Panthenol Spray may be available in the countries listed below.
Dexpanthenol is reported as an ingredient of Panthenol Spray in the following countries:
International Drug Name Search
Nonalges may be available in the countries listed below.
Tramadol is reported as an ingredient of Nonalges in the following countries:
International Drug Name Search
Orciprenalina may be available in the countries listed below.
Orciprenalina (DCIT) is also known as Orciprenaline (Rec.INN)
International Drug Name Search
Glossary
| DCIT | Denominazione Comune Italiana |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
Generic Name: senna (SEN nah)
Brand Names: Black Draught, Dr Caldwell Laxative, Ex-Lax Chocolated, Ex-Lax Maximum Relief Formula, Ex-Lax Regular Strength Pills, Fletchers Castoria, Innerclean, Pedia-Lax, Perdiem Overnight, Senexon, Senna, Senna Lax, Senna Smooth, Senna Soft, Senna-gen, Senokot, Senokot Extra, SenokotXTRA, SenoSol, SenoSol-X
Senna is also known as Cassia senna, tinnevelly senna, India senna, Alexandrian senna, and Khartoum senna.
Senna has been used in alternative medicine as an aid to treat constipation.
Senna is often sold as an herbal supplement. There are no regulated manufacturing standards in place for many herbal compounds and some marketed supplements have been found to be contaminated with toxic metals or other drugs. Herbal/health supplements should be purchased from a reliable source to minimize the risk of contamination.
Senna may also be used for other purposes not listed in this product guide.
Senna is often sold as an herbal supplement. There are no regulated manufacturing standards in place for many herbal compounds and some marketed supplements have been found to be contaminated with toxic metals or other drugs. Herbal/health supplements should be purchased from a reliable source to minimize the risk of contamination.
Use senna as directed on the label, or as your healthcare provider has prescribed. Do not use this product in larger amounts or for longer than recommended.
Ask a doctor, pharmacist, herbalist, or other healthcare provider if it is safe for you to use this product if you have:
a bowel disorder such as Crohn's disease or ulcerative colitis;
heart disease; or
stomach pain, nausea, or vomiting.
Before using senna, talk to your doctor, pharmacist, herbalist, or other healthcare provider. You may not be able to use senna if you have any other medical conditions, allergies, or if you take other medicines or herbal/health supplements.
When considering the use of herbal supplements, seek the advice of your doctor. You may also consider consulting a practitioner who is trained in the use of herbal/health supplements.
If you choose to use senna, use it as directed on the package or as directed by your doctor, pharmacist, or other healthcare provider. Do not use more of this product than is recommended on the label.
Senna is usually taken before bed to produce a bowel movement 6 to 12 hours later when you wake up.
Skip the missed dose if it is almost time for your next scheduled dose. Do not use extra medicine to make up the missed dose.
Follow your healthcare provider's instructions about any restrictions on food, beverages, or activity.
severe stomach pain, severe diarrhea, watery diarrhea;
weight loss;
worsening constipation after you stop taking senna;
enlargement of your fingers and toes;
low potassium (confusion, uneven heart rate, extreme thirst, increased urination, leg discomfort, muscle weakness or limp feeling); or
nausea, upper stomach pain, itching, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes).
Less serious side effects may include:
stomach cramps, bloating, gas, mild diarrhea;
numbness or tingly feeling;
joint pain; or
discolored urine.
This is not a complete list of side effects and others may occur. Tell your doctor, pharmacist, herbalist, or other healthcare provider about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.
digoxin (Lanoxin);
a diuretic (water pill); or
a blood thinner such as warfarin (Coumadin).
This list is not complete and other drugs may interact with senna. Tell your healthcare provider 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: Senexon side effects (in more detail)
Thioguanin Glaxo Wellcome may be available in the countries listed below.
Tioguanine is reported as an ingredient of Thioguanin Glaxo Wellcome in the following countries:
International Drug Name Search
Prindace may be available in the countries listed below.
Perindopril is reported as an ingredient of Prindace in the following countries:
International Drug Name Search
MCP Hexal may be available in the countries listed below.
Metoclopramide hydrochloride (a derivative of Metoclopramide) is reported as an ingredient of MCP Hexal in the following countries:
International Drug Name Search
Generic Name: azelastine nasal (a ZEL uh steen)
Brand Names: Astelin, Astepro
Azelastine is an antihistamine. It blocks the effects of the chemical histamine in your body.
Azelastine prevents sneezing, itching, runny nose, and other nasal symptoms of allergies.
Azelastine nasal may also be used for other purposes not listed in this medication guide.
Before using azelastine nasal, tell your doctor if you regularly use other medicines that make you sleepy (such as 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 azelastine nasal.
Talk with your doctor if your allergy symptoms do not improve or if they get worse.
Use azelastine exactly as it was prescribed for you. Do not use it in larger doses or for longer than recommended by your doctor. Follow the directions on your prescription label.
To use the azelastine nasal spray:
Gently blow your nose before using the nasal spray.
The first time you use a new bottle, screw the pump device onto the bottle. Prime the unit by pumping 4 sprays into the air, away from your face, until a fine mist appears. Prime the spray pump any time it has been longer than 3 days since you last used it.
Insert the spray tip into your nostril, pointing it straight up into your nose. Press your other nostril closed with your finger and keep your head upright. Pump the spray and gently inhale at the same time.
Use only the number of sprays prescribed by your doctor.
Clean the pump nozzle with a clean, damp tissue and recap it.
Try not to sneeze or blow your nose just after using the spray.
Talk with your doctor if your symptoms do not improve or if they get worse.
Use the medication as soon as you remember. If it is almost time for the next dose, skip the missed dose and wait until your next regularly scheduled dose. Do not use extra medicine to make up the missed dose.
Overdose symptoms may include extreme sleepiness.
bronchospasm (shortness of breath, tightness in chest, wheezing); or
fast or uneven heartbeats.
Less serious side effects may include:
a bitter taste in your mouth;
headache;
drowsiness or dizziness;
dry mouth, sore throat;
burning in your nose;
weight gain;
nausea;
nosebleed;
cough, sneezing, runny nose, cold symptoms; or
eye redness.
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 Allergic Rhinitis:
Seasonal allergic rhinitis:
0.1% spray: 1 or 2 sprays in each nostril twice a day.
0.15% spray: 2 sprays per nostril once daily.
Perennial allergic rhinitis:
0.15% spray: 2 sprays per nostril twice a day.
Usual Pediatric Dose for Allergic Rhinitis:
Seasonal allergic rhinitis:
Astelin 0.1% spray:
5 to 11 years: 1 spray in each nostril twice a day.
12 years or older: 1 or 2 sprays in each nostril twice a day.
Astepro Nasal Spray 0.1% and 0.15%
12 years or older: 1 or 2 sprays per nostril twice daily for seasonal allergic rhinitis. Astepro Nasal Spray 0.15% may also be administered as 2 sprays per nostril once daily.
Perennial allergic rhinitis:
0.1% spray and 0.15% spray:
12 years or older: 2 sprays in each nostril twice a day.
Also tell your doctor if you are using cimetidine (Tagamet).
There may be other drugs that can interact with azelastine. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.
Panthenol-Augensalbe Jenapharm may be available in the countries listed below.
Dexpanthenol is reported as an ingredient of Panthenol-Augensalbe Jenapharm in the following countries:
International Drug Name Search
Doxazosin Arcana may be available in the countries listed below.
Doxazosin mesilate (a derivative of Doxazosin) is reported as an ingredient of Doxazosin Arcana in the following countries:
International Drug Name Search
Metoclopramida Genfar may be available in the countries listed below.
Metoclopramide is reported as an ingredient of Metoclopramida Genfar in the following countries:
Metoclopramide hydrochloride (a derivative of Metoclopramide) is reported as an ingredient of Metoclopramida Genfar in the following countries:
International Drug Name Search
Azathioprine Cf may be available in the countries listed below.
Azathioprine is reported as an ingredient of Azathioprine Cf in the following countries:
International Drug Name Search
Piktum may be available in the countries listed below.
Retinol palmitate (a derivative of Retinol) is reported as an ingredient of Piktum in the following countries:
International Drug Name Search
Nardil is a brand name of phenelzine, approved by the FDA in the following formulation(s):
Yes. The following products are equivalent to Nardil:
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Nardil. 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.
There are no current U.S. patents associated with Nardil.
Latof may be available in the countries listed below.
Latanoprost is reported as an ingredient of Latof in the following countries:
International Drug Name Search
Primodian may be available in the countries listed below.
Estradiol 17ß-valerate (a derivative of Estradiol) is reported as an ingredient of Primodian in the following countries:
Testosterone 17ß-enantate (a derivative of Testosterone) is reported as an ingredient of Primodian in the following countries:
International Drug Name Search
Pramiracetam Sulfate may be available in the countries listed below.
Pramiracetam Sulfate (USAN) is also known as Pramiracetam (Rec.INN)
International Drug Name Search
Glossary
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
| USAN | United States Adopted Name |
Pyralen may be available in the countries listed below.
Paracetamol is reported as an ingredient of Pyralen in the following countries:
International Drug Name Search
Pharmacetine may be available in the countries listed below.
Chloramphenicol is reported as an ingredient of Pharmacetine in the following countries:
International Drug Name Search
Pyrévalgine may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Acetylsalicylic Acid calcium salt (a derivative of Acetylsalicylic Acid) is reported as an ingredient of Pyrévalgine in the following countries:
Ascorbic Acid sodium salt (a derivative of Ascorbic Acid) is reported as an ingredient of Pyrévalgine in the following countries:
International Drug Name Search
Dietary management of osteopenia and osteoporosis (weak bones).
Cholecalciferol/Genistein/Zinc Chelazome is a medical food. It works by slowing down bone breakdown activity and speeding up bone building activity.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Cholecalciferol/Genistein/Zinc Chelazome. 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 Cholecalciferol/Genistein/Zinc Chelazome. 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 Cholecalciferol/Genistein/Zinc Chelazome 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 Cholecalciferol/Genistein/Zinc Chelazome 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 Cholecalciferol/Genistein/Zinc Chelazome.
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.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).
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: Cholecalciferol/Genistein/Zinc Chelazome 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 increased thirst; increased urination; lethargy; loss of appetite; severe or persistent nausea or vomiting; weakness.
Store Cholecalciferol/Genistein/Zinc Chelazome 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 Cholecalciferol/Genistein/Zinc Chelazome out of the reach of children and away from pets.
This information is summary only. It does not contain all information about Cholecalciferol/Genistein/Zinc Chelazome. 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.
Relieving symptoms of sinus congestion, 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.
BroveX PB C is a decongestant, antihistamine, and cough suppressant combination. The decongestant works by constricting blood vessels and reducing swelling in the nasal passages. 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 to reduce 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 BroveX PB C. 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 BroveX PB C. 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 BroveX PB C 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 BroveX PB C 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 BroveX PB C.
Some people who use BroveX PB C for a long time may develop a need to continue taking it. People who take high doses are also at risk. This is known as DEPENDENCE or addiction.
If you stop taking BroveX PB C suddenly, you may have WITHDRAWAL symptoms. These may include anxiety, irregular heartbeat, irritability, restlessness, trouble sleeping, and unusual sweating.
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; nervousness or anxiety; trouble sleeping; upset stomach; vomiting; weakness.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); confusion; difficulty urinating or inability to urinate; fast, slow, or irregular heartbeat; hallucinations; loss of coordination; mental or mood changes (eg, irritability); 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; vision changes or blurred vision.
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. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at http://www.fda.gov/medwatch .
See also: BroveX PB C 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; cold and clammy skin; coma; confusion; hallucinations; seizures; severe dizziness, lightheadedness, or headache; severe drowsiness; shallow breathing; unusually fast, slow, or irregular heartbeat; vomiting.
Store BroveX PB C 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 BroveX PB C out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about BroveX PB C. 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.
Amantix may be available in the countries listed below.
Amantadine sulfate (a derivative of Amantadine) is reported as an ingredient of Amantix in the following countries:
International Drug Name Search
Lorazepam Almus may be available in the countries listed below.
Lorazepam is reported as an ingredient of Lorazepam Almus in the following countries:
International Drug Name Search
Acetil colina intraocular may be available in the countries listed below.
Acetylcholine Chloride is reported as an ingredient of Acetil colina intraocular in the following countries:
International Drug Name Search
Polmonin may be available in the countries listed below.
Tolfenamic Acid is reported as an ingredient of Polmonin in the following countries:
International Drug Name Search
0055049-48-4
C30-H28-K6-Na6-O30
1241
Alkalinizer
Hexapotassium hexasodium pentacitrate hydrate complex
International Drug Name Search
Glossary
| IS | Inofficial Synonym |
Visiren may be available in the countries listed below.
Ofloxacin is reported as an ingredient of Visiren in the following countries:
International Drug Name Search
Porosimax may be available in the countries listed below.
Alendronic Acid sodium trihydrate (a derivative of Alendronic Acid) is reported as an ingredient of Porosimax in the following countries:
International Drug Name Search
Pilokarpin Unimed Pharma may be available in the countries listed below.
Pilocarpine hydrochloride (a derivative of Pilocarpine) is reported as an ingredient of Pilokarpin Unimed Pharma in the following countries:
International Drug Name Search
Naproxen beta may be available in the countries listed below.
Naproxen is reported as an ingredient of Naproxen beta in the following countries:
International Drug Name Search
Anodan-HC may be available in the countries listed below.
Hydrocortisone 21-acetate (a derivative of Hydrocortisone) is reported as an ingredient of Anodan-HC in the following countries:
Zinc Sulfate is reported as an ingredient of Anodan-HC in the following countries:
International Drug Name Search
Colohiponarine may be available in the countries listed below.
Etilefrine hydrochloride (a derivative of Etilefrine) is reported as an ingredient of Colohiponarine in the following countries:
International Drug Name Search
Bixon may be available in the countries listed below.
Ceftriaxone disodium salt (a derivative of Ceftriaxone) is reported as an ingredient of Bixon in the following countries:
International Drug Name Search
Generic Name: oxycodone (Oral route)
ox-i-KOE-done hye-droe-KLOR-ide
Oxycodone hydrochloride is an opioid agonist and a Schedule II controlled substance with an abuse potential similar to morphine. Patients should be assessed for their clinical risks for opioid abuse or addiction prior to being prescribed opioids. Oxycodone hydrochloride controlled-release tablets are indicated for continuous, around the clock analgesia for an extended period of time; not for use on an as needed basis. The 60 mg and 80 mg tablets, a single dose greater than 40 mg, or a total daily dose greater than 80 mg, are only for use in opioid-tolerant patients as they may cause fatal respiratory depression when administered to patients who are not tolerant to the respiratory depressant effects of opioids. Oxycodone hydrochloride controlled-release tablets must be swallowed whole to avoid a rapid release of the drug which can be potentially fatal. Concomitant use with CYP3A4 inhibitors may result in an increase in oxycodone plasma concentrations and may cause potentially fatal respiratory depression .
In the U.S.
In Canada
Available Dosage Forms:
Therapeutic Class: Analgesic
Chemical Class: Oxycodone
Oxycodone is used to relieve moderate to severe pain. It belongs to the group of medicines called narcotic analgesics (pain medicines). Oxycodone acts on the central nervous system (CNS) to relieve pain.
When oxycodone is used for a long time, it may become habit-forming, causing mental or physical dependence. However, people who have continuing pain should not let the fear of dependence keep them from using narcotics to relieve their pain. Mental dependence (addiction) is not likely to occur when narcotics are used for this purpose. Physical dependence may lead to withdrawal side effects if treatment is stopped suddenly. However, severe withdrawal side effects can usually be prevented by gradually reducing the dose over a period of time before treatment is stopped completely.
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 have not been performed on the relationship of age to the effects of oxycodone in the pediatric population. Safety and efficacy have not been established.
Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of oxycodone in the elderly. However, elderly patients are more likely to have age-related liver or kidney problems, which may require caution and an adjustment in the dose for patients receiving oxycodone.
| 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 breastfeeding have demonstrated harmful infant effects. An alternative to this medication should be prescribed or you should stop breastfeeding while using this medicine.
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.
Using this medicine with any of the following is usually not recommended, but may be unavoidable in some cases. If used together, your doctor may change the dose or how often you use this medicine, or give you special instructions about the use of 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 oxycodone. It may not be specific to Oxecta. Please read with care.
Take this medicine only 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. This is especially important for elderly patients, who may be more sensitive to the effects of pain medicines. If too much of this medicine is taken for a long time, it may become habit-forming (causing mental or physical dependence).
This medicine comes with a patient information leaflet. Read and follow these instructions carefully. Ask your doctor if you have any questions.
Oxycodone extended-release tablets should only be used by patients who have already been taking narcotic pain medicines, also called opioids. These patients are called opioid-tolerant. If you are uncertain whether or not you are opioid-tolerant, check with your doctor before using this medicine.
Measure the oral liquid concentrate with the calibrated dropper that comes with the package. Your doctor may have you mix the concentrate with a small amount of liquid or food. Carefully follow the instructions and take the medicine mixture right away.
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.
Swallow the Oxecta® or OxyContin® tablet whole with water. Do not break, crush, cut, chew, or dissolve it. Do not pre-soak, lick, or wet the tablet before placing it in the mouth. Take one tablet at a time. Also, do not give this medicine through nasogastric or feeding tubes.
Oxycodone extended-release tablets work differently from the regular oxycodone oral solution or tablets, even at the same dose. Do not switch from one brand or form to the other unless your doctor tells you to.
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.
Oxycodone can cause serious unwanted effects if taken by adults who are not used to strong narcotic pain medicines, children, or pets. Make sure you store the medicine in a safe and secure place to prevent others from getting it.
Flush the unused extended-release tablets and immediate-release tablets down the toilet.
It is very important that your doctor check your progress while you are taking this medicine. This will allow your doctor to see if the medicine is working properly and to decide if you should continue to take it.
This medicine will add to the effects of alcohol and other CNS depressants (medicines that can make you drowsy or less alert). Some examples of CNS depressants are antihistamines or medicine for allergies or colds; sedatives, tranquilizers, or sleeping medicine; other prescription pain medicine or narcotics; medicine for seizures or barbiturates; muscle relaxants; or anesthetics, including some dental anesthetics. Check with your doctor before taking any of these medicines while you are using this medicine.
This medicine may be habit-forming. If you feel that the medicine is not working as well, do not use more than your prescribed dose. Call your doctor for instructions.
Dizziness, lightheadedness, or fainting may occur when you get up suddenly from a lying or sitting position. Getting up slowly may help lessen this problem. Also, lying down for a while may relieve the dizziness or lightheadedness.
This medicine may make you dizzy, drowsy, or lightheaded. Make sure you know how you react to this medicine before you drive, use machines, or do anything else that could be dangerous if you are dizzy or not alert.
Using narcotics for a long time can cause severe constipation. To prevent this, your doctor may direct you to take laxatives, drink a lot of fluids, or increase the amount of fiber in your diet. Be sure to follow the directions carefully, because continuing constipation can lead to more serious problems.
If you have been using this medicine regularly for several weeks or longer, do not change your dose or suddenly stop using it without checking with your doctor. Your doctor may want you to gradually reduce the amount you are using before stopping it completely. This may help prevent worsening of your condition and reduce the possibility of withdrawal symptoms, such as abdominal or stomach cramps, anxiety, fever, nausea, runny nose, sweating, tremors, or trouble with sleeping.
Using this medicine while you are pregnant may cause serious unwanted effects in your newborn baby. Tell your doctor right away if you think you are pregnant or if you plan to become pregnant while using this medicine.
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:
Get emergency help immediately if any of the following symptoms of overdose 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: Oxecta side effects (in more detail)
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Pilules de Vichy may be available in the countries listed below.
Sodium Picosulfate is reported as an ingredient of Pilules de Vichy in the following countries:
International Drug Name Search
Phardine may be available in the countries listed below.
Cimetidine hydrochloride (a derivative of Cimetidine) is reported as an ingredient of Phardine in the following countries:
International Drug Name Search
Injecting insulin (and other solutions as determined by your doctor) into a preselected site of the body.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Novofine. 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 Novofine. However, no specific interactions with Novofine are known at this time.
Ask your health care provider if Novofine 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 Novofine 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 Novofine.
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:
Redness, swelling, or itching at injection sites.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).
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.
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center or emergency room immediately.
Store the needles at room temperature, between 59 and 86 degrees F (15 and 30 degrees C), in the original package. Store away from heat, moisture, and light. Keep Novofine and needles out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Novofine. 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.
