Does NORGESTREL Cause Product use in unapproved indication? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Product use in unapproved indication have been filed in association with NORGESTREL (Opill). This represents 4.4% of all adverse event reports for NORGESTREL.
18
Reports of Product use in unapproved indication with NORGESTREL
4.4%
of all NORGESTREL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product use in unapproved indication From NORGESTREL?
Of the 18 reports.
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 NORGESTREL. However, 18 reports have been filed with the FAERS database.
What Other Side Effects Does NORGESTREL Cause?
Heavy menstrual bleeding (85)
Intermenstrual bleeding (57)
Polymenorrhoea (53)
Nausea (32)
Headache (28)
Pregnancy on oral contraceptive (26)
Product dose omission issue (26)
Dysmenorrhoea (21)
Vaginal haemorrhage (18)
Depression (17)
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 NORGESTREL Alternatives Have Lower Product use in unapproved indication Risk?
NORGESTREL vs NORTRIPTYLINE
NORGESTREL vs NORVASC
NORGESTREL vs NORVIR
NORGESTREL vs NOSCAPINE
NORGESTREL vs NOVOLOG