Oroxadin Side Effects

Report Oroxadin Side Effects

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

Examples: headache, dizziness

Oroxadin Side Effects reported to FDA

The following Oroxadin 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 Oroxadin 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.

Venous Thrombosis, Hypertriglyceridaemia, Hypercholesterolaemia, Hyperglycaemia
on Oct 08, 2012 Male from MX , 65 years of age, weighting 196.2 lb, was diagnosed with and was treated with Oroxadin. Directly after, patient experienced the unwanted or unexpected Oroxadin side effects: venous thrombosis, hypertriglyceridaemia, hypercholesterolaemia, hyperglycaemia. Oroxadin dosage: N/A. Patient was hospitalized.

Myocardial Infarction, Blood Pressure Increased
Patient was taking Oroxadin. Patient felt the following Oroxadin side effects: myocardial infarction, blood pressure increased on Jan 17, 2012 from MEXICO Additional patient health information: Female , 62 years of age, was diagnosed with and. Oroxadin dosage: Unk.
Multiple prescriptions taken: Patient was hospitalized.

Blood Pressure Increased, Myocardial Infarction
Adverse event was reported on Jan 31, 2011 by a Female taking Oroxadin (Dosage: Unk) . Location: MEXICO , 62 years of age, After Oroxadin was administered, patient encountered several Oroxadin side effects: blood pressure increased, myocardial infarction.
Multiple concurrent drugs taken: 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 Oroxadin

Side Effects reported to FDA: 3

Oroxadin safety alerts: No

Reported hospitalizations: 3

Latest Oroxadin clinical trials

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