Lipenil may be available in the countries listed below.
Ingredient matches for Lipenil
Simvastatin is reported as an ingredient of Lipenil in the following countries:
- Italy
International Drug Name Search
Lipenil may be available in the countries listed below.
Simvastatin is reported as an ingredient of Lipenil in the following countries:
International Drug Name Search
Rec.INN
G03DC01
0000432-60-0
C21-H32-O
300
Progestin
Estr-4-en-17-ol, 17-(2-propenyl)-, (17ß)-
International Drug Name Search
Glossary
| BAN | British Approved Name |
| DCF | Dénomination Commune Française |
| DCIT | Denominazione Comune Italiana |
| IS | Inofficial Synonym |
| OS | Official Synonym |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
Teveten Comp. may be available in the countries listed below.
Eprosartan mesilate (a derivative of Eprosartan) is reported as an ingredient of Teveten Comp. in the following countries:
Hydrochlorothiazide is reported as an ingredient of Teveten Comp. in the following countries:
International Drug Name Search
Paroxetine A may be available in the countries listed below.
Paroxetine hydrochloride (a derivative of Paroxetine) is reported as an ingredient of Paroxetine A in the following countries:
International Drug Name Search
Lorfan may be available in the countries listed below.
Levallorphan tartrate (a derivative of Levallorphan) is reported as an ingredient of Lorfan in the following countries:
International Drug Name Search
Sandoz Allopurinol may be available in the countries listed below.
Allopurinol is reported as an ingredient of Sandoz Allopurinol in the following countries:
International Drug Name Search
Butalbital is reported as an ingredient of Butapap in the following countries:
Paracetamol is reported as an ingredient of Butapap in the following countries:
International Drug Name Search
Generic Name: bevacizumab (bev a CIZ oo mab)
Brand Names: Avastin
Bevacizumab is a cancer medicine that interferes with the growth of cancer cells and slows their growth and spread in the body.
Bevacizumab is used to treat a certain type of brain tumor, and certain types of cancers of the kidney, lung, colon and rectum. It is usually given as part of a combination of cancer medicines.
Bevacizumab may also be used for purposes not listed in this medication guide.
Before being treated with bevacizumab, tell your doctor if you have a bleeding or blood-clotting disorder, heart disease, congestive heart failure, high blood pressure, or a history of heart attack, stroke, blood clots, or stomach or intestinal bleeding (including perforation).
Call your doctor at once if you have: any unusual bleeding or bruising, blood in your urine or stools, coughing up blood, any bleeding that will not stop, severe stomach pain with fever and vomiting, sudden numbness or weakness, leg pain or swelling, chest pain, severe headache, problems with speech or balance, swelling or rapid weight gain, urinating less than usual, loss of bladder or bowel control, or missed menstrual periods.
To be sure this medication is not causing harmful effects, your blood pressure will need to be checked often. Your urine may also need to be tested. Visit your doctor regularly.
untreated or uncontrolled high blood pressure;
severe or uncontrolled bleeding;
an open skin wound;
an open surgical incision;
if you have had surgery within the past 4 weeks (28 days);
if you have recently been coughing up blood; or
if you plan to have surgery within the next 4 weeks (28 days).
To make sure you can safely receive bevacizumab, tell your doctor if you have any of these other conditions:
a bleeding or blood-clotting disorder;
a history of stomach or intestinal bleeding;
a history of perforation (a hole or tear) in your esophagus, stomach, or intestines;
heart disease, congestive heart failure;
high blood pressure; or
a history of heart attack, stroke, or blood clots.
Bevacizumab is injected into a vein through an IV. You will receive this injection in a clinic or hospital setting. Bevacizumab must be given slowly, and the IV infusion can take up to 90 minutes to complete.
Bevacizumab is usually given once every 2 weeks.
To be sure this medication is not causing harmful effects, your blood pressure will need to be checked often. Your urine may also need to be tested. Visit your doctor regularly.
Call your doctor for instructions if you miss an appointment for your bevacizumab injection.
Some people receiving a bevacizumab injection have had a reaction to the infusion (when the medicine is injected into the vein). Tell your caregiver right away if you feel dizzy, nauseated, light-headed, sweaty, or have a headache, wheezing, or chest pain during the injection.
any wound that will not heal;
severe stomach pain with fever, vomiting, and constipation;
blood in your urine or stools, vomit that looks like blood or coffee grounds;
easy bruising, unusual bleeding (nose, mouth, vagina, rectum), purple or red pinpoint spots under your skin, or any bleeding that will not stop;
fever, chills, body aches, flu symptoms, sores in your mouth and throat;
sudden numbness or weakness, severe headache, confusion, or problems with vision, speech, or balance;
pain, swelling, warmth, or redness in one or both legs;
chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, general ill feeling;
dangerously high blood pressure (severe headache, blurred vision, buzzing in your ears, anxiety, confusion, shortness of breath, uneven heartbeats, seizure);
puffy eyes, swelling in your stomach, arms, or legs;
rapid weight gain, urinating less than usual or not at all;
urine that looks foamy;
pain or burning when you urinate, loss of bladder or bowel control;
ongoing vaginal discharge, itching, or other irritation; or
missed menstrual periods.
Less serious side effects may include:
mild headache;
back pain;
diarrhea, loss of appetite;
cold symptoms such as stuffy nose, sneezing, sore throat;
dry or watery eyes;
dry or flaky skin, hair loss;
changes in your sense of taste; or
jaw pain, swelling, numbness, loose teeth, gum infection.
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.
Usual Adult Dose for Colorectal Cancer:
Initial dose: 5 mg/kg in combination with intravenous fluorouracil-based chemotherapy
The recommended dose of bevacizumab is based on a rate of 5 mg/kg or 10 mg/kg when used in combination with irinotecan, fluorouracil, and leucovorin in the IFL regimen.
The recommended dose of bevacizumab is based on a rate of 10 mg/kg when used in combination with oxaliplatin, folinic acid, and fluorouracil in the FOLFOX4 regimen.
A dose may be given once every 14 days as an IV infusion until disease progression is detected.
The first dose of bevacizumab should be delivered over 90 minutes as an intravenous infusion following chemotherapy. If the first infusion is well tolerated, the second infusion may be administered over 60 minutes. If the 60 minute infusion is well tolerated, all subsequent infusions may be administered over 30 minutes.
Usual Adult Dose for Non-Small Cell Lung Cancer:
For use in combination with carboplatin and paclitaxel for the treatment of non-squamous, non-small cell lung cancer:
Initial dose: 15 mg/kg as an intravenous infusion every 3 weeks
The first dose of bevacizumab should be delivered over 90 minutes as an intravenous infusion following chemotherapy. If the first infusion is well tolerated, the second infusion may be administered over 60 minutes. If the 60 minute infusion is well tolerated, all subsequent infusions may be administered over 30 minutes.
Usual Adult Dose for Breast Cancer:
(Not approved by FDA)
Recommended dose: 10 mg/kg as an IV infusion every 14 days in combination with paclitaxel.
Usual Adult Dose for Glioblastoma Multiforme:
Recommended dose: 10 mg/kg every 2 weeks
Usual Adult Dose for Ovarian Cancer:
15 mg/kg IV every 3 weeks
Usual Adult Dose for Renal Cell Carcinoma:
10 mg/kg IV every 2 weeks in combination with interferon alfa
Usual Pediatric Dose for Solid Tumors:
Monotherapy: 15 mg/kg IV every 2 weeks in 28 day cycles
Combination therapy: 5 to 10 mg/kg IV every 2 weeks as a part of combination chemotherapy regimens
There may be other drugs that can interact with bevacizumab. 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.
See also: bevacizumab side effects (in more detail)
Oxacil may be available in the countries listed below.
Oxacillin is reported as an ingredient of Oxacil in the following countries:
International Drug Name Search
Losartan/Hydrochlorothiazide Qualimed may be available in the countries listed below.
Hydrochlorothiazide is reported as an ingredient of Losartan/Hydrochlorothiazide Qualimed in the following countries:
Losartan potassium salt (a derivative of Losartan) is reported as an ingredient of Losartan/Hydrochlorothiazide Qualimed in the following countries:
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Pinamet may be available in the countries listed below.
Cimetidine is reported as an ingredient of Pinamet in the following countries:
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Alna retard may be available in the countries listed below.
Tamsulosin hydrochloride (a derivative of Tamsulosin) is reported as an ingredient of Alna retard in the following countries:
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Cytarabine Hydrochloride may be available in the countries listed below.
Cytarabine Hydrochloride (USAN) is known as Cytarabine in the US.
International Drug Name Search
Glossary
| USAN | United States Adopted Name |
Fluxacina L.CH. may be available in the countries listed below.
Flucloxacillin is reported as an ingredient of Fluxacina L.CH. in the following countries:
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Tramadol-Mepha may be available in the countries listed below.
Tramadol hydrochloride (a derivative of Tramadol) is reported as an ingredient of Tramadol-Mepha in the following countries:
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Deldrax may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Nitroxinil is reported as an ingredient of Deldrax in the following countries:
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Clotiazépam may be available in the countries listed below.
Clotiazépam (DCF) is also known as Clotiazepam (Prop.INN)
International Drug Name Search
Glossary
| DCF | Dénomination Commune Française |
| Prop.INN | Proposed International Nonproprietary Name (World Health Organization) |
Nystaform may be available in the countries listed below.
Chlorhexidine dihydrochloride (a derivative of Chlorhexidine) is reported as an ingredient of Nystaform in the following countries:
Nystatin is reported as an ingredient of Nystaform in the following countries:
International Drug Name Search
Vitamin B1 Winthrop may be available in the countries listed below.
Thiamine hydrochloride (a derivative of Thiamine) is reported as an ingredient of Vitamin B1 Winthrop in the following countries:
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Venotrulan Trox may be available in the countries listed below.
Troxerutin is reported as an ingredient of Venotrulan Trox in the following countries:
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Paroxetine ratiopharm may be available in the countries listed below.
Paroxetine is reported as an ingredient of Paroxetine ratiopharm in the following countries:
Paroxetine hydrochloride (a derivative of Paroxetine) is reported as an ingredient of Paroxetine ratiopharm in the following countries:
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Anatifen may be available in the countries listed below.
Ketotifen fumarate (a derivative of Ketotifen) is reported as an ingredient of Anatifen in the following countries:
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Ucol may be available in the countries listed below.
Tolterodine tartrate (a derivative of Tolterodine) is reported as an ingredient of Ucol in the following countries:
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Negaflox may be available in the countries listed below.
Norfloxacin is reported as an ingredient of Negaflox in the following countries:
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Propyl may be available in the countries listed below.
Propylthiouracil is reported as an ingredient of Propyl in the following countries:
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Vicks Hoestsiroop may be available in the countries listed below.
Dextromethorphan hydrobromide (a derivative of Dextromethorphan) is reported as an ingredient of Vicks Hoestsiroop in the following countries:
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Wellcoprim may be available in the countries listed below.
Trimethoprim is reported as an ingredient of Wellcoprim in the following countries:
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Lansoprazole ratiopharm may be available in the countries listed below.
Lansoprazole is reported as an ingredient of Lansoprazole ratiopharm in the following countries:
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Grefen may be available in the countries listed below.
Ibuprofen is reported as an ingredient of Grefen in the following countries:
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Dixamid may be available in the countries listed below.
Indapamide is reported as an ingredient of Dixamid in the following countries:
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Omeprazol Domesco may be available in the countries listed below.
Omeprazole is reported as an ingredient of Omeprazol Domesco in the following countries:
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Fertinorm P may be available in the countries listed below.
Menotropins is reported as an ingredient of Fertinorm P in the following countries:
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Buflomédil Zydus may be available in the countries listed below.
Buflomedil hydrochloride (a derivative of Buflomedil) is reported as an ingredient of Buflomédil Zydus in the following countries:
International Drug Name Search
Metabolin G may be available in the countries listed below.
Thiamine hydrochloride (a derivative of Thiamine) is reported as an ingredient of Metabolin G in the following countries:
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Paroxetina Pharmakern may be available in the countries listed below.
Paroxetine hydrochloride (a derivative of Paroxetine) is reported as an ingredient of Paroxetina Pharmakern in the following countries:
International Drug Name Search
Generic Name: salicylic acid (Topical route)
sal-i-SIL-ik AS-id
In the U.S.
In Canada
Available Dosage Forms:
Therapeutic Class: Antiacne
Pharmacologic Class: NSAID
Chemical Class: Salicylate, Non-Aspirin
Salicylic acid is used to treat many skin disorders, such as acne, dandruff, psoriasis, seborrheic dermatitis of the skin and scalp, calluses, corns, common warts, and plantar warts, depending on the dosage form and strength of the preparation.
Some of these preparations are available only with your doctor's prescription.
In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:
Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.
Young children may be at increased risk of unwanted effects because of increased absorption of salicylic acid through the skin. Also, young children may be more likely to get skin irritation from salicylic acid. Salicylic acid should not be applied to large areas of the body, used for long periods of time, or used under occlusive dressing (air-tight covering, such as kitchen plastic wrap) in infants and children. Salicylic acid should not be used in children younger than 2 years of age.
Elderly people are more likely to have age-related blood vessel disease. This may increase the chance of problems during treatment with this medicine.
There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.
Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.
Using this medicine with any of the following medicines is usually not recommended, but may be required in some cases. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.
Using this medicine with any of the following medicines may cause an increased risk of certain side effects, but using both drugs may be the best treatment for you. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.
Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.
The presence of other medical problems may affect the use of this medicine. Make sure you tell your doctor if you have any other medical problems, especially:
This section provides information on the proper use of a number of products that contain salicylic acid. It may not be specific to Dr. Scholl's Cushlin Ultra Slim Corn Removers. Please read with care.
It is very important that you use this medicine only as directed. Do not use more of it, do not use it more often, and do not use it for a longer time than recommended on the label, unless otherwise directed by your doctor. To do so may increase the chance of absorption through the skin and the chance of salicylic acid poisoning.
If your doctor has ordered an occlusive dressing (airtight covering, such as kitchen plastic wrap) to be applied over this medicine, make sure you know how to apply it. Since an occlusive dressing will increase the amount of medicine absorbed through your skin and the possibility of salicylic acid poisoning, use it only as directed. If you have any questions about this, check with your doctor.
Keep this medicine away from the eyes and other mucous membranes, such as the mouth and inside of the nose. If you should accidentally get some in your eyes or on other mucous membranes, immediately flush them with water for 15 minutes.
To use the cream, lotion, or ointment form of salicylic acid:
To use the gel form of salicylic acid:
To use the pad form of salicylic acid:
To use the plaster form of salicylic acid for warts, corns, or calluses:
To use the shampoo form of salicylic acid:
To use the soap form of salicylic acid:
To use the topical solution form of salicylic acid for acne:
To use the topical solution form of salicylic acid for warts, corns, or calluses:
Unless your hands are being treated, wash them immediately after applying this medicine to remove any medicine that may be on them.
The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.
The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.
If you miss a dose of this medicine, apply it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule.
Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.
Keep out of the reach of children.
Do not keep outdated medicine or medicine no longer needed.
When using salicylic acid, do not use any of the following preparations on the same affected area as this medicine, unless otherwise directed by your doctor:
To use any of the above preparations on the same affected area as salicylic acid may cause severe irritation of the skin.
Check with your doctor right away if you have nausea, vomiting, dizziness, loss of hearing, tinnitus, lethargy hyperpnea, diarrhea, and psychic disturbances. These could be symptoms of a serious condition called salicylate toxicity, especially in children under 12 years of age and patients with kidney or liver problems.
Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.
Check with your doctor as soon as possible if any of the following side effects occur:
Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:
Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.
Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.
See also: Dr. Scholl's Cushlin Ultra Slim Corn Removers Topical side effects (in more detail)
The information contained in the Thomson Reuters Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.
The use of the Thomson Reuters Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Reuters Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON REUTERS HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Reuters Healthcare does not assume any responsibility or risk for your use of the Thomson Reuters Healthcare products.
Canifug Cremolum may be available in the countries listed below.
Clotrimazole is reported as an ingredient of Canifug Cremolum in the following countries:
International Drug Name Search
In some countries, this medicine may only be approved for veterinary use.
In the US, Lamisil (terbinafine systemic) is a member of the drug class miscellaneous antifungals and is used to treat Cutaneous Candidiasis, Onychomycosis - Fingernail, Onychomycosis - Toenail, Tinea Capitis, Tinea Corporis, Tinea Cruris and Tinea Pedis.
US matches:
UK matches:
Terbinafine is reported as an ingredient of Lamisil in the following countries:
Terbinafine hydrochloride (a derivative of Terbinafine) is reported as an ingredient of Lamisil in the following countries:
International Drug Name Search
Glossary
| SPC | Summary of Product Characteristics (UK) |
Carboplatin Gerolymatos may be available in the countries listed below.
Carboplatin is reported as an ingredient of Carboplatin Gerolymatos in the following countries:
International Drug Name Search
Claritromicina Cuve may be available in the countries listed below.
Clarithromycin is reported as an ingredient of Claritromicina Cuve in the following countries:
International Drug Name Search
Enalapril axcount may be available in the countries listed below.
Enalapril maleate (a derivative of Enalapril) is reported as an ingredient of Enalapril axcount in the following countries:
International Drug Name Search
Generic Name: decitabine (de SIT a been)
Brand Names: Dacogen
Decitabine is a cancer medication that interferes with the growth and spread of cancer cells in the body.
Decitabine is used to treat myelodysplastic syndromes (certain types of blood or bone marrow cancer).
Decitabine may also be used for purposes not listed in this medication guide.
Before receiving this medication, tell your doctor if you have liver or kidney disease.
Decitabine can lower blood cells that help your body fight infections. Avoid being near people who are sick or have infections. Avoid activities that may increase your risk of bleeding or injury. Your blood may need to be tested often. Visit your doctor regularly.
To make sure you can safely take decitabine, tell your doctor if you have any of these other conditions:
kidney disease; or
liver disease.
Decitabine is injected into a vein through an IV. You will receive this injection in a clinic or hospital setting. Decitabine must be given slowly, and the IV infusion can take up to 3 hours to complete.
In most cases, a decitabine injection is given every 8 hours for 3 days. This 3-day treatment is usually repeated every 6 weeks. You will most likely receive at least 4 of these treatments.
You may be given other medications to prevent nausea or vomiting while you are receiving decitabine.
Call your doctor for instructions if you miss an appointment for your decitabine injection.
Overdose symptoms may include some of the serious side effects listed in this medication guide.
Avoid being near people who are sick or have infections. Tell your doctor at once if you develop signs of infection.
fever, chills, body aches, cough, sore throat, flu symptoms;
easy bruising, unusual bleeding (nose, mouth, vagina, or rectum), purple or red pinpoint spots under your skin;
pale skin, feeling light-headed or short of breath, rapid heart rate, trouble concentrating;
white patches or sores inside your mouth or on your lips; or
stabbing chest pain, wheezing, feeling short of breath, cough with yellow or green mucus;
swelling, pain, tenderness, or redness anywhere on your body; or
electrolyte imbalance (confusion, uneven heart rate, extreme thirst, increased urination, jerking muscle movements, leg discomfort, muscle weakness or limp feeling).
Less serious side effects may include:
headache, dizziness;
tired feeling;
nausea, vomiting, stomach pain, diarrhea, constipation;
cough;
increased thirst, increased urination, hunger, dry mouth, drowsiness;
joint pain; or
sleep problems (insomnia).
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.
There may be other drugs that can interact with decitabine. 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.
See also: Dacogen side effects (in more detail)
Basteen may be available in the countries listed below.
Norfloxacin is reported as an ingredient of Basteen in the following countries:
International Drug Name Search
Serevent Rotadisk may be available in the countries listed below.
Salmeterol xinafoate (a derivative of Salmeterol) is reported as an ingredient of Serevent Rotadisk in the following countries:
International Drug Name Search
Primogyna may be available in the countries listed below.
Estradiol 17ß-valerate (a derivative of Estradiol) is reported as an ingredient of Primogyna in the following countries:
International Drug Name Search
Natrijev hidrogenkarbonat may be available in the countries listed below.
Sodium Bicarbonate is reported as an ingredient of Natrijev hidrogenkarbonat in the following countries:
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Clorpromazina Duncan may be available in the countries listed below.
Chlorpromazine hydrochloride (a derivative of Chlorpromazine) is reported as an ingredient of Clorpromazina Duncan in the following countries:
International Drug Name Search
Vibranord may be available in the countries listed below.
Doxycycline hyclate (a derivative of Doxycycline) is reported as an ingredient of Vibranord in the following countries:
International Drug Name Search
Oxitocina may be available in the countries listed below.
Oxitocina (DCIT) is known as Oxytocin in the US.
International Drug Name Search
Glossary
| DCIT | Denominazione Comune Italiana |
In some countries, this medicine may only be approved for veterinary use.
In the US, Prednisol (prednisolone ophthalmic) is a member of the drug class ophthalmic steroids and is used to treat Postoperative Ocular Inflammation.
US matches:
Prednisolone 21-acetate (a derivative of Prednisolone) is reported as an ingredient of Prednisol in the following countries:
International Drug Name Search
Ciprofloxacine Apotex may be available in the countries listed below.
Ciprofloxacin hydrochloride (a derivative of Ciprofloxacin) is reported as an ingredient of Ciprofloxacine Apotex in the following countries:
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Flavost may be available in the countries listed below.
Ipriflavone is reported as an ingredient of Flavost in the following countries:
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Oxifungol may be available in the countries listed below.
Fluconazole is reported as an ingredient of Oxifungol in the following countries:
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Rosazol may be available in the countries listed below.
Metronidazole is reported as an ingredient of Rosazol in the following countries:
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Prazosina may be available in the countries listed below.
Prazosin is reported as an ingredient of Prazosina in the following countries:
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Predxal may be available in the countries listed below.
Telmisartan is reported as an ingredient of Predxal in the following countries:
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Gestoden/Ethinylestradiol 75/30 Schering may be available in the countries listed below.
Ethinylestradiol is reported as an ingredient of Gestoden/Ethinylestradiol 75/30 Schering in the following countries:
Gestodene is reported as an ingredient of Gestoden/Ethinylestradiol 75/30 Schering in the following countries:
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Prednitex may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Prednisolone is reported as an ingredient of Prednitex in the following countries:
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Flubex may be available in the countries listed below.
Flucloxacillin sodium salt (a derivative of Flucloxacillin) is reported as an ingredient of Flubex in the following countries:
International Drug Name Search
Bastion may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Iron Dextran is reported as an ingredient of Bastion in the following countries:
International Drug Name Search
Eubron may be available in the countries listed below.
Ambroxol is reported as an ingredient of Eubron in the following countries:
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In some countries, this medicine may only be approved for veterinary use.
Sulfachlorpyridazine is reported as an ingredient of Pyradan in the following countries:
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Apo-Bicalutamide may be available in the countries listed below.
Bicalutamide is reported as an ingredient of Apo-Bicalutamide in the following countries:
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Anuar may be available in the countries listed below.
Chloramphenicol succinate sodium (a derivative of Chloramphenicol) is reported as an ingredient of Anuar in the following countries:
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Ketesgel may be available in the countries listed below.
Dexketoprofen tromethamine (a derivative of Dexketoprofen) is reported as an ingredient of Ketesgel in the following countries:
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Generic Name: metformin (Oral route)
met-FOR-min hye-droe-KLOR-ide
Fortamet(R), Glucophage(R), Glucophage XR(R), Riomet(R): Lactic acidosis is a rare, but serious, metabolic complication that can occur due to metformin accumulation during treatment with metformin hydrochloride; when it occurs, it is fatal in approximately 50% of cases. Lactic acidosis may also occur in association with pathophysiologic conditions, including diabetes mellitus, characterized by significant tissue hypoperfusion and hypoxemia. The risk of lactic acidosis increases with renal impairment, increased age, congestive heart failure, and hepatic insufficiency. Treatment with metformin should not be initiated in patients 80 years old or older, unless measurement of creatinine clearance demonstrates that renal function is normal. Therapy should temporarily be discontinued prior to any intravascular radiocontrast study or surgical procedure. Excessive alcohol use should be avoided, because alcohol potentiates the effects of metformin on lactate metabolism. Discontinue therapy immediately and institute supportive measures promptly for suspected lactic acidosis .
Glumetza(R): Lactic acidosis is a rare, but serious, complication that can occur due to metformin accumulation. The risk of lactic acidosis increases with renal or hepatic impairment, acute congestive heart failure, sepsis, dehydration, and excess alcohol intake. Onset may be subtle and include nonspecific symptoms such as malaise, myalgia, respiratory distress, somnolence, and abdominal distress; laboratory abnormalities include low pH, increased anion gap and elevated blood lactate. If lactic acidosis is suspected, Glumetza(R) should be discontinued and the patient immediately hospitalized .
In the U.S.
Available Dosage Forms:
Therapeutic Class: Hypoglycemic
Chemical Class: Metformin
Metformin is used to treat high blood sugar levels that are caused by a type of diabetes mellitus or sugar diabetes called type 2 diabetes. With this type of diabetes, insulin produced by the pancreas is not able to get sugar into the cells of the body where it can work properly. Using metformin alone, with a type of oral antidiabetic medicine called a sulfonylurea, or with insulin, will help to lower blood sugar when it is too high and help restore the way you use food to make energy.
Many people can control type 2 diabetes with diet and exercise. Following a specially planned diet and exercise will always be important when you have diabetes, even when you are taking medicines. To work properly, the amount of metformin you take must be balanced against the amount and type of food you eat and the amount of exercise you do. If you change your diet or exercise, you will want to test your blood sugar to find out if it is too low. Your doctor will teach you what to do if this happens.
Metformin does not help patients does not help patients who have insulin-dependent or type 1 diabetes because they cannot produce insulin from their pancreas gland. Their blood glucose is best controlled by insulin injections.
This medicine is available only with your doctor's prescription.
Once a medicine has been approved for marketing for a certain use, experience may show that it is also useful for other medical problems. Although this use is not included in product labeling, metformin is used in certain patients with the following medical conditions:
In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:
Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.
Appropriate studies performed to date have not demonstrated pediatric-specific problems that would limit the usefulness of metformin oral solution and tablets in children 10 to 16 years of age. However, safety and efficacy of metformin extended-release tablets in the pediatric population have not been established.
Although appropriate studies on the relationship of age to the effects of metformin have not been performed in the geriatric population, geriatric-specific problems are not expected to limit the usefulness of metformin in the elderly. However, elderly patients are more likely to have age-related kidney problems, which may require caution in patients receiving metformin. This medicine is not recommended in patients 80 years of age and older who have kidney problems.
| Pregnancy Category | Explanation | |
|---|---|---|
| All Trimesters | B | Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate studies in pregnant women OR animal studies have shown an adverse effect, but adequate studies in pregnant women have failed to demonstrate a risk to the fetus. |
Studies in women suggest that this medication poses minimal risk to the infant when used during breastfeeding.
Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.
Using this medicine with any of the following medicines is not recommended. Your doctor may decide not to treat you with this medication or change some of the other medicines you take.
Using this medicine with any of the following medicines is usually not recommended, but may be required in some cases. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.
Using this medicine with any of the following medicines may cause an increased risk of certain side effects, but using both drugs may be the best treatment for you. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.
Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.
The presence of other medical problems may affect the use of this medicine. Make sure you tell your doctor if you have any other medical problems, especially:
This section provides information on the proper use of a number of products that contain metformin. It may not be specific to Riomet. Please read with care.
This medicine usually comes with a patient information insert. Read the information carefully and make sure you understand it before taking this medicine. If you have any questions, ask your doctor.
Carefully follow the special meal plan your doctor gave you. This is a very important part of controlling your condition, and is necessary if the medicine is to work properly. Also, exercise regularly and test for sugar in your blood or urine as directed.
Metformin should be taken with meals to help reduce stomach or bowel side effects that may occur during the first few weeks of treatment.
Swallow the extended-release tablet whole with a full glass of water. Do not crush, break, or chew it.
While taking the extended-release tablet, part of the tablet may pass into your stool after your body has absorbed the medicine. This is normal and nothing to worry about.
Measure the oral liquid with a marked measuring spoon, oral syringe, or medicine cup. The average household teaspoon may not hold the right amount of liquid.
Use only the brand of this medicine that your doctor prescribed. Different brands may not work the same way.
You may notice improvement in your blood glucose control in 1 to 2 weeks, but the full effect of blood glucose control may take up to 2 to 3 months. Ask your doctor if you have any questions about this.
The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.
The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.
If you miss a dose of this medicine, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.
Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.
Keep out of the reach of children.
Do not keep outdated medicine or medicine no longer needed.
Ask your healthcare professional how you should dispose of any medicine you do not use.
It is very important that your doctor check your progress at regular visits, especially during the first few weeks that you take this medicine. Blood and urine tests may be needed to check for unwanted effects.
This medicine may interact with the dye used for an X-ray or CT scan. Your doctor should advise you to stop taking it before you have any medical exams or diagnostic tests that might cause less urine output than usual. You may be advised to start taking the medicine again 48 hours after the exams or tests if your kidney function is tested and found to be normal.
Make sure any doctor or dentist who treats you knows that you are using this medicine. You may need to stop using this medicine several days before having surgery or medical tests.
It is very important to carefully follow any instructions from your health care team about:
Under certain conditions, too much metformin can cause lactic acidosis. The symptoms of lactic acidosis are severe and quick to appear, and usually occur when other health problems not related to the medicine are present and are very severe, such as a heart attack or kidney failure. Symptoms of lactic acidosis include abdominal or stomach discomfort, decreased appetite; diarrhea; fast or shallow breathing; a general feeling of discomfort; severe muscle pain or cramping; and unusual sleepiness, tiredness, or weakness.
If symptoms of lactic acidosis occur, you should get immediate emergency medical help.
Metformin can cause low blood sugar (hypoglycemia). However, this can also occur if you delay or miss a meal or snack, drink alcohol, exercise more than usual, cannot eat because of nausea or vomiting, take certain medicines, or take metformin with another type of diabetes medicine. The symptoms of low blood sugar must be treated before they lead to unconsciousness (passing out). Different people feel different symptoms of low blood sugar. It is important that you learn which symptoms of low blood sugar you usually have so that you can treat it quickly.
Symptoms of hypoglycemia (low blood sugar) include anxiety; behavior change similar to being drunk; blurred vision; cold sweats; confusion; cool, pale skin; difficulty with thinking; drowsiness; excessive hunger; fast heartbeat; headache (continuing); nausea; nervousness; nightmares; restless sleep; shakiness; slurred speech; or unusual tiredness or weakness.
If symptoms of low blood sugar occur, eat glucose tablets or gel, corn syrup, honey, or sugar cubes; or drink fruit juice, non-diet soft drink, or sugar dissolved in water. Also, check your blood for low blood sugar. Glucagon is used in emergency situations when severe symptoms such as seizures (convulsions) or unconsciousness occur. Have a glucagon kit available, along with a syringe or needle, and know how to use it. The members of your household also should know how to use it.
High blood sugar (hyperglycemia) is another problem related to uncontrolled diabetes. Symptoms of mild high blood sugar appear more slowly than those of low blood sugar. These may include blurred vision; drowsiness; dry mouth; flushed, dry skin; fruit-like breath odor; increased urination (frequency and volume); ketones in the urine; loss of appetite; sleepiness; stomachache, nausea or vomiting; tiredness; troubled breathing (rapid and deep); unconsciousness; or unusual thirst.
High blood sugar may occur if you do not exercise as much as usual, have a fever or infection, do not take enough or skip a dose of your diabetes medicine, or overeat or do not follow your meal plan.
If symptoms of high blood sugar occur, check your blood sugar level and then call your doctor for instructions.
This medicine is only part of a complete program for controlling diabetes. It is important that you always eat a healthy diet, watch your weight, and get regular exercise.
Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.
Check with your doctor immediately if any of the following side effects occur:
Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:
Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.
Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.
See also: Riomet side effects (in more detail)
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