Idrofos Side Effects

Report Idrofos Side Effects

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

Examples: headache, dizziness

The most commonly reported Idrofos side effects are:
Jaw Pain (1 reports)

If you have experienced a side effect listed above, you can check a box to report it.

To view a complete list of submitted side effects, please follow the link Idrofos side effects . You can also compare Idrofos side effects or view FDA reports.

Idrofos Side Effects reported to FDA

The following Idrofos 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 Idrofos 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.

Bone Pain, Movement Disorder
on Jan 27, 2010 Female from UNITED STATES , 64 years of age, weighting 119.0 lb, was diagnosed with and was treated with Idrofos (ibandronate) -sun Pharma. Boneva Nda# 21-455. Directly after, patient experienced the unwanted or unexpected Idrofos side effects: bone pain, movement disorder. Idrofos (ibandronate) -sun Pharma. Boneva Nda# 21-455 dosage: Monthly, Oral. 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 Idrofos

Side Effects reported to FDA: 1

Idrofos safety alerts: No

Reported hospitalizations: 1

Latest Idrofos clinical trials

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