Does ROZANOLIXIZUMAB-NOLI Cause Device issue? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Device issue have been filed in association with ROZANOLIXIZUMAB-NOLI. This represents 2.3% of all adverse event reports for ROZANOLIXIZUMAB-NOLI.
8
Reports of Device issue with ROZANOLIXIZUMAB-NOLI
2.3%
of all ROZANOLIXIZUMAB-NOLI reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device issue From ROZANOLIXIZUMAB-NOLI?
Of the 8 reports, 2 (25.0%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROZANOLIXIZUMAB-NOLI. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does ROZANOLIXIZUMAB-NOLI Cause?
Myasthenia gravis (57)
Drug ineffective (51)
Headache (48)
Nausea (29)
Diarrhoea (27)
Fatigue (27)
Dyspnoea (19)
Hospitalisation (19)
Vomiting (17)
Therapy interrupted (15)
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 ROZANOLIXIZUMAB-NOLI Alternatives Have Lower Device issue Risk?
ROZANOLIXIZUMAB-NOLI vs RUBIDIUM RB-82
ROZANOLIXIZUMAB-NOLI vs RUCAPARIB
ROZANOLIXIZUMAB-NOLI vs RUCAPARIB CAMSYLATE
ROZANOLIXIZUMAB-NOLI vs RUFINAMIDE
ROZANOLIXIZUMAB-NOLI vs RUPATADINE