Does INSULIN GLARGINE-YFGN Cause Device breakage? 164 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 164 reports of Device breakage have been filed in association with INSULIN GLARGINE-YFGN. This represents 9.1% of all adverse event reports for INSULIN GLARGINE-YFGN.
164
Reports of Device breakage with INSULIN GLARGINE-YFGN
9.1%
of all INSULIN GLARGINE-YFGN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device breakage From INSULIN GLARGINE-YFGN?
Of the 164 reports, 1 (0.6%) required hospitalization.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN GLARGINE-YFGN. However, 164 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 issue (279)
Device delivery system issue (236)
Device defective (215)
Product storage error (212)
Wrong technique in product usage process (181)
Incorrect dose administered (152)
Blood glucose increased (115)
Product dose omission issue (110)
What Other Drugs Cause Device breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
Which INSULIN GLARGINE-YFGN Alternatives Have Lower Device breakage 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