Does MORNIFLUMATE Cause Device malfunction? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Device malfunction have been filed in association with MORNIFLUMATE. This represents 5.9% of all adverse event reports for MORNIFLUMATE.
23
Reports of Device malfunction with MORNIFLUMATE
5.9%
of all MORNIFLUMATE reports
0
Deaths
23
Hospitalizations
How Dangerous Is Device malfunction From MORNIFLUMATE?
Of the 23 reports, 23 (100.0%) required hospitalization, and 14 (60.9%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MORNIFLUMATE. However, 23 reports have been filed with the FAERS database.
What Other Side Effects Does MORNIFLUMATE Cause?
Dyspnoea (242)
Asthma (234)
Obstructive airways disorder (229)
Wheezing (229)
Therapeutic product effect incomplete (227)
Full blood count abnormal (216)
Loss of personal independence in daily activities (201)
Productive cough (159)
Vasculitis (145)
Condition aggravated (144)
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 MORNIFLUMATE Alternatives Have Lower Device malfunction Risk?
MORNIFLUMATE vs MORPHINE
MORNIFLUMATE vs MORPHINE\NALTREXONE
MORNIFLUMATE vs MOSAPRIDE
MORNIFLUMATE vs MOSUNETUZUMAB
MORNIFLUMATE vs MOSUNETUZUMAB-AXGB