Does ALISKIREN HEMIFUMARATE Cause Wrong technique in product usage process? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Wrong technique in product usage process have been filed in association with ALISKIREN HEMIFUMARATE (Aliskiren). This represents 1.8% of all adverse event reports for ALISKIREN HEMIFUMARATE.
9
Reports of Wrong technique in product usage process with ALISKIREN HEMIFUMARATE
1.8%
of all ALISKIREN HEMIFUMARATE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ALISKIREN HEMIFUMARATE?
Of the 9 reports.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALISKIREN HEMIFUMARATE. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does ALISKIREN HEMIFUMARATE Cause?
Nausea (227)
Fall (214)
Cerebrovascular accident (196)
Anxiety (195)
Fatigue (186)
Confusional state (185)
Muscular weakness (184)
Hemiparesis (181)
Hemiplegia (181)
Muscle spasticity (181)
What Other Drugs Cause Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which ALISKIREN HEMIFUMARATE Alternatives Have Lower Wrong technique in product usage process Risk?
ALISKIREN HEMIFUMARATE vs ALISKIREN\HYDROCHLOROTHIAZIDE
ALISKIREN HEMIFUMARATE vs ALIZAPRIDE
ALISKIREN HEMIFUMARATE vs ALLANTOIN
ALISKIREN HEMIFUMARATE vs ALLEGRA
ALISKIREN HEMIFUMARATE vs ALLEGRA 24 HOUR