Does BISOPROLOL\HYDROCHLOROTHIAZIDE Cause Product prescribing error? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product prescribing error have been filed in association with BISOPROLOL\HYDROCHLOROTHIAZIDE. This represents 2.4% of all adverse event reports for BISOPROLOL\HYDROCHLOROTHIAZIDE.
14
Reports of Product prescribing error with BISOPROLOL\HYDROCHLOROTHIAZIDE
2.4%
of all BISOPROLOL\HYDROCHLOROTHIAZIDE reports
0
Deaths
10
Hospitalizations
How Dangerous Is Product prescribing error From BISOPROLOL\HYDROCHLOROTHIAZIDE?
Of the 14 reports, 10 (71.4%) required hospitalization.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BISOPROLOL\HYDROCHLOROTHIAZIDE. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does BISOPROLOL\HYDROCHLOROTHIAZIDE Cause?
Pruritus (82)
Fall (75)
Dizziness (67)
Insomnia (65)
Diarrhoea (56)
Off label use (55)
Asthenia (54)
Vomiting (54)
Erectile dysfunction (53)
Bradycardia (52)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which BISOPROLOL\HYDROCHLOROTHIAZIDE Alternatives Have Lower Product prescribing error Risk?
BISOPROLOL\HYDROCHLOROTHIAZIDE vs BIVALIRUDIN
BISOPROLOL\HYDROCHLOROTHIAZIDE vs BLEOMYCIN
BISOPROLOL\HYDROCHLOROTHIAZIDE vs BLINATUMOMAB
BISOPROLOL\HYDROCHLOROTHIAZIDE vs BLONANSERIN
BISOPROLOL\HYDROCHLOROTHIAZIDE vs --BLOOD-COAGULATION FACTOR VIII FUSION PROTEIN WITH IMMUNOGLOBULIN G1 , ,-BIS WITH IMMUNOGLOBULIN G1