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Toprec Side Effects

Report Toprec Side Effects

If you experienced any harmful or unwanted effects of Toprec, please share your experience. This could help to raise awareness about Toprec side effects, identify uknown risks and inform health professionals and patients taking Toprec.

Examples: headache, dizziness


Toprec Side Effects reported to FDA

The following Toprec reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
The FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.


The appearance of Toprec on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has identified a causal relationship between the drug and the listed risk.

Abdominal Pain, Colitis, Diarrhoea Haemorrhagic
on Apr 24, 2006 Female from , 40 years of age, was diagnosed with and was treated with Toprec. Directly after, patient experienced the unwanted or unexpected Toprec side effects: abdominal pain, colitis, diarrhoea haemorrhagic. Toprec dosage: Dose: 4 Df Daily.
Associated medications used:
  • Nasacort
  • Birodogyl (Dose: 6 Df Daily)
  • Efferalgan Codeine (Dose: 6 Df Daily)
  • Vogalene
  • Vogalene
Patient was hospitalized.

Record and Track Your Side Effects

It is very important to keep track of all side effects and discuss them with your doctor. If you think you may have a medical emergency, call your doctor or 911 immediately.

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Most drugs have a large list of nonsevere or mild adverse effects which do not rule out continued usage. These effects depend on individual sensitivity, and can include nausea, dizziness, diarrhea, malaise, vomiting, headache, dermatitis, dry mouth, etc. Check commonly reported side effects . These can be considered a form of pseudo-allergic reaction, as not all users experience these effects; many users experience none at all.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

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Safety Alerts, Active Ingredients, Usage Information

More About Toprec

Side Effects reported to FDA: 1

Toprec safety alerts: No

Reported hospitalizations: 1

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