Does SULFAGUANIDINE Cause Product dose omission issue? 61 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 61 reports of Product dose omission issue have been filed in association with SULFAGUANIDINE. This represents 93.9% of all adverse event reports for SULFAGUANIDINE.
61
Reports of Product dose omission issue with SULFAGUANIDINE
93.9%
of all SULFAGUANIDINE reports
21
Deaths
61
Hospitalizations
How Dangerous Is Product dose omission issue From SULFAGUANIDINE?
Of the 61 reports, 21 (34.4%) resulted in death, 61 (100.0%) required hospitalization, and 21 (34.4%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SULFAGUANIDINE. However, 61 reports have been filed with the FAERS database.
What Other Side Effects Does SULFAGUANIDINE Cause?
Abdominal discomfort (63)
Arthropathy (62)
Lower respiratory tract infection (62)
Pulmonary pain (62)
Rash (62)
Off label use (60)
Drug abuse (59)
Intentional product misuse (59)
Overdose (59)
Knee arthroplasty (46)
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)