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Idrofos Side Effects and Adverse Effects reported to US Food and Drug Administration (FDA)

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Bone Pain, Movement Disorder (6602863-8)
on Jan 27, 2010 Female from UNITED STATES , 64 years of age, weighting 119.0 lb, was diagnosed with
  • bone density decreased
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.

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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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