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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 TRAVOPROST Cause Product container issue? 67 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 67 reports of Product container issue have been filed in association with TRAVOPROST (Travoprost Ophthalmic Soluton). This represents 1.0% of all adverse event reports for TRAVOPROST.

67
Reports of Product container issue with TRAVOPROST
1.0%
of all TRAVOPROST reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product container issue From TRAVOPROST?

Of the 67 reports.

Is Product container issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TRAVOPROST. However, 67 reports have been filed with the FAERS database.

What Other Side Effects Does TRAVOPROST Cause?

Treatment failure (2,364) Ocular hyperaemia (478) Drug ineffective (467) Eye irritation (448) Intraocular pressure increased (335) Hypersensitivity (305) Glaucoma (286) Eye pain (284) Visual impairment (264) Vision blurred (180)

What Other Drugs Cause Product container issue?

CYCLOSPORINE (910) MINOXIDIL (556) MOMETASONE FUROATE (450) FORMOTEROL\MOMETASONE FUROATE (375) LIFITEGRAST (244) ALBUTEROL (192) LATANOPROST (158) CARBOXYMETHYLCELLULOSE\GLYCERIN (123) BRIMONIDINE (121) ACETAMINOPHEN (118)

Which TRAVOPROST Alternatives Have Lower Product container issue Risk?

TRAVOPROST vs TRAZODONE TRAVOPROST vs TREANDA TRAVOPROST vs TREMELIMUMAB TRAVOPROST vs TREMELIMUMAB\TREMELIMUMAB-ACTL TRAVOPROST vs TRENBOLONE

Related Pages

TRAVOPROST Full Profile All Product container issue Reports All Drugs Causing Product container issue TRAVOPROST Demographics