Does ATROPINE Cause Product administration error? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product administration error have been filed in association with ATROPINE (Hepaticol Drops 5008). This represents 0.4% of all adverse event reports for ATROPINE.
11
Reports of Product administration error with ATROPINE
0.4%
of all ATROPINE reports
1
Deaths
2
Hospitalizations
How Dangerous Is Product administration error From ATROPINE?
Of the 11 reports, 1 (9.1%) resulted in death, 2 (18.2%) required hospitalization, and 6 (54.5%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ATROPINE. However, 11 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which ATROPINE Alternatives Have Lower Product administration error Risk?
ATROPINE vs ATROPINE\ATROPINE
ATROPINE vs ATROPINE\DIPHENOXYLATE
ATROPINE vs AUBAGIO
ATROPINE vs AUGMENTIN
ATROPINE vs AUTOLOGOUS CULTURED CHONDROCYTES