Does INSULIN DETEMIR Cause Product quality issue? 160 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 160 reports of Product quality issue have been filed in association with INSULIN DETEMIR (Levemir). This represents 1.7% of all adverse event reports for INSULIN DETEMIR.
160
Reports of Product quality issue with INSULIN DETEMIR
1.7%
of all INSULIN DETEMIR reports
0
Deaths
25
Hospitalizations
How Dangerous Is Product quality issue From INSULIN DETEMIR?
Of the 160 reports, 25 (15.6%) required hospitalization, and 1 (0.6%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN DETEMIR. However, 160 reports have been filed with the FAERS database.
What Other Side Effects Does INSULIN DETEMIR Cause?
Blood glucose increased (1,975)
Blood glucose decreased (603)
Hypoglycaemia (418)
Foetal exposure during pregnancy (367)
Glycosylated haemoglobin increased (301)
Drug ineffective (298)
Cerebrovascular accident (294)
Dizziness (290)
Malaise (288)
Visual impairment (275)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which INSULIN DETEMIR Alternatives Have Lower Product quality issue Risk?
INSULIN DETEMIR vs INSULIN GLARGINE
INSULIN DETEMIR vs INSULIN GLARGINE-YFGN
INSULIN DETEMIR vs INSULIN GLARGINE\LIXISENATIDE
INSULIN DETEMIR vs INSULIN GLULISINE
INSULIN DETEMIR vs INSULIN HUMAN