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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 TIMOLOL Cause Product quality issue? 106 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 106 reports of Product quality issue have been filed in association with TIMOLOL (Timoptic). This represents 1.4% of all adverse event reports for TIMOLOL.

106
Reports of Product quality issue with TIMOLOL
1.4%
of all TIMOLOL reports
0
Deaths
3
Hospitalizations

How Dangerous Is Product quality issue From TIMOLOL?

Of the 106 reports, 3 (2.8%) required hospitalization.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TIMOLOL. However, 106 reports have been filed with the FAERS database.

What Other Side Effects Does TIMOLOL Cause?

Treatment failure (3,690) Drug ineffective (684) Hypersensitivity (526) Eye irritation (421) Ocular hyperaemia (262) Intraocular pressure increased (231) Eye pain (229) Eye pruritus (228) Vision blurred (212) Dizziness (201)

What Other Drugs Cause Product quality issue?

ETONOGESTREL (4,651) ALBUTEROL (4,466) TIOTROPIUM (3,821) MOMETASONE FUROATE (3,406) LIDOCAINE (3,126) FLUTICASONE\SALMETEROL (2,986) FORMOTEROL\MOMETASONE FUROATE (2,458) FENTANYL (2,450) NICOTINE (1,987) EXENATIDE (1,839)

Which TIMOLOL Alternatives Have Lower Product quality issue Risk?

TIMOLOL vs TIMOLOL\TRAVOPROST TIMOLOL vs TINIDAZOLE TIMOLOL vs TINZAPARIN TIMOLOL vs TIOCONAZOLE TIMOLOL vs TIOPRONIN

Related Pages

TIMOLOL Full Profile All Product quality issue Reports All Drugs Causing Product quality issue TIMOLOL Demographics