Does SCOPOLAMINE Cause Incorrect product administration duration? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Incorrect product administration duration have been filed in association with SCOPOLAMINE (Scopolamine). This represents 0.4% of all adverse event reports for SCOPOLAMINE.
11
Reports of Incorrect product administration duration with SCOPOLAMINE
0.4%
of all SCOPOLAMINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product administration duration From SCOPOLAMINE?
Of the 11 reports.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SCOPOLAMINE. However, 11 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which SCOPOLAMINE Alternatives Have Lower Incorrect product administration duration Risk?
SCOPOLAMINE vs SCOPOLAMINE HYDROBROMIDE
SCOPOLAMINE vs SEBELIPASE ALFA
SCOPOLAMINE vs SECNIDAZOLE
SCOPOLAMINE vs SECUKINUMAB
SCOPOLAMINE vs SELADELPAR LYSINE