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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 ATROPINE Cause Product use issue? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product use issue have been filed in association with ATROPINE (Hepaticol Drops 5008). This represents 0.5% of all adverse event reports for ATROPINE.

14
Reports of Product use issue with ATROPINE
0.5%
of all ATROPINE reports
0
Deaths
7
Hospitalizations

How Dangerous Is Product use issue From ATROPINE?

Of the 14 reports, 7 (50.0%) required hospitalization, and 1 (7.1%) were considered life-threatening.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ATROPINE. However, 14 reports have been filed with the FAERS database.

What Other Side Effects Does ATROPINE Cause?

Drug ineffective (572) Off label use (289) Toxicity to various agents (231) Macular degeneration (221) Hypotension (216) Nausea (167) Pain (166) Bradycardia (150) Constipation (146) Pyrexia (141)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which ATROPINE Alternatives Have Lower Product use issue Risk?

ATROPINE vs ATROPINE\ATROPINE ATROPINE vs ATROPINE\DIPHENOXYLATE ATROPINE vs AUBAGIO ATROPINE vs AUGMENTIN ATROPINE vs AUTOLOGOUS CULTURED CHONDROCYTES

Related Pages

ATROPINE Full Profile All Product use issue Reports All Drugs Causing Product use issue ATROPINE Demographics