Does PHENTERMINE\TOPIRAMATE Cause Product administration interrupted? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product administration interrupted have been filed in association with PHENTERMINE\TOPIRAMATE. This represents 0.2% of all adverse event reports for PHENTERMINE\TOPIRAMATE.
11
Reports of Product administration interrupted with PHENTERMINE\TOPIRAMATE
0.2%
of all PHENTERMINE\TOPIRAMATE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product administration interrupted From PHENTERMINE\TOPIRAMATE?
Of the 11 reports, 1 (9.1%) 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 PHENTERMINE\TOPIRAMATE. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does PHENTERMINE\TOPIRAMATE Cause?
Headache (333)
Paraesthesia (309)
Insomnia (274)
Dry mouth (264)
Weight increased (250)
Dizziness (245)
Feeling abnormal (210)
Fatigue (194)
Inappropriate schedule of product administration (194)
Constipation (188)
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 PHENTERMINE\TOPIRAMATE Alternatives Have Lower Product administration interrupted Risk?
PHENTERMINE\TOPIRAMATE vs PHENTOLAMINE
PHENTERMINE\TOPIRAMATE vs PHENYLEPHRINE
PHENTERMINE\TOPIRAMATE vs PHENYLEPHRINE\PHENYLEPHRINE
PHENTERMINE\TOPIRAMATE vs PHENYLPROPANOLAMINE
PHENTERMINE\TOPIRAMATE vs PHENYTOIN