Index of reports
> Disability (1)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Zanaflex (Tizanidine) disability. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Zanaflex side effects in female
Reported by a consumer/non-health professional from United States on 2012-05-23
Patient: female, weighing 72.6 kg (159.6 pounds)
Reactions: Migraine, Nerve Injury, Intervertebral Disc Protrusion, Hypersensitivity, Drug Ineffective, Gastric Disorder, Intervertebral Disc Disorder, Intervertebral Disc Injury, Spinal Cord Disorder
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Oxycodone HCL
Dosage: unk
Effexor XR
Dosage: unk
Administration route: Oral
Start date: 2009-01-01
Fexmid
Dosage: unk
Indication: Muscle Relaxant Therapy
Zanaflex
Dosage: unk
Indication: Muscle Disorder
Effexor XR
Dosage: 300 mg, daily
Administration route: Oral
Indication: Depression
Start date: 2002-01-01
Other drugs received by patient: Ascorbic Acid
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