Does SCOPOLAMINE Cause Wrong technique in product usage process? 157 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 157 reports of Wrong technique in product usage process have been filed in association with SCOPOLAMINE (Scopolamine). This represents 5.7% of all adverse event reports for SCOPOLAMINE.
157
Reports of Wrong technique in product usage process with SCOPOLAMINE
5.7%
of all SCOPOLAMINE reports
3
Deaths
4
Hospitalizations
How Dangerous Is Wrong technique in product usage process From SCOPOLAMINE?
Of the 157 reports, 3 (1.9%) resulted in death, 4 (2.5%) required hospitalization, and 1 (0.6%) were considered life-threatening.
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 SCOPOLAMINE. However, 157 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 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 SCOPOLAMINE Alternatives Have Lower Wrong technique in product usage process Risk?
SCOPOLAMINE vs SCOPOLAMINE HYDROBROMIDE
SCOPOLAMINE vs SEBELIPASE ALFA
SCOPOLAMINE vs SECNIDAZOLE
SCOPOLAMINE vs SECUKINUMAB
SCOPOLAMINE vs SELADELPAR LYSINE