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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 power source issue: Which Medications Cause It? (2,343 Reports Across 28 Drugs)

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Device power source issue has been reported as an adverse event with 28 different drugs in the FDA's FAERS database, with 2,343 total reports. 24 of these reports resulted in death.The drugs most commonly associated with Device power source issue are SOMATROPIN, PEGFILGRASTIM, and TREPROSTINIL.

2,343
Total Reports
28
Drugs Involved
24
Deaths
197
Hospitalizations
35.1 yrs
Average Patient Age
48.8% / 51.2%
Female / Male

Which Drugs Cause Device power source issue Most Often?

Drug Reports % of Drug Reports Deaths Hosp. Life-Threat.
SOMATROPIN 1,219 1.8% 1 3 1
PEGFILGRASTIM 486 0.6% 1 0 0
TREPROSTINIL 299 0.3% 4 83 2
CARBIDOPA\LEVODOPA 62 0.1% 4 27 0
ETANERCEPT 54 0.0% 0 4 0
BACLOFEN 50 0.2% 3 27 9
GLYCOPYRROLATE 39 0.8% 1 2 0
DEVICE 20 0.2% 0 5 0
FOSCARBIDOPA\FOSLEVODOPA 14 0.4% 0 9 0
INTERFERON BETA-1B 13 0.1% 0 0 0
LECITHIN\POLOXAMER 407 11 6.3% 0 1 0
HYDROMORPHONE 10 0.0% 0 2 2
BUPIVACAINE 9 0.1% 0 2 1
CLONIDINE 9 0.1% 0 3 1
MACITENTAN 8 0.0% 0 4 0
NITRIC 8 0.3% 0 0 0
APIXABAN 7 0.0% 0 1 0
ADALIMUMAB 6 0.0% 0 2 0
AMIKACIN 6 0.1% 3 6 0
GABAPENTIN 6 0.0% 0 2 0

View all 28 drugs →

Top 3 Drugs Associated With Device power source issue

1,219 reports
486 reports
299 reports

Related Side Effects

Drug ineffective (1,049,718) Off label use (762,782) Death (660,423) Fatigue (599,248) Nausea (562,301) Diarrhoea (491,550) Pain (471,975) Headache (460,069) Dyspnoea (409,496) Dizziness (352,922)