Does SCOPOLAMINE Cause Product use in unapproved indication? 163 Reports in FDA Database
Boost Your Natural Energy & Metabolism
Mitolyn — 6 exotic plants to unlock your body's fat-burning power. 90-day guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 163 reports of Product use in unapproved indication have been filed in association with SCOPOLAMINE (Scopolamine). This represents 5.9% of all adverse event reports for SCOPOLAMINE.
163
Reports of Product use in unapproved indication with SCOPOLAMINE
5.9%
of all SCOPOLAMINE reports
4
Deaths
19
Hospitalizations
How Dangerous Is Product use in unapproved indication From SCOPOLAMINE?
Of the 163 reports, 4 (2.5%) resulted in death, 19 (11.7%) required hospitalization, and 3 (1.8%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SCOPOLAMINE. However, 163 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)
Headache (158)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which SCOPOLAMINE Alternatives Have Lower Product use in unapproved indication Risk?
SCOPOLAMINE vs SCOPOLAMINE HYDROBROMIDE
SCOPOLAMINE vs SEBELIPASE ALFA
SCOPOLAMINE vs SECNIDAZOLE
SCOPOLAMINE vs SECUKINUMAB
SCOPOLAMINE vs SELADELPAR LYSINE