The most commonly reported side effects of technetium tc-99m mertiatide kit include radioisotope scan abnormal, renal scan abnormal, and syncope, based on 110 FDA adverse event reports from 2004 to 2025. 8.2% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for technetium tc-99m mertiatide kit.
These are voluntary reports and do not establish that technetium tc-99m mertiatide kit caused these reactions.
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Other drugs that appear in adverse event reports alongside technetium tc-99m mertiatide 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.
34.5% of technetium tc-99m mertiatide kit adverse event reports involve female patients and 36.4% involve male patients. The largest age group is adult at 49%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking technetium tc-99m mertiatide kit when the adverse event was reported.
Technetium Tc-99m Mertiatide Kit is sold under the brand name Technetium Tc99m Mertiatide Kit.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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