Does LEVALBUTEROL Cause Device delivery system issue? 459 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 459 reports of Device delivery system issue have been filed in association with LEVALBUTEROL (Levalbuterol tartrate HFA inhalation). This represents 31.8% of all adverse event reports for LEVALBUTEROL.
459
Reports of Device delivery system issue with LEVALBUTEROL
31.8%
of all LEVALBUTEROL reports
0
Deaths
7
Hospitalizations
How Dangerous Is Device delivery system issue From LEVALBUTEROL?
Of the 459 reports, 7 (1.5%) required hospitalization, and 1 (0.2%) were considered life-threatening.
Is Device delivery system issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVALBUTEROL. However, 459 reports have been filed with the FAERS database.
What Other Side Effects Does LEVALBUTEROL Cause?
Drug dose omission by device (395)
No adverse event (393)
Dyspnoea (224)
Drug ineffective (181)
Asthma (105)
Off label use (97)
Cough (70)
Device issue (68)
Incorrect dose administered by device (59)
Product use in unapproved indication (56)
What Other Drugs Cause Device delivery system issue?
ALBUTEROL (9,509)
SOMATROPIN (1,848)
EXENATIDE (1,533)
BUDESONIDE\FORMOTEROL (1,260)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (1,181)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (523)
MOMETASONE FUROATE\OLOPATADINE (347)
ABATACEPT (342)
PEGFILGRASTIM (323)
ALBUTEROL\BUDESONIDE (244)
Which LEVALBUTEROL Alternatives Have Lower Device delivery system issue Risk?
LEVALBUTEROL vs LEVAMISOLE
LEVALBUTEROL vs LEVAQUIN
LEVALBUTEROL vs LEVEMIR
LEVALBUTEROL vs LEVETIRACETAM
LEVALBUTEROL vs LEVOBUNOLOL