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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does CLINDAMYCIN Cause Product dose omission issue? 62 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 62 reports of Product dose omission issue have been filed in association with CLINDAMYCIN (XACIATO). This represents 0.4% of all adverse event reports for CLINDAMYCIN.

62
Reports of Product dose omission issue with CLINDAMYCIN
0.4%
of all CLINDAMYCIN reports
0
Deaths
20
Hospitalizations

How Dangerous Is Product dose omission issue From CLINDAMYCIN?

Of the 62 reports, 20 (32.3%) required hospitalization.

Is Product dose omission issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CLINDAMYCIN. However, 62 reports have been filed with the FAERS database.

What Other Side Effects Does CLINDAMYCIN Cause?

Drug hypersensitivity (3,900) Drug ineffective (1,894) Rash (1,325) Diarrhoea (1,206) Off label use (901) Nausea (803) Pruritus (776) Dyspnoea (607)