Does LEVALBUTEROL Cause Device issue? 68 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 68 reports of Device issue have been filed in association with LEVALBUTEROL (Levalbuterol tartrate HFA inhalation). This represents 4.7% of all adverse event reports for LEVALBUTEROL.
68
Reports of Device issue with LEVALBUTEROL
4.7%
of all LEVALBUTEROL reports
0
Deaths
5
Hospitalizations
How Dangerous Is Device issue From LEVALBUTEROL?
Of the 68 reports, 5 (7.4%) required hospitalization, and 1 (1.5%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVALBUTEROL. However, 68 reports have been filed with the FAERS database.
What Other Side Effects Does LEVALBUTEROL Cause?
Device delivery system issue (459)
Drug dose omission by device (395)
No adverse event (393)
Dyspnoea (224)
Drug ineffective (181)
Asthma (105)
Off label use (97)
Cough (70)
Incorrect dose administered by device (59)
Product use in unapproved indication (56)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which LEVALBUTEROL Alternatives Have Lower Device issue Risk?
LEVALBUTEROL vs LEVAMISOLE
LEVALBUTEROL vs LEVAQUIN
LEVALBUTEROL vs LEVEMIR
LEVALBUTEROL vs LEVETIRACETAM
LEVALBUTEROL vs LEVOBUNOLOL