Does ATROPINE Cause Wrong product administered? 19 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Wrong product administered have been filed in association with ATROPINE (Hepaticol Drops 5008). This represents 0.7% of all adverse event reports for ATROPINE.
19
Reports of Wrong product administered with ATROPINE
0.7%
of all ATROPINE reports
0
Deaths
6
Hospitalizations
How Dangerous Is Wrong product administered From ATROPINE?
Of the 19 reports, 6 (31.6%) required hospitalization, and 6 (31.6%) were considered life-threatening.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ATROPINE. However, 19 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 product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which ATROPINE Alternatives Have Lower Wrong product administered Risk?
ATROPINE vs ATROPINE\ATROPINE
ATROPINE vs ATROPINE\DIPHENOXYLATE
ATROPINE vs AUBAGIO
ATROPINE vs AUGMENTIN
ATROPINE vs AUTOLOGOUS CULTURED CHONDROCYTES