DEVICE for Relapsing-remitting multiple sclerosis: Side Effects & Safety Data

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There are 63 adverse event reports in the FDA FAERS database where DEVICE was used for Relapsing-remitting multiple sclerosis.

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