Does BEROTRALSTAT Cause Product dose omission issue? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Product dose omission issue have been filed in association with BEROTRALSTAT (Orladeyo). This represents 2.7% of all adverse event reports for BEROTRALSTAT.
15
Reports of Product dose omission issue with BEROTRALSTAT
2.7%
of all BEROTRALSTAT reports
0
Deaths
7
Hospitalizations
How Dangerous Is Product dose omission issue From BEROTRALSTAT?
Of the 15 reports, 7 (46.7%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BEROTRALSTAT. However, 15 reports have been filed with the FAERS database.
What Other Side Effects Does BEROTRALSTAT Cause?
Hereditary angioedema (124)
Diarrhoea (45)
Nausea (45)
Abdominal pain (33)
Gastrointestinal disorder (32)
Condition aggravated (31)
Headache (31)
Vomiting (28)
Fatigue (26)
Abdominal pain upper (25)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which BEROTRALSTAT Alternatives Have Lower Product dose omission issue Risk?
BEROTRALSTAT vs BESIFLOXACIN
BEROTRALSTAT vs BETA CAROTENE
BEROTRALSTAT vs BETA GLUCAN
BEROTRALSTAT vs BETAHISTINE
BEROTRALSTAT vs BETAINE