Does TIMOLOL Cause Recalled product administered? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Recalled product administered have been filed in association with TIMOLOL (Timoptic). This represents 0.3% of all adverse event reports for TIMOLOL.
22
Reports of Recalled product administered with TIMOLOL
0.3%
of all TIMOLOL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Recalled product administered From TIMOLOL?
Of the 22 reports.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIMOLOL. However, 22 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 Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which TIMOLOL Alternatives Have Lower Recalled product administered Risk?
TIMOLOL vs TIMOLOL\TRAVOPROST
TIMOLOL vs TINIDAZOLE
TIMOLOL vs TINZAPARIN
TIMOLOL vs TIOCONAZOLE
TIMOLOL vs TIOPRONIN