Does GUANIDINE Cause Product administration error? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product administration error have been filed in association with GUANIDINE. This represents 6.2% of all adverse event reports for GUANIDINE.
5
Reports of Product administration error with GUANIDINE
6.2%
of all GUANIDINE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product administration error From GUANIDINE?
Of the 5 reports, 5 (100.0%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUANIDINE. However, 5 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)
Product dose omission issue (75)
Off label use (74)
Drug abuse (72)
Intentional product misuse (72)
Overdose (72)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)