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Index of reports
> Cases resulting in disability (17)
> Cases with Fall (5)
Below is the selection of adverse event reports related to Voltaren (Diclofenac) that includes cases resulting in disability where reactions include fall.
Adverse event in 80 year old female receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-06-20
Patient: 80 year old female, weighing 36.9 kg (81.2 pounds)
Adverse reactions / side effects: Angina Pectoris, Anaemia, Gastric Ulcer Haemorrhage, Pain, Muscular Weakness, Fall, Stress
Adverse event resulted in: disablity
Suspect drug(s):
Azulfidine
Dosage: 1 g, oral
Administration route: Oral
Indication: Rheumatoid Arthritis
End date: 2006-12-21
Methotrexate
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
End date: 2006-12-21
Methotrexate
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2006-12-29
End date: 2007-03-05
Prednisolone
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2006-12-04
End date: 2006-12-21
Prednisolone
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
End date: 2006-12-21
Prednisolone
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2006-12-23
Tacrolimus Capsules (Tacrolimus Capsule) Capsules
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2006-12-04
End date: 2006-12-27
Tacrolimus Capsules (Tacrolimus Capsule) Capsules
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2006-12-28
End date: 2007-01-12
Tacrolimus Capsules (Tacrolimus Capsule) Capsules
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2007-01-13
Voltaren
Dosage: 75 mg, oral
Administration route: Oral
Indication: Rheumatoid Arthritis
End date: 2006-12-21
Adverse event in 80 year old female receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-03-26
Patient: 80 year old female, weighing 36.9 kg (81.2 pounds)
Adverse reactions / side effects: Angina Pectoris, Gastric Ulcer Haemorrhage, Fall, Stress
Adverse event resulted in: disablity
Suspect drug(s):
Azulfidine EN (Sulfasalazine) PER Oral NOS
Dosage: 1 g, d, oral
Administration route: Oral
Indication: Rheumatoid Arthritis
Methotrexate
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
End date: 2006-12-21
Methotrexate
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2006-12-29
Prednisolone
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
End date: 2006-12-03
Prednisolone
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2006-12-04
End date: 2006-12-21
Prednisolone
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2006-12-23
Tacrolimus
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2006-12-04
End date: 2006-12-27
Tacrolimus
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2006-12-28
End date: 2007-01-12
Tacrolimus
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2007-01-13
Voltaren
Dosage: 75 mg, d, oral
Indication: Rheumatoid Arthritis
End date: 2006-12-21
Other drugs received by patient: Rabeprazole Sodium; Folic Acid; Mucosta (Rebamipide); Baktar (Sulfamethoxazole, Trimethoprim); Risedronate Sodium
Adverse event in 80 year old female receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-03-16
Patient: 80 year old female, weighing 36.9 kg (81.2 pounds)
Adverse reactions / side effects: Angina Pectoris, Gastric Ulcer Haemorrhage, Fall
Adverse event resulted in: disablity
Suspect drug(s):
Tacrolimus Capsules (Tacrolimus) Capsule
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2006-12-04
End date: 2006-12-27
Tacrolimus Capsules (Tacrolimus) Capsule
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2006-12-28
End date: 2007-01-12
Tacrolimus Capsules (Tacrolimus) Capsule
Dosage: see image
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2007-01-13
Voltaren
Dosage: 75 mg, unknown/d, oral
Administration route: Oral
End date: 2006-12-21
Other drugs received by patient: Prednisolone; Methotrexate (Methotrexate Sodium) PER Oral NOS; Azulfidine EN PER Oral NOS; Pariet (Rabeprazole Sodium) PER Oral NOS; Foliamin (Folic Acid) PER Oral NOS; Mucosta (Rebamipide) PER Oral NOS; Baktar (Sulfamethoxazole, Trimethoprim) PER Oral NOS; Benet (Risedronate Sodium) PER Oral NOS; Cytotec (Misoprostol) PER Oral NOS
Adverse event in 79 year old male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Australia on 2007-03-13
Patient: 79 year old male
Adverse reactions / side effects: Bone Scan Abnormal, Impaired Healing, Tooth Extraction, Fall
Adverse event resulted in: disablity
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Fosamax
Adverse event in 79 year old male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Australia on 2007-03-10
Patient: 79 year old male
Adverse reactions / side effects: Bone Scan Abnormal, Impaired Healing, Tooth Extraction, Fall
Adverse event resulted in: disablity
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Fosamax
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