Does TERBUTALINE Cause Product administration error? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Product administration error have been filed in association with TERBUTALINE (Terbutaline Sulfate). This represents 1.5% of all adverse event reports for TERBUTALINE.
24
Reports of Product administration error with TERBUTALINE
1.5%
of all TERBUTALINE reports
0
Deaths
24
Hospitalizations
How Dangerous Is Product administration error From TERBUTALINE?
Of the 24 reports, 24 (100.0%) required hospitalization, and 1 (4.2%) 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 TERBUTALINE. However, 24 reports have been filed with the FAERS database.
What Other Side Effects Does TERBUTALINE Cause?
Dyspnoea (404)
Asthma (371)
Wheezing (265)
Loss of personal independence in daily activities (186)
Therapeutic product effect incomplete (168)
Sleep disorder due to a general medical condition (149)
Drug ineffective (148)
Cough (138)
Pneumonia (128)
Full blood count abnormal (103)
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 TERBUTALINE Alternatives Have Lower Product administration error Risk?
TERBUTALINE vs TERCONAZOLE
TERBUTALINE vs TERIFLUNOMIDE
TERBUTALINE vs TERIPARATIDE
TERBUTALINE vs TERIZIDONE
TERBUTALINE vs TERLIPRESSIN