DrugLib.com — Drug Information Portal

Rx drug information, pharmaceutical research, clinical trials, news, and more

Crestor (Rosuvastatin) - Adverse Event Reports - Disability - Myalgia

 



Index of reports > Cases resulting in disability (66) > Cases with Myalgia (13)

Below is the selection of adverse event reports related to Crestor (Rosuvastatin) that includes cases resulting in disability where reactions include myalgia.

Adverse event in 78 year old female receiving Crestor (Rosuvastatin)

Reported by a consumer/non-health professional from United States on 2007-10-30

Patient: 78 year old female, weighing 68.0 kg (149.6 pounds)

Adverse reactions / side effects: Myalgia, Hemiplegia

Adverse event resulted in: disablity

Suspect drug(s):
Crestor (Rosuvastatin)

Other drugs received by patient: Synthroid



Adverse event in 69 year old male receiving Crestor (Rosuvastatin)

Reported by a physician from Belgium on 2007-10-24

Patient: 69 year old male

Adverse reactions / side effects: Myalgia, Fatigue, Muscle Swelling, Arthralgia, Bradycardia, Muscle Spasms

Adverse event resulted in: disablity

Suspect drug(s):
Crestor (Rosuvastatin)

Other drugs received by patient: Amlor; Persantine



Adverse event in 605 month old male receiving Crestor (Rosuvastatin)

Reported by a physician from United Kingdom on 2007-10-18

Patient: 605 month old male

Adverse reactions / side effects: Weight Decreased, Muscle Atrophy, Nasopharyngitis, Diabetes Mellitus, Haemorrhage, Dyskinesia, Wheezing, Eczema, Pyrexia, Feeling Cold, Speech Disorder, Conjunctivitis Allergic, Myalgia, Balance Disorder, Carpal Tunnel Syndrome, Rhinorrhoea, Psoriasis, Ill-Defined Disorder, Hepatocellular Damage, Tremor, Dysgeusia, Arthralgia, Sleep Disorder, Ocular Hyperaemia, Psoriatic Arthropathy

Adverse event resulted in: disablity

Suspect drug(s):
Crestor
    Administration route: Oral
    Start date: 2004-01-05
    End date: 2004-05-14

Atorvastatin Calcium
    Administration route: Oral
    Start date: 2002-11-18
    End date: 2004-01-01

Cerivastatin
    Administration route: Oral
    Start date: 2000-05-03
    End date: 2001-08-28

Fenofibrate
    Administration route: Oral
    Start date: 2000-03-22
    End date: 2000-08-01

Other drugs received by patient: Calcipotriene; Gliclazide; Gliclazide; Sulfasalazine



Adverse event in 80 year old female receiving Crestor (Rosuvastatin)

Reported by a individual with unspecified qualification from United States on 2007-07-27

Patient: 80 year old female, weighing 55.8 kg (122.8 pounds)

Adverse reactions / side effects: Abdominal Pain, Rhabdomyolysis, Dyslexia, Speech Disorder, Myalgia, Fatigue, Tongue Disorder, DRY Mouth, Bone Disorder, Myositis, Chondropathy, Dyspnoea, Dysphagia, Atrial Fibrillation, Myopathy, Hepatic Enzyme Increased, Tremor, Dysphemia, Diarrhoea, Dysphonia, Dysuria, Vaginal Infection, Asthenia

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Crestor
    Administration route: Oral
    Indication: Hypercholesterolaemia
    Start date: 2006-03-21
    End date: 2006-08-18

Crestor
    Administration route: Oral
    Indication: Hyperlipidaemia
    Start date: 2006-03-21
    End date: 2006-08-18

Crestor
    Administration route: Oral
    Indication: Dyslipidaemia
    Start date: 2006-03-21
    End date: 2006-08-18

Other drugs received by patient: Flecainide Acetate; Antivert; Xanax; Warfarin Sodium; Cholestyramine; Carafate; M.v.i.; Namenda; Citracal + D; Verapamil; Halcion



Adverse event in 80 year old female receiving Crestor (Rosuvastatin)

Reported by a individual with unspecified qualification from United States on 2007-07-26

Patient: 80 year old female, weighing 55.8 kg (122.8 pounds)

Adverse reactions / side effects: Abdominal Pain, Rhabdomyolysis, Dyslexia, Speech Disorder, Myalgia, Fatigue, Tongue Disorder, DRY Mouth, Bone Disorder, Myositis, Chondropathy, Dyspnoea, Dysphagia, Atrial Fibrillation, Myopathy, Hepatic Enzyme Increased, Tremor, Dysphemia, Diarrhoea, Dysphonia, Dysuria, Vaginal Infection, Asthenia

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Crestor
    Administration route: Oral
    Indication: Hypercholesterolaemia
    Start date: 2006-03-21
    End date: 2006-08-18

Crestor
    Administration route: Oral
    Indication: Hyperlipidaemia
    Start date: 2006-03-21
    End date: 2006-08-18

Crestor
    Administration route: Oral
    Indication: Dyslipidaemia
    Start date: 2006-03-21
    End date: 2006-08-18

Other drugs received by patient: Flecainide Acetate; Antivert; Xanax; Warfarin Sodium; Cholestyramine; Carafate; M.v.i.; Namenda; Citracal + D; Verapamil; Halcion



Adverse event in female receiving Crestor (Rosuvastatin)

Reported by a physician from Ireland on 2007-07-23

Patient: female

Adverse reactions / side effects: Myalgia, Pernicious Anaemia

Adverse event resulted in: disablity

Suspect drug(s):
Crestor (Rosuvastatin)



Adverse event in 80 year old female receiving Crestor (Rosuvastatin)

Reported by a individual with unspecified qualification from United States on 2007-06-25

Patient: 80 year old female, weighing 55.8 kg (122.8 pounds)

Adverse reactions / side effects: Myalgia, Abdominal Pain, Myositis, Fatigue, Rhabdomyolysis, Diarrhoea, Asthenia, Hepatic Enzyme Increased, Tremor

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Crestor
    Administration route: Oral
    Indication: Hypercholesterolaemia
    Start date: 2006-03-21
    End date: 2006-08-18

Crestor
    Administration route: Oral
    Indication: Hyperlipidaemia
    Start date: 2006-03-21
    End date: 2006-08-18

Other drugs received by patient: Flecainide Acetate; Antivert; Xanax; Warfarin Sodium; Cholestyramine; Carafate; M.v.i.; Namenda; Citracal + D; Verapamil; Halcion



Adverse event in male receiving Crestor (Rosuvastatin)

Reported by a consumer/non-health professional from United States on 2007-06-11

Patient: male

Adverse reactions / side effects: Myalgia, Drug Ineffective, Abasia, Intervertebral Disc Degeneration, Muscular Weakness, Muscle Spasms

Adverse event resulted in: disablity

Suspect drug(s):
Lipitor

Crestor



Adverse event in 33 year old male receiving Crestor (Rosuvastatin)

Reported by a individual with unspecified qualification from United States on 2007-05-31

Patient: 33 year old male, weighing 102.1 kg (224.5 pounds)

Adverse reactions / side effects: Myalgia, Muscle Swelling, Contusion, Oedema Peripheral, Muscular Weakness, Testicular Swelling, Excessive Exercise, Muscle Enzyme Increased

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

Suspect drug(s):
Crestor (Rosuvastatin)



Adverse event in male receiving Crestor (Rosuvastatin)

Reported by a consumer/non-health professional from United States on 2007-04-28

Patient: male

Adverse reactions / side effects: Myalgia, Drug Ineffective, Abasia, Intervertebral Disc Degeneration

Adverse event resulted in: disablity

Suspect drug(s):
Lipitor

Crestor



Adverse event in 57 year old male receiving Crestor (Rosuvastatin)

Reported by a physician from France on 2007-04-28

Patient: 57 year old male

Adverse reactions / side effects: Myalgia, Amyotrophy, Muscular Weakness

Adverse event resulted in: disablity

Suspect drug(s):
Tahor
    Indication: Hypercholesterolaemia

Crestor



Adverse event in male receiving Crestor (Rosuvastatin)

Reported by a pharmacist from Canada on 2007-02-02

Patient: male

Adverse reactions / side effects: Myalgia, Drug Ineffective, Blood Glucose Increased

Adverse event resulted in: disablity

Suspect drug(s):
Lantus
    Start date: 2007-01-24

Crestor
    Administration route: Oral

Other drugs received by patient: Altace



Adverse event in 658 month old female receiving Crestor (Rosuvastatin)

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

Patient: 658 month old female

Adverse reactions / side effects: Cytomegalovirus Antibody Positive, Weight Decreased, Blood Creatine Phosphokinase Increased, Eye Irritation, Fall, Transaminases Increased, Muscle Enzyme Increased, Myalgia, Skin Discolouration, Skeletal Injury, Peripheral Vascular Disorder, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Varicose Vein, Mucosal Erosion, Ocular Hyperaemia, Aspartate Aminotransferase Increased, Herpes Virus Infection

Adverse event resulted in: disablity

Suspect drug(s):
Crestor
    Administration route: Oral
    Indication: Hypercholesterolaemia
    Start date: 2005-12-21
    End date: 2006-01-31

Zelitrex
    Administration route: Oral
    Indication: Antiviral Prophylaxis
    Start date: 2005-12-01
    End date: 2006-01-31

Other drugs received by patient: Seresta; Mepronizine; Motilium; Lamaline

-- advertisement -- The American Red Cross
We comply with
HONcode standard.
Verify here.
Home | About Us | Contact Us | Site usage policy | Privacy policy

All Rights reserved - Copyright DrugLib.com, 2006-2009