Spersadexolina may be available in the countries listed below.
Ingredient matches for Spersadexolina
Chloramphenicol is reported as an ingredient of Spersadexolina in the following countries:
- Colombia
- Peru
International Drug Name Search
Spersadexolina may be available in the countries listed below.
Chloramphenicol is reported as an ingredient of Spersadexolina in the following countries:
International Drug Name Search
Ramipril may cause injury or death to the fetus if taken after the third month of pregnancy. If you think you may be pregnant, contact your doctor right away.
Treating high blood pressure or decreasing the risk of heart attack, stroke, and death in certain patients. It may be used alone or with other medicines. It is used along with other medicines to manage heart failure and improve survival after a heart attack. It may also be used for other conditions as determined by your doctor.
Ramipril is an angiotensin-converting enzyme (ACE) inhibitor. It works by relaxing blood vessels. This helps to lower blood pressure.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Ramipril. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with Ramipril. Tell your health care provider if you are taking any other medicines, especially any of the following:
This may not be a complete list of all interactions that may occur. Ask your health care provider if Ramipril 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.
Use Ramipril as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use Ramipril.
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:
Cough; dizziness; headache; tiredness.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the hands, eyes, mouth, face, lips, throat, or tongue; hoarseness); chest pain; dark urine; decreased urination; difficulty swallowing; infection (eg, fever, chills, persistent sore throat); irregular heartbeat; loss of appetite; pale stools; red, swollen, blistered, or peeling skin; seizures; stomach pain (with or without nausea or vomiting); symptoms of low blood pressure (eg, fainting, severe dizziness, lightheadedness); yellowing of the skin or eyes.
This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.
See also: Ramipril side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include fainting; severe dizziness or lightheadedness; weakness.
Store Ramipril between 68 and 77 degrees F (20 and 25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Ramipril out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Ramipril. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.
Diconten may be available in the countries listed below.
Flupentixol is reported as an ingredient of Diconten in the following countries:
Melitracen is reported as an ingredient of Diconten in the following countries:
International Drug Name Search
Toradiur may be available in the countries listed below.
Torasemide is reported as an ingredient of Toradiur in the following countries:
International Drug Name Search
Promycine may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Colistin sulfate (a derivative of Colistin) is reported as an ingredient of Promycine in the following countries:
International Drug Name Search
Veteusan may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Crotamiton is reported as an ingredient of Veteusan in the following countries:
International Drug Name Search
Humulin 30/70 may be available in the countries listed below.
Insulin Injection, Biphasic Isophane human (a derivative of Insulin Injection, Biphasic Isophane) is reported as an ingredient of Humulin 30/70 in the following countries:
International Drug Name Search
Salicylic Acid is reported as an ingredient of Wart-Off in the following countries:
International Drug Name Search
Carbo activatus may be available in the countries listed below.
Charcoal, Activated is reported as an ingredient of Carbo activatus in the following countries:
International Drug Name Search
Artrozan may be available in the countries listed below.
Meloxicam is reported as an ingredient of Artrozan in the following countries:
International Drug Name Search
Acido Clodronico Sandoz may be available in the countries listed below.
Clodronic Acid disodium tetrahydrate (a derivative of Clodronic Acid) is reported as an ingredient of Acido Clodronico Sandoz in the following countries:
International Drug Name Search
Prilenor may be available in the countries listed below.
Enalapril maleate (a derivative of Enalapril) is reported as an ingredient of Prilenor in the following countries:
International Drug Name Search
Clorexidine may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Chlorhexidine digluconate (a derivative of Chlorhexidine) is reported as an ingredient of Clorexidine in the following countries:
International Drug Name Search
Acyrax may be available in the countries listed below.
Aciclovir is reported as an ingredient of Acyrax in the following countries:
Aciclovir sodium salt (a derivative of Aciclovir) is reported as an ingredient of Acyrax in the following countries:
International Drug Name Search
Captoprilan may be available in the countries listed below.
Captopril is reported as an ingredient of Captoprilan in the following countries:
International Drug Name Search
Ditec may be available in the countries listed below.
Cromoglicic Acid disodium salt (a derivative of Cromoglicic Acid) is reported as an ingredient of Ditec in the following countries:
Fenoterol hydrobromide (a derivative of Fenoterol) is reported as an ingredient of Ditec in the following countries:
Torasemide is reported as an ingredient of Ditec in the following countries:
International Drug Name Search
Vetalgina may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Metamizole is reported as an ingredient of Vetalgina in the following countries:
International Drug Name Search
Relieving runny nose, sneezing, and cough due to colds, upper respiratory infections, and allergies. It may also be used for other conditions as determined by your doctor.
Brompheniramine/Codeine Syrup is an antihistamine and narcotic cough suppressant combination. The antihistamine works by blocking the action of histamine, which helps reduce symptoms, such as watery eyes and sneezing. The cough suppressant works in the brain to help decrease the cough reflex, which reduces a dry cough.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Brompheniramine/Codeine Syrup. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with Brompheniramine/Codeine Syrup. Tell your health care provider if you are taking any other medicines, especially any of the following:
This may not be a complete list of all interactions that may occur. Ask your health care provider if Brompheniramine/Codeine Syrup 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.
Use Brompheniramine/Codeine Syrup as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use Brompheniramine/Codeine Syrup.
When used for long periods of time or at high doses, Brompheniramine/Codeine Syrup may not work as well and may require higher doses to obtain the same effect as when originally taken. This is known as TOLERANCE. Talk with your doctor if Brompheniramine/Codeine Syrup stops working well. Do not take more than prescribed.
When used for long periods of time or at high doses, some people develop a need to continue taking Brompheniramine/Codeine Syrup. This is known as DEPENDENCE or addiction.
If you suddenly stop taking Brompheniramine/Codeine Syrup, you may experience WITHDRAWAL symptoms including anxiety; diarrhea; fever, runny nose, or sneezing; goose bumps and abnormal skin sensations; nausea; vomiting; pain; rigid muscles; rapid heartbeat; seeing, hearing or feeling things that are not there; shivering or tremors; sweating; trouble sleeping.
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; dry mouth, nose, or throat; excitability; headache; loss of appetite; nausea; thickening of mucus secretions; upset stomach; vomiting.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred vision, double vision, or other vision changes; confusion; difficulty urinating or inability to urinate; fast, slow, or irregular heartbeat; loss of coordination; mood or mental changes; nervousness; ringing in the ears; seizures; severe dizziness, lightheadedness, or headache; severe drowsiness; shallow breathing; tremor; trouble sleeping; uncontrolled muscle movements; unusual bruising or bleeding; unusual weakness or tiredness.
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. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.
See also: Brompheniramine/Codeine side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include blurred vision; confusion; hallucinations; seizures; severe dizziness, lightheadedness, or headache; severe drowsiness; shallow breathing; unusually fast, slow, or irregular heartbeat; vomiting.
Store Brompheniramine/Codeine Syrup at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Brompheniramine/Codeine Syrup out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Brompheniramine/Codeine Syrup. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.
Velkaderm may be available in the countries listed below.
Clindamycin dihydrogen phosphate (a derivative of Clindamycin) is reported as an ingredient of Velkaderm in the following countries:
International Drug Name Search
Uromykol may be available in the countries listed below.
Clotrimazole is reported as an ingredient of Uromykol in the following countries:
International Drug Name Search
In the US, Orphenadrine (orphenadrine systemic) is a member of the drug class skeletal muscle relaxants and is used to treat Migraine and Muscle Spasm.
US matches:
UK matches:
Rec.INN
0000083-98-7
C18-H23-N-O
269
Treatment of Parkinson's disease: Central anticholinergic
Ethanamine, N,N-dimethyl-2-[(2-methylphenyl)phenylmethoxy]-
International Drug Name Search
Glossary
| BAN | British Approved Name |
| BANM | British Approved Name (Modified) |
| DCF | Dénomination Commune Française |
| DCIT | Denominazione Comune Italiana |
| OS | Official Synonym |
| PH | Pharmacopoeia Name |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
| SPC | Summary of Product Characteristics (UK) |
| USAN | United States Adopted Name |
Proinfark may be available in the countries listed below.
Dopamine hydrochloride (a derivative of Dopamine) is reported as an ingredient of Proinfark in the following countries:
International Drug Name Search
Phoenix Xylazine may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Xylazine is reported as an ingredient of Phoenix Xylazine in the following countries:
International Drug Name Search
Epirazole may be available in the countries listed below.
Omeprazole is reported as an ingredient of Epirazole in the following countries:
International Drug Name Search
Tekilon may be available in the countries listed below.
Anetholtrithion is reported as an ingredient of Tekilon in the following countries:
International Drug Name Search
Steripet may be available in the countries listed below.
Fludeoxyglucose (18F) is reported as an ingredient of Steripet in the following countries:
International Drug Name Search
Duro Tuss Dry Cough may be available in the countries listed below.
Cetylpyridinium chloride (a derivative of Cetylpyridinium) is reported as an ingredient of Duro Tuss Dry Cough in the following countries:
Pholcodine is reported as an ingredient of Duro Tuss Dry Cough in the following countries:
Pseudoephedrine hydrochloride (a derivative of Pseudoephedrine) is reported as an ingredient of Duro Tuss Dry Cough in the following countries:
International Drug Name Search
Premique may be available in the countries listed below.
UK matches:
Estrogens, conjugated is reported as an ingredient of Premique in the following countries:
Medroxyprogesterone 17α-acetate (a derivative of Medroxyprogesterone) is reported as an ingredient of Premique in the following countries:
International Drug Name Search
Glossary
| SPC | Summary of Product Characteristics (UK) |
Carcopa may be available in the countries listed below.
Carbidopa is reported as an ingredient of Carcopa in the following countries:
Levodopa is reported as an ingredient of Carcopa in the following countries:
International Drug Name Search
See also: Generic Taclonex Scalp
Taclonex is a brand name of betamethasone/calcipotriene topical, approved by the FDA in the following formulation(s):
No. There is currently no therapeutically equivalent version of Taclonex available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Taclonex. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: About generic drugs.
Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.
Stomédine may be available in the countries listed below.
Cimetidine is reported as an ingredient of Stomédine in the following countries:
International Drug Name Search
Mirtazapine Mylan may be available in the countries listed below.
Mirtazapine is reported as an ingredient of Mirtazapine Mylan in the following countries:
International Drug Name Search
Metkar may be available in the countries listed below.
Metformin hydrochloride (a derivative of Metformin) is reported as an ingredient of Metkar in the following countries:
International Drug Name Search
Methylfenidaathydrochloride PCH may be available in the countries listed below.
Methylphenidate hydrochloride (a derivative of Methylphenidate) is reported as an ingredient of Methylfenidaathydrochloride PCH in the following countries:
International Drug Name Search
Buflox may be available in the countries listed below.
Buflomedil hydrochloride (a derivative of Buflomedil) is reported as an ingredient of Buflox in the following countries:
International Drug Name Search
Ryth may be available in the countries listed below.
Roxithromycin is reported as an ingredient of Ryth in the following countries:
International Drug Name Search
Dispeptal may be available in the countries listed below.
Pancreatin is reported as an ingredient of Dispeptal in the following countries:
International Drug Name Search
Warfarin Norton may be available in the countries listed below.
Warfarin sodium salt (a derivative of Warfarin) is reported as an ingredient of Warfarin Norton in the following countries:
International Drug Name Search
Teprix may be available in the countries listed below.
Ibuprofen is reported as an ingredient of Teprix in the following countries:
International Drug Name Search
Enabeta may be available in the countries listed below.
Enalapril maleate (a derivative of Enalapril) is reported as an ingredient of Enabeta in the following countries:
International Drug Name Search
Calcitugg may be available in the countries listed below.
Calcium Carbonate is reported as an ingredient of Calcitugg in the following countries:
International Drug Name Search
Profamid may be available in the countries listed below.
Flutamide is reported as an ingredient of Profamid in the following countries:
International Drug Name Search
Phloroglucinol Qualimed may be available in the countries listed below.
Phloroglucinol is reported as an ingredient of Phloroglucinol Qualimed in the following countries:
International Drug Name Search
Pantoprazol G.L. may be available in the countries listed below.
Pantoprazole is reported as an ingredient of Pantoprazol G.L. in the following countries:
International Drug Name Search
Fluvean may be available in the countries listed below.
Fluocinolone Acetonide is reported as an ingredient of Fluvean in the following countries:
International Drug Name Search
Pantoprazol AbZ may be available in the countries listed below.
Pantoprazole sodium (a derivative of Pantoprazole) is reported as an ingredient of Pantoprazol AbZ in the following countries:
International Drug Name Search
Lisinopril/Hydroklortiazid Actavis may be available in the countries listed below.
Hydrochlorothiazide is reported as an ingredient of Lisinopril/Hydroklortiazid Actavis in the following countries:
Lisinopril dihydrate (a derivative of Lisinopril) is reported as an ingredient of Lisinopril/Hydroklortiazid Actavis in the following countries:
International Drug Name Search
Oracyn-K may be available in the countries listed below.
Phenoxymethylpenicillin potassium (a derivative of Phenoxymethylpenicillin) is reported as an ingredient of Oracyn-K in the following countries:
International Drug Name Search
Bonacal may be available in the countries listed below.
Calcium Carbonate is reported as an ingredient of Bonacal in the following countries:
International Drug Name Search
Ocuson may be available in the countries listed below.
Betamethasone is reported as an ingredient of Ocuson in the following countries:
Dexchlorpheniramine maleate (a derivative of Dexchlorpheniramine) is reported as an ingredient of Ocuson in the following countries:
International Drug Name Search
Pulmicort Turbuhaler Orifarm may be available in the countries listed below.
Budesonide is reported as an ingredient of Pulmicort Turbuhaler Orifarm in the following countries:
International Drug Name Search
Plivit C may be available in the countries listed below.
Ascorbic Acid is reported as an ingredient of Plivit C in the following countries:
International Drug Name Search
Panaldine may be available in the countries listed below.
Ticlopidine hydrochloride (a derivative of Ticlopidine) is reported as an ingredient of Panaldine in the following countries:
International Drug Name Search
Yakuzol may be available in the countries listed below.
Benzalkonium chloride (a derivative of Benzalkonium) is reported as an ingredient of Yakuzol in the following countries:
International Drug Name Search
Carbon Medical may be available in the countries listed below.
Charcoal, Activated is reported as an ingredient of Carbon Medical in the following countries:
International Drug Name Search
In the US, Tolazamide (tolazamide systemic) is a member of the drug class sulfonylureas and is used to treat Diabetes, Type 2.
US matches:
Rec.INN
A10BB05
0001156-19-0
C14-H21-N3-O3-S
311
Oral antidiabetic agent, sulfonylurea
Benzenesulfonamide, N-[[(hexahydro-1H-azepin-1-yl)amino]carbonyl]-4-methyl-
International Drug Name Search
Glossary
| BAN | British Approved Name |
| DCF | Dénomination Commune Française |
| DCIT | Denominazione Comune Italiana |
| IS | Inofficial Synonym |
| JAN | Japanese Accepted Name |
| OS | Official Synonym |
| PH | Pharmacopoeia Name |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
| USAN | United States Adopted Name |
Generic Name: ofloxacin otic (oh FLOCKS a sin OH tic)
Brand names: Floxin Otic, Floxin Otic Singles
Ofloxacin is a fluoroquinolone antibiotic. Ofloxacin fights bacteria in the body.
Ofloxacin is used to treat ear infections.
Ofloxacin otic may also be used for purposes other than those listed in this medication guide.
Notify your doctor if the condition does not improve or appears to worsen.
ciprofloxacin (Cipro, CiproDex, Cipro HC), gatifloxacin (Tequin), levofloxacin (Levaquin), lomefloxacin (Maxaquin), moxifloxacin (Avelox), norfloxacin (Noroxin), ofloxacin (Floxin), sparfloxacin (Zagam), or trovafloxacin (Trovan).
You may not be able to use ofloxacin otic, or you may require a dosage adjustment or special monitoring during treatment.
In general, ofloxacin otic should be used as follows:
Warm the drops slightly by holding the bottle in the hands for 1 or 2 minutes. Administration of cold drops into the ear may cause dizziness.
Have another person administer the drops whenever possible. Have the affected person lie on their side or tilt the ear up to make administering a drop easier.
For adults, gently hold the earlobe up and back. For children, gently hold the earlobe down and back. This will allow the drops to run into the ear canal. Carefully instill the prescribed number of drops in the first ear.
Keep the ear tilted for at least 5 minutes to allow the medication to penetrate the ear.
If the patient being treated has ear tubes, the doctor may recommend gently pressing the tragus (part of the ear in front of the opening of the ear canal) four to five times in a pumping motion after administration of the drops. This may allow the drops to pass through the tubes into the middle ear. Follow the doctor's instructions.
Repeat the process in the other ear if prescribed.
Ofloxacin ear drops are usually used twice a day, about 12 hours apart. Follow your doctor's instructions.
Use all of the medication that has been prescribed. Symptoms may begin to improve before the condition is completely treated. If you do not use all of the medication prescribed, the condition could return or worsen.
It is important to use ofloxacin otic regularly to get the most benefit.
Notify your doctor if the condition does not improve or appears to worsen.
Store ofloxacin otic at room temperature, away from moisture, heat, and direct light. Keep the bottle properly capped.
Use the missed dose as soon as you remember. However, if it is almost time for the next dose, skip the missed dose and use only the next regularly scheduled dose. Do not use a double dose of ofloxacin otic unless otherwise directed by your doctor.
Symptoms of a ofloxacin otic overdose are not known.
an allergic reaction (difficulty breathing; closing of the throat; swelling of the lips, tongue, or face; or hives);
skin rash; or
ear drainage, discharge, or worsening pain.
Other less serious side effects may also occur such as ear discomfort or itching, and headache. Continue to use the medication and talk to your doctor if these side effects seem excessive or unusual.
Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome. You may report side effects to FDA at 1-800-FDA-1088.
Usual Adult Dose for Acute Otitis Externa:
Instill 10 drops into the affected ear(s) once daily for 7 days.
Before administration, the solution should be warmed by holding the bottle in the hand for 1 to 2 minutes. The drops should be instilled with the patient lying on his/her side with the affected ear upward. The patient should stay on his/her side for 5 minutes. Repeat for the opposite ear, if necessary.
Usual Adult Dose for Otitis Media:
Chronic suppurative otitis media with perforated tympanic membrane:
Instill 10 drops into the affected ear(s) twice daily for 14 days.
Before administration, the solution should be warmed by holding the bottle in the hand for 1 to 2 minutes. The drops should be instilled with the patient lying on his/her side with the affected ear upward. After administration, the tragus should be gently pressed 4 times to allow the solution to flow through the tympanic membrane into the middle ear. The patient should stay on his/her side for 5 minutes. Repeat for the opposite ear, if necessary.
Usual Pediatric Dose for Acute Otitis Externa:
6 months to 12 years: Instill 5 drops into the affected ear(s) once daily for 7 days.
>=13 years: Instill 10 drops into the affected ear(s) once daily for 7 days.
Before administration, the solution should be warmed by holding the bottle in the hand for 1 to 2 minutes. The drops should be instilled with the patient lying on his/her side with the affected ear upward. The patient should stay on his/her side for 5 minutes. Repeat for the opposite ear, if necessary.
Usual Pediatric Dose for Otitis Media:
Acute otitis media in patients with tympanostomy tubes:
1 to 12 years: Instill 5 drops into the affected ear(s) twice daily for 10 days.
Chronic suppurative otitis media with perforated tympanic membranes:
>12 years: Instill 10 drops into the affected ear(s) twice daily for 14 days.
Before administration, the solution should be warmed by holding the bottle in the hand for 1 to 2 minutes. The drops should be instilled with the patient lying on his/her side with the affected ear upward. After administration, the outer ear should be gently pulled upward and backward to allow the solution to flow down into the ear canal. The patient should stay on his/her side for 5 minutes. Repeat for the opposite ear, if necessary.
Drugs other than those listed here may also interact with ofloxacin otic. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines, including vitamins, minerals, and herbal products.
Generic Name: prednisolone (Oral route)
pred-NIS-oh-lone
In the U.S.
In Canada
Available Dosage Forms:
Therapeutic Class: Endocrine-Metabolic Agent
Pharmacologic Class: Adrenal Glucocorticoid
Prednisolone provides relief for inflamed areas of the body. It is used to treat a number of different conditions, such as inflammation (swelling), severe allergies, adrenal problems, arthritis, asthma, blood or bone marrow problems, eye or vision problems, lupus, skin conditions, kidney problems, ulcerative colitis, and flare-ups of multiple sclerosis. Prednisolone is a corticosteroid (cortisone-like medicine or steroid). It works on the immune system to help relieve swelling, redness, itching, and allergic reactions.
This medicine is 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.
Appropriate studies performed to date have not demonstrated pediatric-specific problems that would limit the usefulness of prednisolone in children. However, pediatric patients are more likely to have slower growth and bone problems if prednisolone is used for a long time. Recommended doses should not be exceeded, and the patient should be carefully monitored during therapy.
Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of prednisolone in the elderly. However, elderly patients are more likely to have age-related kidney and bone problems, which may require caution and an adjustment in the dose for elderly patients receiving prednisolone.
| Pregnancy Category | Explanation | |
|---|---|---|
| All Trimesters | C | Animal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women. |
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. 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 prednisolone. It may not be specific to Orapred. Please read with care.
Take this medicine exactly as directed by your doctor. Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered. To do so may increase the chance for unwanted effects.
This medicine comes with a patient instruction insert. Read and follow the instructions in the insert carefully. Ask your doctor if you have any questions.
This medicine should be taken with food to avoid stomach irritation.
Measure the oral liquid with the special oral syringe that comes with the package. The average household teaspoon may not hold the right amount of liquid.
If you use this medicine for a long time, do not suddenly stop using it without checking first with your doctor. You may need to slowly decrease your dose before stopping it completely.
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.
If you will be taking this medicine for a long time, it is very important that your doctor check you at regular visits for any unwanted effects that may be caused by this medicine. Blood or urine tests may be needed to check for unwanted effects.
Using this medicine while you are pregnant can harm your unborn baby. Use an effective form of birth control to keep from getting pregnant. If you think you have become pregnant while using this medicine, tell your doctor right away.
Using too much of this medicine or using it for a long time may increase your risk of having adrenal gland problems. Talk to your doctor right away if you have more than one of these symptoms while you are using this medicine: blurred vision; dizziness or fainting; a fast, irregular, or pounding heartbeat; increased thirst or urination; irritability; or unusual tiredness or weakness.
This medicine may cause you to get more infections than usual. Avoid people who are sick or have infections and wash your hands often. If you are exposed to chickenpox or measles, tell your doctor right away. If you start to have a fever, chills, sore throat, or any other sign of an infection, call your doctor right away.
This medicine may cause changes in mood or behavior for some patients. Tell your doctor right away if you have depression; mood swings; a false or unusual sense of well-being; trouble with sleeping; or personality changes while taking this medicine.
This medicine might cause thinning of the bones (osteoporosis) or slow growth in children if used for a long time. Tell your doctor if you have any bone pain or if you have an increased risk for osteoporosis. If your child is using this medicine, tell the doctor if you think your child is not growing properly.
If you are using this medicine for a long time, tell your doctor about any extra stress or anxiety in your life, including other health concerns and emotional stress. Your dose of this medicine might need to be changed for a short time while you have extra stress.
Check with your doctor right away if blurred vision, difficulty in reading, or any other change in vision occurs during or after treatment. Your doctor may want you to have your eyes checked by an ophthalmologist (eye doctor).
While you are being treated with prednisolone, do not have any immunizations (vaccines) without your doctor's approval. Prednisolone may lower your body's resistance and the vaccine may not work as well or you might get the infection the vaccine is meant to prevent. In addition, you should not be around other persons living in your household who receive live virus vaccines because there is a chance they could pass the virus on to you. Some examples of live vaccines include measles, mumps, influenza (nasal flu vaccine), poliovirus (oral form), rotavirus, and rubella. Do not get close to them and do not stay in the same room with them for very long. If you have questions about this, talk to your doctor.
Make sure any doctor or dentist who treats you knows that you are using this medicine. This medicine may affect the results of certain skin tests.
Do not take other medicines unless they have been discussed with your doctor. This includes prescription or nonprescription (over-the-counter [OTC]) medicines and herbal or vitamin supplements.
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.
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