Does GRANISETRON Cause Product use in unapproved indication? 103 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 103 reports of Product use in unapproved indication have been filed in association with GRANISETRON (Granisetron Hydrochloride). This represents 4.0% of all adverse event reports for GRANISETRON.
103
Reports of Product use in unapproved indication with GRANISETRON
4.0%
of all GRANISETRON reports
1
Deaths
6
Hospitalizations
How Dangerous Is Product use in unapproved indication From GRANISETRON?
Of the 103 reports, 1 (1.0%) resulted in death, 6 (5.8%) required hospitalization, and 1 (1.0%) 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 GRANISETRON. However, 103 reports have been filed with the FAERS database.
What Other Side Effects Does GRANISETRON Cause?
Nausea (433)
Product adhesion issue (395)
Death (319)
Vomiting (185)
Drug ineffective (177)
Wrong technique in product usage process (172)
Constipation (129)
Inappropriate schedule of drug administration (115)
No adverse event (111)
Diarrhoea (102)
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 GRANISETRON Alternatives Have Lower Product use in unapproved indication Risk?
GRANISETRON vs GRANULOCYTE COLONY-STIMULATING FACTOR NOS
GRANISETRON vs GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR
GRANISETRON vs GRAZOPREVIR
GRANISETRON vs GRISEOFULVIN
GRANISETRON vs GUAIFENESIN