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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 Device issue? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Device issue have been filed in association with ATROPINE (Hepaticol Drops 5008). This represents 0.3% of all adverse event reports for ATROPINE.

8
Reports of Device issue with ATROPINE
0.3%
of all ATROPINE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Device issue From ATROPINE?

Of the 8 reports.

Is Device issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ATROPINE. However, 8 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 Device issue?

ADALIMUMAB (17,630) SOMATROPIN (5,131) PEGFILGRASTIM (5,071) ETANERCEPT (4,143) INSULIN GLARGINE (3,175) EXENATIDE (2,862) LEVONORGESTREL (2,623) CARBIDOPA\LEVODOPA (2,574) GOLIMUMAB (1,827) USTEKINUMAB (1,716)

Which ATROPINE Alternatives Have Lower Device 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 Device issue Reports All Drugs Causing Device issue ATROPINE Demographics