Does SCOPOLAMINE Cause Wrong patient received product? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Wrong patient received product have been filed in association with SCOPOLAMINE (Scopolamine). This represents 0.6% of all adverse event reports for SCOPOLAMINE.
17
Reports of Wrong patient received product with SCOPOLAMINE
0.6%
of all SCOPOLAMINE reports
17
Deaths
0
Hospitalizations
How Dangerous Is Wrong patient received product From SCOPOLAMINE?
Of the 17 reports, 17 (100.0%) resulted in death.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SCOPOLAMINE. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does SCOPOLAMINE Cause?
Off label use (418)
Nausea (313)
Dizziness (293)
Product adhesion issue (254)
Drug ineffective (231)
Vision blurred (212)
Vomiting (201)
Product quality issue (189)
Mydriasis (180)
Product use in unapproved indication (163)
What Other Drugs Cause Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
Which SCOPOLAMINE Alternatives Have Lower Wrong patient received product Risk?
SCOPOLAMINE vs SCOPOLAMINE HYDROBROMIDE
SCOPOLAMINE vs SEBELIPASE ALFA
SCOPOLAMINE vs SECNIDAZOLE
SCOPOLAMINE vs SECUKINUMAB
SCOPOLAMINE vs SELADELPAR LYSINE