Does SOLRIAMFETOL Cause Product administration interrupted? 40 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Product administration interrupted have been filed in association with SOLRIAMFETOL (SUNOSI). This represents 1.9% of all adverse event reports for SOLRIAMFETOL.
40
Reports of Product administration interrupted with SOLRIAMFETOL
1.9%
of all SOLRIAMFETOL reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product administration interrupted From SOLRIAMFETOL?
Of the 40 reports, 5 (12.5%) required hospitalization.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOLRIAMFETOL. However, 40 reports have been filed with the FAERS database.
What Other Side Effects Does SOLRIAMFETOL Cause?
Drug ineffective (440)
Off label use (186)
Headache (184)
Anxiety (174)
Fatigue (123)
Nausea (95)
Blood pressure increased (82)
Somnolence (82)
Depression (71)
Insomnia (62)
What Other Drugs Cause Product administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
Which SOLRIAMFETOL Alternatives Have Lower Product administration interrupted Risk?
SOLRIAMFETOL vs SOLU-MEDROL
SOLRIAMFETOL vs SOMATREM
SOLRIAMFETOL vs SOMATROPIN
SOLRIAMFETOL vs SONIDEGIB
SOLRIAMFETOL vs SORAFENIB