Does REMODULIN Cause Device malfunction? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Device malfunction have been filed in association with REMODULIN. This represents 2.0% of all adverse event reports for REMODULIN.
14
Reports of Device malfunction with REMODULIN
2.0%
of all REMODULIN reports
2
Deaths
13
Hospitalizations
How Dangerous Is Device malfunction From REMODULIN?
Of the 14 reports, 2 (14.3%) resulted in death, 13 (92.9%) required hospitalization.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REMODULIN. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does REMODULIN Cause?
Death (95)
Dyspnoea (79)
Device related infection (64)
Drug dose omission (42)
Nausea (32)
Headache (30)
Diarrhoea (28)
Pulmonary arterial hypertension (28)
Vomiting (28)
Fluid retention (27)
What Other Drugs Cause Device malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which REMODULIN Alternatives Have Lower Device malfunction Risk?
REMODULIN vs REPAGLINIDE
REMODULIN vs REPOTRECTINIB
REMODULIN vs REQUIP
REMODULIN vs RESLIZUMAB
REMODULIN vs RESMETIROM