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Zanaflex (Tizanidine) - Disability - Suspected Cause - Side Effect Reports

 
 



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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