Does GUANIDINE Cause Product dose omission issue? 75 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 75 reports of Product dose omission issue have been filed in association with GUANIDINE. This represents 92.6% of all adverse event reports for GUANIDINE.
75
Reports of Product dose omission issue with GUANIDINE
92.6%
of all GUANIDINE reports
32
Deaths
73
Hospitalizations
How Dangerous Is Product dose omission issue From GUANIDINE?
Of the 75 reports, 32 (42.7%) resulted in death, 73 (97.3%) required hospitalization, and 30 (40.0%) 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 GUANIDINE. However, 75 reports have been filed with the FAERS database.
What Other Side Effects Does GUANIDINE Cause?
Abdominal discomfort (76)
Arthropathy (76)
Lower respiratory tract infection (76)
Pulmonary pain (76)
Rash (76)
Off label use (74)
Drug abuse (72)
Intentional product misuse (72)
Overdose (72)
Knee arthroplasty (58)
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)