SOMA Side Effects

6907736-9 | Convulsion
on Feb 23, 2010 Female patient from UNITED STATES , 62 years of age, was diagnosed with neck pain and was treated with Soma (View Usage). Patient experienced the following unwanted or unexpected effects: convulsion. Soma dosage: 1000 Mg (250 Mg, 1 In 6 Hr), Oral. During the same period patient was treated with TOPIRAMATE (View Topiramate Review and Topiramate Label ), FLEXERIL (View Flexeril Review and Flexeril Label ), LANTUS (View Lantus Review and Lantus Label ), JANUMET (SITAGLIPTIN, METFORMIN) (View Janumet (sitagliptin, Metformin) Review and Janumet (sitagliptin, Metformin) Label ), AVANDIA (View Avandia Review and Avandia Label ), CELEBREX (View Celebrex Review and Celebrex Label ), AMBIEN (View Ambien Review and Ambien Label ), VOLTAREN (View Voltaren Review and Voltaren Label ). Patient was hospitalized.

6907735-7 | Amnesia, Contusion, Dizziness, Fall, Grand Mal Convulsion, Periorbital Haematoma
Patient was taking Soma (View Usage). Patient had the following side effects: amnesia, contusion, dizziness (What is dizziness?), fall (What is fall?), grand mal convulsion, periorbital haematoma on Nov 23, 2009 from UNITED STATES Additional patient health information: Male patient , 36 years of age, weighting 260.0 lb, was diagnosed with back pain (What is back pain?) and. Soma dosage: Q1d (350 Mg, 4 In 1 D), Oral. During the same period patient was treated with TRAMADOL HCL (360 Mg (60 Mg, 1 In 4 Hr), Oral) (View Tramadol Hcl Review and Tramadol Hcl Label ), CYMBALTA (DULOXETINE HC1) (View Cymbalta (duloxetine Hc1) Review and Cymbalta (duloxetine Hc1) Label ). Patient was hospitalized.

6907732-1 | Withdrawal Syndrome
Adverse event was reported on Oct 22, 2009 by a Male patient taking Soma (View Usage) (Dosage: 1400 Mg (350 Mg, 4 In 1 As Required), Oral) was diagnosed with back pain (What is back pain?) and. Location: UNITED STATES , 52 years of age, weighting 185.0 lb, After Soma was administered, patient had the following side effects: withdrawal syndrome. Patient was hospitalized.

6907731-X | Convulsion
on Sep 08, 2009 Female patient from UNITED STATES , 40 years of age, was treated with Soma (View Usage). Patient experienced the following unwanted or unexpected effects: convulsion. Soma dosage: Daily. During the same period patient was treated with TRANXENE (Daily) (View Tranxene Review and Tranxene Label ).


6771220-6 | Accidental Overdose, Unresponsive To Stimuli
on Jun 01, 2010 Female patient from UNITED STATES , 48 years of age, was diagnosed with muscle spasms, pain (What is pain?) and was treated with Soma (View Usage). Patient had the following side effects: accidental overdose, unresponsive to stimuli. Soma dosage: 350 Mg, Q6 Hours Prn), Oral. During the same period patient was treated with OXYCONTIN (30 Mg (15 Mg, 2 In 1 D),oral) (View Oxycontin Review and Oxycontin Label ), CYMBALTA (DULOXETINE HC1) (View Cymbalta (duloxetine Hc1) Review and Cymbalta (duloxetine Hc1) Label ), LYRICA (View Lyrica Review and Lyrica Label ). Patient was hospitalized.

6671449-1 | Gait Disturbance, Musculoskeletal Stiffness
Patient was taking Soma (View Usage). After Soma was administered, patient had the following side effects: gait disturbance, musculoskeletal stiffness on Apr 06, 2010 from UNITED STATES Additional patient health information: Female patient , 68 years of age, weighting 161.0 lb, was diagnosed with sleep disorder (What is sleep disorder?) and. Soma dosage: 125 Mg. (1/2) 1 Eye. 125 Mg. (1/2) 2nd. Eye..

6670923-1 | Skin Discolouration
Adverse event was reported on Apr 06, 2010 by a Male patient taking Soma (View Usage) (Dosage: 1 Pill As Needed Po) was diagnosed with back pain (What is back pain?) and. Location: UNITED STATES , weighting 220.0 lb, Patient experienced the following unwanted or unexpected effects: skin discolouration. Patient was hospitalized.

6656840-1 | Activities Of Daily Living Impaired, Disturbance In Attention, Family Stress, Fibromyalgia, Impaired Work Ability, Influenza Like Illness, Insomnia, Ligament Pain, Social Problem
on Mar 15, 2010 Female patient from UNITED STATES , 71 years of age, was treated with Soma (View Usage). Patient had the following side effects: activities of daily living impaired, disturbance in attention, family stress, fibromyalgia, impaired work ability, influenza like illness, insomnia, ligament pain, social problem. Soma dosage: . During the same period patient was treated with XANAX (1 Mg) (View Xanax Review and Xanax Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), MORPHINE SULFATE INJ (View Morphine Sulfate Inj Review and Morphine Sulfate Inj Label ), OXYCODONE HCL (3 Mg) (View Oxycodone Hcl Review and Oxycodone Hcl Label ), ROXICODONE (View Roxicodone Review and Roxicodone Label ), OPANA (View Opana Review and Opana Label ).

6656741-9 | Balance Disorder, Brain Injury, Condition Aggravated, Convulsion, Dermal Cyst, Dry Skin, Feeling Abnormal, Insomnia, Memory Impairment
on Mar 10, 2010 Male patient from UNITED STATES , 30 years of age, weighting 190.1 lb, was diagnosed with myalgia, convulsion and was treated with Soma (View Usage). After Soma was administered, patient had the following side effects: balance disorder, brain injury, condition aggravated, convulsion, dermal cyst, dry skin, feeling abnormal, insomnia, memory impairment. Soma dosage: Oral. During the same period patient was treated with CHANTIX (0.5 Mg (0.5 Mg, 1 In 1 D), Oral; 1 Mg (0.5 Mg, 2 In 1 D0, Oral; 2 Mg (1 Mg, 2 In 1 D), Oral) (View Chantix Review and Chantix Label ), KLONOPIN (2 Mg (1 Mg, 2 In 1 D), Oral) (View Klonopin Review and Klonopin Label ), KEPPRA ((750 Mg)) (View Keppra Review and Keppra Label ), VALIUM (20 Mg (10 Mg, 2 In 1 D)) (View Valium Review and Valium Label ), LYRICA (View Lyrica Review and Lyrica Label ), DILANTIN (View Dilantin Review and Dilantin Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), XANAX (View Xanax Review and Xanax Label ). Patient was hospitalized.

6552428-1 | Blood Albumin Decreased, Blood Calcium Decreased, Blood Glucose Increased, Blood Sodium Decreased, Cardiovascular Disorder, Circulatory Collapse, Completed Suicide, Hypotension, Infusion Site Haemorrhage
Patient was taking Soma (View Usage). Patient experienced the following unwanted or unexpected effects: blood albumin decreased, blood calcium decreased, blood glucose increased, blood sodium decreased, cardiovascular disorder, circulatory collapse, completed suicide, hypotension, infusion site haemorrhage on Jan 07, 2010 from UNITED STATES Additional patient health information: Female patient , 54 years of age, . Soma dosage: (250 Mg), Oral. During the same period patient was treated with PLAVIX (Oral) (View Plavix Review and Plavix Label ), METOPROLOL SUCCINATE EXTENDED RELEASE ((25 Mg), Oral) (View Metoprolol Succinate Extended Release Review and Metoprolol Succinate Extended Release Label ), VALIUM ((1 Tablet), Oral) (View Valium Review and Valium Label ).

6552427-X | Anxiety, Asthma, Bladder Disorder, Psychotic Disorder, Urinary Retention
Adverse event was reported on Jan 13, 2010 by a Female patient taking Soma (View Usage) (Dosage: ) . Location: UNITED STATES , 36 years of age, Patient had the following side effects: anxiety (What is anxiety?), asthma (What is asthma?), bladder disorder, psychotic disorder (What is psychotic disorder?), urinary retention. During the same period patient was treated with CHANTIX (View Chantix Review and Chantix Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), IPRATROPIUM BROMIDE (View Ipratropium Bromide Review and Ipratropium Bromide Label ), SPIRIVA (View Spiriva Review and Spiriva Label ), SEROQUEL (View Seroquel Review and Seroquel Label ). Patient was hospitalized.

6429515-1 | Blood Calcium Decreased, Blood Glucose Decreased, Blood Magnesium Decreased, Blood Potassium Decreased, Discomfort, Electrocardiogram Abnormal, Facial Pain, Fatigue, Joint Swelling
on Oct 26, 2009 Female patient from UNITED STATES , 46 years of age, weighting 230.0 lb, was diagnosed with pain (What is pain?), osteoarthritis (What is osteoarthritis?) and was treated with Soma (View Usage). After Soma was administered, patient had the following side effects: blood calcium decreased, blood glucose decreased, blood magnesium decreased, blood potassium decreased, discomfort, electrocardiogram abnormal, facial pain, fatigue, joint swelling. Soma dosage: (350 Mg,once),oral ; (350 Mg,once),oral. During the same period patient was treated with VOLTAREN ((2 Gm),topical) (View Voltaren Review and Voltaren Label ), METHADONE (METHADONE) (Qd (80 Mg,1 In 1 D),oral) (View Methadone (methadone) Review and Methadone (methadone) Label ), VITAMINS (View Vitamins Review and Vitamins Label ), ROXICODONE (OXYCODONE HC1) (View Roxicodone (oxycodone Hc1) Review and Roxicodone (oxycodone Hc1) Label ), CYMBALTA (DULOXETINE HC1) (View Cymbalta (duloxetine Hc1) Review and Cymbalta (duloxetine Hc1) Label ), WELLBUTRIN (BUPROPION HC1) (View Wellbutrin (bupropion Hc1) Review and Wellbutrin (bupropion Hc1) Label ), PROTONIX (View Protonix Review and Protonix Label ). Patient was hospitalized.

6408867-2 | Brain Injury, Liver Injury, Lung Disorder, Renal Disorder
on Oct 09, 2009 Male patient from UNITED STATES , 30 years of age, was treated with Soma (View Usage). Patient experienced the following unwanted or unexpected effects: brain injury, liver injury, lung disorder, renal disorder. Soma dosage: . During the same period patient was treated with EXTRA STRENGTH TYLENOL (View Extra Strength Tylenol Review and Extra Strength Tylenol Label ). Patient was hospitalized.

6369371-3 | Intentional Overdose, Respiratory Arrest
Patient was taking Soma (View Usage). Patient had the following side effects: intentional overdose, respiratory arrest on Sep 10, 2009 from UNITED STATES Additional patient health information: Female patient , 18 years of age, . Soma dosage: . Patient was hospitalized.

6310804-6 | Fall, International Normalised Ratio Increased, Prothrombin Time Prolonged, Subdural Haematoma
Adverse event was reported on Aug 05, 2009 by a Female patient taking Soma (View Usage) (Dosage: 2800 Mg (700 Mg,4 In 1 D), Oral) was diagnosed with back pain (What is back pain?), breast cancer (What is breast cancer?) and. Location: UNITED STATES , 69 years of age, weighting 178.0 lb, After Soma was administered, patient had the following side effects: fall (What is fall?), international normalised ratio increased, prothrombin time prolonged, subdural haematoma. During the same period patient was treated with EXEMESTANE (25 Mg (25 Mg, 1 In 1 D),oral) (View Exemestane Review and Exemestane Label ), TYLENOL WITH CODEINE NO 4 (PARACETAMOL, CODEINE PHOSPHATE) (View Tylenol With Codeine No 4 (paracetamol, Codeine Phosphate) Review and Tylenol With Codeine No 4 (paracetamol, Codeine Phosphate) Label ), PROTONIX (View Protonix Review and Protonix Label ), GLUCOPHAGE (View Glucophage Review and Glucophage Label ), CARDIZEM CD (View Cardizem Cd Review and Cardizem Cd Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), RESTORIL (View Restoril Review and Restoril Label ). Patient was hospitalized.

6298674-6 | Dyspnoea, Memory Impairment, Refusal Of Treatment By Patient, Rheumatoid Arthritis, Somnolence, Urinary Incontinence, Urinary Retention, Vomiting
on Jul 29, 2009 Female patient from UNITED STATES , 47 years of age, weighting 200.0 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Soma (View Usage). Patient experienced the following unwanted or unexpected effects: dyspnoea, memory impairment, refusal of treatment by patient, rheumatoid arthritis (What is rheumatoid arthritis?), somnolence, urinary incontinence (What is urinary incontinence?), urinary retention, vomiting. Soma dosage: 2-3 Tablets Per Day (350 Mg, As Required), Oral. During the same period patient was treated with AMRIX (30 Mg (30 Mg, 1 In 1 D), Oral) (View Amrix Review and Amrix Label ), AMITRIPTYLINE HYDROCHLORIDE (50 Mg (50 Mg, At Bedtime)) (View Amitriptyline Hydrochloride Review and Amitriptyline Hydrochloride Label ), LORCET (HYDROCODONE BITATRATE, ACETAMINOPHEN) (22.5 Mg (7.5 Mg, 3 In 1 D)) (View Lorcet (hydrocodone Bitatrate, Acetaminophen) Review and Lorcet (hydrocodone Bitatrate, Acetaminophen) Label ), XANAX (Twice Or Three Times Daily (0.5 Mg)) (View Xanax Review and Xanax Label ), LYRICA (200 Mg (100 Mg, 3 In 1 D)) (View Lyrica Review and Lyrica Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), FLUTICASONE PROPIONATE (View Fluticasone Propionate Review and Fluticasone Propionate Label ).

6264227-9 | Overdose
on Feb 09, 2009 Female patient from UNITED STATES , 24 years of age, was diagnosed with pain (What is pain?) and was treated with Soma (View Usage). Patient had the following side effects: overdose. Soma dosage: 1050 Mg (350 Mg, 3 In 1 D), Oral. During the same period patient was treated with LORCET HD (View Lorcet-hd Review and Lorcet-hd Label ), XANAX (View Xanax Review and Xanax Label ).

6264225-5 | Overdose
Patient was taking Soma (View Usage). After Soma was administered, patient had the following side effects: overdose on Jan 28, 2009 from UNITED STATES Additional patient health information: Female patient , 39 years of age, was diagnosed with back pain (What is back pain?) and. Soma dosage: Oral. During the same period patient was treated with VALIUM (View Valium Review and Valium Label ).

6264214-0 | Loss Of Consciousness
Adverse event was reported on Aug 25, 2008 by a Female patient taking Soma (View Usage) (Dosage: Oral) . Location: UNITED STATES , 35 years of age, Patient experienced the following unwanted or unexpected effects: loss of consciousness. During the same period patient was treated with TYLENOL W/ CODEINE NO. 3 ((every 4 Hours)) (View Tylenol W/ Codeine No. 3 Review and Tylenol W/ Codeine No. 3 Label ), DARVOCET N 100 (View Darvocet-n 100 Review and Darvocet-n 100 Label ).

6243980-4 | Dyspnoea, Memory Impairment, Somnolence, Urinary Incontinence, Urinary Retention, Vomiting
on Jun 16, 2009 Female patient from UNITED STATES , 47 years of age, weighting 200.0 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Soma (View Usage). Patient had the following side effects: dyspnoea, memory impairment, somnolence, urinary incontinence (What is urinary incontinence?), urinary retention, vomiting. Soma dosage: 350 Mg (350 Mg, 1 In 1 As Required). During the same period patient was treated with AMRIX (CYCLOBENZAPRINE HCL) (15 Mg (15 Mg, 1 In 1 D), Oral) (View Amrix (cyclobenzaprine Hcl) Review and Amrix (cyclobenzaprine Hcl) Label ), AMITRIPTYLINE HYDROCHLORIDE (50 Mg (50 Mg, 1 In 1 D),) (View Amitriptyline Hydrochloride Review and Amitriptyline Hydrochloride Label ), LORCET HD (10 Mg (10 Mg, 1 In 1 As Required)) (View Lorcet-hd Review and Lorcet-hd Label ), XANAX (2 Mg (1 Mg, 2 In 1 D)) (View Xanax Review and Xanax Label ), LYRICA (100 Mg (100 Mg, 1 In 1 D)) (View Lyrica Review and Lyrica Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ).

6162961-2 | Chest Pain, Muscular Weakness, Rash, Vomiting
on Apr 07, 2009 Female patient from UNITED STATES , 49 years of age, weighting 75.00 lb, was diagnosed with pain (What is pain?), multiple sclerosis (What is multiple sclerosis?) and was treated with Soma (View Usage). After Soma was administered, patient had the following side effects: chest pain (What is chest pain?), muscular weakness, rash (What is rash?), vomiting. Soma dosage: Oral. During the same period patient was treated with REBIF (9.4286 Mcg (22 Mcg, 3 In 1 Wka), Subcutaneous) (View Rebif Review and Rebif Label ), CELEXA (View Celexa Review and Celexa Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ), CELLCEPT (View Cellcept Review and Cellcept Label ), BACLOFEN (View Baclofen Review and Baclofen Label ), FOSAMAX (View Fosamax Review and Fosamax Label ), DITROPAN (View Ditropan Review and Ditropan Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ). Patient was hospitalized.

6153085-9 | Asthenia, Chest Pain, Rash, Vomiting
Patient was taking Soma (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, chest pain (What is chest pain?), rash (What is rash?), vomiting on Apr 01, 2009 from UNITED STATES Additional patient health information: Female patient , 49 years of age, weighting 75.00 lb, was diagnosed with pain (What is pain?), multiple sclerosis (What is multiple sclerosis?) and. Soma dosage: 1 Dose, Oral. During the same period patient was treated with REBIF (9.4286 Mcg (22 Mcg, 3 In 1 Wk), Subcutaneous) (View Rebif Review and Rebif Label ), CELEXA (View Celexa Review and Celexa Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ), CELLCEPT/MYCOPENOLATE MOFETIL) (View Cellcept/mycopenolate Mofetil) Review and Cellcept/mycopenolate Mofetil) Label ), BACLOFEN (View Baclofen Review and Baclofen Label ), FOSAMAX (View Fosamax Review and Fosamax Label ), DITROPAN (View Ditropan Review and Ditropan Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ). Patient was hospitalized.

6149197-6 | Overdose, Somnolence
Adverse event was reported on Apr 06, 2009 by a Female patient taking Soma (View Usage) (Dosage: 3 A Day Im) was diagnosed with inflammation, pain (What is pain?) and. Location: UNITED STATES , 46 years of age, weighting 138.0 lb, Patient had the following side effects: overdose, somnolence. Patient was hospitalized.

6140468-6 | Blood Potassium Decreased, Blood Sodium Decreased, Convulsion
on Mar 18, 2009 Female patient from UNITED STATES , 44 years of age, weighting 128.0 lb, was diagnosed with back pain (What is back pain?) and was treated with Soma (View Usage). After Soma was administered, patient had the following side effects: blood potassium decreased, blood sodium decreased, convulsion. Soma dosage: 1000 Mg (250 Mg, 4 In 1 D), Oral. During the same period patient was treated with SOMA (CARISOPRODOL, USP) (CARISOPRODOL) (View Soma (carisoprodol, Usp) (carisoprodol) Review and Soma (carisoprodol, Usp) (carisoprodol) Label ), PROZAC (View Prozac Review and Prozac Label ). Patient was hospitalized.

6051137-5 | Angina Pectoris, Dyspnoea, Tachycardia
on Jan 21, 2009 Female patient from UNITED STATES , 61 years of age, weighting 154.0 lb, was diagnosed with temporomandibular joint syndrome and was treated with Soma (View Usage). Patient experienced the following unwanted or unexpected effects: angina pectoris, dyspnoea, tachycardia. Soma dosage: 1 Tablet As Needed Buccal.

6046427-6 | Product Quality Issue
Patient was taking Soma (View Usage). Patient had the following side effects: product quality issue on Jan 21, 2009 from UNITED STATES Additional patient health information: Male patient , 61 years of age, weighting 125.0 lb, was diagnosed with pain (What is pain?) and. Soma dosage: 2 Qid Po.

6015272-X | Swelling
Adverse event was reported on Dec 19, 2008 by a Female patient taking Soma (View Usage) (Dosage: 250mg 4 Times Daily Po) was diagnosed with inflammation, whiplash injury and. Location: UNITED STATES , 59 years of age, weighting 152.0 lb, After Soma was administered, patient had the following side effects: swelling.

5980181-9 | Abnormal Behaviour, Amnesia, Balance Disorder, Contusion, Fall, Imprisonment, Insomnia, Intentional Self-injury
on Dec 02, 2008 Female patient from UNITED STATES , 29 years of age, weighting 120.0 lb, was diagnosed with back pain (What is back pain?), insomnia, myalgia and was treated with Soma (View Usage). Patient experienced the following unwanted or unexpected effects: abnormal behaviour, amnesia, balance disorder, contusion, fall (What is fall?), imprisonment, insomnia, intentional self-injury. Soma dosage: 250mg 3 Po.

5955888-X | Ejaculation Failure
on Nov 05, 2008 Male patient from UNITED STATES , 36 years of age, weighting 189.6 lb, was diagnosed with muscle spasms, neuropathy peripheral and was treated with Soma (View Usage). Patient had the following side effects: ejaculation failure. Soma dosage: 1050 Mg (350 Mg, 3 In 1 D), Oral. During the same period patient was treated with GABAPENTIN (1200 Mg (400 Mg, 3 In1 D), Oral) (View Gabapentin Review and Gabapentin Label ).

5943889-7 | Depression, Pain, Refusal Of Treatment By Patient, Suicide Attempt
Patient was taking Soma (View Usage). After Soma was administered, patient had the following side effects: depression (What is depression?), pain (What is pain?), refusal of treatment by patient, suicide attempt on Oct 20, 2008 from UNITED STATES Additional patient health information: Male patient , 51 years of age, weighting 188.1 lb, was diagnosed with hepatitis c (What is hepatitis c?) and. Soma dosage: 1050 Mg (350 Mg, 3 In 1 D), Oral. During the same period patient was treated with PEGASYS (25/7143 Mcg (180 Mcg, 1 In 1 Wk), Subcutaneous) (View Pegasys Review and Pegasys Label ), COPEGUS (600 Mg (600 Mg, Am), Oral) (View Copegus Review and Copegus Label ), LUNESTA (3 Mg (3 Mg, 1 In 1 D)) (View Lunesta Review and Lunesta Label ), TRAZODONE HCL (100 Mg (100 Mg, 1 In 1 D)) (View Trazodone Hcl Review and Trazodone Hcl Label ), XANAX (View Xanax Review and Xanax Label ), FLEXERIL (View Flexeril Review and Flexeril Label ), WELLBUTRIN XL (View Wellbutrin Xl Review and Wellbutrin Xl Label ), PHENERGAN HCL (View Phenergan Hcl Review and Phenergan Hcl Label ).

5933981-5 | Accident At Work, Alcohol Problem, Artificial Crown Procedure, Bruxism, Dental Caries, Depression, Dry Mouth
Adverse event was reported on Oct 13, 2008 by a Male patient taking Soma (View Usage) (Dosage: See Image) was diagnosed with analgesia, muscle spasms, neck pain and. Location: UNITED STATES , 31 years of age, weighting 189.0 lb, Patient experienced the following unwanted or unexpected effects: accident at work, alcohol problem, artificial crown procedure, bruxism, dental caries, depression (What is depression?), dry mouth. During the same period patient was treated with ACTIQ (800 Mcg (800 Mcg, 1 In 1 D), Bu; 1600mcg (800 Mcg, 2 In 1 D), Bu; 2400mcg (800 Mcg, 3 In 1 D), Bu) (View Actiq Review and Actiq Label ). Patient was hospitalized and became disabled.

5931799-0 | Amnesia, Cognitive Disorder, Loss Of Consciousness, Pain
on Oct 06, 2008 Male patient from PAKISTAN , 23 years of age, was treated with Soma (View Usage). Patient had the following side effects: amnesia, cognitive disorder, loss of consciousness, pain (What is pain?). Soma dosage: 2100 Mg, Daily Oral. Patient was hospitalized.

5892285-X | Dental Caries, Legal Problem, Major Depression, Mental Disorder, Road Traffic Accident, Suicide Attempt
on Sep 10, 2008 Male patient from UNITED STATES , 30 years of age, weighting 189.0 lb, was diagnosed with muscle spasms, neck pain and was treated with Soma (View Usage). After Soma was administered, patient had the following side effects: dental caries, legal problem, major depression, mental disorder, road traffic accident, suicide attempt. Soma dosage: 700 Mg (700 Mg, At Bedtime), Oral, 1050 Mg (1050 Mg, 1 In 1 D), Oral, 1750 Mg (1750 Mg, 1 In 1 D), O. During the same period patient was treated with ACTIQ (800 Mcg (800 Mcg, 1 In 1 D), Bu, 1600 Mcg (800 Mcg, 2 In 1 D), Bu, 2400 Mcg (800 Mcg, 3 In 1 D), Bu) (View Actiq Review and Actiq Label ), OXYCONTIN (360 Mg (120 Mg, 3 In 1 D), Oral, 480 Mg (160 Mg, 3 In 1 D), Oral) (View Oxycontin Review and Oxycontin Label ), DILAUDID (20 Mg (20 Mg, 1 In 1 D), Oral) (View Dilaudid Review and Dilaudid Label ). Patient was hospitalized and became disabled.

5868787-9 | Agitation, Dizziness, Headache, Insomnia, Nausea, Somnolence, Syncope, Tremor
Patient was taking Soma (View Usage). Patient experienced the following unwanted or unexpected effects: agitation, dizziness (What is dizziness?), headache (What is headache?), insomnia, nausea (What is nausea?), somnolence, syncope, tremor on Sep 02, 2008 from UNITED STATES Additional patient health information: Female patient , 47 years of age, weighting 130.0 lb, was diagnosed with back injury and. Soma dosage: 1 Tablet 3-4 X Day Po.

5825299-6 | Pyrexia, Suicidal Ideation
Adverse event was reported on Jul 11, 2008 by a Female patient taking Soma (View Usage) (Dosage: 4 In 1 D) . Location: UNITED STATES , 47 years of age, Patient had the following side effects: pyrexia, suicidal ideation. During the same period patient was treated with XANAX (6 Mg (2 Mg, 3 In 1 D)) (View Xanax Review and Xanax Label ), OXYCONTIN (100 Mg (50 Mg, 2 In 1 D)) (View Oxycontin Review and Oxycontin Label ), ROXICODONE (120 Mg (30 Mg, 4 In 1 D)) (View Roxicodone Review and Roxicodone Label ), WELLBUTRIN (3 In 1 D) (View Wellbutrin Review and Wellbutrin Label ), ADDERALL 10 (3 In 1 D) (View Adderall 10 Review and Adderall 10 Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), YASMIN (View Yasmin Review and Yasmin Label ).

5809767-9 | Road Traffic Accident
on Oct 02, 2007 Female patient from UNITED STATES , 53 years of age, was diagnosed with fibromyalgia and was treated with Soma (View Usage). After Soma was administered, patient had the following side effects: road traffic accident. Soma dosage: 2100 Mg (700 Mg, 3 In 1 D), Oral. Patient was hospitalized.

5809761-8 | Overdose
on May 22, 2007 Female patient from UNITED STATES , 16 years of age, was diagnosed with ill-defined disorder and was treated with Soma (View Usage). Patient experienced the following unwanted or unexpected effects: overdose. Soma dosage: Oral. Patient was hospitalized.

5729072-9 | Nausea, Oedema Peripheral
Patient was taking Soma (View Usage). Patient had the following side effects: nausea (What is nausea?), oedema peripheral on May 05, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 118.0 lb, was diagnosed with muscle spasms and. Soma dosage: .

5712993-0 | Fall, International Normalised Ratio Increased, Loss Of Consciousness, Prothrombin Time Prolonged, Subdural Haematoma
Adverse event was reported on Apr 03, 2008 by a Female patient taking Soma (View Usage) (Dosage: 2800 Mg (700 Mg, 4 In 1 D), Oral) was diagnosed with back pain (What is back pain?), breast cancer (What is breast cancer?) and. Location: UNITED STATES , 69 years of age, weighting 178.0 lb, After Soma was administered, patient had the following side effects: fall (What is fall?), international normalised ratio increased, loss of consciousness, prothrombin time prolonged, subdural haematoma. During the same period patient was treated with EXEMESTANE (25 Mg (25 Mg, 1 In 1 D), Oral) (View Exemestane Review and Exemestane Label ), TYLENOL WITH CODEINE NO 4 (View Tylenol With Codeine No 4 Review and Tylenol With Codeine No 4 Label ), PROTONIX (View Protonix Review and Protonix Label ), GLUCOPHAGE (View Glucophage Review and Glucophage Label ), CARDIZEM CD (View Cardizem Cd Review and Cardizem Cd Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), RESTORIL (View Restoril Review and Restoril Label ). Patient was hospitalized.

5571097-0 | Acute Hepatic Failure
on Dec 03, 2007 Male patient from UNITED STATES , 26 years of age, was diagnosed with ill-defined disorder and was treated with Soma (View Usage). Patient experienced the following unwanted or unexpected effects: acute hepatic failure. Soma dosage: . During the same period patient was treated with VICODIN (View Vicodin Review and Vicodin Label ), XANAX (View Xanax Review and Xanax Label ). Patient was hospitalized.

5571020-9 | Acute Hepatic Failure, Anorexia, Asthenia, Convulsion, Gastroenteritis, Hepatic Necrosis, Malaise, Mental Status Changes
on Dec 03, 2007 Male patient from UNITED STATES , 45 years of age, weighting 149.0 lb, was diagnosed with back pain (What is back pain?) and was treated with Soma (View Usage). Patient had the following side effects: acute hepatic failure, anorexia, asthenia, convulsion, gastroenteritis (What is gastroenteritis?), hepatic necrosis, malaise, mental status changes. Soma dosage: . During the same period patient was treated with LORTAB (View Lortab Review and Lortab Label ). Patient was hospitalized.

5570922-7 | Acute Hepatic Failure, Anaemia Macrocytic, Chills, Crepitations, Delirium, Disorientation, Disturbance In Attention, Dyskinesia, Hallucination, Visual
Patient was taking Soma (View Usage). After Soma was administered, patient had the following side effects: acute hepatic failure, anaemia macrocytic, chills, crepitations, delirium, disorientation, disturbance in attention, dyskinesia, hallucination, visual on Dec 03, 2007 from UNITED STATES Additional patient health information: Male patient , 21 years of age, was diagnosed with ill-defined disorder, back pain (What is back pain?) and. Soma dosage: . During the same period patient was treated with LORTAB (View Lortab Review and Lortab Label ), BENADRYL (View Benadryl Review and Benadryl Label ), HALDOL (View Haldol Review and Haldol Label ), COGENTIN (View Cogentin Review and Cogentin Label ), BENTYL (View Bentyl Review and Bentyl Label ), LIBRIUM (View Librium Review and Librium Label ), ATARAX (View Atarax Review and Atarax Label ), PHENERGAN HCL (View Phenergan Hcl Review and Phenergan Hcl Label ). Patient was hospitalized.

5553920-9 | Diarrhoea, Headache, Nausea
Adverse event was reported on Dec 12, 2007 by a Female patient taking Soma (View Usage) (Dosage: 3x/day) was diagnosed with blood cholesterol increased, myalgia and. Location: UNITED STATES , 37 years of age, weighting 147.0 lb, Patient experienced the following unwanted or unexpected effects: diarrhoea, headache (What is headache?), nausea (What is nausea?). During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ).

5336624-7 | Autoimmune Thyroiditis, Cardio-respiratory Arrest, Cerebral Infarction, Contusion, Dehydration, Fall, Gastroenteritis Viral
on May 11, 2007 Female patient from UNITED STATES , 39 years of age, weighting 177.9 lb, was diagnosed with back pain (What is back pain?), insomnia, ill-defined disorder, influenza and was treated with Soma (View Usage). Patient had the following side effects: autoimmune thyroiditis, cardio-respiratory arrest, cerebral infarction, contusion, dehydration, fall (What is fall?), gastroenteritis viral. Soma dosage: Oral. During the same period patient was treated with CHLORAL HYDRATE (View Chloral Hydrate Review and Chloral Hydrate Label ), DIPHENHYDRAMINE HCL (View Diphenhydramine Hcl Review and Diphenhydramine Hcl Label ), CLONAZEPAM (View Clonazepam Review and Clonazepam Label ), DIAZEPAM (View Diazepam Review and Diazepam Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ), METHOCARBAMOL (View Methocarbamol Review and Methocarbamol Label ), TAMIFLU (View Tamiflu Review and Tamiflu Label ), METHADONE HCL (View Methadone Hcl Review and Methadone Hcl Label ).

5279846-6 | Nausea
on Mar 26, 2007 Female patient from UNITED STATES , weighting 151.0 lb, was diagnosed with pain (What is pain?) and was treated with Soma (View Usage). After Soma was administered, patient had the following side effects: nausea (What is nausea?). Soma dosage: 1 Qid Po Prn.

5208944-8 | Amnesia, Choking, Facial Palsy, Musculoskeletal Stiffness, Overdose, Speech Disorder, Vomiting
Patient was taking Soma (View Usage). Patient experienced the following unwanted or unexpected effects: amnesia, choking (What is choking?), facial palsy, musculoskeletal stiffness, overdose, speech disorder, vomiting on Jan 11, 2007 from UNITED STATES Additional patient health information: Female patient , weighting 110.0 lb, was diagnosed with back pain (What is back pain?) and. Soma dosage: .

5041248-5 | Completed Suicide, Muscle Rigidity
Adverse event was reported on Jun 12, 2006 by a Female patient taking Soma (View Usage) (Dosage: ) was diagnosed with ill-defined disorder and. Location: UNITED STATES , 42 years of age, Patient had the following side effects: completed suicide, muscle rigidity. During the same period patient was treated with CODEINE (CODEINE) (View Codeine (codeine) Review and Codeine (codeine) Label ), DIAZEPAM (View Diazepam Review and Diazepam Label ), MEPROBAMATE (View Meprobamate Review and Meprobamate Label ), MORPHINE (View Morphine Review and Morphine Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), CAFFEINE (View Caffeine Review and Caffeine Label ), DIPHENHYDRAMINE HCL (View Diphenhydramine Hcl Review and Diphenhydramine Hcl Label ), DOXEPIN (View Doxepin Review and Doxepin Label ). Patient was hospitalized.

5005407-X | Acute Myocardial Infarction, Arteriosclerosis, Asthma, Chest Pain, Chronic Fatigue Syndrome, Chronic Obstructive Pulmonary Disease, Confusional State, Constipation, Coronary Artery Disease
on Jan 30, 2006 Female patient from UNITED STATES , 61 years of age, weighting 183.0 lb, was diagnosed with muscle tightness, asthma (What is asthma?), bacterial infection (What is bacterial infection?), depression (What is depression?), prophylaxis and was treated with Soma (View Usage). After Soma was administered, patient had the following side effects: acute myocardial infarction, arteriosclerosis, asthma (What is asthma?), chest pain (What is chest pain?), chronic fatigue syndrome (What is chronic fatigue syndrome?), chronic obstructive pulmonary disease, confusional state, constipation (What is constipation?), coronary artery disease (What is coronary artery disease?). Soma dosage: . During the same period patient was treated with VIOXX (View Vioxx Review and Vioxx Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label ), BACTRIM (View Bactrim Review and Bactrim Label ), CELEXA (View Celexa Review and Celexa Label ), CLIMARA (View Climara Review and Climara Label ), COZAAR (View Cozaar Review and Cozaar Label ). Patient was hospitalized.

4993516-0 | Nausea
on May 03, 2006 Female patient from UNITED STATES , weighting 159.0 lb, was diagnosed with pain (What is pain?) and was treated with Soma (View Usage). Patient experienced the following unwanted or unexpected effects: nausea (What is nausea?). Soma dosage: One Tid Po.

4983851-4 | Blood Cholesterol Increased, Hypersensitivity, Myocardial Infarction
Patient was taking Soma (View Usage). Patient had the following side effects: blood cholesterol increased, hypersensitivity, myocardial infarction on Oct 19, 2005 from UNITED STATES Additional patient health information: Female patient , 45 years of age, weighting 145.5 lb, was diagnosed with myalgia, back pain (What is back pain?), joint injury and. Soma dosage: . During the same period patient was treated with VIOXX (View Vioxx Review and Vioxx Label ), HYDROCODONE BITARTRATE (View Hydrocodone Bitartrate Review and Hydrocodone Bitartrate Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized and became disabled.