Does INSULIN GLARGINE-YFGN Cause Device issue? 279 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 279 reports of Device issue have been filed in association with INSULIN GLARGINE-YFGN. This represents 15.5% of all adverse event reports for INSULIN GLARGINE-YFGN.
279
Reports of Device issue with INSULIN GLARGINE-YFGN
15.5%
of all INSULIN GLARGINE-YFGN reports
1
Deaths
0
Hospitalizations
How Dangerous Is Device issue From INSULIN GLARGINE-YFGN?
Of the 279 reports, 1 (0.4%) resulted in death.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN GLARGINE-YFGN. However, 279 reports have been filed with the FAERS database.
What Other Side Effects Does INSULIN GLARGINE-YFGN Cause?
Device mechanical issue (853)
Product quality issue (426)
Device delivery system issue (236)
Device defective (215)
Product storage error (212)
Wrong technique in product usage process (181)
Device breakage (164)
Incorrect dose administered (152)
Blood glucose increased (115)
Product dose omission issue (110)
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 INSULIN GLARGINE-YFGN Alternatives Have Lower Device issue Risk?
INSULIN GLARGINE-YFGN vs INSULIN GLARGINE\LIXISENATIDE
INSULIN GLARGINE-YFGN vs INSULIN GLULISINE
INSULIN GLARGINE-YFGN vs INSULIN HUMAN
INSULIN GLARGINE-YFGN vs INSULIN LISPRO
INSULIN GLARGINE-YFGN vs INSULIN LISPRO-AABC