The most commonly reported side effects of technetium tc-99m medronate kit include off label use, urticaria, and radioisotope uptake increased, based on 42 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for technetium tc-99m medronate kit.
These are voluntary reports and do not establish that technetium tc-99m medronate kit caused these reactions.
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Other drugs that appear in adverse event reports alongside technetium tc-99m medronate kit. 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.
57.1% of technetium tc-99m medronate kit adverse event reports involve female patients and 35.7% involve male patients. The largest age group is adult at 64%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking technetium tc-99m medronate kit when the adverse event was reported.
Technetium Tc-99m Medronate Kit is sold under the brand name Technetium Tc 99m Mpi Mdp.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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