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Caduet (Amlodipine / Atorvastatin) - Disability - Suspected Cause - Side Effect Reports

 
 



Index of reports > Disability (5)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Caduet (Amlodipine / Atorvastatin) disability. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Caduet side effects in male

Reported by a consumer/non-health professional from United States on 2012-07-30

Patient: male, weighing 97.5 kg (214.6 pounds)

Reactions: Myopathy, Tremor, Myalgia, Balance Disorder, Depression, Coordination Abnormal, Multiple Sclerosis, Muscle Spasms

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Caduet
    Dosage: 10/20mg qd po
    Administration route: Oral
    Indication: Blood Cholesterol Increased
    Start date: 2010-10-19
    End date: 2012-06-21

Caduet
    Dosage: 10/20mg qd po
    Administration route: Oral
    Indication: Hypertension
    Start date: 2010-10-19
    End date: 2012-06-21

Other drugs received by patient: Statin Based Drugs



Possible Caduet side effects in 75 year old male

Reported by a physician from Australia on 2012-04-06

Patient: 75 year old male

Reactions: Pruritus, Photodermatosis

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Caduet
    Indication: Hypercholesterolaemia

Caduet
    Dosage: amlodipine 5 mg/atorvastatin 20 mg, 1x/day
    Administration route: Oral
    Indication: Hypertension
    Start date: 2010-01-01
    End date: 2012-02-28

Amlodipine Besylate

Other drugs received by patient: Micardis



Possible Caduet side effects in female

Reported by a consumer/non-health professional from United States on 2012-01-23

Patient: female

Reactions: Limb Operation

Adverse event resulted in: disablity

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

Caduet
    Dosage: unk

Relpax
    Dosage: unk

Protonix
    Dosage: unk



Possible Caduet side effects in female

Reported by a consumer/non-health professional from United States on 2012-01-17

Patient: female

Reactions: Limb Operation

Adverse event resulted in: disablity

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

Caduet
    Dosage: unk

Protonix
    Dosage: unk

Relpax
    Dosage: unk



Possible Caduet side effects in 46 year old male

Reported by a physician from Japan on 2011-12-15

Patient: 46 year old male, weighing 69.7 kg (153.3 pounds)

Reactions: Becker's Muscular Dystrophy, Fall

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Caduet

Other drugs received by patient: Micardis; Norvasc; Urinorm

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