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Robaxin (Methocarbamol) - Side Effect Reports to FDA

 
 



This is an index of side effect / adverse reaction reports (a.k.a. adverse event reports) related to Robaxin (Methocarbamol) and submitted to the FDA during the sample period of about a year. The information is not vetted and should not be considered as verified clinical evidence.

Reports by Event Outcome

All Cases (11)

Reports by Reaction Type

Mental Status Changes (6)Hypokalaemia (6)Polymedication (6)Dysarthria (6)Hypertension (6)Condition Aggravated (4)Headache (2)Medication Error (2)Drug Dispensing Error (2)Drug Hypersensitivity (2)Asthenia (2)Rectal Haemorrhage (1)

Possible Robaxin side effects in 48 year old female

Reported by a consumer/non-health professional from United States on 2012-07-03

Patient: 48 year old female

Reactions: Wrong Drug Administered, Somnolence

Drug(s) suspected as cause:
Fentanyl
    Dosage: 50 mg patch

Robaxin
    Dosage: unk

Percocet
    Dosage: unk

Rimadyl

Lyrica
    Dosage: unk

Cymbalta
    Dosage: unk



Possible Robaxin side effects in female

Reported by a physician from United States on 2012-06-29

Patient: female

Reactions: Drug Hypersensitivity

Drug(s) suspected as cause:
Celebrex
    Dosage: unk

Robaxin
    Dosage: unk

Seroquel
    Dosage: unk

Doxepin HCL
    Dosage: unk

Haloperidol
    Dosage: unk

Abilify
    Dosage: unk

Amitriptyline HCL
    Dosage: unk

Stelazine
    Dosage: unk

Allegra
    Dosage: unk

Mellaril
    Dosage: unk

Thorazine
    Dosage: unk



Possible Robaxin side effects in

Reported by a individual with unspecified qualification from United States on 2012-04-10

Patient:

Reactions: Medication Error, Drug Name Confusion, Rectal Haemorrhage, Chest Pain, Drug Dispensing Error

Drug(s) suspected as cause:
Biaxin
    Dosage: tablet
    Administration route: Oral

Robaxin
    Dosage: tablet
    Administration route: Oral



Possible Robaxin side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-03-15

Patient: female, weighing 89.4 kg (196.7 pounds)

Reactions: Dysarthria, Polymedication, Mental Status Changes, Headache, Hypertension, Asthenia, Hypokalaemia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Lexapro
    Administration route: Oral
    Indication: Post-Traumatic Stress Disorder

Ambien
    Administration route: Oral
    Indication: Insomnia

Lyrica
    Administration route: Oral
    Indication: Fibromyalgia

Clonazepam
    Administration route: Oral
    Indication: Bipolar Disorder

Ibuprofen
    Administration route: Oral
    Indication: Fibromyalgia

Placebo
    Administration route: Oral
    Start date: 2008-11-29
    End date: 2008-12-24

Lexapro
    Administration route: Oral
    Indication: Bipolar Disorder

Robaxin
    Indication: Fibromyalgia

Zestoretic
    Dosage: 20/12.5 daily
    Administration route: Oral
    Indication: Hypertension
    Start date: 2008-12-04

Desvenlafaxine Succinate Monohydrate
    Administration route: Oral
    Indication: Menopausal Symptoms
    Start date: 2008-09-09
    End date: 2008-11-22

Placebo
    Administration route: Oral
    Indication: Menopausal Symptoms
    Start date: 2008-09-09
    End date: 2008-11-22

Loratadine
    Administration route: Oral
    Indication: Seasonal Allergy

Vicodin
    Dosage: 5/500 as needed
    Administration route: Oral
    Indication: Fibromyalgia

Vivelle
    Indication: Hormone Replacement Therapy

Desvenlafaxine Succinate Monohydrate
    Administration route: Oral
    Start date: 2008-11-29
    End date: 2008-12-24

Abilify
    Administration route: Oral
    Indication: Bipolar I Disorder

Fluticasone
    Indication: Seasonal Allergy



Possible Robaxin side effects in female

Reported by a physician from United States on 2012-03-13

Patient: female, weighing 89.4 kg (196.7 pounds)

Reactions: Dysarthria, Polymedication, Mental Status Changes, Condition Aggravated, Hypertension, Hypokalaemia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Abilify
    Dosage: 15 mg, 2x/day
    Administration route: Oral
    Indication: Bipolar I Disorder

Blinded Desvenlafaxine Succinate Monohydrate
    Dosage: blinded therapy daily
    Administration route: Oral
    Start date: 2008-11-29
    End date: 2008-12-24

Lexapro
    Dosage: 20 mg, 1x/day
    Administration route: Oral
    Indication: Post-Traumatic Stress Disorder

Fluticasone
    Dosage: 2 sprays daily route: in
    Indication: Seasonal Allergy

Blinded Placebo
    Dosage: blinded therapy daily
    Administration route: Oral
    Start date: 2008-11-29
    End date: 2008-12-24

Lyrica
    Dosage: 75 mg, 1x/day
    Administration route: Oral
    Indication: Fibromyalgia

Robaxin
    Dosage: 750 mg, 3x/day
    Administration route: Oral
    Indication: Fibromyalgia

Clonazepam
    Dosage: 1 mg, 2x/day
    Administration route: Oral
    Indication: Bipolar Disorder

Vicodin
    Dosage: 5/500 prn
    Administration route: Oral
    Indication: Fibromyalgia

Blinded Placebo
    Dosage: blinded therapy daily
    Administration route: Oral
    Indication: Menopausal Symptoms
    Start date: 2008-09-09
    End date: 2008-11-22

Loratadine
    Dosage: 10 mg, 1x/day
    Administration route: Oral
    Indication: Seasonal Allergy

Robaxin
    Dosage: unknown

Lexapro
    Indication: Bipolar Disorder

Vivelle
    Dosage: 0.1 mg, unk
    Indication: Hormone Replacement Therapy

Ibuprofen
    Dosage: 800 mg, 3x/day
    Administration route: Oral
    Indication: Fibromyalgia

Ambien
    Dosage: 10 mg, 1x/day
    Administration route: Oral
    Indication: Insomnia

Blinded Desvenlafaxine Succinate Monohydrate
    Dosage: blinded therapy daily
    Administration route: Oral
    Indication: Menopausal Symptoms
    Start date: 2008-09-09
    End date: 2008-11-22

Blinded NO Subject Drug
    Dosage: blinded therapy daily
    Administration route: Oral
    Indication: Menopausal Symptoms
    Start date: 2008-09-09
    End date: 2008-11-22

Zestoretic
    Dosage: 20/12.5 daily
    Administration route: Oral
    Indication: Hypertension
    Start date: 2008-12-04

Blinded NO Subject Drug
    Dosage: blinded therapy daily
    Administration route: Oral
    Start date: 2008-11-29
    End date: 2008-12-24



Possible Robaxin side effects in

Reported by a physician from United States on 2012-03-01

Patient:

Reactions: Vomiting, Nausea, Drug Hypersensitivity

Drug(s) suspected as cause:
Voltaren
    Dosage: unk

Flexeril
    Dosage: unk

Benadryl
    Dosage: unk

Pseudoephedrine Hydrochloride
    Dosage: unk

Promethazine Hydrochloride
    Dosage: unk

Acetaminophen
    Dosage: unk

Procardia
    Dosage: unk

Robaxin
    Dosage: unk

Codeine Sulfate
    Dosage: unk

Diphenhydramine Citrate

Ultram
    Dosage: unk



Possible Robaxin side effects in

Reported by a individual with unspecified qualification from United States on 2012-01-25

Patient:

Reactions: Medication Error, Drug Dispensing Error

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Relafen
    Dosage: tablet oral
    Administration route: Oral

Robaxin
    Dosage: tablet oral



Possible Robaxin side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2011-12-23

Patient: female, weighing 89.4 kg (196.7 pounds)

Reactions: Dysarthria, Polymedication, Mental Status Changes, Headache, Hypertension, Asthenia, Hypokalaemia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Desvenlafaxine Succinate Monohydrate
    Administration route: Oral
    Start date: 2008-09-09
    End date: 2008-11-22

Lexapro
    Indication: Ill-Defined Disorder

Fluticasone Furoate
    Indication: Ill-Defined Disorder

Loratadine
    Indication: Ill-Defined Disorder

Vicodin
    Dosage: 5/500 as needed
    Indication: Ill-Defined Disorder

Ambien
    Administration route: Oral
    Indication: Ill-Defined Disorder

Lyrica
    Indication: Ill-Defined Disorder

Placebo
    Administration route: Oral
    Indication: Menopausal Symptoms
    Start date: 2008-09-09
    End date: 2008-11-22

Abilify
    Indication: Ill-Defined Disorder

Vivelle
    Indication: Ill-Defined Disorder

Zestoretic
    Dosage: 20/12.5 daily
    Indication: Ill-Defined Disorder

Desvenlafaxine Succinate Monohydrate
    Administration route: Oral
    Indication: Menopausal Symptoms
    Start date: 2008-11-29
    End date: 2008-12-24

Robaxin
    Indication: Ill-Defined Disorder

Ibuprofen
    Indication: Ill-Defined Disorder

Placebo
    Administration route: Oral
    Start date: 2008-11-29
    End date: 2008-12-24

Clonazepam
    Indication: Ill-Defined Disorder



Possible Robaxin side effects in female

Reported by a physician from United States on 2011-12-20

Patient: female, weighing 89.4 kg (196.7 pounds)

Reactions: Dysarthria, Polymedication, Mental Status Changes, Condition Aggravated, Hypertension, Hypokalaemia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Blinded Desvenlafaxine Succinate Monohydrate
    Dosage: blinded therapy daily
    Administration route: Oral
    Indication: Menopausal Symptoms
    Start date: 2008-09-09
    End date: 2008-11-22

Blinded NO Subject Drug
    Dosage: blinded therapy daily
    Administration route: Oral
    Indication: Menopausal Symptoms
    Start date: 2008-09-09
    End date: 2008-11-22

Blinded Desvenlafaxine Succinate Monohydrate
    Dosage: blinded therapy daily
    Administration route: Oral
    Start date: 2008-11-29
    End date: 2008-12-24

Ibuprofen
    Dosage: 800 mg, 3x/day

Robaxin
    Dosage: unknown

Blinded Placebo
    Dosage: blinded therapy daily
    Administration route: Oral
    Start date: 2008-11-29
    End date: 2008-12-24

Clonazepam
    Dosage: 1 mg, 2x/day

Lexapro
    Dosage: 20 mg, 1x/day

Vicodin
    Dosage: 5/500 prn

Ambien
    Dosage: 10 mg, 1x/day
    Administration route: Oral

Blinded Placebo
    Dosage: blinded therapy daily
    Administration route: Oral
    Indication: Menopausal Symptoms
    Start date: 2008-09-09
    End date: 2008-11-22

Blinded NO Subject Drug
    Dosage: blinded therapy daily
    Administration route: Oral
    Start date: 2008-11-29
    End date: 2008-12-24

Zestoretic
    Dosage: 20/12.5 daily

Lyrica
    Dosage: 75 mg, 1x/day

Fluticasone Furoate
    Dosage: 2 sprays daily

Abilify
    Dosage: 15 mg, 2x/day

Vivelle
    Dosage: 0.1 mg, unk

Loratadine
    Dosage: 10 mg, 1x/day

Robaxin
    Dosage: 750 mg, 3x/day
    Administration route: Oral



Possible Robaxin side effects in female

Reported by a physician from United States on 2011-12-19

Patient: female, weighing 89.4 kg (196.7 pounds)

Reactions: Dysarthria, Polymedication, Mental Status Changes, Condition Aggravated, Hypertension, Hypokalaemia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Abilify
    Dosage: 15 mg, 2x/day

Blinded Placebo
    Dosage: blinded therapy daily
    Administration route: Oral
    Indication: Menopausal Symptoms
    Start date: 2008-09-09
    End date: 2008-11-22

Fluticasone Propionate
    Dosage: 2 sprays daily

Vicodin
    Dosage: 5/500 prn

Ambien
    Dosage: 10 mg, 1x/day
    Administration route: Oral

Blinded Desvenlafaxine Succinate Monohydrate
    Dosage: blinded therapy daily
    Administration route: Oral
    Indication: Menopausal Symptoms
    Start date: 2008-09-09
    End date: 2008-11-22

Lyrica
    Dosage: 75 mg, 1x/day

Vivelle
    Dosage: 0.1 mg, unk

Blinded Desvenlafaxine Succinate Monohydrate
    Dosage: blinded therapy daily
    Administration route: Oral
    Start date: 2008-11-29
    End date: 2008-12-24

Blinded NO Subject Drug
    Dosage: blinded therapy daily
    Administration route: Oral
    Start date: 2008-11-29
    End date: 2008-12-24

Robaxin
    Dosage: 750 mg, 3x/day
    Administration route: Oral

Blinded Placebo
    Dosage: blinded therapy daily
    Administration route: Oral
    Start date: 2008-11-29
    End date: 2008-12-24

Ibuprofen
    Dosage: 800 mg, 3x/day

Clonazepam
    Dosage: 1 mg, 2x/day

Loratadine
    Dosage: 10 mg, 1x/day

Zestoretic
    Dosage: 20/12.5 daily

Blinded NO Subject Drug
    Dosage: blinded therapy daily
    Administration route: Oral
    Indication: Menopausal Symptoms
    Start date: 2008-09-09
    End date: 2008-11-22

Lexapro
    Dosage: 20 mg, 1x/day



Possible Robaxin side effects in female

Reported by a physician from United States on 2011-12-16

Patient: female, weighing 89.4 kg (196.7 pounds)

Reactions: Dysarthria, Polymedication, Condition Aggravated, Mental Status Changes, Hypertension, Hypokalaemia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Lexapro
    Dosage: 20 mg, 1x/day

Vivelle
    Dosage: 0.1 mg, unk

Blinded NO Subject Drug
    Dosage: blinded therapy daily
    Administration route: Oral
    Indication: Menopausal Symptoms
    Start date: 2008-09-09
    End date: 2008-11-22

Blinded Desvenlafaxine Succinate Monohydrate
    Dosage: blinded therapy daily
    Administration route: Oral
    Indication: Menopausal Symptoms
    Start date: 2008-09-09
    End date: 2008-11-22

Blinded NO Subject Drug
    Dosage: blinded therapy daily
    Administration route: Oral
    Start date: 2008-11-29
    End date: 2008-12-24

Blinded Placebo
    Dosage: blinded therapy daily
    Administration route: Oral
    Start date: 2008-11-29
    End date: 2008-12-24

Loratadine
    Dosage: 10 mg, 1x/day

Robaxin
    Dosage: unknown

Abilify
    Dosage: 15 mg, 2x/day

Ibuprofen
    Dosage: 800 mg, 3x/day

Clonazepam
    Dosage: 1 mg, 2x/day

Fluticasone
    Dosage: 2 sprays daily

Zestoretic
    Dosage: 20/12.5 daily

Ambien
    Dosage: 10 mg, 1x/day
    Administration route: Oral

Lyrica
    Dosage: 75 mg, 1x/day

Robaxin
    Dosage: 750 mg, 3x/day
    Administration route: Oral

Blinded Placebo
    Dosage: blinded therapy daily
    Administration route: Oral
    Indication: Menopausal Symptoms
    Start date: 2008-09-09
    End date: 2008-11-22

Blinded Desvenlafaxine Succinate Monohydrate
    Dosage: blinded therapy daily
    Administration route: Oral
    Start date: 2008-11-29
    End date: 2008-12-24

Vicodin
    Dosage: 5/500 prn

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