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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

DEVICE for Type 2 diabetes mellitus: Side Effects & Safety Data

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There are 3,625 adverse event reports in the FDA FAERS database where DEVICE was used for Type 2 diabetes mellitus.

Most Reported Side Effects for DEVICE

Side Effect Reports % Deaths Hosp.
Blood glucose increased 2,114 16.6% 5 161
Device issue 1,417 11.1% 7 85
Product use issue 1,076 8.4% 5 94
Intercepted product preparation error 1,033 8.1% 1 1
Wrong technique in product usage process 935 7.3% 1 25
Device leakage 795 6.2% 0 9
Injection site pain 751 5.9% 1 40
Syringe issue 634 5.0% 0 1
Product quality issue 567 4.5% 2 9
Drug ineffective 488 3.8% 22 94
Dyspnoea 482 3.8% 28 135
Cough 458 3.6% 15 58
Off label use 443 3.5% 22 63
Visual impairment 437 3.4% 5 31
Device use issue 396 3.1% 0 24

Other Indications for DEVICE

Product used for unknown indication (942) Prostate cancer (852) Diabetes mellitus (660) Type 1 diabetes mellitus (495) Dyslipidaemia (172) Keratoconus (139) Multiple sclerosis (104) Precocious puberty (103) Dermatitis atopic (89) Pulmonary arterial hypertension (63)

Other Drugs Used for Type 2 diabetes mellitus

INSULIN GLARGINE (41,731) METFORMIN (25,080) DULAGLUTIDE (24,742) SEMAGLUTIDE (17,910) INSULIN LISPRO (16,871) EXENATIDE (16,403) TIRZEPATIDE (14,571) EMPAGLIFLOZIN (12,176) CANAGLIFLOZIN (10,795) PIOGLITAZONE (8,418)

Related Pages

DEVICE Full Profile All Type 2 diabetes mellitus Drugs DEVICE Demographics DEVICE Timeline