTAL:

Los efectos reportados por sobredosis son somnolencia dolor de cabeza y taquicardia.

En caso de sobredosis se recomienda aplicar medidas de soporte bajo vigilancia mпїЅdica (incluyendo respiraciпїЅn artificial si es necesario).

Si el paciente estпїЅ consciente y no tiene convulsiones se debe inducir el vпїЅmito.

El jarabe de ipecacuana es efectivo si se administra dentro de la primera hora de haber ingerido la sobredosis y antes de que los efectos tпїЅxicos aparezcan. Debe tenerse cuidado para evitar la broncoaspiraciпїЅn. Si no se puede inducir el vпїЅmito se recomienda el lavado gпїЅstrico y administraciпїЅn de carbпїЅn activado.

Los catпїЅrticos salinos (ejemplo: sulfato de magnesio) son пїЅtiles para la rпїЅpida diluciпїЅn del contenido intestinal.

La loratadina no es removida por hemodiпїЅlisis y se desconoce si se elimina por diпїЅlisis peritoneal.

Caja con 10 y 20 tabletas para venta al pпїЅblico y GenпїЅrico Intercambiable (GI).

RECOMENDACIONES SOBRE ALMACENAMIENTO:

ConsпїЅrvese a temperatura ambiente a no mпїЅs de 30пїЅC y en lugar seco.

LEYENDAS DE PROTECCIпїЅN:

Su venta requiere receta mпїЅdica. No se deje al alcance de los niпїЅos. No se use durante el embarazo y la lactancia. No se administre a menores de 12 aпїЅos. Literatura exclusiva para mпїЅdicos.

LABORATORIOS KENDRICK S. A.

Reg. NпїЅm. 642M98 S. S. A. IV

Zocor - Cholesterol Lowering, Lovanil

Zocor is used for lowering high cholesterol and triglycerides in certain patients. It also increases high-density lipoprotein (HDL, "good") cholesterol levels. It is used along with an appropriate diet. It is used in certain patients to reduce the risk of heart attack, stroke, and death due to coronary heart disease. It is also used to reduce the need for medical procedures to open blocked blood vessels. It is also used in certain patients to reduce the risk of heart attack, stroke, blood vessel blockage, or chest pain caused by angina. Zocor is an HMG-CoA reductase inhibitor, also known as a "statin." It works by reducing the production of certain fatty substances in the body, including cholesterol.

Use Zocor as directed by your doctor.

Take Zocor by mouth with or without food.

Eating grapefruit or drinking grapefruit juice may increase the amount of Zocor in your blood, which may increase your risk for serious side effects. The risk may be greater with large amounts of grapefruit or grapefruit juice. Avoid large amounts of grapefruit or grapefruit juice (eg, more than one quart daily). Talk with your doctor or pharmacist if you have questions about including grapefruit or grapefruit juice in your diet while you are taking Zocor.

Continue to take Zocor even if you feel well. Do not miss any doses.

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

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

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

Active Ingredient: Simvastatin.

Do NOT use Zocor if:

you are allergic to any ingredient in Zocor

you have liver problems or unexplained abnormal liver function tests

you are pregnant or breast-feeding

you are taking a macrolide antibiotic (eg, clarithromycin, erythromycin), an HIV protease inhibitor (eg, ritonavir), itraconazole, ketoconazole, mibefradil, nefazodone, or telithromycin.

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

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

if you are planning to become pregnant

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 low blood pressure, kidney problems, diabetes, a serious infection, or a history of seizures

if you have metabolism, hormonal, or electrolyte problems

if you drink alcohol or have a history of liver problems or alcohol abuse

if you have recently had major surgery or a serious injury.

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

Amiodarone, certain azole antifungals (eg, itraconazole, ketoconazole), danazol, diltiazem, fibrates (eg, gemfibrozil, clofibrate), fluconazole, HIV protease inhibitors (eg, ritonavir), imatinib, immunosuppressants (eg, cyclosporine), macrolide antibiotics (eg, clarithromycin, erythromycin), mibefradil, nefazodone, niacin, non-nucleoside reverse transcriptase inhibitors (eg, delavirdine), risperidone, streptogramins (eg, dalfopristin), telithromycin, vasopressin receptor antagonists (eg, conivaptan), verapamil, or voriconazole because they may increase the risk of muscle or kidney problems

Bosentan, carbamazepine, rifampin, or St. John's wort because they may decrease Zocor's effectiveness

Anticoagulants (eg, warfarin), digoxin, macrolide immunosuppressants (eg, tacrolimus), or spironolactone because the risk of their side effects may be increased by Zocor.

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

Drinking alcohol daily or in large amounts may increase the risk of liver problems with Zocor. Check with your doctor before drinking alcohol while you are taking Zocor.

Follow the diet and exercise program given to you by your health care provider.

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

Women who may become pregnant should use effective birth control while taking Zocor. Check with your doctor if you have questions about using birth control.

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

Report any unexplained muscle pain, tenderness, or weakness to your doctor right away, especially if you also have a fever or general body discomfort.

Rarely, changes to the skin, hair, and nails (eg, discoloration, dryness, hair loss) may occur. Check with your doctor if these effects become bothersome or cause you concern.

Lab tests, including blood cholesterol levels, liver function tests, and creatine phosphokinase (CPK) blood levels, may be performed while you use Zocor. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Zocor should be used with extreme caution in children younger 10 years and in those who have not reached puberty; safety and effectiveness in these children have not been confirmed.

Pregnancy and breast-feeding: Do not use Zocor if you are pregnant. It may cause harm to the fetus. Avoid becoming pregnant while you are taking it. If you think you may be pregnant, contact your doctor right away. It is not known if Zocor is found in breast milk. Do not breastfeed while taking Zocor.

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:

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); chest pain; dark urine; muscle pain, tenderness, or weakness (with or without fever and fatigue); pale stools; red, swollen, blistered, or peeling skin; severe or persistent stomach pain; yellowing of 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.

Anacin - Pain Relief, Cefekons

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

Availability: In Stock (17 packs)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Do NOT use Anacin if:

you are allergic to any ingredient in Anacin

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

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

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

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

Before using Anacin:

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

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

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

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

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

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

if you have anxiety, trouble sleeping, or heart problems

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

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

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

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

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

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

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

Pantomime - Definition Of Pantomime By The Free Dictionary, Panto

pantomime

1. Communication by means of gesture and facial expression: Some tourists make themselves understood abroad by pantomime.

a. The telling of a story without words, by means of bodily movements, gestures, and facial expressions.

b. A play, dance, or other theatrical performance characterized by such wordless storytelling.

c. An ancient Roman theatrical performance in which one actor played all the parts by means of gesture and movement, accompanied by a narrative chorus.

d. A player in such a performance.

3. A traditional British Christmas entertainment for children, usually based on nursery tales and featuring stock characters in costume who sing, dance, and perform skits.

To represent or express by pantomime: pantomime a story on the stage; pantomimed "baby" by cradling an imaginary infant.

To express oneself in pantomime.

[Latin pantomīmus . a pantomimic actor . from Greek pantomīmos . panto - . all (from pās , pant - ; see pan - ) + mīmos . mime .]

pan′to·mim′ic (-mĭm′ĭk) adj.

pan′to·mim′ist (-mī′mĭst) n.

pantomime

1. (Theatre) (in Britain)

a. a kind of play performed at Christmas time characterized by farce, music, lavish sets, stock roles, and topical jokes. Sometimes shortened to: panto

b. ( as modifier ): a pantomime horse.

2. (Theatre) a theatrical entertainment in which words are replaced by gestures and bodily actions

3. action without words as a means of expression

4. (Theatre) (in ancient Rome) an actor in a dumb show

5. informal chiefly Brit a confused or farcical situation

another word for mime 5

[C17: via Latin from Greek pantomimos; see panto-, mime]

pantomimic . pantomimical adj

pan•to•mime

1. the art of conveying emotions, actions, and thoughts by gestures without speech.

2. a play or entertainment in which the performers express themselves by gesture alone, often to the accompaniment of music.

3. significant gesture without speech.

4. (in the Roman Empire)

a. a masked dancer, accompanied by a chorus.

b. a dramatic performance by such a dancer and chorus.

5. a theatrical spectacle common in England at Christmastime, with stock characters who sing, dance, and tell jokes.

6. a pantomimist.

7. to express in pantomime.

8. to express oneself in pantomime.

[1580–90; earlier pantomimus < Latin < Greek pantomīmos ]

pan`to•mim′ic (-ˈmɪm ɪk) adj.

pantomime

the art of mute acting. — pantomimist, n.

pantomime

Past participle: pantomimed Gerund: pantomiming

B. CPD pantomime dame N ( Brit ) papel femenino en comedia musical navidena, tradicionalmente interpretado por un hombre

Una pantomime, abreviada en ingles como panto, es una obra teatral que se representa normalmente en Navidades ante un publico familiar. Suele estar basada en un cuento de hadas u otra historia conocida y en ella nunca faltan personajes como la dama (dame), papel que siempre interpreta un actor, el protagonista joven (principal boy), normalmente interpretado por una actriz, y el malvado (villain). Aunque es un espectaculo familiar dirigido fundamentalmente a los ninos, en el se alienta la participacion de todo el publico y posee una gran dosis de humor para adultos.

pantomime

[ˈpæntəmaɪm] n (British)

pantomime

pantomime

pantomime

1. a play performed at Christmas time, usually based on a popular fairy tale, with music, dancing, comedy etc . pantomime ??? ?????????? ???????? коледна сценка pantomima (vanocni) pohadkova revue die Pantomime, weihnachtliches Laienspiel eventyrkomedie ???????? ?????????? ????????? revista musical en epoca de Navidades (Brit) joulunaidend ????? ????? ? ??????? joulunaytelma spectacle de Noel ???????? ????????, ???????? muzicki igrokaz na temu iz bajke pantomim pantomim latbrag?sleikur (spettacolo natalizio) ????? ??? kaledinis vaidinimas vaikams pantomima; uzvedums pantomim pantomime gjoglerspill. eventyrspill pantomima ??? ???? ?? ???? ???? ???? ???? ????? ????? ????? ??? ??? ??? pantomima (spectacol de) pantomima рождественская пьеса-сказка (vianocna) rozpravkova revue bozicna predstava Bozicna predstava julshow ????????????????????????? peri masal? temsili ???,?? вистава для дітей; п'єса-казка ????? ?? ???? ?? ??? ????? k?ch th?n tho?i ???,??

2. ( also mime ) a performance by an actor done without using words. He studied pantomime in acting school. pantomime ?????? ?????? пантомима pantomina pantomima die Pantomime pantomime ????????? pantomima pantomiim ????? ???? pantomiimi pantomime ???????? ??? ???????, ??? ????? pantomima pantomim pantomim pantomima ?????????? ???(???), ???? pantomima, gestu kalba pantomima pantomim pantomime pantomime pantomima ???? ?? ??? ?????? пантомима pantomima pantomima pantomima pantomim ??????? pandomim ???? пантоміма ????? ??????? k?ch cam ????

to act out a scene without using words. Since she couldn't speak French, she had to pantomime her request for water. uitbeeld, met gebare praat ???????? ??????? ????????? играя в пантомима gesticular hrat pantomimu gebarden, mit Korpersprache darstellen mimerere ???? ????????? hacer una pantomima zestikuleerima ?? ???? ???????? ???? ???? esittaa pantomiimina mimer ???????? ????????????? ??? ????? ????, ?????? ?? ???? ??? ?????? ???? nijemo prikazivanje tatogat berpantomim mimare ??????? ???(???)? ?? parodyti gestais attelot ar kustibam menggunakan bahasa badan zich in gebarentaal uitdrukken mime grac mimicznie ??? ???? ?? ???? ???? ???? ???? ???? изъясняться жестами vyjadrit pantomimicky, naznacit posunkami izraziti (se) z mimiko pokazati pantomimom askadliggora med gester, mima ??????????? hareketlerle anlatmak ???,??? порозумітися жестами ????? ??????? ???? ra hi?u ???,???

pantomime

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He was then bound and fastened to the body of the sapling, on whose branches Magua had acted the pantomime of the falling Huron.

A staid, steadfast man, whose life for the most part was a telling pantomime of action, and not a tame chapter of sounds.

Whether flat on her stomach, or head down, heels in the air, the Simpson baby knew she was in the hands of an expert, and continued gurgling placidly while aunt Jane regarded the pantomime with a kind of dazed awe.

A ceremony followed, in dumb show, in which it was easy to recognise the pantomime of a marriage.

It was Covent Garden Theatre that I chose; and there, from the back of a centre box, I saw Julius Caesar and the new Pantomime .

I expressed in pantomime the greatest astonishment.

A sprightly tramp promised greater difficulty, and nothing but some ferocious pantomime and a shilling persuaded him to forego a choice fantasia of cockney humour.

He tapped his forehead with a distressful forefinger, to convey his opinion that the widow Jules Giry was most certainly mad, a piece of pantomime which confirmed M.

He leaped upon me with the most savage growls I ever heard, lifted me completely above his head, hurled me upon his bed, and after going through a pantomime indicative of choking me to death he stood upon my prostrate form and gave voice to a most fearsome shriek, which he explained was the victory cry of a bull ape.

All that Grimaud gained by this momentary pantomime was to pass from the rear guard to the vanguard.

It was too far to hear a word, but I had no doubt that this pantomime could only refer to the strange new captain.

So David, with a promptitude equal to the occasion, drew out his box of yellow lozenges, lifted the lid, and performed a pantomime with his mouth and fingers, which was meant to imply that he was delighted to see his dear brother Jacob, and seized the opportunity of making him a small present, which he would find particularly agreeable to the taste.

Metrazole Oral Uses, Side Effects, Interactions, Pictures, Warnings - Dosing, Metazole

Metrazole

Uses

Metronidazole is an antibiotic that is used to treat a wide variety of infections. It works by stopping the growth of certain bacteria and parasites .

This antibiotic treats only certain bacterial and parasitic infections. It will not work for viral infections (such as common cold. flu ). Using any antibiotic when it is not needed can cause it to not work for future infections.

Metronidazole may also be used with other medications to treat certain stomach /intestinal ulcers caused by a bacteria (H. pylori).

How to use Metrazole

Take this medication by mouth as directed by your doctor. To prevent stomach upset, take this medication with food or a full glass of water or milk. The dosage is based on your medical condition and response to treatment.

Antibiotics work best when the amount of medicine in your body is kept at a constant level. Take this drug at evenly spaced intervals.

Continue to take this medication until the full prescribed amount is finished, even if symptoms disappear after a few days. Stopping the medication too early may result in a return of the infection.

Tell your doctor if your condition lasts or gets worse.

Side Effects

Dizziness. headache. stomach upset, nausea. vomiting. loss of appetite, diarrhea. constipation. or metallic taste in your mouth may occur. If any of these effects last or get worse, tell your doctor or pharmacist promptly.

This medication may cause your urine to turn darker in color. This effect is harmless and will disappear when the medication is stopped.

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.

Tell your doctor right away if you have any serious side effects, including: signs of a new infection (such as sore throat that doesn't go away, fever), easy bruising/bleeding, stomach/abdominal pain. painful urination .

Get medical help right away if you have any very serious side effects, including: unsteadiness, seizures. mental/mood changes (such as confusion), trouble speaking, numbness/tingling of arms/legs, eye pain. sudden vision changes, headache that is severe or doesn't go away, stiff/painful neck.

Use of this medication for prolonged or repeated periods may result in oral thrush or a new yeast infection. Contact your doctor if you notice white patches in your mouth. a change in vaginal discharge. or other new symptoms.

A very serious allergic reaction to this drug is rare. However, get medical help right away if you notice any symptoms of a serious allergic reaction. including: rash. itching /swelling (especially of the face/tongue /throat), severe 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.

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 metronidazole, tell your doctor or pharmacist if you are allergic to it; or to other antibiotics (such as tinidazole ); 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: liver disease, kidney disease. certain blood disorders (low blood cell counts).

Avoid alcoholic beverages and products containing propylene glycol while taking this medication and for at least 3 days after finishing this medicine because severe stomach upset/cramps. nausea, vomiting, headache. and flushing may occur.

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.

Before having surgery, tell your doctor or dentist about all the products you use (including prescription drugs, nonprescription drugs, and herbal products).

During pregnancy. this medication should be used only when clearly needed. Discuss the risks and benefits with your doctor.

This medication passes into breast milk. Discuss the risks and benefits with your doctor before breast - feeding. If you are prescribed the single-dose treatment, your doctor may direct you to stop breast-feeding for a short time after the dose. Consult your doctor for more details.

Interactions

See also Precautions section.

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: alcohol-containing products (such as cough and cold syrups, aftershave), products containing propylene glycol, lopinavir/ritonavir solution, lithium.

Do not take metronidazole if you are also taking disulfiram or if you have taken disulfiram within the last 2 weeks.

Although most antibiotics are unlikely to affect hormonal birth control such as pills, patch, or ring, a few antibiotics (such as rifampin, rifabutin) can decrease their effectiveness. This could result in pregnancy. If you use hormonal birth control, ask your doctor or pharmacist for more details.

This medication may interfere with certain lab tests, possibly causing false test results. Make sure lab 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: nausea, vomiting, unsteadiness.

Notes

Do not share this medication with others.

If you are being treated for a certain infection (trichomoniasis), all sexual partners may also need to be treated to avoid re-infection. During treatment, avoid sexual intercourse, or always use a latex or polyurethane condom.

This medication has been prescribed for your current condition only. Do not use it later for another infection unless your doctor directs you to do so. A different medication may be necessary in that case.

If you are taking this medication for a longer time, lab tests (such as blood cell counts) may be done while you are taking this medication. Keep all medical and lab appointments. 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. Take your next dose at the regular time. 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 February 2016. Copyright(c) 2016 First Databank, Inc.

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

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

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Antix-Linux Download, Antix

antiX-Linux

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I have an old Dell Inspiron 1200 Notebook that I use as a backup/side-tool that struggles with just about any OS given to it. It's low spec and it's upgrade ability is severely limited. All versions of Windows after XP were too much for this computer. I spent months trying to find an OS that would suffice for this old computer. Even Lubuntu was too much. All other Linux distros aimed at older computers either simply would not work or required too much knowledge of Linux for a new or average user. I was about to give up completely on using this old computer when I decided one more time to give all the small distros another chance. How or why I overlooked antiX is beyond me, but I'm glad I took another run at this. antiX was easy enough to install and runs smoothly and quickly. iceWM is still a wee bit lacking, but they've added enough scripts and GUI windows for dealing with settings and the applications menu. Once you take care of settings, update the system and programs and install what you want/need, then it's smooth sailing from then on. I've got some old towers and desktops sitting in a closet that might now benefit from antiX.

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antiX has long been one of the finest distributions available. I say that for many reasons. Here are a few: it is reasonably easy to install (trivial for a veteran, reasonable for a novice), yet it extremely easy to customize to make it just the way you want it. You can run it live or you can install it. The forum is helpful and the people respond to feature requests. Of course, anticapitalista is an excellent distribution creator, who has created small to medium sized implementations with great success. I have used the Beta 3 version of antiX 15 plus nearly every version and build since 2006 and I can personally vouch for any of them and heartily recommend antiX!

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Buy Cobapolas (Oxytrol) Online Without A Prescription, Cobapolas

Buy Cobapolas (Oxytrol) Without Prescription

Cobapolas (Oxytrol) Description

Cobapolas medicine contains oxybutynin which reduces muscle spasms of the bladder and urinary tract.

Cobapolas works by reducing muscle spasms of the bladder and urinary tract.

Generic name of Cobapolas is Oxybutynin.

Brand name of Cobapolas is Cobapolas.

Cobapolas (Oxytrol) Dosage

Cobapolas is available in:

2.5mg Low Dosage

5mg Standard Dosage

To use the Cobapolas patch, open the sealed pouch and remove the protective liner.

Apply the Cobapolas patch to a clean, dry area on your stomach, hip or buttock. Avoid skin that is oily, irritated or damaged. Avoid placing the patch on a skin area that will be rubbed by a waistband or tight clothing.

Press the Cobapolas patch onto the skin and press it down firmly with your fingers. Make sure the patch is well sealed around the edges. When properly applied, the patch should stay on while swimming or bathing.

Leave the patch in place and wear it for 3 to 4 days. You should change the patch twice per week. Each time you apply a new patch, choose a different skin area on your stomach, hip or buttock. Do not apply a patch to the same skin twice within one week.

Try to change your Cobapolas patch on the same two days each week (such as every Sunday and Thursday). There is a calendar printed on the package of this medication to help you establish a steady patch-changing schedule.

If the patch falls off, try sticking it back on. If it does not stay on, replace it with a new one and wear it until your next regular patch-changing day. Do not change your schedule, even if you apply a new patch to replace one that has fallen off.

After removing a patch, fold it in half so it sticks together and throw it away in a place where children or pets cannot get to it.

Cobapolas (Oxytrol) Missing of dose

Do not take double dose. If you miss a dose you should take it as soon as you remember about your missing. If it is the time for the next dose you should continue your regular dosing schedule.

Cobapolas (Oxytrol) Overdose

If you overdose Cobapolas and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Cobapolas overdosage: restlessness, tingly feeling, fever, uneven heart rate, vomiting, urinating less than usual or not at all.

Cobapolas (Oxytrol) Storage

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture, humidity and heat Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Cobapolas (Oxytrol) Side effects

Cobapolas has its side effects. The most common are:

mild skin itching, burning, redness or discoloration where a patch was worn

dizziness

drowsiness

weakness

blurred vision

dry mouth

warmth, tingling or redness under your skin

nausea

vomiting

stomach pain

constipation or diarrhea

dry eyes

stuffy nose

back pain

feeling restless

insomnia

Less common but more serious side effects during taking Cobapolas:

allergy reactions (urticaria, breathing difficulties, rash, and eruption)

fever with hot, dry skin

uneven heart rate

pain, burning or other difficulty when urinating

severe itching, burning or blistering that does not clear up within several hours after removing the skin patch

Side effects manifestations are not only depend on medicine you are taking but also depend on your health state and on the other factors.

Cobapolas (Oxytrol) Contra-indications

Do not take Cobapolas if you are allergic to Cobapolas components.

Be careful with Cobapolas while you are pregnant or have nurseling.

Do not take Cobapolas if you have untreated or uncontrolled glaucoma.

Do not take Cobapolas if you have a blockage in your digestive tract (stomach or intestines).

Do not take Cobapolas if you have decreased urination or are unable to urinate.

Be careful with Cobapolas while you have glaucoma, liver disease, kidney disease, myasthenia gravis, enlarged prostate, intestinal disorder, such as ulcerative colitis, stomach disorder such as gastroesophageal reflux disease (GERD) or slow digestion.

Be careful with Cobapolas while you take atropine (Donnatal, and others), belladonna;, clidinium (Quarzan), dicyclomine (Bentyl), glycopyrrolate (Robinul), hyoscyamine (Anaspaz, Cystospaz, Levsin and others), mepenzolate (Cantil), methantheline (Provocholine), methscopolamine (Pamine), propantheline (Pro-Banthine), scopolamine (Transderm-Scop), clarithromycin (Biaxin), erythromycin (E-Mycin, E. E.S. Ery-Tab, Erythrocin), itraconazole (Sporanox) or ketoconazole (Nizoral).

Avoid using harsh soaps, alcohol, nail polish remover or other solvents that could irritate your skin.

Avoid becoming overheated or dehydrated during exercise and in hot weather.

Avoid machine driving.

It can be dangerous to stop Cobapolas taking suddenly.

Cobapolas (Oxytrol) Frequently asked questions

Q: What is Cobapolas?

A: Cobapolas medicine contains oxybutynin which reduces muscle spasms of the bladder and urinary tract.

Q: What is Cobapolas used for?

A: Cobapolas is used to treat symptoms of overactive bladder: frequent or urgent urination, incontinence (urine leakage), increased nighttime urination.

Q: How does Cobapolas work?

A: Cobapolas works by reducing muscle spasms of the bladder and urinary tract.

Q: What is the generic name of Cobapolas?

A: Generic name is Oxybutynin.

Q: What should I do in case of dose missing?

A: If you forget to change a patch on your scheduled day, remove and replace the patch as soon as you remember. Wear the patch until your next regular patch-changing day. Do not change your schedule, even if you wear the new patch for less than 3 days. Do not apply two patches at the same time to make up the missed dose.

Q: What are the symptoms of Cobapolas overdosage?

A: Possible symptoms of overdosage: restlessness, tingly feeling, fever, uneven heart rate, vomiting, urinating less than usual or not at all.

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Setiral, Setiral

Zyrtec (cetirizine) is an antihistamine that reduces the effects of natural chemical histamine in the body. Histamine can produce symptoms of sneezing, itching, watery eyes, and runny nose.

Zyrtec is used to treat cold or allergy symptoms such as sneezing, itching, watery eyes, or runny nose.

Zyrtec is also used to treat itching and swelling caused by chronic urticaria (hives).

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

Use Zyrtec exactly as directed on the label, or as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended.

You may take Zyrtec with or without food.

The chewable tablet must be chewed before you swallow it.

Do not swallow the Zyrtec dissolving tablet whole. Allow it to dissolve in your mouth without chewing. Swallow several times as the tablet dissolves. If desired, you may drink liquid to help swallow the dissolved tablet.

Call your doctor if your symptoms do not improve, if they get worse, or if you also have a fever. Store this medicine at room temperature away from moisture and heat. Do not allow the liquid form of this medicine to freeze.

Use Zyrtec exactly as directed on the label, or as prescribed by your doctor.

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

Store at room temperature between 68-77 degrees F (20-25 degrees C) away from light and moisture. Brief storage between 59-86 degrees F (15-30 degrees C) is permitted. Or store in the refrigerator between 36-46 degrees F (2-8 degrees C). Do not store in the bathroom. Keep all medicines 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 for more details about how to safely discard your product.

Active ingredient: Cetirizine

Inactive ingredients: colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide

Do NOT use Zyrtec if:

You are allergic to any ingredient in Zyrtec or to hydroxyzine Contact your doctor or health care provider right away if any of these apply to you. Some medical conditions may interact with Zyrtec. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you: if you are pregnant, plan 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 kidney or liver problems, or are receiving dialysis

Do not drink alcohol or use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are using Zyrtec ; it may add to their effects.

Ask a doctor or pharmacist if it is safe for you to take this medicine if you have any medical conditions.

Tell your doctor if you regularly use other medicines that make you sleepy (such as other cold or allergy medicine, narcotic pain medicine, sleeping pills, muscle relaxers, and medicine for seizures, depression, or anxiety). They can add to sleepiness caused by Zyrtec.

This list is not complete and other drugs may interact with Zyrtec. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.

Important safety information:

Do not use with any other antihistamines applied to the skin (such as diphenhydramine cream, ointment, spray) because increased side effects may occur.

If you are scheduled for allergy testing, ask your doctor if you should stop taking this medication for several days before testing. This drug may affect your allergy test results.

This document does not contain all possible interactions. Therefore, before using this product, tell your doctor or pharmacist of all the products you use. Keep a list of all your medications with you, and share the list with your doctor and health care provider.

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 when using Zyrtec:

Drowsiness; dry mouth; stomach pain (in children); tiredness; trouble sleeping (in children).

Seek medical attention right away if any of these SEVERE side effects occur when using Zyrtec:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); dark urine; fainting; fast or irregular heartbeat; mental or mood changes; persistent fatigue; seizures; severe dizziness; unusual bruising or bleeding; yellowing of eyes or skin.

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

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Biography

Larenz Tate was born on the west side of Chicago to Larry and Peggy Tate, the youngest of three brothers. His brothers are actors Larron Tate and Lahmard J. Tate. In 1984, Larenz and his family moved to California. It was while living in California that Larenz's parents got him and his brothers involved in a drama program at the Inner City Cultural Center. At first, the boys were interested just to meet girls. However, when they saw classmate Malcolm-Jamal Warner get cast in the role of "Theo Huxtable" on The Cosby Show (1984), they began to take it more seriously. From then on, the brothers began getting other small roles. Larenz's career first took off in a Christmas episode of The Twilight Zone (1985), after which roles began pouring in. He has gone on to star in both television series and movies.

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Flutinax Capsulas Para Que Sirve, Flutinax

FLUTINAX CAPSULAS

Acceso rapido al contenido

Precaucion con mayores de 65 anos

Especial antencion con menores de 14 anos

Tenga especial cuidado durante el embarazo .

No usar FLUTINAX CAPSULAS con lactantes.

Revise siempre que no sea alergico a ninguno de los componentes de FLUTINAX CAPSULAS . podria poner en peligro su salud

Recuerda antes de tomar este medicamento consultar siempre con su medico, la informacion que ofrecemos es orientativa y no sustituye en ningun caso la de su medico u otro profesional de la salud.

Prospecto e indicaciones

DENOMINACION GENERICA:

FORMA FARMACEUTICA Y FORMULACION:

Cada capsula contiene:

Clorhidrato de fluoxetina equivalente a. 20 mg de fluoxetina

Excipiente, cbp. 1 capsula

INDICACIONES TERAPEUTICAS:

FLUTINAX es fluoxetina, antidepresivo clasificado como inhibidor de la recaptacion de serotonina.

FLUTINAX esta indicado en las siguientes entidades:

Depresion leve o moderada, trastornos depresivos mayores, depresion asociada con ansiedad.

Bulimia nerviosa: En el manejo de los excesos en comer y las acciones relacionadas con la bulimia.

Trastorno obsesivo-compulsivo.

FARMACOCINETICA Y FARMACODINAMIA EN HUMANOS:

La fluoxetina esta clasificada como una fenilpropilamina de cadena recta, es un inhibidor potente y selectivo de la captura de serotonina, lo cual permite la accion bioquimica de esta ultima cuya funcion en la enfermedad depresiva es fundamental.

La fluoxetina sobrelleva metabolismo hepatico, originando varios metabolitos, siendo uno de los mas conocidos la norfluoxetina, la cual se forma por una desmetilacion de la molecula de fluoxetina.

Cuando la fluoxetina se administra por via oral se absorbe bien por el aparato gastrointestinal, despues de una dosis de 40 mg se alcanzan concentraciones hematicas de 15 a 55 ng/ml a las 8 horas. Aparentemente, la biodisponibilidad de la fluoxetina no es afectada por la ingesta de alimentos, sin embargo, en estas circunstancias la velocidad de absorcion si resulta afectada.

La fluoxetina se liga extensamente a las proteinas plasmaticas y tiene una distribucion amplia en el organismo. La vida media del farmaco y del metabolito norfluoxetina es de 24 a 72 horas en pacientes con funcion hepatica normal. Dado que el higado es el sitio principal de metabolismo del producto, este puede verse afectado en presencia de insuficiencia hepatica. La vida media de eliminacion de la fluoxetina es de 4 a 6 dias y la de su metabolito norfluoxetina es de 4 a 16 dias.

En pacientes con hepatopatias la administracion de fluoxetina debera ser cautelosa, utilizando dosis bajas y espaciadas, con el objeto de evitar dano renal en el paciente.

En pacientes mayores de 65 anos de edad, debido a la prolongada vida media del farmaco, la dosis debera ajustarse, sobre todo en pacientes que esten recibiendo farmacos multiples para el tratamiento de otros padecimientos.

El mecanismo de accion de la fluoxetina consiste en inhibir la incorporacion de la serotonina en la neurona presinaptica, con ello facilita la transmision serotoninergica. El efecto en el sistema noradrenergico es muy escaso. La fluoxetina tiene afinidad por otros tipos de receptores, tales como: muscarinicos, histaminicos H1, serotoninergicos 5-HT1 o 5-HT2, noradrenergicos ?1 o ?2.

Existe evidencia de que la deficiencia de serotonina es causa primaria de alteraciones afectivas y se ha demostrado que existen efectos antidepresivos posteriores a la administracion de farmacos que incrementan la serotonina en las terminaciones sinapticas.

CONTRAINDICACIONES:

La fluoxetina no debera administrarse en pacientes con historia de hipersensibilidad al farmaco o a cualquiera de los componentes de la formula.

La fluoxetina no se debe combinar con inhibidores de la monoaminooxidasa, incluso se deben dejar pasar 2 semanas despues de suspender el tratamiento con un IMAO para reiniciar la terapia con fluoxetina.

RESTRICCIONES DE USO DURANTE EL EMBARAZO Y LA LACTANCIA:

La seguridad y eficacia de la fluoxetina no han sido determinadas en pacientes pediatricos, por lo que no debera administrarse en pacientes menores de 14 anos.

Los estudios efectuados en ratas y conejos en fases de reproduccion utilizando fluoxetina a la dosis maxima empleada en humanos (80 mg) no han reportado evidencia de dano al producto. Con todo, no existen estudios realizados en la mujer embarazada, en consecuencia, dado que los estudios en animales de experimentacion no siempre son predictivos de la respuesta en seres humanos se concluye que la fluoxetina no debera emplearse durante el embarazo.

La fluoxetina no debera administrarse durante la lactancia debido a que este farmaco asi como su metabolito norfluoxetina se excretan en leche materna.

REACCIONES SECUNDARIAS Y ADVERSAS:

La administracion de fluoxetina ha sido asociada con los siguientes efectos adversos, los cuales pueden ocurrir tambien con otros inhibidores de la recaptura de serotonina:

Reacciones generales: Boca seca, sudoracion, escalofrios, vasodilatacion (sintomatologia autonomica); hipersensibilidad (erupcion cutanea, prurito, reaccion anafilactoide); sindrome serotoninergico, el cual se caracteriza por alteraciones del estado mental y en la actividad neuromuscular; fotosensibilidad. Bostezos.

Sistema endocrino: Se ha observado que puede haber secrecion anormal de hormona antidiuretica.

Sistema digestivo: Nausea, diarrea, disfagia, dispepsia, sentido del gusto alterado.

Piel y anexos: Equimosis y alopecia.

Sistema nervioso: Mareo, movimientos anormales (espasmos musculares, ataxia, mioclonus), anorexia, perdida de peso, ansiedad, fatiga, somnolencia, astenia, alteraciones del proceso de pensamiento o de la concentracion, suenos anormales, insomnio, reaccion maniaca, midriasis, vision borrosa.

Sistema urinario: Cambios en la miccion.

Sistema genital: Disfuncion sexual incluyendo cambios en la libido, priapismo, disminucion o ausencia de eyaculacion, impotencia, anorgasmia.

INTERACCIONES MEDICAMENTOSAS Y DE OTRO GENERO:

En pacientes tratados con fluoxetina y un inhibidor de la monoaminooxidasa se han reportado casos graves y fatales de sindrome serotoninergico, lo cual ha ocurrido cuando no se toma la precaucion de espaciar cuando menos 5 semanas posteriores a la suspension de fluoxetina para el inicio de tratamiento con el IMAO.

Se debera tener en mente que la fluoxetina tiene la particularidad de inhibir la isoenzima del citocromo P450IID6, en consecuencia, el tratamiento con los medicamentos que son metabolizados por este sistema enzimatico y que poseen indice terapeutico estrecho debera comenzarse en el limite inferior del rango de dosificacion si el paciente esta siendo tratado con fluoxetina o si ha tomado este farmaco las 5 semanas anteriores. En caso de ser necesario el tratamiento concomitante de fluoxetina con alguno de los farmacos mencionados, debera ajustarse la dosis.

El tratamiento simultaneo de fluoxetina con farmacos con actividad en SNC tales como carbamacepina, fenitoina, diacepam, imipramina, litio, clozapina, desipramina, alprazolam y haloperidol puede provocar cambios en los niveles hematicos de estos medicamentos, incluyendo en algunas ocasiones manifestaciones clinicas de toxicidad.

La coadministracion de ketorolaco y fluoxetina debera evitarse puesto que ha habido reportes de alucinaciones en algunos pacientes.

En cualquier caso, los pacientes cuyo tratamiento implique el uso concomitante de fluoxetina y otros farmacos debera ser vigilado con el proposito de detectar cualquier efecto adverso lo mas pronto posible y actuar en consecuencia.

La administracion conjunta de warfarina y fluoxetina obliga a tener estrecho monitoreo en las pruebas de coagulacion del paciente debido a que, aunque raras veces, se han reportado alteraciones del efecto anticoagulante.

Se han reportado en raras ocasiones convulsiones prolongadas en pacientes que estan en tratamiento con fluoxetina y que tambien estaban bajo terapia electroconvulsiva.

ALTERACIONES EN LOS RESULTADOS DE PRUEBAS DE LABORATORIO:

En casos aislados se ha reportado alteracion de pruebas de funcionamiento hepatico y cambios en los hemoniveles de acido urico, aunque estos ultimos no han tenido trascendencia clinica.

PRECAUCIONES EN RELACION CON EFECTOS DE CARCINOGENESIS, MUTAGENESIS, TERATOGENESIS Y SOBRE LA FERTILIDAD:

Los estudios realizados en ratas y conejos con dosis de 12.5 y 15 mg/kg respectivamente no reportaron que la fluoxetina pueda producir efectos de carcinogenicidad, teratogenicidad, mutagenicidad y sobre la fertilidad en dichas especies animales durante la etapa de organogenesis. Estudios realizados en conejas y ratas embarazadas obtuvieron la conclusion de que las malformaciones observadas no tuvieron incremento en el grupo de los animales tratados con fluoxetina durante el embarazo.

DOSIS Y VIA DE ADMINISTRACION:

Dosis: La dosis de inicio de FLUTINAX varia de 20 a 80 mg/dia.

Depresion: La dosis oral de inicio de FLUTINAX es de 20 mg/24 horas, en caso de que la respuesta no fuera la adecuada despues de 3 a 6 semanas, se puede incrementar la dosis en multiplos de 20, no excediendo de 80 mg, la cual es la dosis maxima. Es recomendable que la toma sea por la manana y en caso de que la dosis sea de mas de 20 mg se puede dividir en dos tomas al dia.

Trastorno obsesivo-compulsivo: Se recomienda comenzar con 20 mg/24 horas, siguiendo el esquema anterior, aumentar 20 mg en caso de respuesta negativa cada 3 a 6 semanas, no excediendo de 80 mg/dia.

Bulimia nerviosa: Se ha observado que este trastorno se maneja adecuadamente cuando se aplican 60 mg.

En pacientes con insuficiencia renal severa se recomienda disminuir la dosis o espaciar los intervalos de dosificacion de fluoxetina.

En funcion de que la fluoxetina es metabolizada en higado, los pacientes con insuficiencia hepatica deberan ser vigilados y reducir la dosis hasta 50%.

La fluoxetina ha sido utilizada exitosamente en geriatria sin necesidad de ajustar la dosis, sin embargo, quedara a juicio del clinico, en funcion del estado general del paciente anciano, el ajuste de la dosificacion.

Via de administracion: Oral.

MANIFESTACIONES Y MANEJO DE LA SOBREDOSIFICACION O INGESTA ACCIDENTAL:

En caso de sobredosificacion se deberan establecer medidas de soporte cardiovascular y respiratorio al paciente. No se sabe cual es el nivel hematico toxico de fluoxetina, sin embargo, los valores hematicos con la dosis habitual son de 400 ng/ml. Se realizara lavado gastrico solamente cuando la ingestion de fluoxetina sea muy reciente.

La aplicacion de carbon activado a dosis de 240 ml de diluente y 30 g de carbon, puede ser de gran utilidad.

PRESENTACIONES:

Cajas con 7, 14 y 28 capsulas de 20 mg de fluoxetina.

RECOMENDACIONES SOBRE ALMACENAMIENTO:

Conservese en lugar fresco y seco, de 15 a 30°C.

LEYENDAS DE PROTECCION:

Literatura exclusiva para medicos. No se deje al alcance de los ninos. Su venta requiere receta medica.

LABORATORIO Y DIRECCION:

IVAX PHARMACEUTICALS MEXICO, S. A. de C. V. Calzada de Tlalpan Num. 3007 Colonia Santa Ursula Coapa 04650 Mexico, D. F.

Reg. Num. 372M2000, SSA IEAR-207427/R2000/IPPA

Buy Belnif (Adalat) Online No Prescription, Belnif

Buy Belnif (Adalat) without Prescription

Belnif Marketing Information

Belnif Description

Belnif is a perfect remedy in struggle against hypertension or high blood pressure, angina or chest pain.

Belnif acts by relaxing blood vessels (such as veins and arteries), which makes it easier for the heart to pump and reduces its workload.

Generic name of Belnif is Nifedipine.

Brand names of Belnif are Belnif CC, Procardia, Procardia XL.

Belnif Dosage

Belnif is available in:

10mg Low Dosage20mg Standard Dosage30mg Increased Dosage

Belnif should be taken orally with or without food.

It is better to take Belnif at the same time every day. Take on an empty stomach.

Avoid grapefruit juice during treatment with Belnif.

If you want to achieve most effective results do not stop taking Belnif suddenly.

Belnif Missing of dose

Do not take double dose. If you miss a dose you should take it as soon as you remember about your missing. If it is the time for the next dose you should continue your regular dosing schedule.

Belnif Overdose

If you overdose Belnif and you don't feel good you should visit your doctor or health care provider immediately.

Belnif Side effects

Belnif has its side effects. The most common are:

migrainefatigueflushingvivid or unusual dreamsnauseaconstipationproblems with urinationtrouble sleepingubnormal heartbeatslightheadednesspsychosisswelling of the legs or anklesyellowing of the skin or eyes

Less common but more serious side effects during taking Belnif: allergy reactions (urticaria, breathing difficulties, rash, and eruption)

Side effects manifestations are not only depend on medicine you are taking but also depend on your health state and on the other factors.

Belnif Contra-indications

Do not take Belnif if you are allergic to Belnif components.

Do not take Belnif if you're pregnant or you plan to have a baby, or you are a nursing mother. Belnif can harm your baby.

Do not use Belnif in combination with salt substitutes or potassium supplements.

If you want to achieve most effective results without any side effects it is better to avoid alcohol.

Avoid grapefruit juice during treatment with Belnif.

Try to be careful using Belnif if you suffer from kidney disease, liver disease, diseases of the heart or blood vessels (sick sinus syndrome), aortic stenosis, heart failure, low blood pressure, or coronary artery disease.

Do not stop taking Belnif suddenly.

Belnif Frequently asked questions

Q: What does Belnif mean?

A: Belnif is a high-quality medication which is taken in treatment of hypertension or high blood pressure, angina or chest pain.

Q: What are brand and generic names of Belnif?

A: Generic name of Belnif is Nifedipine. Brand names of Belnif are Belnif CC, Procardia, Procardia XL.

Q: What is necessary to avoid?

A: Do not use Belnif in combination with salt substitutes or potassium supplements. If you want to achieve most effective results without any side effects it is better to avoid alcohol. Avoid grapefruit juice during treatment with Belnif.

Q: In what way does Belnif operate?

A: Belnif acts by relaxing blood vessels (such as veins and arteries), which makes it easier for the heart to pump and reduces its workload.

Pediaflor Oral Uses, Side Effects, Interactions, Pictures, Warnings - Dosing, Pediachlor

Pediaflor

Uses

This medication is used to prevent cavities. It makes teeth stronger and more resistant to decay caused by acid and bacteria. Talk to your dentist or doctor about the benefits and risks of this product.

This medication is not recommended for use in infants less than 6 months of age.

This medication is not recommended for use in areas where the fluoride content in the water supply is greater than 0.6 parts per million. See Notes section for more information.

How to use Pediaflor

Take this medication by mouth. usually once daily as directed by your doctor/dentist.

The dosage is based on your age and the fluoride content in your water supply.

If you are using the liquid form of this medication, measure the dose carefully using the specially marked medicine dropper that is provided. Drops may be swallowed directly, added to a small amount of juice, or mixed with a small amount of food such as applesauce. Do not mix with food containing milk or other dairy products.

If you are using the chewable form of this medication, chew or dissolve it in the mouth before swallowing so that the teeth will also absorb the fluoride. If you are using the lozenge, place the lozenge in your mouth and allow it to dissolve. Take the chewable medication or lozenge at bedtime after brushing your teeth or as directed by your doctor/dentist. For best results, do not rinse your mouth, eat, or drink for 30 minutes after taking these forms of the medication.

Take this medication 1 hour apart from products that contain calcium. aluminum, or magnesium. Some examples include dairy products (such as milk, yogurt), antacids, laxatives. and vitamins /minerals. These products can bind with fluoride, preventing its full absorption.

Use this medication regularly in order to get the most benefit from it. To help you remember, take it at the same time each day.

Side Effects

Stomach upset may occur. If this effect persists or worsens, contact your doctor/dentist or pharmacist promptly.

Tell your doctor/dentist right away if your teeth become stained or pitted. This is often a result of too much fluoride.

Remember that your doctor/dentist has prescribed this medicine 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 very serious allergic reaction to this drug is unlikely, but seek immediate medical attention if it occurs. Symptoms of a serious allergic reaction may include: rash. itching /swelling (especially of the face/tongue /throat), severe dizziness. trouble breathing .

This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor/dentist 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 this medication, tell your doctor/dentist or pharmacist if you are allergic to it; or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

Before using this medication, tell your doctor/dentist or pharmacist your medical history, especially of: mouth problems (e. g. sores, mucositis).

Tell your doctor if you are pregnant before using this medication.

This medication passes into breast milk. While there have been no reports of harm to nursing infants, consult your doctor before breast - feeding.

Interactions

See also How to Use section.

Your healthcare professionals (e. g. doctor or pharmacist) may already be aware of any possible drug interactions and may be monitoring you for them. Do not start, stop, or change the dosage of any medicine before checking with them first.

Before using this medication, tell your doctor/dentist or pharmacist of all prescription and nonprescription/herbal products you may use.

Keep a list of all your medications with you, and share the list with your doctor and pharmacist.

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: burning in the mouth, sore tongue. nausea. vomiting. diarrhea. increased saliva. stomach pain /cramping, muscle weakness. shaking, seizures .

Notes

Do not share this medication with others.

Taking this medication does not replace good dental habits. Continue to brush and floss your teeth regularly as directed by your dentist, and have regular dental checkups.

Check the fluoride content of your water supply by asking local town or city officials. Fluoride supplements are not necessary if the fluoride content in the water supply is greater than 0.6 parts per million. If your water supply changes or if you move, check with your doctor or dentist to determine if extra fluoride is still necessary.

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 between 68-77 degrees F (20-25 degrees C) away from heat and moisture. Store the liquid form in the original plastic container. Do not store in the bathroom. Keep all medicines 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 for more details about how to safely discard your product.

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

Images

No data available at this time.

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

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

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ADHD Drug Side Effects

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Buy Diklonat P - Diclofenac - Online Without Prescriptions, Diklonat P

Diclofenac (Diklonat p)

Diclofenac is used primarily for the treatment of inflammation and pain caused by conditions such as rheumatoid arthritis, osteoarthritis, and ankylosing spondylitis. It is also effective in treating soft tissue inflammations due to tendinitis and bursitis, and treating dysmenorrhea (menstrual cramps). Diclofenac is an NSAID. NSAIDs treat the symptoms of pain and inflammation. They do not treat the disease that causes those symptoms.

Use Diclofenac as directed by your doctor!

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

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

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

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

Do NOT use Diclofenac if:

you are allergic to any ingredient in Diclofenac or to bovine (cow) protein

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 have severe kidney problems

you are in the last 3 months of pregnancy.

Contact your doctor or health care provider right away if this applies to you.

Some medical conditions may interact with Diclofenac. 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 a history of kidney or liver problems, diabetes, or stomach or bowel problems (eg, bleeding, perforation, ulcers)

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

if you have high blood pressure, blood disorders (eg, porphyria), 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 smoke, drink alcohol, or have a history of alcohol abuse

if you are taking an antibiotic or an anti-seizure medicine. The risk of liver problems may be increased with some of these medicines.

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

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

Acetaminophen because the risk of liver problems may be increased

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

Cyclosporine, lithium, metformin, methotrexate, oral NSAIDs (eg, ibuprofen), or quinolones (eg, ciprofloxacin) because the risk of their side effects may be increased by Diclofenac

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

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

Diclofenac may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Diclofenac 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 Diclofenac. Taking it in high doses, for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Diclofenac with food will NOT reduce the risk of these effects. If you have severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling, contact your doctor or emergency room right away.

Do NOT take more than the recommended dose or use for longer than prescribed without checking with your doctor.

Diclofenac 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 Diclofenac unless your doctor tells you to.

Check with your doctor or pharmacist before you take acetaminophen while you are taking Diclofenac. The risk of liver problems may be increased.

Do not switch between different forms of Diclofenac (eg, enteric-coated tablets, immediate-release tablets, capsules) unless your doctor tells you to. They may not provide the same amount of medicine to your body.

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

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

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

Pregnancy and breast-feeding: Diclofenac 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 Diclofenac while you are pregnant. It is not known if Diclofenac is found in breast milk. Do not breastfeed while taking Diclofenac.

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:

Constipation; diarrhea; dizziness; drowsiness; headache; mild stomach pain or heartburn; nausea; vomiting.

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; 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; persistent flu-like symptoms; red, swollen, blistered, or peeling skin; ringing in the ears; seizures; severe headache or dizziness; severe or persistent stomach pain or nausea; severe vomiting or diarrhea; shortness of breath; sudden or unexplained weight gain; swelling of the hands, legs, or feet; symptoms of liver problems (eg, dark urine, pale stools, persistent loss of appetite, yellowing of the skin or eyes); unusual bruising or bleeding; unusual joint or muscle pain; unusual tiredness or weakness; vision or speech changes; vomit that looks like coffee grounds.

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.

Customers who bought this product also bought

Diflucan (Fluconazole) Drug Side Effects, Interactions, And Medication Information On Emedicinehealt

Generic Name: fluconazole (Pronunciation: floo KOE na zole)

What is fluconazole (Diflucan)?

Fluconazole is an antifungal antibiotic.

Fluconazole is used to treat infections caused by fungus, which can invade any part of the body including the mouth, throat, esophagus, lungs, bladder, genital area, and the blood.

Fluconazole is also used to prevent fungal infection in people with weak immune systems caused by cancer treatment, bone marrow transplant, or diseases such as AIDS.

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

Diflucan 100 mg

trapezoid, pink, imprinted with DIFLUCAN 100, ROERIG

Diflucan 150 mg

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Diflucan 200 mg

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Diflucan 50 mg

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Fluconazole 100 mg-GRE

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Fluconazole 100 mg-IVA

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What are the possible side effects of fluconazole (Diflucan)?

Get emergency medical help if you have any of these signs of an allergic reaction . hives; difficult breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if you have any of these serious side effects:

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

fever. chills, body aches, flu symptoms;

severe blistering, peeling, and red skin rash ;

easy bruising or bleeding. unusual weakness; or

seizure (convulsions).

Less serious side effects may include:

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.

What is the most important information I should know about fluconazole (Diflucan)?

Do not use this medication if you are allergic to fluconazole, or similar drugs such as clotrimazole (Lotrimin), econazole (Spectazole), ketoconazole (Nizoral), miconazole (Monistat, Oravig), sertaconazole (Ertaczo), sulconazole (Exelderm), terconazole (Terazol), tioconazole (Vagistat-1), or voriconazole (Vfend).

You should not use fluconazole if you are also taking cisapride (Propulsid).

Before taking fluconazole, tell your doctor if you have liver disease, kidney disease. a heart rhythm disorder, or a history of Long QT syndrome.

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

Medical Dictionary

Macroxam Piroxicam 48mg Patch Review, Macroxam

by coolynch78 TRUSTWORTHY

A few months ago, my mom had a severe left ankle pain and swelling. It was already giving her problems for more than a week. I tried giving her the usual non-steroidal analgesics such as Naproxen and Ibuprofen but she complained developing some epigastric pains after intake of the said medications.

Because of this I scanned my

MIMS (a book of current drugs and medications available in our country) and saw this ad on the back page of the book. It is about Macroxam Piroxicam 48mg transdermal patch which my mom can just put on her affected ankle and forget about it for three days.

I bought her one and put it on her painful.

ankle. After a few hours, the pain gradually subsided and the inflammation became lesser in intensity. After three days she was already pain free and she was very happy because she was not able to take even a single medication per orem.

What I really like about this Macroxam transdermal patch is that it gives the relief

from pain even to patients who don’t like taking medications. It is a put-and-forget transdermal patch which is as effective as its oral medication counterpart.

Thus I highly recommend this medication to those patients who want to have relief from joint pains and muscle pains. This is a very good medication that will surely work for you.

Dentron, Dentron

Dentron Innovative Healthcare

Dentron Limited manufactured specialist medical devices and supplied them to the dental, podiatric, veterinary and acupuncture professions from 1989.

PLEASE NOTE THAT DENTRON LIMITED BECAME DORMANT ON 1ST AUGUST 2015.

Details of equipment and other information are left here for reference, but most of the devices shown are no longer available.

However, in order not to leave former customers 'stranded', sales of consumables, accessories, spares and repairs have been taken over by 'Dentron Partnership', which can be found at www. dentronpartnership. co. uk

It must be stressed that Dentron Partnership is a separate entity from Dentron Limited, and cannot accept any liability arising from the limited company's products, services or other activities.

The Directors of Dentron limited are grateful to all former customers for their support, and wish them well for the future.

The Directors would also like to thank customers for their concern, but would like to make clear that the reasons for putting the company into dormancy are twofold: first, the cost of maintaining registration under EU rules is becoming prohibitive for small medical equipment manufacturers; and secondly, having reached 70 we feel we deserve a less hectic life!

Someone rang in anxious that a safety issue might have arisen with Dentron equipment, but we can emphatically state that this is not the case.

Kerlofin, Kerlofin

Product Description Common use This medicine is a proton pump inhibitor (PPI) used to treat ulcers, heartburn, gastroesophageal reflux, erosive esophagitis, or Zollinger-Ellison syndrome and also ulcers generated by long-term use of non-steroidal anti-inflammatory drugs (NSAIDs). To treat ulcers caused by bacterial infections this medicine may be used in combination with antibiotics such as amoxicillin or clarithromycin. Prilosek significantly alleviates such their symptoms as heartburn, difficulty swallowing, coughing, and sleep problems. Prilosek works by blocking acid production in the stomach. The medicine may be used to treat other conditions diagnosed by your doctor.

Dosage and directions Follow all the directions provided by your doctor. Take this medication (15-30 mg) orally once a day in morning before a meal with a full glass of water or according to your doctor's recommendations. Swallow the tab whole, do not chew, crush, or open the capsule as may destroy the drug and/or increase side effects. Antacids drugs can be taken together with this medicine, if necessary. Dosage and duration of treatment depends on your medical condition and response to the therapy. Take it the same time each day to avoid missing a dose. In the case of aggravation or worsening of your illness notify your doctor immediately. It may take 1 - 4 days before Prilosek acts in full measure. Treatment with Prilosec should not be stopped even if certain amelioration is achieved. Improvement of symptoms is observed within 4 to 8 weeks in treatment of gastric ulcers or reflux disease. Treatment of heartburn usually lasts for 14 days. If heartburn persists after this period of time or even worsens, or if you need more than one course of treatment every 4 months, contact your doctor or pharmacist.

Precautions Prilosec is not recommended during pregnancy. Breastfeeding when using this drug is not recommended as it is not known whether it gets into breast milk. Tell your doctor if allergic reaction appears. Your doctor or pharmacist should be aware of your health problems, to provide health care, especially if you have problems such as liver disease, other stomach problems (e. g. tumors), heartburn over 3 months, unexplained weight loss, constant nausea/vomiting /stomach pain, blood in vomit or black stools. Some symptoms may witness about a more serious condition. This medicine may cause dizziness. Be careful performing work associated with concentration of attention, such as driving or operating mechanisms. Restrict consumption of alcoholic beverages. Start or interruption in taking any medicine should be be approved by your doctor. If you do not notice any improvement of your symptoms or if they even become worse, inform your doctor about it. Do not share this medicine with anybody with similar symptoms. Do not use this medicine to treat other diseases.

Possible side effects Adverse reactions that may disappear during treatment include headache, constipation, cough, dizziness, or rash. If they continue or are bothersome, let your doctor know about it. An allergic reaction to this medicine is not expected, but seek immediate medical help if it happens. Symptoms of an allergic reaction appear as rash, itching, dizziness, swelling, or difficult breathing. If you notice other reactions of your body which are not listed above, contact your doctor or pharmacist.

Prilosec can decreases elimination of diazepam, warfarin and phenytoin. These are medications metabolized in the liver by oxidation. Drugs which are metabolized with help of cytochrome P-450 system (e. g. cyclosporine, disulfiram, benzodiazepines) may also interact with Prilosec because it is metabolized the same way. Clarithromycin is also metabolized by cytochrome P450, concomitant administration of clarithromycin with Prilosec may result in increases in plasma levels of Prilosec. Concomitant use of Prilosec and clarithromycin may result in increases in plasma levels of erithromycin, and 14-hydroxy-clarithromycin. You may need additional monitoring of your condition if you are taking ampicillin, cilostazol, cyclosporine, diazepam, digoxin, disulfiram, iron, itraconazole, ketoconazole, moclobemide, phenytoin, sucralfate, vorconizole, or warfarin. This medicine may be combined with antacids if they were prescribed by your doctor. Potent acid-reducing drugs such as Prilosec diminish the effectiveness of sucralfate, and other medicaitons such as the antifungals ketoconazole and itraconazole. If instructed to take any of these medicines while taking Prilosec, consult your doctor or pharmacist regarding the proper timing of each dose, usually Prilosec is taken 30 minutes before sucralfate.

Missed dose If you missed a dose take the medication as soon as you remember. If it is almost time of your next dose, just skip its intake and return to your regular schedule.

Overdose If suppose that took too much of Prilosec contact your local poison control center or emergency room immediately. Symptoms of overdose are confusion, blurred vision, unusual sweating, or unusually fast heartbeat.

Storage Store at room temperature between 59-77 F (15-25 C). Do not expose to high humidity or keep in a bathroom. Hide Prilosec away from children and pets. If your treatment requires an extended period of time, take care about refills before your supply is over.

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.

Product Description Common use This medicine is a proton pump inhibitor (PPI) used to treat ulcers, heartburn, gastroesophageal reflux, erosive esophagitis, or Zollinger-Ellison syndrome and also ulcers generated by long-term use of non-steroidal anti-inflammatory drugs (NSAIDs). To treat ulcers caused by bacterial infections this medicine may be used in combination with antibiotics such as amoxicillin or clarithromycin. Prilosek significantly alleviates such their symptoms as heartburn, difficulty swallowing, coughing, and sleep problems. Prilosek works by blocking acid production in the stomach. The medicine may be used to treat other conditions diagnosed by your doctor.

Dosage and directions Follow all the directions provided by your doctor. Take this medication (15-30 mg) orally once a day in morning before a meal with a full glass of water or according to your doctor's recommendations. Swallow the tab whole, do not chew, crush, or open the capsule as may destroy the drug and/or increase side effects. Antacids drugs can be taken together with this medicine, if necessary. Dosage and duration of treatment depends on your medical condition and response to the therapy. Take it the same time each day to avoid missing a dose. In the case of aggravation or worsening of your illness notify your doctor immediately. It may take 1 - 4 days before Prilosek acts in full measure. Treatment with Prilosec should not be stopped even if certain amelioration is achieved. Improvement of symptoms is observed within 4 to 8 weeks in treatment of gastric ulcers or reflux disease. Treatment of heartburn usually lasts for 14 days. If heartburn persists after this period of time or even worsens, or if you need more than one course of treatment every 4 months, contact your doctor or pharmacist.

Precautions Prilosec is not recommended during pregnancy. Breastfeeding when using this drug is not recommended as it is not known whether it gets into breast milk. Tell your doctor if allergic reaction appears. Your doctor or pharmacist should be aware of your health problems, to provide health care, especially if you have problems such as liver disease, other stomach problems (e. g. tumors), heartburn over 3 months, unexplained weight loss, constant nausea/vomiting /stomach pain, blood in vomit or black stools. Some symptoms may witness about a more serious condition. This medicine may cause dizziness. Be careful performing work associated with concentration of attention, such as driving or operating mechanisms. Restrict consumption of alcoholic beverages. Start or interruption in taking any medicine should be be approved by your doctor. If you do not notice any improvement of your symptoms or if they even become worse, inform your doctor about it. Do not share this medicine with anybody with similar symptoms. Do not use this medicine to treat other diseases.

Possible side effects Adverse reactions that may disappear during treatment include headache, constipation, cough, dizziness, or rash. If they continue or are bothersome, let your doctor know about it. An allergic reaction to this medicine is not expected, but seek immediate medical help if it happens. Symptoms of an allergic reaction appear as rash, itching, dizziness, swelling, or difficult breathing. If you notice other reactions of your body which are not listed above, contact your doctor or pharmacist.

Prilosec can decreases elimination of diazepam, warfarin and phenytoin. These are medications metabolized in the liver by oxidation. Drugs which are metabolized with help of cytochrome P-450 system (e. g. cyclosporine, disulfiram, benzodiazepines) may also interact with Prilosec because it is metabolized the same way. Clarithromycin is also metabolized by cytochrome P450, concomitant administration of clarithromycin with Prilosec may result in increases in plasma levels of Prilosec. Concomitant use of Prilosec and clarithromycin may result in increases in plasma levels of erithromycin, and 14-hydroxy-clarithromycin. You may need additional monitoring of your condition if you are taking ampicillin, cilostazol, cyclosporine, diazepam, digoxin, disulfiram, iron, itraconazole, ketoconazole, moclobemide, phenytoin, sucralfate, vorconizole, or warfarin. This medicine may be combined with antacids if they were prescribed by your doctor. Potent acid-reducing drugs such as Prilosec diminish the effectiveness of sucralfate, and other medicaitons such as the antifungals ketoconazole and itraconazole. If instructed to take any of these medicines while taking Prilosec, consult your doctor or pharmacist regarding the proper timing of each dose, usually Prilosec is taken 30 minutes before sucralfate.

Missed dose If you missed a dose take the medication as soon as you remember. If it is almost time of your next dose, just skip its intake and return to your regular schedule.

Overdose If suppose that took too much of Prilosec contact your local poison control center or emergency room immediately. Symptoms of overdose are confusion, blurred vision, unusual sweating, or unusually fast heartbeat.

Storage Store at room temperature between 59-77 F (15-25 C). Do not expose to high humidity or keep in a bathroom. Hide Prilosec away from children and pets. If your treatment requires an extended period of time, take care about refills before your supply is over.

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.

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European Medicines Agency - Suramox 15 % La And Its Associated Name Stabox 15 % La, Suramox

Suramox 15 % LA and its associated name Stabox 15 % LA

Suramox 15% LA is an injectable suspension containing amoxicillin, which is a beta-lactam antibiotic belonging to the penicillin group. The product is used in the treatment of respiratory infections caused by Pasteurella multocida and Mannheimia haemolytica in cattle and for the treatment of respiratory infections due to Pasteurella multocida in pigs. In both species the product is administered intramuscularly at a dose of 15 mg amoxicillin/kg bw (equivalent to 1 ml of Suramox 15% LA / 10 kg bw) twice with a 48 hour interval between doses.

A Marketing Authorisation for Suramox 15% LA was previously granted to Virbac S. A. in France on 6 July 2004 based on an abridged application citing Duphamox LA as reference medicinal product. The withdrawal periods established for Suramox 15% LA were 58 days in cattle for meat and offal and 35 days in pigs for meat and offal. The withdrawal period for milk was 2.5 days.

A mutual recognition procedure was started on 28 April 2005. The Reference Member State was France and the Concerned Member States were Belgium, the Czech Republic, Germany, Italy, Spain and the United Kingdom. The product was accepted by the Czech Republic, Italy and Spain. Concerns were raised by Belgium, Germany and the United Kingdom regarding the inadequacy of the withdrawal periods and the applications were withdrawn from these countries. Belgium referred the issue to the EMEA on 28 July 2005.

The scope of the referral was to agree whether the proposed withdrawal periods of 58 days for cattle and 35 days for pigs were adequately established.

The arbitration procedure started on 8 September 2005 with the adoption of a list of questions. The rapporteur was Mr. J. Schefferlie and the co-rapporteur was Prof. R. Kroker. The Marketing Authorisation Holder (MAH) subsequently provided written explanations to the Committee on 16 January 2006.

During its May 2006 meeting, the CVMP, in light of the overall data submitted and the scientific discussion within the Committee, adopted by consensus an opinion recommending the suspension of the marketing authorisations for Suramox 15% LA and the Stabox 15% LA, for cattle and pigs. The reasons being the following:

it was not possible to establish a withdrawal period for cattle and pigs based on the data available; 1 Article 35 of Directive 2001/82/EC, as amended

the currently established withdrawal periods for cattle and pigs are inadequate to ensure that residues do not exceed the MRLs;

the currently authorised withdrawal periods are inadequate to ensure that foodstuffs obtained from treated animals do not contain residues which might constitute a health hazard to the consumer.

On 1 June 2006, the MAH notified the EMEA of its intention to request the reexamination of the CVMP opinion in accordance with Article 36(4)2. During its June 2006 meeting, the CVMP appointed Dr. R. Breathnach as rapporteur for the assessment of the grounds for the request for re-examination of the opinion. The detailed grounds for the request were submitted to the EMEA on 18 July 2006 and the evaluation procedure for the re-examination started on 19 July 2006.

On 13 September 2006 the CVMP considered the detailed grounds for the re-examination of the opinion and confirmed its previous opinion concluding that the marketing authorisations for Suramox 15% LA should be suspended. The reasons for the suspension were the same as those identified in the May 2006 CVMP meeting.

On 25 October 2006 the European Commission forwarded a draft decision to the Standing Committee on Veterinary Medicinal Products for adoption by written procedure. During the written procedure a request was received from France for a scientific assessment of new studies made available by the Marketing Authorisation Holder.

On 14 November 2006 the European Commission suspended the written procedure and on 16 November 2006, requested the CVMP to consider the new residue studies in the assessment of the referral and to revise as appropriate the opinion of 13 September 2006.

The Marketing Authorisation Holder submitted the new residue studies to the CVMP on 9 January 2007 and provided oral explanations to the Committee on 13 March 2007.

On 14 March 2007 the CVMP, having considered the new residue studies, concluded that it was not possible to set a withdrawal period for Suramox 15% LA and Stabox 15% LA, for either cattle or pig meat and offal and therefore recommended by consensus the suspension of the above marketing authorisations for the above-mentioned products.

On 13 June 2007 the European Commission adopted a Commission Decision suspending the national marketing authorisations for Suramox 15% LA and Stabox 15% LA, but providing an opportunity for the decision to be reviewed further to a new opinion formulated by the CVMP on the basis of the assessment of new residue depletion studies.

The Marketing Authorisation Holder submitted further new residue studies to the CVMP on 14 April 2008. The procedure for evaluation of the new data started on 15 April 2008. The rapporteur was Mrs. R. Kearsley and the co-rapporteur was Prof. C. Friis.

During its June 2008 meeting the CVMP considered the new residue studies submitted with regard to Suramox 15% LA and concluded that withdrawal periods can now be set for both cattle and pigs for Suramox 15% LA and Stabox 15% LA. Therefore, the Committee adopted by consensus an opinion recommending the lifting of the suspension of the marketing authorisations for the above-mentioned product.

Furthermore, the Committee recommends varying the marketing authorisations of the veterinary medicinal products referred to in Annex I in accordance with the Summary of Product Characteristics (SPC) as set out in Annex III.

The list of product names concerned is given in Annex I. The scientific conclusions are provided in Annex II, together with the SPC in Annex III.

The final opinion was converted into a Decision by the European Commission on 5 September 2008.

Opinion - contains the opinion of the Committee for Medicinal Products for Veterinary use (CVMP) on the referred medicine(s)

List of the medicines affected by the referral (annex I)

Scientific conclusions of the Committee (annex II)

The following two documents may not always be available:

Changes to the summary of product characteristics, labeling or package leaflet ('annex III') - available when changes have been recommended by the Committee

Conditions of the marketing authorisation (Annex IV) - available when the Committee recommends measures to be taken for the marketing authorisation(s) such as safety measures or extra studies

Current status: European Commission final decision

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Utinor (Norfloxacin), Utinor

Utinor (norfloxacin)

What is it used for?

How does it work?

Utinor tablets contain the active ingredient norfloxacin, which is a type of medicine called a quinolone antibiotic. Antibiotics are used to treat infections caused by bacteria. (NB. Norfloxacin is also available without a brand name, ie as the generic medicine.)

Norfloxacin works by killing the bacteria that are causing an infection. It does this by entering the bacterial cells and inhibiting a bacterial enzyme called DNA-gyrase. This enzyme is involved in replicating and repairing the genetic material (DNA) of the bacteria. If this enzyme doesn't work, the bacteria cannot reproduce or repair themselves and this kills the bacteria.

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Norfloxacin is filtered out of the blood and into the urine by the kidneys. High levels of the medicine pass into the urine, which means norfloxacin can be used to treat bacterial infections in the urinary tract.

Your doctor may ask you for a urine sample to make sure the bacteria causing the infection are susceptible to norfloxacin.

How do I take it?

The dose of this medicine and how long it needs to be taken for depends on the type of infection you have. Follow the instructions given by your doctor. These will be printed on the dispensing label that your pharmacist has put on the packet of medicine.

Norfloxacin is usually taken twice a day (every 12 hours), though this may be reduced to once a day in chronic recurrent infections. You should try to space the doses evenly.

Norfloxacin tablets should be taken with a glass of water on an empty stomach. This means at least one hour before or two hours after a meal or consuming milk or other dairy products.

Do not take indigestion remedies, or medicines containing calcium, iron or zinc at the same time of day as this medicine. This is because these can reduce the absorption of norfloxacin from the gut and make it less effective.

Unless your doctor tells you otherwise, it is important that you finish the prescribed course of this antibiotic medicine, even if you feel better or it seems the infection has cleared up. Stopping the course early increases the chance that the infection will come back and that the bacteria will grow resistant to the antibiotic.

Warning!

This medicine may reduce your ability to drive or operate machinery safely. Do not drive or operate machinery until you know how this medicine affects you and you are sure it won't affect your performance.

Avoid exposing your skin to excessive sunlight, sunlamps or sunbeds while taking norfloxacin, as it may increase the sensitivity of your skin to UV light. If you get a rash or other skin reaction on exposure to sunlight you should stop taking this medicine and consult your doctor.

Treatment with antibiotics can sometimes cause overgrowth of other organisms that are not susceptible to the antibiotic, for example fungi or yeasts such as Candida. This may sometimes cause infections such as thrush. Tell your doctor if you think you have developed a new infection during or after taking this antibiotic.

Quinolone antibiotics may rarely cause tendon inflammation (tendinitis) and tendon rupture. People aged over 60, people who have had a kidney, heart, or lung transplant and those taking corticosteroid medication are most at risk of this. You should stop taking this medicine immediately if you experience any pain or inflammation in your joints during treatment. Rest the affected limb(s) and consult a doctor immediately.

Broad-spectrum antibiotics can sometimes cause inflammation of the bowel (colitis). For this reason, if you get diarrhoea that becomes severe or persistent or contains blood or mucus, either during or after taking this medicine, you should consult your doctor immediately.

Use with caution in

People over 60 years of age.

People using corticosteroid medicines.

People who have had a kidney, heart, or lung transplant.

Severely decreased kidney function.

History of seizures (fits), eg epilepsy .

People with a risk of seizures.

Abnormal muscle weakness (myasthenia gravis) .

History of psychiatric illness.

People who a lack an enzyme called G6PD in their blood.

People with a personal or family history of an abnormal heart rhythm seen on a heart monitoring trace (ECG ) as a 'prolonged QT interval'.

People with a very slow heart rate (bradycardia).

People with low levels of potassium in their blood (hypokalaemia).

Not to be used in

Children who have not yet reached puberty.

Growing adolescents.

Allergy to other quinolone-type antibiotics. eg ciprofloxacin, ofloxacin.

People with a history of tendon disorders caused by previous treatment with a quinolone-type antibiotic.

This medicine should not be used if you are allergic to one or any of its ingredients. Please inform your doctor or pharmacist if you have previously experienced such an allergy. If you feel you have experienced an allergic reaction, stop using this medicine and inform your doctor or pharmacist immediately.

Pregnancy and breastfeeding

Certain medicines should not be used during pregnancy or breastfeeding. However, other medicines may be safely used in pregnancy or breastfeeding providing the benefits to the mother outweigh the risks to the unborn baby. Always inform your doctor if you are pregnant or planning a pregnancy, before using any medicine.

This medicine is not recommended for use in pregnancy. This is because norfloxacin has been shown to cause joint disease in immature animals and may therefore have this effect in humans. There are usually safer alternative antibiotics available. Seek medical advice from your doctor.

It is not known if this medicine passes into breast milk. It is not recommended for use during breastfeeding, as there are usually safer alternative antibiotics available. Seek medical advice from your doctor.

Side effects

Medicines and their possible side effects can affect individual people in different ways. The following are some of the side effects that are known to be associated with this medicine. Just because a side effect is stated here does not mean that all people using this medicine will experience that or any side effect.

Gut disturbances such as feeling sick, abdominal pain, heartburn, diarrhoea.

Headache.

Dizziness.

Rash.

Itching (pruritus).

Increased sensitivity of the skin the UV light (photosensitivity - see warning section above).

Loss of appetite.

Changes in taste.

Watery eyes, visual disturbances.

Hearing disturbances, including sensation of ringing or other noise in the ears (tinnitus).

Disturbed sleep.

Depression, anxiety or nervousness. Tell your doctor straight away if you notice any change in your mood, feelings or thoughts while taking this medicine.

Irritability.

Feeling disorientated.

Hallucinations.

Pins and needles, burning or numb sensations. Tell your doctor straight away if you notice any strange sensations while taking this medicine.

Tremor.

Convulsions.

Disturbances in the numbers of blood cells in the blood.

Inflammation or rupture of tendons (see warning section above).

Vaginal thrush.

Inflammation of the bowel lining (colitis - see warning section above).

Liver or kidney disorders. Tell your doctor if you experience any of the following symptoms while taking this medicine, as they may suggest a problem with your liver: rapidly feeling weak or unwell, unexplained itching, loss of appetite, abdominal pain, yellowing of the skin or whites of the eyes (jaundice) or unusually dark urine.

Severe skin reactions. Consult your doctor immediately if you get a severe rash, skin peeling, or painful blisters in the mouth/nose or genitals while taking this medicine.

Abnormal heart rhythm (very rare).

The side effects listed above may not include all of the side effects reported by the medicine's manufacturer. For more information about any other possible risks associated with this medicine, please read the information provided with the medicine or consult your doctor or pharmacist.

How can this medicine affect other medicines?

It is important to tell your doctor or pharmacist what medicines you are already taking, including those bought without a prescription and herbal medicines, before you start treatment with this medicine. Similarly, check with your doctor or pharmacist before taking any new medicines while taking this one, to ensure that the combination is safe .

The following medicines may reduce the absorption of norfloxacin from the gut, which could make it less effective. If you are taking medicines containing any of the following ingredients they should be taken at least two hours before or after your norfloxacin dose:

antacids for indigestion or heartburn

calcium supplements

iron supplements, eg ferrous sulphate, ferrous gluconate, ferrous fumarate

medicines containing calcium, magnesium, aluminium, zinc or iron

sucralfate

Videx chewable/dispersible tablets (these contain an antacid)

zinc supplements .

Strontium ranelate may also reduce the absorption of norfloxacin from the gut and could make it less effective. If you are taking strontium for osteoporosis its manufacturer recommends that you stop taking it temporarily while you are taking a course of norfloxacin.

Norfloxacin may increase the blood levels of the medicines listed below. If you are taking one of these your doctor may want to check the level of the medicine in your blood after you start a course of norfloxacin, and may need to alter your dose:

If norfloxacin is used in combination with any of the following medicines there may be an increased risk of seizures (fits):

theophylline

non-steroidal anti-inflammatory drugs (NSAIDs) such as indometacin, fenbufen, naproxen .

Norfloxacin may enhance the anti-blood-clotting effect of anticoagulant medicines such as warfarin . As this may increase the risk of bleeding, your blood clotting time (INR) should be monitored more frequently if you are taking norfloxacin with an anticoagulant.

If norfloxacin is taken in combination with glibenclamide for diabetes it may very rarely cause a large drop in blood sugar (hypoglycaemia). If you are taking glibenclamide your doctor may recommend that you monitor your blood sugar while taking a course of norfloxacin.

There may be an increased chance of abnormal heart rhythms ('prolonged QT interval' on a heart monitoring trace or ECG) if this medicine is taken in combination with other medicines that can increase the risk of this, for example those listed below:

atomoxetine

medicines to treat abnormal heart rhythms (antiarrhythmics), eg amiodarone, procainamide, quinidine, disopyramide, sotalol

the antihistamines astemizole, terfenadine or mizolastine

certain antidepressants, eg maprotiline, amitriptyline, imipramine

certain antipsychotics, eg thioridazine, chlorpromazine, sertindole, haloperidol, pimozide

certain antimalarials, eg halofantrine, chloroquine, quinine, Riamet, mefloquine

certain other antimicrobials, eg erythromycin by injection, voriconazole, moxifloxacin or pentamidine

cisapride .

Oral typhoid vaccine ( Vivotif ) should not be taken until at least three days after you have finished a course of this antibiotic, because the antibiotic could make the vaccine less effective.

In the past, women using hormonal contraception such as the pill or patch would be advised to use an extra method of contraception (eg condoms) while having treatment with an antibiotic like this one and for seven days after finishing the course. However, this advice has now changed. You no longer need to use an extra method of contraception with the pill, patch or vaginal ring while you have a course of antibiotics. This change in advice comes because to date there is no evidence to prove that antibiotics (other than rifampicin or rifabutin) affect these contraceptives. This is the latest guidance from the Faculty of Sexual & Reproductive Healthcare.

However, if you are taking the contraceptive pill and experience vomiting or diarrhoea as a result of treatment with this antibiotic, you should follow the instructions for vomiting and diarrhoea described in the leaflet provided with your pills.

Other medicines containing the same active ingredient

Norfloxacin tablets are also available without a brand name, ie as the generic medicine.

Last updated 09.06.2011

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