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Index of reports
> Cases resulting in disability (17)
Below is the selection of adverse event reports related to Voltaren (Diclofenac) that includes cases resulting in disability.
Adverse event in receiving Voltaren (Diclofenac)
Reported by a physician from Turkey on 2007-10-29
Patient:
Adverse reactions / side effects: Sciatic Nerve Palsy
Adverse event resulted in: disablity
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in male receiving Voltaren (Diclofenac)
Reported by a physician from Turkey on 2007-10-29
Patient: male
Adverse reactions / side effects: Peripheral Nerve Lesion
Adverse event resulted in: disablity
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in 55 year old female receiving Voltaren (Diclofenac)
Reported by a consumer/non-health professional from Brazil on 2007-07-02
Patient: 55 year old female
Adverse reactions / side effects: Cerebrovascular Accident
Adverse event resulted in: disablity
Suspect drug(s):
Valium
Dosage: dosing frequency: as necessary
Administration route: Oral
Indication: Epilepsy
Start date: 1995-06-01
Voltaren
Indication: Back Pain
Other drugs received by patient: Salicin; Glibenclamide; Lisinopril
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):
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
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
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
Azulfidine
Dosage: 1 g, oral
Administration route: Oral
Indication: Rheumatoid Arthritis
End date: 2006-12-21
Adverse event in 75 year old male receiving Voltaren (Diclofenac)
Reported by a consumer/non-health professional from France on 2007-04-30
Patient: 75 year old male
Adverse reactions / side effects: Incisional Drainage, Impaired Healing, Insomnia, Pain, Gait Disturbance, Wound Secretion
Adverse event resulted in: disablity
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Tramadol HCL; Seresta; Allopurinol
Adverse event in 56 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-04-04
Patient: 56 year old male, weighing 65.0 kg (143.0 pounds)
Adverse reactions / side effects: Abdominal Pain, Blood Alkaline Phosphatase Increased, Enterocolitis Haemorrhagic, Blood Creatine Phosphokinase Increased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Colonoscopy, Drug Interaction, Liver Disorder, Glycosylated Haemoglobin Increased, Colonic Stenosis, Gamma-Glutamyltransferase Increased, Aspartate Aminotransferase Increased, Pancreatitis, Melaena, White Blood Cell Count Increased
Adverse event resulted in: disablity
Suspect drug(s):
Rocephin
Dosage: 2 g/day
Indication: Pyrexia
Start date: 2007-02-07
End date: 2007-02-13
Voltaren
Dosage: 100 mg/day
Indication: Pyrexia
Start date: 2007-02-06
End date: 2007-02-13
Other drugs received by patient: Futhan
Adverse event in 56 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-03-28
Patient: 56 year old male, weighing 65.0 kg (143.0 pounds)
Adverse reactions / side effects: Abdominal Pain, Blood Alkaline Phosphatase Increased, Enterocolitis Haemorrhagic, Blood Creatine Phosphokinase Increased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Colonoscopy, Drug Interaction, Glycosylated Haemoglobin Increased, Colonic Stenosis, Gamma-Glutamyltransferase Increased, Aspartate Aminotransferase Increased, Pancreatitis, Melaena, White Blood Cell Count Increased
Adverse event resulted in: disablity
Suspect drug(s):
Rocephin
Dosage: 2 g/day
Indication: Pyrexia
Start date: 2007-02-07
End date: 2007-02-13
Voltaren
Dosage: 100 mg/day
Indication: Pyrexia
Start date: 2007-02-06
End date: 2007-02-13
Other drugs received by patient: Futhan
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):
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
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
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
Azulfidine EN (Sulfasalazine) PER Oral NOS
Dosage: 1 g, d, oral
Administration route: Oral
Indication: Rheumatoid Arthritis
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
Adverse event in 49 year old male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from United States on 2007-02-15
Patient: 49 year old male, weighing 99.8 kg (219.5 pounds)
Adverse reactions / side effects: Burning Sensation, Abdominal Discomfort, Panic Attack, Pain, Dizziness, Feeling Abnormal
Adverse event resulted in: disablity
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in 31 year old female receiving Voltaren (Diclofenac)
Reported by a physician from Netherlands on 2007-02-02
Patient: 31 year old female
Adverse reactions / side effects: Muscle Swelling, Monoplegia, Pain, Scar
Adverse event resulted in: disablity
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in 40 year old male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Finland on 2007-02-01
Patient: 40 year old male
Adverse reactions / side effects: Pain, Musculoskeletal Discomfort, Hypoaesthesia, Neoplasm
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Norflex
Dosage: (60 mg, single dose)
Indication: Back Pain
Start date: 2006-11-26
End date: 2006-11-26
Voltaren
Dosage: (75 mg, single dose)
Indication: Back Pain
Start date: 2006-11-26
End date: 2006-11-26
Other drugs received by patient: Burana
Adverse event in 80 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Norway on 2007-01-30
Patient: 80 year old female
Adverse reactions / side effects: Paraplegia, Spinal Epidural Haemorrhage, Urinary Tract Infection, Drug Interaction, Conus Medullaris Syndrome
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Voltaren
Administration route: Oral
Morphine
Administration route: Oral
Neurontin
Dosage: 400 mg, 5qd
Administration route: Oral
Paracet
Administration route: Oral
Levaxin
Administration route: Oral
Simvastatin
Dosage: 40 mg, qd
Administration route: Oral
Tegretol
Dosage: 100 mg, bid
Administration route: Oral
Warfarin Sodium
Dosage: 2.5 mg, 3 to 4 times/day
Administration route: Oral
Indication: Atrial Fibrillation
End date: 2006-11-30
Adverse event in 80 year old female receiving Voltaren (Diclofenac)
Reported by a health professional (non-physician/pharmacist) from Norway on 2007-01-26
Patient: 80 year old female
Adverse reactions / side effects: Blood Pressure Increased, Paraplegia, Blood Potassium Decreased, Spinal Epidural Haemorrhage, International Normalised Ratio Increased, Drug Interaction
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Zocor
Administration route: Oral
Voltaren
Administration route: Oral
Levaxin
Administration route: Oral
Marevan
Administration route: Oral
Indication: Atrial Fibrillation
End date: 2006-11-30
Paracet
Administration route: Oral
Tegretol
Administration route: Oral
Other drugs received by patient: Morfin; Neurontin
Adverse event in 40 year old male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Finland on 2007-01-26
Patient: 40 year old male
Adverse reactions / side effects: Injection Site Mass, Injection Site Discomfort, Injection Site Pain, Injection Site Anaesthesia
Adverse event resulted in: disablity
Suspect drug(s):
Voltaren
Dosage: 75 mg/day
Indication: Back Pain
Start date: 2006-11-26
Norflex
Indication: Back Pain
Start date: 2006-11-26
Other drugs received by patient: Burana
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