Temerit Side Effects

If You had Temerit side effect, You are not alone. Other patients reported side effects.

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Temerit adverse events reported to FDA.

Have You Experienced unusual Temerit symptoms? PatientsVille.com collects and analyzes Temerit side effect and adverse reports submitted by Temerit users, such as .

Summary

FDA Adverse Reports: 2. View All

Temerit FDA safety alerts: No

Reported hospitalizations: 5

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Often additional risks of using a medication, such as Temerit, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Temerit users, Learn more about unwanted side effects & find ways to reduce them. Browse Temerit Adverse Reports reported to FDA and participate in Temerit discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Temerit. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

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Temerit Adverse Effect Reports (FDA)

5720833-9 | Anaemia, Blood Creatinine Increased, Blood Urea Increased, Haemoglobin Decreased, Overdose, Renal Failure Acute, Transaminases Increased
on Apr 22, 2008 Female patient from FRANCE , 58 years of age, was diagnosed with hyperuricaemia and was treated with Temerit (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia, blood creatinine increased, blood urea increased, haemoglobin decreased, overdose, renal failure acute, transaminases increased. Temerit dosage: . During the same period patient was treated with ARIMIDEX (View Arimidex Review and Arimidex Label ), ESIDRIX (25 Mg, Bid) (View Esidrix Review and Esidrix Label ), BURINEX (1 Mg, Tid) (View Burinex Review and Burinex Label ), COZAAR (50 Mg, Qd) (View Cozaar Review and Cozaar Label ), COLCHIMAX /FRA/ (View Colchimax /fra/ Review and Colchimax /fra/ Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ). Patient was hospitalized.

5691806-X | Anaemia, Blood Creatinine Increased, Blood Urea Increased, Haemoglobin Decreased, Overdose, Renal Failure Acute, Transaminases Increased
Patient was taking Temerit (View Usage). Patient had the following side effects: anaemia, blood creatinine increased, blood urea increased, haemoglobin decreased, overdose, renal failure acute, transaminases increased on Mar 25, 2008 from FRANCE Additional patient health information: Female patient , 58 years of age, was diagnosed with hyperuricaemia and. Temerit dosage: . During the same period patient was treated with ARIMIDEX (View Arimidex Review and Arimidex Label ), ESIDRIX (25 Mg, Bid) (View Esidrix Review and Esidrix Label ), BURINEX (1 Mg, Tid) (View Burinex Review and Burinex Label ), COZAAR (50 Mg, Qd) (View Cozaar Review and Cozaar Label ), COLCHIMAX /FRA/ (View Colchimax /fra/ Review and Colchimax /fra/ Label ), ZYLORIC (View Zyloric Review and Zyloric Label ). Patient was hospitalized.

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Temerit Questions, Answers, Feedback and Comments

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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Temerit risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Temerit quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Temerit use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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TEMERIT Side Effects

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Temerit adverse events reported to FDA.

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Temerit Adverse Effect Reports (FDA)

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Temerit Reactions

Anaemia
Blood Creatinine Increased
Blood Urea Increased
Haemoglobin Decreased
Overdose
Renal Failure Acute
Transaminases Increased

TEMERIT Side Effects

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Common Temerit Side Effects

Detailed Reporting will help others get complete information and find alternative treatments to avoid or reduce side effects associated with it.

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Temerit adverse events reported to FDA.

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Search By Drug Names, Symptoms or a Health Condition

Temerit Adverse Effect Reports (FDA)

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Temerit Reactions