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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