Does UNSPECIFIED INGREDIENT Cause Mobility decreased? 179 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 179 reports of Mobility decreased have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.7% of all adverse event reports for UNSPECIFIED INGREDIENT.
179
Reports of Mobility decreased with UNSPECIFIED INGREDIENT
0.7%
of all UNSPECIFIED INGREDIENT reports
84
Deaths
122
Hospitalizations
How Dangerous Is Mobility decreased From UNSPECIFIED INGREDIENT?
Of the 179 reports, 84 (46.9%) resulted in death, 122 (68.2%) required hospitalization, and 74 (41.3%) were considered life-threatening.
Is Mobility decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 179 reports have been filed with the FAERS database.
What Other Side Effects Does UNSPECIFIED INGREDIENT Cause?
Death (2,090)
Off label use (1,306)
Drug ineffective (1,227)
Completed suicide (1,190)
Nausea (1,041)
Fatigue (1,020)
Dyspnoea (934)
Pneumonia (903)
Asthenia (894)
Vomiting (877)
What Other Drugs Cause Mobility decreased?
ADALIMUMAB (8,829)
ETANERCEPT (8,321)
METHOTREXATE (5,936)
ABATACEPT (4,519)
TOCILIZUMAB (4,403)
LEFLUNOMIDE (4,354)
HYDROXYCHLOROQUINE (4,105)
RITUXIMAB (4,067)
INFLIXIMAB (3,784)
TOFACITINIB (3,734)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Mobility decreased Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN