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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 Wrong technique in product usage process? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Wrong technique in product usage process have been filed in association with ATROPINE (Hepaticol Drops 5008). This represents 0.2% of all adverse event reports for ATROPINE.

6
Reports of Wrong technique in product usage process with ATROPINE
0.2%
of all ATROPINE reports
1
Deaths
2
Hospitalizations

How Dangerous Is Wrong technique in product usage process From ATROPINE?

Of the 6 reports, 1 (16.7%) resulted in death, 2 (33.3%) required hospitalization.

Is Wrong technique in product usage process Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ATROPINE. However, 6 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 Wrong technique in product usage process?

EVOLOCUMAB (21,664) ALBUTEROL (17,114) ADALIMUMAB (11,766) PEGFILGRASTIM (10,217) ETANERCEPT (9,835) ERENUMAB-AOOE (9,359) SACUBITRIL\VALSARTAN (8,022) LEUPROLIDE (5,062) FENTANYL (2,812) SEMAGLUTIDE (2,538)

Which ATROPINE Alternatives Have Lower Wrong technique in product usage process 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 Wrong technique in product usage process Reports All Drugs Causing Wrong technique in product usage process ATROPINE Demographics