Does RILMENIDINE Cause Product administration error? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product administration error have been filed in association with RILMENIDINE. This represents 1.6% of all adverse event reports for RILMENIDINE.
14
Reports of Product administration error with RILMENIDINE
1.6%
of all RILMENIDINE reports
9
Deaths
9
Hospitalizations
How Dangerous Is Product administration error From RILMENIDINE?
Of the 14 reports, 9 (64.3%) resulted in death, 9 (64.3%) required hospitalization, and 1 (7.1%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RILMENIDINE. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does RILMENIDINE Cause?
Acute kidney injury (214)
Lactic acidosis (121)
Fall (120)
Hyperkalaemia (86)
Hypotension (85)
Hypoglycaemia (59)
Diarrhoea (49)
Bradycardia (45)
Rhabdomyolysis (44)
Drug ineffective (41)
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)
Which RILMENIDINE Alternatives Have Lower Product administration error Risk?
RILMENIDINE vs RILONACEPT
RILMENIDINE vs RILPIVIRINE
RILMENIDINE vs RILUZOLE
RILMENIDINE vs RIMABOTULINUMTOXINB
RILMENIDINE vs RIMEGEPANT