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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 BIMATOPROST Cause Product packaging quantity issue? 177 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 177 reports of Product packaging quantity issue have been filed in association with BIMATOPROST (Bimatoprost). This represents 1.2% of all adverse event reports for BIMATOPROST.

177
Reports of Product packaging quantity issue with BIMATOPROST
1.2%
of all BIMATOPROST reports
0
Deaths
2
Hospitalizations

How Dangerous Is Product packaging quantity issue From BIMATOPROST?

Of the 177 reports, 2 (1.1%) required hospitalization.

Is Product packaging quantity issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BIMATOPROST. However, 177 reports have been filed with the FAERS database.

What Other Side Effects Does BIMATOPROST Cause?

Drug ineffective (3,067) Treatment failure (3,062) Ocular hyperaemia (1,447) Eye irritation (1,212) Madarosis (847) Eye pruritus (779) Hypersensitivity (719) Erythema of eyelid (585) Wrong technique in product usage process (512) Eye pain (506)

What Other Drugs Cause Product packaging quantity issue?

LEUPROLIDE (523) ALBUTEROL (431) BUDESONIDE\FORMOTEROL (301) FENTANYL (286) BUPRENORPHINE (225) CYCLOSPORINE (206) ESTRADIOL (201) RIVAROXABAN (174) EXENATIDE (154) LIFITEGRAST (153)

Which BIMATOPROST Alternatives Have Lower Product packaging quantity issue Risk?

BIMATOPROST vs BIMATOPROST\TIMOLOL BIMATOPROST vs BIMEKIZUMAB BIMATOPROST vs BIMEKIZUMAB-BKZX BIMATOPROST vs BINIMETINIB BIMATOPROST vs BIOFLAVONOIDS

Related Pages

BIMATOPROST Full Profile All Product packaging quantity issue Reports All Drugs Causing Product packaging quantity issue BIMATOPROST Demographics