The most commonly reported side effects of tiludronate include fall, fall, and dependence, based on 15 FDA adverse event reports from 2005 to 2013.
Percentages show how often each reaction appears relative to total reports for tiludronate.
These are voluntary reports and do not establish that tiludronate caused these reactions.
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Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside tiludronate. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
Also suspected
Taken alongside
Co-occurrence in adverse event reports does not establish a drug interaction. Patients often take multiple medications, and these lists reflect prescribing patterns rather than causal relationships. Consult a healthcare provider about potential drug interactions.
46.7% of tiludronate adverse event reports involve female patients and 46.7% involve male patients. The largest age group is elderly at 89%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking tiludronate when the adverse event was reported.
Tiludronate is sold under the brand name Skelid.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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