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Zocor (Simvastatin) - Adverse Event Reports - Disability

 



Index of reports > Cases resulting in disability (76)

     Myalgia (18)Rhabdomyolysis (15)Drug Interaction (10)Blood Creatine Phosphokinase Increased (9)Pain in Extremity (9)Asthenia (9)Arthralgia (8)Pain (7)Muscular Weakness (7)Amyotrophic Lateral Sclerosis (6)

Below is the selection of adverse event reports related to Zocor (Simvastatin) that includes cases resulting in disability.

 Reports 1 - 25 of 76   Next >>

Adverse event in 57 year old female receiving Zocor (Simvastatin)

Reported by a individual with unspecified qualification from United States on 2007-10-29

Patient: 57 year old female

Adverse reactions / side effects: Myalgia, Pain in Extremity

Adverse event resulted in: disablity

Suspect drug(s):
Zocor
    Administration route: Oral
    Indication: Blood Cholesterol
    Start date: 2006-01-01
    End date: 2007-10-11

Zocor
    Administration route: Oral
    Start date: 2007-10-18

Other drugs received by patient: Metformin; Actos; Prinivil; Cyclobenzaprine Hydrochloride; Ibuprofen; Sulfamethoxazole and Trimethoprim; Cymbalta; Aspirin; Vitamins (Unspecified); Asian Ginseng; Caltrate + D; Vitamins (Unspecified)



Adverse event in 67 year old female receiving Zocor (Simvastatin)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-25

Patient: 67 year old female, weighing 95.0 kg (209.0 pounds)

Adverse reactions / side effects: Emotional Distress, Syncope, Headache

Adverse event resulted in: disablity

Suspect drug(s):
Zocor
    Administration route: Oral
    Indication: Lipids Increased
    Start date: 2007-04-22
    End date: 2007-04-23

Zocor
    Administration route: Oral
    Start date: 2007-04-03
    End date: 2007-04-20

Zocor
    Administration route: Oral

Other drugs received by patient: Aspirin; Albuterol Sulfate and Ipratropium Bromide; Rimonabant; Ramipril



Adverse event in 49 year old female receiving Zocor (Simvastatin)

Reported by a health professional (non-physician/pharmacist) from Denmark on 2007-10-24

Patient: 49 year old female

Adverse reactions / side effects: Neuropathy, Pain, Biopsy Muscle Abnormal, Adverse Event, Asthenia

Adverse event resulted in: disablity

Suspect drug(s):
Zocor (Simvastatin)

Other drugs received by patient: Simvastatin



Adverse event in 49 year old female receiving Zocor (Simvastatin)

Reported by a health professional (non-physician/pharmacist) from Denmark on 2007-10-22

Patient: 49 year old female

Adverse reactions / side effects: Neuropathy, Pain, Biopsy Muscle Abnormal, Asthenia, Hysterotomy

Adverse event resulted in: disablity

Suspect drug(s):
Zocor (Simvastatin)

Other drugs received by patient: Simvastatin



Adverse event in 82 year old male receiving Zocor (Simvastatin)

Reported by a pharmacist from Belgium on 2007-10-16

Patient: 82 year old male

Adverse reactions / side effects: Pain in Extremity

Adverse event resulted in: disablity

Suspect drug(s):
Zocor (Simvastatin)

Other drugs received by patient: Mometasone Furoate; Aspirin



Adverse event in male receiving Zocor (Simvastatin)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-12

Patient: male

Adverse reactions / side effects: Rhabdomyolysis, Aspartate Aminotransferase Increased, Troponin T Increased

Adverse event resulted in: disablity

Suspect drug(s):
Zocor (Simvastatin)

Other drugs received by patient: Erythromycin



Adverse event in 68 year old male receiving Zocor (Simvastatin)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-08

Patient: 68 year old male

Adverse reactions / side effects: Affective Disorder, Feeling Abnormal, Tearfulness

Adverse event resulted in: disablity

Suspect drug(s):
Zocor
    Administration route: Oral
    Indication: Coronary Artery Bypass
    Start date: 2007-07-01
    End date: 2007-08-27

Zocor
    Administration route: Oral
    Indication: Prophylaxis
    Start date: 2007-07-01
    End date: 2007-08-27

Other drugs received by patient: Aspirin; Ramipril



Adverse event in 64 year old male receiving Zocor (Simvastatin)

Reported by a physician from United States on 2007-10-02

Patient: 64 year old male, weighing 84.0 kg (184.8 pounds)

Adverse reactions / side effects: Gallbladder Enlargement, Pancreatic Carcinoma

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
Zocor
    Administration route: Oral
    Indication: Blood Cholesterol Increased
    Start date: 1992-01-01

Zocor
    Administration route: Oral
    End date: 2007-08-01

Other drugs received by patient: Zyloprim; Cozaar; Cozaar; Atenolol; Aspirin; Urocit-K



Adverse event in 90 year old male receiving Zocor (Simvastatin)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-01

Patient: 90 year old male

Adverse reactions / side effects: Haematuria

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Zocor (Simvastatin)

Other drugs received by patient: Aspirin



Adverse event in 66 year old male receiving Zocor (Simvastatin)

Reported by a physician from United States on 2007-07-27

Patient: 66 year old male, weighing 93.0 kg (204.6 pounds)

Adverse reactions / side effects: Diplopia, Myalgia, Ivth Nerve Paresis

Adverse event resulted in: disablity

Suspect drug(s):
Zocor
    Administration route: Oral
    Indication: Hypercholesterolaemia
    Start date: 2007-05-17
    End date: 2007-07-08

Zocor
    Administration route: Oral
    Start date: 2005-01-01
    End date: 2007-05-16

Other drugs received by patient: Propranolol Hydrochloride; Benazepril Hydrochloride; Clonidine; Hydrochlorothiazide and Triamterene; Allopurinol



Adverse event in 71 year old female receiving Zocor (Simvastatin)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-25

Patient: 71 year old female

Adverse reactions / side effects: Optic Neuropathy, Blindness

Adverse event resulted in: disablity

Suspect drug(s):
Zocor (Simvastatin)

Other drugs received by patient: Aspirin; Candesartan; Estrogens (Unspecified)



Adverse event in 54 year old female receiving Zocor (Simvastatin)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-20

Patient: 54 year old female

Adverse reactions / side effects: Myalgia, Rhabdomyolysis, Angioedema

Adverse event resulted in: life threatening event, disablity

Suspect drug(s):
Zocor
    Administration route: Oral
    Indication: Blood Cholesterol Increased
    Start date: 2007-05-01
    End date: 2007-06-12

Amitriptyline Hydrochloride
    Indication: Pain

Amitriptyline Hydrochloride
    Indication: Sleep Disorder

Ascorbic Acid and Vitamin B Complex
    Indication: Vitamin Supplementation

Ubidecarenone

Atropine Sulfate and Diphenoxylate Hydrochloride
    Indication: Irritable Bowel Syndrome

Atropine Sulfate and Diphenoxylate Hydrochloride
    Indication: Pain

Acetaminophen and Propoxyphene Hydrochloride
    Indication: Analgesia

Furosemide
    Indication: Fluid Retention

Ginger

Hydroxocobalamin
    Indication: Vitamin B12 Deficiency

Magnesium (Unspecified)
    Indication: Chronic Fatigue Syndrome

Vitamins (Unspecified)
    Indication: Vitamin Supplementation

Acetaminophen
    Indication: Analgesia

Selenium (Unspecified)
    Indication: Medical Diet

Albuterol
    Indication: Asthma

Niacinamide

Vitamin E

Zinc (Unspecified)
    Indication: Medical Diet

Cetyl Myristoleate and Cetylated Fatty Acids

Glucametacin

Ascorbic Acid

Omega-3 Marine Triglycerides
    Indication: Arthralgia



Adverse event in 66 year old male receiving Zocor (Simvastatin)

Reported by a physician from United States on 2007-07-20

Patient: 66 year old male

Adverse reactions / side effects: Ivth Nerve Paresis

Adverse event resulted in: disablity

Suspect drug(s):
Zocor
    Administration route: Oral
    Indication: Blood Cholesterol Increased
    Start date: 2005-01-01
    End date: 2007-01-01

Zocor
    Administration route: Oral
    Start date: 2007-01-01
    End date: 2007-07-06

Other drugs received by patient: [therapy Unspecified]



Adverse event in 60 year old female receiving Zocor (Simvastatin)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-19

Patient: 60 year old female, weighing 60.0 kg (132.0 pounds)

Adverse reactions / side effects: Myositis

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Zocor (Simvastatin)

Other drugs received by patient: Aspirin; Thiamine; Vitamin B (Unspecified)



Adverse event in 50 year old male receiving Zocor (Simvastatin)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-11

Patient: 50 year old male

Adverse reactions / side effects: Tendonitis

Adverse event resulted in: disablity

Suspect drug(s):
Zocor
    Administration route: Oral
    Start date: 2007-05-30
    End date: 2007-06-28

Atorvastatin
    Administration route: Oral
    Start date: 2005-09-14
    End date: 2007-05-30

Other drugs received by patient: Amlodipine Besylate; Bendroflumethiazide; Moxonidine; Perindopril



Adverse event in 60 year old female receiving Zocor (Simvastatin)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-05

Patient: 60 year old female, weighing 70.0 kg (154.0 pounds)

Adverse reactions / side effects: Myalgia, Arthralgia, Musculoskeletal Stiffness, Joint Stiffness

Adverse event resulted in: disablity

Suspect drug(s):
Zocor (Simvastatin)

Other drugs received by patient: Atenolol; Ibuprofen; Lansoprazole; Tildiem



Adverse event in 41 year old male receiving Zocor (Simvastatin)

Reported by a individual with unspecified qualification from Norway on 2007-07-02

Patient: 41 year old male

Adverse reactions / side effects: Myalgia, Nervous System Disorder, Headache

Adverse event resulted in: disablity

Suspect drug(s):
Zocor
    Administration route: Oral
    Indication: Hypercholesterolaemia
    Start date: 1993-09-01
    End date: 1996-06-01

Zocor
    Administration route: Oral
    Start date: 1996-06-01
    End date: 1998-01-01

Lipitor
    Administration route: Oral
    Indication: Hypercholesterolaemia
    Start date: 1998-01-01
    End date: 2003-09-01

Lescol
    Administration route: Oral
    Indication: Hypercholesterolaemia
    Start date: 2003-09-01
    End date: 2003-10-01

Lescol
    Administration route: Oral
    Start date: 2003-10-21
    End date: 2004-01-13

Mevacor
    Administration route: Oral
    Indication: Hypercholesterolaemia
    Start date: 2003-10-01
    End date: 2003-10-01

Other drugs received by patient: Albyl-E; Sorbangil; Kredex; Selo-ZOK



Adverse event in 87 year old female receiving Zocor (Simvastatin)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-06-29

Patient: 87 year old female, weighing 65.0 kg (143.0 pounds)

Adverse reactions / side effects: Rheumatoid Arthritis, Polymyalgia Rheumatica

Adverse event resulted in: disablity

Suspect drug(s):
Zocor (Simvastatin)

Other drugs received by patient: Candesartan



Adverse event in 81 year old female receiving Zocor (Simvastatin)

Reported by a consumer/non-health professional from United States on 2007-06-28

Patient: 81 year old female

Adverse reactions / side effects: Myalgia, Dysstasia

Adverse event resulted in: disablity

Suspect drug(s):
Zocor (Simvastatin)



Adverse event in 54 year old male receiving Zocor (Simvastatin)

Reported by a physician from Sweden on 2007-06-21

Patient: 54 year old male, weighing 93.0 kg (204.6 pounds)

Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Muscle Atrophy, Angina Unstable, Erectile Dysfunction, Palpitations, Multiple Injuries, Carpal Tunnel Syndrome, Nerve Root Compression, Demyelination, Intervertebral Disc Protrusion, Back Pain, Benign Prostatic Hyperplasia, Bursitis, Myopathy, Antinuclear Antibody Positive, Joint Swelling, Nervous System Disorder, Penis Disorder, Pain, Fall, Dermatitis Contact, Concussion, Joint Crepitation, Amyotrophic Lateral Sclerosis, Application Site Vesicles, Acute Coronary Syndrome, Neuropathy, Humerus Fracture, Hyperreflexia, Anxiety, Skin Laceration, Arthralgia, Joint Sprain, Spinal Osteoarthritis

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Zocor
    Administration route: Oral
    Indication: Blood Cholesterol Increased
    Start date: 1999-09-24
    End date: 2000-05-30

Zocor
    Administration route: Oral
    Start date: 2000-07-13
    End date: 2001-09-01

Other drugs received by patient: Vasotec; Catapres; Lopressor; Xanax; Vicodin; Aspirin; Lortab; Tricor; Pravachol; Influenza Virus Vaccine (Unspecified); Pneumococcal Vaccine (Unspecified); Lasix; Slow-K; Mestinon; Nortriptyline; Lopid; Verapamil



Adverse event in 73 year old male receiving Zocor (Simvastatin)

Reported by a physician from Sweden on 2007-06-20

Patient: 73 year old male

Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Muscle Atrophy, Rhabdomyolysis, Pain in Extremity, Abasia, Polyneuropathy, Dysstasia, Peroneal Nerve Palsy, Amyotrophic Lateral Sclerosis, Chest Pain, Electromyogram Abnormal, Asthenia

Adverse event resulted in: disablity

Suspect drug(s):
Zocor
    Administration route: Oral
    Indication: Blood Cholesterol Increased
    Start date: 1999-01-01
    End date: 2000-01-01

Zocor
    Administration route: Oral
    Start date: 2000-01-01

Other drugs received by patient: Hydrodiuril



Adverse event in 71 year old female receiving Zocor (Simvastatin)

Reported by a physician from Sweden on 2007-06-20

Patient: 71 year old female

Adverse reactions / side effects: Dysarthria, Amyotrophic Lateral Sclerosis

Adverse event resulted in: death, life threatening event, disablity

Suspect drug(s):
Zocor (Simvastatin)

Other drugs received by patient: Lotrel; Ecotrin; Rilutek



Adverse event in 69 year old female receiving Zocor (Simvastatin)

Reported by a physician from Sweden on 2007-06-20

Patient: 69 year old female

Adverse reactions / side effects: Brachial Plexopathy, Muscle Contractions Involuntary, Amyotrophic Lateral Sclerosis, Asthenia, Paraesthesia

Adverse event resulted in: disablity

Suspect drug(s):
Zocor (Simvastatin)

Other drugs received by patient: Tenormin; Magnesium Hydroxide



Adverse event in 54 year old male receiving Zocor (Simvastatin)

Reported by a physician from Sweden on 2007-06-20

Patient: 54 year old male, weighing 93.0 kg (204.6 pounds)

Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Muscle Atrophy, Angina Unstable, Erectile Dysfunction, Palpitations, Multiple Injuries, Carpal Tunnel Syndrome, Nerve Root Compression, Demyelination, Intervertebral Disc Protrusion, Back Pain, Benign Prostatic Hyperplasia, Bursitis, Myopathy, Antinuclear Antibody Positive, Joint Swelling, Nervous System Disorder, Penis Disorder, Pain, Fall, Dermatitis Contact, Concussion, Joint Crepitation, Amyotrophic Lateral Sclerosis, Application Site Vesicles, Acute Coronary Syndrome, Neuropathy, Humerus Fracture, Hyperreflexia, Anxiety, Skin Laceration, Arthralgia, Joint Sprain, Spinal Osteoarthritis

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Zocor
    Administration route: Oral
    Indication: Blood Cholesterol Increased
    Start date: 1999-09-24
    End date: 2000-05-30

Zocor
    Administration route: Oral
    Start date: 2000-07-13
    End date: 2001-09-01

Other drugs received by patient: Vasotec; Catapres; Lopressor; Xanax; Vicodin; Aspirin; Lortab; Tricor; Pravachol; Influenza Virus Vaccine (Unspecified); Pneumococcal Vaccine (Unspecified); Lasix; Slow-K; Mestinon; Nortriptyline; Lopid; Verapamil



Adverse event in 40 year old male receiving Zocor (Simvastatin)

Reported by a physician from United States on 2007-06-20

Patient: 40 year old male, weighing 102.0 kg (224.4 pounds)

Adverse reactions / side effects: Gait Spastic, Blood Creatine Phosphokinase Increased, Balance Disorder, Amyotrophic Lateral Sclerosis, Electromyogram Abnormal, Asthenia, Fall, Muscle Spasms

Adverse event resulted in: disablity

Suspect drug(s):
Zocor
    Administration route: Oral
    Indication: Hypertension
    Start date: 2001-01-01

Lipitor
    Indication: Blood Cholesterol Increased
    Start date: 1999-01-01

Other drugs received by patient: Accupril



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