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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 POLYVINYL ALCOHOL Cause Recalled product administered? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Recalled product administered have been filed in association with POLYVINYL ALCOHOL (MINIDROPS). This represents 11.0% of all adverse event reports for POLYVINYL ALCOHOL.

8
Reports of Recalled product administered with POLYVINYL ALCOHOL
11.0%
of all POLYVINYL ALCOHOL reports
0
Deaths
2
Hospitalizations

How Dangerous Is Recalled product administered From POLYVINYL ALCOHOL?

Of the 8 reports, 2 (25.0%) required hospitalization.

Is Recalled product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for POLYVINYL ALCOHOL. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does POLYVINYL ALCOHOL Cause?

Vision blurred (12) Eye irritation (9) Recalled product (8) Eye pain (7) Adverse event (5) Eye pruritus (5) Muscle spasticity (5) Pain (5) Visual impairment (5)

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)

Related Pages

POLYVINYL ALCOHOL Full Profile All Recalled product administered Reports All Drugs Causing Recalled product administered POLYVINYL ALCOHOL Demographics