Does ROPIVACAINE Cause Product administration error? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product administration error have been filed in association with ROPIVACAINE (Ropivacaine Hydrochloride). This represents 0.4% of all adverse event reports for ROPIVACAINE.
12
Reports of Product administration error with ROPIVACAINE
0.4%
of all ROPIVACAINE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product administration error From ROPIVACAINE?
Of the 12 reports, 3 (25.0%) required hospitalization, and 1 (8.3%) 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 ROPIVACAINE. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does ROPIVACAINE Cause?
Vomiting (483)
Dyspnoea (458)
Drug hypersensitivity (448)
Oedema (446)
Pneumonia (445)
Asthma (430)
Wheezing (418)
Drug ineffective (262)
Pain (187)
Hypotension (178)
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 ROPIVACAINE Alternatives Have Lower Product administration error Risk?
ROPIVACAINE vs ROSIGLITAZONE
ROPIVACAINE vs ROSUVASTATIN
ROPIVACAINE vs ROSUVASTATIN\ROSUVASTATIN
ROPIVACAINE vs ROTIGOTINE
ROPIVACAINE vs ROXADUSTAT