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Index of reports
> Cases resulting in death (52)
Below is the selection of adverse event reports related to Voltaren (Diclofenac) that includes cases resulting in death.
Reports 1 - 25 of 52 Next >>
Adverse event in female receiving Voltaren (Diclofenac)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-10-30
Patient: female
Adverse reactions / side effects: Gastrointestinal Infection, Toxic Epidermal Necrolysis
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Cravit
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Olmetec
Administration route: Oral
Indication: Hypertension
Lansoprazole
Indication: Gastric Ulcer
Lansoprazole
Administration route: Oral
Apresoline
Administration route: Oral
Indication: Hypertension
Omegacin
Indication: Interstitial Lung Disease
Dormicum
Indication: Sedation
Pentazocine Lactate
Indication: Sedation
Voltaren
Indication: Hyperthermia
Prodif
Indication: Interstitial Lung Disease
Baktar
Administration route: Oral
Indication: Interstitial Lung Disease
Norvasc
Administration route: Oral
Indication: Hypertension
Other drugs received by patient: Rheumatrex; Rimatil; Solu-Medrol; Elaspol; Predonine; Predonine
Adverse event in 85 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Norway on 2007-10-29
Patient: 85 year old female
Adverse reactions / side effects: Tachycardia, Tricuspid Valve Incompetence, C-Reactive Protein Increased, Dyspepsia, Blood Creatinine Increased, White Blood Cell Count Increased, Anuria, Hiatus Hernia, Diastolic Dysfunction, Renal Cyst, Computerised Tomogram Abnormal, Organ Failure, Haemoglobin Decreased, Hepatic Cyst, Cardiac Failure, Mitral Valve Incompetence, Ejection Fraction Decreased, Peptic Ulcer Perforation
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Ibux
Indication: Myalgia
Prednisolone
Dosage: 10 mg/day
Indication: Myalgia
Voltaren
Indication: Myalgia
Other drugs received by patient: Zantac
Adverse event in 58 year old female receiving Voltaren (Diclofenac)
Reported by a consumer/non-health professional from United States on 2007-10-23
Patient: 58 year old female
Adverse reactions / side effects: Vomiting, Dyspnoea, Nausea, Atrial Fibrillation, Gastric Ulcer, Cardiac Failure, Chest Pain, Pleural Effusion, Melaena, Ulcer Haemorrhage
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Voltaren
Indication: Rheumatoid Arthritis
Kineret
Indication: Rheumatoid Arthritis
Start date: 2003-04-01
End date: 2003-05-01
Prednisolone
Other drugs received by patient: Methotrexate; Plasmapheresis; Hydroxychloroquine Sulfate; Metoprolol Succinate; Furosemide; Levothyroxine Sodium; Esomeprazole Magnesium
Adverse event in receiving Voltaren (Diclofenac)
Reported by a pharmacist from Japan on 2007-10-15
Patient:
Adverse reactions / side effects: Cardiac Failure
Adverse event resulted in: death
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in 53 year old female receiving Voltaren (Diclofenac)
Reported by a consumer/non-health professional from Brazil on 2007-10-03
Patient: 53 year old female, weighing 90.0 kg (198.0 pounds)
Adverse reactions / side effects: Upper Limb Deformity, Application Site Anaesthesia, Metastases TO Liver, Application Site Necrosis, Gastrointestinal Carcinoma, Application Site Erythema, Application Site Pain
Adverse event resulted in: death
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-07-31
Patient: male, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Shock
Adverse event resulted in: death
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in 70 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-07-31
Patient: 70 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Sepsis, Liver Disorder, Stevens-Johnson Syndrome
Adverse event resulted in: death
Suspect drug(s):
Naproxen
Administration route: Oral
Indication: Pyrexia
Start date: 2006-09-20
End date: 2006-09-26
Rohypnol
Administration route: Oral
Start date: 2006-09-13
End date: 2006-09-15
Rohypnol
Administration route: Oral
Start date: 2006-09-18
End date: 2006-09-19
Rohypnol
Administration route: Oral
Start date: 2006-09-21
End date: 2006-09-21
Rohypnol
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-26
Cercine
Administration route: Oral
Indication: Convulsion Prophylaxis
Start date: 2006-09-24
End date: 2006-09-26
Perdipine
Dosage: dose increased or decreased based on blood pressure, on an as needed basis
Indication: Hypertension
Start date: 2006-08-24
End date: 2006-08-24
Amoban
Dosage: drug name: amoban tablets 7.5.
Administration route: Oral
Start date: 2006-09-20
End date: 2006-09-20
Amoban
Administration route: Oral
Start date: 2006-09-22
End date: 2006-09-23
Amoban
Administration route: Oral
Start date: 2006-09-25
End date: 2006-09-25
Magmitt
Administration route: Oral
Indication: Constipation
Start date: 2006-08-29
End date: 2006-09-26
Phenobarbital TAB
Administration route: Oral
Indication: Convulsion Prophylaxis
Start date: 2006-08-28
End date: 2006-09-23
Myslee
Administration route: Oral
Start date: 2006-08-22
End date: 2006-08-22
Myslee
Administration route: Oral
Start date: 2006-08-31
End date: 2006-08-31
Myslee
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-23
Ubretid
Administration route: Oral
Indication: Neurogenic Bladder
Start date: 2006-09-08
End date: 2006-09-29
Spelear
Administration route: Oral
Indication: Sputum Retention
Start date: 2006-09-14
End date: 2006-09-24
Selbex
Administration route: Oral
Indication: Gastritis
Start date: 2006-09-24
End date: 2006-09-24
Lansoprazole
Administration route: Oral
Indication: Gastric Ulcer
Start date: 2006-08-24
End date: 2006-08-24
Lansoprazole
Administration route: Oral
Start date: 2006-09-06
End date: 2006-09-29
Tegretol
Administration route: Oral
Indication: Wound Complication
Start date: 2006-09-22
End date: 2006-09-23
Aspirin
Administration route: Oral
Indication: Cerebral Infarction
Start date: 2006-08-30
End date: 2006-09-30
Polaramine
Administration route: Oral
Indication: Pruritus
Start date: 2006-09-23
End date: 2006-09-23
Loxonin
Administration route: Oral
Indication: Wound Complication
Start date: 2006-09-18
End date: 2006-09-20
Loxonin
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-24
Voltaren
Indication: Wound Complication
Start date: 2006-08-24
End date: 2006-08-24
Voltaren
Dosage: form: rectal suppository.
Start date: 2006-09-04
Voltaren
Start date: 2006-09-17
End date: 2006-09-17
Voltaren
Start date: 2006-09-18
End date: 2006-09-19
Voltaren
Start date: 2006-09-20
End date: 2006-09-22
Voltaren
Start date: 2006-09-23
End date: 2006-09-23
Ketoprofen
Dosage: form: tape. dose: adjusted 10 x 14 cm.
Indication: Wound Complication
Start date: 2006-09-17
Laxoberon
Dosage: dose: as needed
Administration route: Oral
Indication: Constipation
Start date: 2006-09-02
Rinderon-VG
Dosage: dose: as needed
Administration route: Topical
Indication: Rash
Start date: 2006-09-18
Solu-Medrol
Indication: Asthma
Start date: 2006-09-20
End date: 2006-09-21
Aminofluid
Indication: Fluid Replacement
Start date: 2006-09-25
End date: 2006-09-26
Pasil
Indication: Infection
Start date: 2006-09-20
End date: 2006-09-20
Finibax
Indication: Infection
Start date: 2006-09-19
End date: 2006-09-20
Flumarin
Indication: Infection
Start date: 2006-09-17
End date: 2006-09-17
NEO-Minophagen C
Indication: Hepatic Function Abnormal
Start date: 2006-09-01
End date: 2006-09-11
NEO-Minophagen C
Start date: 2006-09-25
End date: 2006-09-27
NEO-Minophagen C
Start date: 2006-09-29
End date: 2006-10-12
Sennoside
Administration route: Oral
Indication: Constipation
Start date: 2006-08-22
End date: 2006-08-22
Humulin 70 / 30
Indication: Hyperglycaemia
Start date: 2006-08-23
End date: 2006-08-24
Mobic
Administration route: Oral
Start date: 2006-08-24
End date: 2006-08-24
Albumin (Human)
Start date: 2006-08-24
End date: 2006-08-24
1 Suspected Drug
Dosage: drug name reported as anapeine (ropivacaine)
Start date: 2006-08-24
End date: 2006-08-26
Omeprazole
Start date: 2006-08-24
End date: 2006-08-30
1 Suspected Drug
Dosage: drug name reported as pansporin (cefotiam hydrochloride)
Indication: Infection Prophylaxis
Start date: 2006-08-24
End date: 2006-08-26
Cataclot
Indication: Cerebral Infarction
Start date: 2006-08-24
End date: 2006-08-24
Multivitamin Additive
Dosage: total daily dose =1 vial
Indication: Vitamin Supplementation
Start date: 2006-08-24
End date: 2006-08-30
Novo-Heparin
Indication: Drug USE FOR Unknown Indication
Start date: 2006-08-24
End date: 2006-08-27
Bisolvon
Dosage: taken on an as needed basis
Start date: 2006-08-24
End date: 2006-08-24
Bisolvon
Dosage: taken on an as needed basis
Start date: 2006-08-29
End date: 2006-09-04
Radicut
Indication: Cerebral Infarction
Start date: 2006-08-24
End date: 2006-09-03
Amino Acid INJ
Indication: Nutritional Support
Start date: 2006-08-24
End date: 2006-08-25
Other drugs received by patient: Unspecified Drug
Adverse event in 70 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-07-31
Patient: 70 year old male
Adverse reactions / side effects: Stevens-Johnson Syndrome
Adverse event resulted in: death
Suspect drug(s):
Perdipine
Dosage: daily dose reported: increased or decreased based on blood pressure, on an as needed basis.
Indication: Hypertension
Start date: 2006-08-24
End date: 2006-08-24
Naproxen
Administration route: Oral
Indication: Pyrexia
Start date: 2006-09-20
End date: 2006-09-26
Rohypnol
Administration route: Oral
Start date: 2006-09-13
End date: 2006-09-15
Rohypnol
Administration route: Oral
Start date: 2006-09-18
End date: 2006-09-19
Rohypnol
Administration route: Oral
Start date: 2006-09-21
End date: 2006-09-21
Rohypnol
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-26
Cercine
Administration route: Oral
Indication: Convulsion Prophylaxis
Start date: 2006-09-24
End date: 2006-09-26
Myslee
Administration route: Oral
Start date: 2006-08-22
End date: 2006-08-22
Myslee
Administration route: Oral
Start date: 2006-08-31
End date: 2006-08-31
Myslee
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-23
Sennoside
Administration route: Oral
Indication: Constipation
Start date: 2006-08-22
End date: 2006-08-22
Humulin 70 / 30
Indication: Hyperglycaemia
Start date: 2006-08-23
End date: 2006-08-24
Lansoprazole
Administration route: Oral
Indication: Gastric Ulcer
Start date: 2006-08-24
End date: 2006-08-24
Lansoprazole
Administration route: Oral
Start date: 2006-09-06
End date: 2006-09-29
Mobic
Administration route: Oral
Start date: 2006-08-24
End date: 2006-08-24
Albumin (Human)
Start date: 2006-08-24
End date: 2006-08-24
Ropivacaine
Dosage: drug reported as anapeine.
Start date: 2006-08-24
End date: 2006-08-26
Omeprazole
Start date: 2006-08-24
End date: 2006-08-30
Pansporin
Indication: Infection Prophylaxis
Start date: 2006-08-24
End date: 2006-08-26
Cataclot
Indication: Cerebral Infarction
Start date: 2006-08-24
End date: 2006-08-24
Multivitamin Additive
Dosage: daily dose reported as 1 vial.
Indication: Vitamin Supplementation
Start date: 2006-08-24
End date: 2006-08-30
Novo-Heparin
Indication: Drug USE FOR Unknown Indication
Start date: 2006-08-24
End date: 2006-08-27
Radicut
Indication: Cerebral Infarction
Start date: 2006-08-24
End date: 2006-09-03
Bisolvon
Dosage: daily dose reported: on an as needed basis.
Start date: 2006-08-24
End date: 2006-08-24
Bisolvon
Dosage: daily dose reported: on an as needed basis.
Start date: 2006-08-29
End date: 2006-09-04
Amino Acid INJ
Indication: Nutritional Support
Start date: 2006-08-24
End date: 2006-08-25
Voltaren
Start date: 2006-08-24
End date: 2006-08-24
Voltaren
Start date: 2006-09-04
End date: 2006-09-23
Voltaren
Start date: 2006-09-17
End date: 2006-09-17
Voltaren
Start date: 2006-09-20
End date: 2006-09-22
Amino Acid INJ
Start date: 2006-08-25
End date: 2006-08-30
Wakobital
Indication: Convulsion Prophylaxis
Start date: 2006-08-25
End date: 2006-08-28
Phenobarbital TAB
Administration route: Oral
Indication: Convulsion Prophylaxis
Start date: 2006-08-28
End date: 2006-09-23
Magium (Magnesium Oxide)
Dosage: drug reported as magmitt.
Administration route: Oral
Indication: Constipation
Start date: 2006-08-29
End date: 2006-09-26
Aspirin
Administration route: Oral
Indication: Prophylaxis
Start date: 2006-08-30
End date: 2006-09-30
NEO-Minophagen C
Start date: 2006-09-01
End date: 2006-09-11
NEO-Minophagen C
Start date: 2006-09-25
End date: 2006-09-27
NEO-Minophagen C
Start date: 2006-09-29
End date: 2006-10-12
Laxoberon
Dosage: daily dose reported: adequate dose as needed.
Administration route: Oral
Indication: Constipation
Start date: 2006-09-02
Ubretid
Administration route: Oral
Indication: Neurogenic Bladder
Start date: 2006-09-08
End date: 2006-09-29
Spelear
Administration route: Oral
Start date: 2006-09-14
End date: 2006-09-24
Ketoprofen
Administration route: Oral
Start date: 2006-09-17
Flumarin
Indication: Infection
Start date: 2006-09-17
End date: 2006-09-17
Loxonin
Administration route: Oral
Start date: 2006-09-18
End date: 2006-09-20
Loxonin
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-24
Rinderon
Dosage: daily dose reported: adequate dose as needed. drug reported as rinderon-vg
Administration route: Topical
Start date: 2006-09-18
Finibax
Indication: Infection
Start date: 2006-09-19
End date: 2006-09-20
Amoban
Administration route: Oral
Start date: 2006-09-20
End date: 2006-09-20
Amoban
Administration route: Oral
Start date: 2006-09-22
End date: 2006-09-23
Amoban
Administration route: Oral
Start date: 2006-09-25
End date: 2006-09-25
Solu-Medrol
Start date: 2006-09-20
End date: 2006-09-21
Pazufloxacin Mesilate
Dosage: drug reported as pasil.
Indication: Infection
Start date: 2006-09-20
End date: 2006-09-20
Tegretol
Administration route: Oral
Start date: 2006-09-22
End date: 2006-09-23
Polaramine
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-23
Selbex
Administration route: Oral
Indication: Gastritis
Start date: 2006-09-24
End date: 2006-09-24
Aminofluid
Indication: Fluid Replacement
Start date: 2006-09-25
End date: 2006-09-26
Adverse event in female receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-07-30
Patient: female, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Hepatorenal Syndrome, Condition Aggravated, Hepatitis B
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Enbrel
Indication: Rheumatoid Arthritis
Start date: 2006-11-30
End date: 2007-03-01
Prograf
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2005-10-27
End date: 2007-03-06
Predonine
Administration route: Oral
Indication: Rheumatoid Arthritis
End date: 2007-03-06
Voltaren
Indication: Rheumatoid Arthritis
End date: 2007-03-06
Hypen
Administration route: Oral
Indication: Rheumatoid Arthritis
End date: 2007-03-06
Methotrexate
Dosage: 2.5 mg, frequency unknown
Indication: Rheumatoid Arthritis
End date: 2007-03-06
Iscotin
Administration route: Oral
Start date: 2006-04-20
End date: 2007-03-06
Other drugs received by patient: Foliamin; Kolantyl; Diovan; ONE-Alpha; Famotidine
Adverse event in 70 year old male receiving Voltaren (Diclofenac)
Reported by a pharmacist from Japan on 2007-07-26
Patient: 70 year old male
Adverse reactions / side effects: Oculomucocutaneous Syndrome, Sepsis, Liver Disorder
Adverse event resulted in: death
Suspect drug(s):
Naproxen
Dosage: unit dose: 100 mg
Administration route: Oral
Indication: Pyrexia
Start date: 2006-09-20
End date: 2006-09-26
Rohypnol
Dosage: unit dose: 1 mg
Administration route: Oral
Indication: Insomnia
Start date: 2006-09-13
End date: 2006-09-26
Cercine
Administration route: Oral
Indication: Convulsion Prophylaxis
Start date: 2006-09-24
End date: 2006-09-26
Amoban
Administration route: Oral
Indication: Insomnia
Start date: 2006-09-20
End date: 2006-09-25
Magmitt
Dosage: unit dose: 330 mg
Administration route: Oral
Indication: Constipation
Start date: 2006-08-29
End date: 2006-09-26
Phenobarbital TAB
Dosage: unit dose: 10 mg
Administration route: Oral
Indication: Convulsion Prophylaxis
Start date: 2006-08-28
End date: 2006-09-23
Myslee
Dosage: unit dose: 5 mg
Administration route: Oral
Indication: Insomnia
Start date: 2006-08-22
End date: 2006-09-23
Ubretid
Dosage: unit dose: 5 mg
Administration route: Oral
Indication: Neurogenic Bladder
Start date: 2006-09-08
End date: 2006-09-29
Spelear
Dosage: unit dose: 400 mg
Administration route: Oral
Indication: Sputum Retention
Start date: 2006-09-14
End date: 2006-09-24
Selbex
Dosage: unit dose: 50 mg
Administration route: Oral
Indication: Gastritis
Start date: 2006-09-24
End date: 2006-09-24
Lansoprazole
Dosage: unit dose: 15 mg
Administration route: Oral
Indication: Stress Ulcer
Start date: 2006-08-24
End date: 2006-09-29
Tegretol
Dosage: unit dose: 100 mg
Administration route: Oral
Indication: Wound Complication
Start date: 2006-09-22
End date: 2006-09-23
Aspirin
Dosage: unit dose: 100 mg
Administration route: Oral
Indication: Cerebral Infarction
Start date: 2006-08-30
End date: 2006-09-30
Polaramine
Dosage: unit dose: 2 mg
Administration route: Oral
Indication: Pruritus
Start date: 2006-09-23
End date: 2006-09-23
Loxonin
Dosage: unit dose: 60 mg
Administration route: Oral
Indication: Wound Complication
Start date: 2006-09-18
End date: 2006-09-24
Voltaren
Dosage: unit dose: 25 mg
Administration route: Oral
Indication: Wound Complication
Start date: 2006-09-04
End date: 2006-09-23
Ketoprofen
Administration route: Topical
Indication: Wound Complication
Start date: 2006-09-17
Laxoberon
Administration route: Oral
Indication: Constipation
Start date: 2006-09-02
Rinderon-VG
Administration route: Topical
Indication: Rash
Start date: 2006-09-18
Solu-Medrol
Dosage: unit dose: 125 mg
Indication: Asthma
Start date: 2006-09-20
End date: 2006-09-21
Aminofluid
Indication: Fluid Replacement
Start date: 2006-09-25
End date: 2006-09-26
Pasil
Dosage: unit dose: 500 mg
Indication: Infection
Start date: 2006-09-20
End date: 2006-09-20
Finibax
Dosage: unit dose: 0.25 mg
Indication: Infection
Start date: 2006-09-19
End date: 2006-09-20
Flumarin
Dosage: unit dose: 1 g
Indication: Infection
Start date: 2006-09-17
End date: 2006-09-17
NEO-Minophagen C
Dosage: unit dose: 20 ml
Indication: Hepatic Function Abnormal
Start date: 2006-09-01
End date: 2006-09-27
Other drugs received by patient: Sennoside; Humulin 70 / 30; Soldem; Mobic; Albumin (Human); Naropin; Aminotripa 1; Omeprazole; Cataclot; Multivitamin Additive; Heparin; Pansporin; Perdipine; Potacol-R; Potacol-R; Radicut; LOW Molecular Dextran; Bisolvon; Bisolvon; Wakobital
Adverse event in 70 year old male receiving Voltaren (Diclofenac)
Reported by a pharmacist from Japan on 2007-07-24
Patient: 70 year old male
Adverse reactions / side effects: Oculomucocutaneous Syndrome, Sepsis, Liver Disorder
Adverse event resulted in: death
Suspect drug(s):
Naproxen
Dosage: unit dose: 100 mg
Administration route: Oral
Indication: Pyrexia
Start date: 2006-09-20
End date: 2006-09-26
Rohypnol
Dosage: unit dose: 1 mg
Administration route: Oral
Indication: Insomnia
Start date: 2006-09-13
End date: 2006-09-26
Cercine
Administration route: Oral
Indication: Convulsion Prophylaxis
Start date: 2006-09-24
End date: 2006-09-26
Amoban
Administration route: Oral
Indication: Insomnia
Start date: 2006-09-20
End date: 2006-09-25
Magmitt
Dosage: unit dose: 330 mg
Administration route: Oral
Indication: Constipation
Start date: 2006-08-29
End date: 2006-09-26
Phenobarbital TAB
Dosage: unit dose: 10 mg
Administration route: Oral
Indication: Convulsion Prophylaxis
Start date: 2006-08-28
End date: 2006-09-23
Myslee
Dosage: unit dose: 5 mg
Administration route: Oral
Indication: Insomnia
Start date: 2006-08-22
End date: 2006-09-23
Ubretid
Dosage: unit dose: 5 mg
Administration route: Oral
Indication: Neurogenic Bladder
Start date: 2006-09-08
End date: 2006-09-29
Spelear
Dosage: unit dose: 400 mg
Administration route: Oral
Indication: Sputum Retention
Start date: 2006-09-14
End date: 2006-09-24
Selbex
Dosage: unit dose: 50 mg
Administration route: Oral
Indication: Gastritis
Start date: 2006-09-24
End date: 2006-09-24
Lansoprazole
Dosage: unit dose: 15 mg
Administration route: Oral
Indication: Stress Ulcer
Start date: 2006-08-24
End date: 2006-09-29
Tegretol
Dosage: unit dose: 100 mg
Administration route: Oral
Indication: Wound Complication
Start date: 2006-09-22
End date: 2006-09-23
Aspirin
Dosage: unit dose: 100 mg
Administration route: Oral
Indication: Cerebral Infarction
Start date: 2006-08-30
End date: 2006-09-30
Polaramine
Dosage: unit dose: 2 mg
Administration route: Oral
Indication: Pruritus
Start date: 2006-09-23
End date: 2006-09-23
Loxonin
Dosage: unit dose: 60 mg
Administration route: Oral
Indication: Wound Complication
Start date: 2006-09-18
End date: 2006-09-24
Voltaren
Dosage: unit dose: 25 mg
Administration route: Oral
Indication: Wound Complication
Start date: 2006-09-04
End date: 2006-09-23
Ketoprofen
Administration route: Topical
Indication: Wound Complication
Start date: 2006-09-17
Laxoberon
Administration route: Oral
Indication: Constipation
Start date: 2006-09-02
Rinderon-VG
Administration route: Topical
Indication: Rash
Start date: 2006-09-18
Solu-Medrol
Dosage: unit dose: 125 mg
Indication: Asthma
Start date: 2006-09-20
End date: 2006-09-21
Aminofluid
Indication: Fluid Replacement
Start date: 2006-09-25
End date: 2006-09-26
Pasil
Dosage: unit dose: 500 mg
Indication: Infection
Start date: 2006-09-20
End date: 2006-09-20
Finibax
Dosage: unit dose: 0.25 mg
Indication: Infection
Start date: 2006-09-19
End date: 2006-09-20
Flumarin
Dosage: unit dose: 1 g
Indication: Infection
Start date: 2006-09-17
End date: 2006-09-17
NEO-Minophagen C
Dosage: unit dose: 20 ml
Indication: Hepatic Function Abnormal
Start date: 2006-09-01
End date: 2006-09-27
Other drugs received by patient: Sennoside; Humulin 70 / 30; Soldem; Mobic; Albumin (Human); Naropin; Aminotripa 1; Omeprazole; Cataclot; Multivitamin Additive; Heparin; Pansporin; Perdipine; Potacol-R; Potacol-R; Radicut; LOW Molecular Dextran; Bisolvon; Bisolvon; Wakobital
Adverse event in 70 year old male receiving Voltaren (Diclofenac)
Reported by a pharmacist from Japan on 2007-07-20
Patient: 70 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Oculomucocutaneous Syndrome, Sepsis, Liver Disorder
Adverse event resulted in: death
Suspect drug(s):
Cercine
Administration route: Oral
Indication: Convulsion Prophylaxis
Start date: 2006-09-24
End date: 2006-09-26
Rohypnol
Administration route: Oral
Start date: 2006-09-13
End date: 2006-09-15
Rohypnol
Administration route: Oral
Start date: 2006-09-18
End date: 2006-09-19
Rohypnol
Administration route: Oral
Start date: 2006-09-21
End date: 2006-09-21
Rohypnol
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-26
Naproxen
Administration route: Oral
Indication: Pyrexia
Start date: 2006-09-20
End date: 2006-09-26
Amoban
Dosage: drug name: amoban tablets 7.5.
Administration route: Oral
Start date: 2006-09-20
End date: 2006-09-20
Amoban
Administration route: Oral
Start date: 2006-09-22
End date: 2006-09-23
Amoban
Administration route: Oral
Start date: 2006-09-25
End date: 2006-09-25
Magmitt
Administration route: Oral
Indication: Constipation
Start date: 2006-08-29
End date: 2006-09-26
Phenobarbital TAB
Administration route: Oral
Indication: Convulsion Prophylaxis
Start date: 2006-08-28
End date: 2006-09-23
Myslee
Administration route: Oral
Start date: 2006-08-22
End date: 2006-08-22
Myslee
Administration route: Oral
Start date: 2006-08-31
End date: 2006-08-31
Myslee
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-23
Ubretid
Administration route: Oral
Indication: Neurogenic Bladder
Start date: 2006-09-08
End date: 2006-09-29
Spelear
Administration route: Oral
Indication: Sputum Retention
Start date: 2006-09-14
End date: 2006-09-24
Selbex
Administration route: Oral
Indication: Gastritis
Start date: 2006-09-24
End date: 2006-09-24
Lansoprazole
Administration route: Oral
Indication: Stress Ulcer
Start date: 2006-08-24
End date: 2006-08-24
Lansoprazole
Administration route: Oral
Start date: 2006-09-06
End date: 2006-09-29
Tegretol
Administration route: Oral
Indication: Wound Complication
Start date: 2006-09-22
End date: 2006-09-23
Aspirin
Administration route: Oral
Indication: Cerebral Infarction
Start date: 2006-08-30
End date: 2006-09-30
Polaramine
Administration route: Oral
Indication: Pruritus
Start date: 2006-09-23
End date: 2006-09-23
Loxonin
Administration route: Oral
Indication: Wound Complication
Start date: 2006-09-18
End date: 2006-09-20
Loxonin
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-24
Voltaren
Dosage: form: rectal suppository.
Administration route: Oral
Indication: Wound Complication
Start date: 2006-09-04
End date: 2006-09-16
Voltaren
Administration route: Oral
Start date: 2006-09-17
End date: 2006-09-17
Voltaren
Administration route: Oral
Start date: 2006-09-18
End date: 2006-09-19
Voltaren
Administration route: Oral
Start date: 2006-09-20
End date: 2006-09-22
Voltaren
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-23
Ketoprofen
Dosage: form: tape. dose: adjusted 10 x 14 cm.
Administration route: Topical
Indication: Wound Complication
Start date: 2006-09-17
Laxoberon
Dosage: dose: adjusted.
Administration route: Oral
Indication: Constipation
Start date: 2006-09-02
Rinderon-VG
Dosage: dosage adjusted.
Administration route: Topical
Indication: Rash
Start date: 2006-09-18
Solu-Medrol
Indication: Asthma
Start date: 2006-09-20
End date: 2006-09-21
Aminofluid
Indication: Fluid Replacement
Start date: 2006-09-25
End date: 2006-09-26
Pasil
Indication: Infection
Start date: 2006-09-20
End date: 2006-09-20
Finibax
Indication: Infection
Start date: 2006-09-19
End date: 2006-09-20
Flumarin
Indication: Infection
Start date: 2006-09-17
End date: 2006-09-17
NEO-Minophagen C
Indication: Hepatic Function Abnormal
Start date: 2006-09-01
End date: 2006-09-11
NEO-Minophagen C
Start date: 2006-09-25
End date: 2006-09-27
Other drugs received by patient: Unspecified Drug
Adverse event in 70 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-07-20
Patient: 70 year old male
Adverse reactions / side effects: Stevens-Johnson Syndrome
Adverse event resulted in: death
Suspect drug(s):
Perdipine
Dosage: daily dose reported: increased or decreased based on blood pressure, on an as needed basis.
Indication: Hypertension
Start date: 2006-08-24
End date: 2006-08-24
Naproxen
Administration route: Oral
Indication: Pyrexia
Start date: 2006-09-20
End date: 2006-09-26
Rohypnol
Administration route: Oral
Start date: 2006-09-13
End date: 2006-09-15
Rohypnol
Administration route: Oral
Start date: 2006-09-18
End date: 2006-09-19
Rohypnol
Administration route: Oral
Start date: 2006-09-21
End date: 2006-09-21
Rohypnol
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-26
Cercine
Administration route: Oral
Indication: Convulsion Prophylaxis
Start date: 2006-09-24
End date: 2006-09-26
Myslee
Administration route: Oral
Start date: 2006-08-22
End date: 2006-08-22
Myslee
Administration route: Oral
Start date: 2006-08-31
End date: 2006-08-31
Myslee
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-23
Sennoside
Administration route: Oral
Indication: Constipation
Start date: 2006-08-22
End date: 2006-08-22
Humulin 70 / 30
Indication: Hyperglycaemia
Start date: 2006-08-23
End date: 2006-08-24
Lansoprazole
Administration route: Oral
Indication: Gastric Ulcer
Start date: 2006-08-24
End date: 2006-08-24
Lansoprazole
Administration route: Oral
Start date: 2006-09-06
End date: 2006-09-29
Mobic
Administration route: Oral
Start date: 2006-08-24
End date: 2006-08-24
Albumin (Human)
Start date: 2006-08-24
End date: 2006-08-24
Ropivacaine
Dosage: drug reported as anapeine.
Start date: 2006-08-24
End date: 2006-08-26
Omeprazole
Start date: 2006-08-24
End date: 2006-08-30
Pansporin
Indication: Infection Prophylaxis
Start date: 2006-08-24
End date: 2006-08-26
Cataclot
Indication: Cerebral Infarction
Start date: 2006-08-24
End date: 2006-08-24
Multivitamin Additive
Dosage: daily dose reported as 1 vial.
Indication: Vitamin Supplementation
Start date: 2006-08-24
End date: 2006-08-30
Novo-Heparin
Indication: Drug USE FOR Unknown Indication
Start date: 2006-08-24
End date: 2006-08-27
Radicut
Indication: Cerebral Infarction
Start date: 2006-08-24
End date: 2006-09-03
Bisolvon
Dosage: daily dose reported: on an as needed basis.
Start date: 2006-08-24
End date: 2006-08-24
Bisolvon
Dosage: daily dose reported: on an as needed basis.
Start date: 2006-08-29
End date: 2006-09-04
Amino Acid INJ
Indication: Nutritional Support
Start date: 2006-08-24
End date: 2006-08-25
Voltaren
Start date: 2006-08-24
End date: 2006-08-24
Voltaren
Start date: 2006-09-04
End date: 2006-09-23
Voltaren
Start date: 2006-09-17
End date: 2006-09-17
Voltaren
Start date: 2006-09-20
End date: 2006-09-22
Amino Acid INJ
Start date: 2006-08-25
End date: 2006-08-30
Wakobital
Indication: Convulsion Prophylaxis
Start date: 2006-08-25
End date: 2006-08-28
Phenobarbital TAB
Administration route: Oral
Indication: Convulsion Prophylaxis
Start date: 2006-08-28
End date: 2006-09-23
Magium (Magnesium Oxide)
Dosage: drug reported as magmitt.
Administration route: Oral
Indication: Constipation
Start date: 2006-08-29
End date: 2006-09-26
Aspirin
Administration route: Oral
Indication: Prophylaxis
Start date: 2006-08-30
End date: 2006-09-30
NEO-Minophagen C
Start date: 2006-09-01
End date: 2006-09-11
NEO-Minophagen C
Start date: 2006-09-25
End date: 2006-09-27
NEO-Minophagen C
Start date: 2006-09-29
End date: 2006-10-12
Laxoberon
Dosage: daily dose reported: adequate dose as needed.
Administration route: Oral
Indication: Constipation
Start date: 2006-09-02
Ubretid
Administration route: Oral
Indication: Neurogenic Bladder
Start date: 2006-09-08
End date: 2006-09-29
Spelear
Administration route: Oral
Start date: 2006-09-14
End date: 2006-09-24
Ketoprofen
Administration route: Oral
Start date: 2006-09-17
Flumarin
Indication: Infection
Start date: 2006-09-17
End date: 2006-09-17
Loxonin
Administration route: Oral
Start date: 2006-09-18
End date: 2006-09-20
Loxonin
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-24
Rinderon
Dosage: daily dose reported: adequate dose as needed. drug reported as rinderon-vg
Administration route: Topical
Start date: 2006-09-18
Finibax
Indication: Infection
Start date: 2006-09-19
End date: 2006-09-20
Amoban
Administration route: Oral
Start date: 2006-09-20
End date: 2006-09-20
Amoban
Administration route: Oral
Start date: 2006-09-22
End date: 2006-09-23
Amoban
Administration route: Oral
Start date: 2006-09-25
End date: 2006-09-25
Solu-Medrol
Start date: 2006-09-20
End date: 2006-09-21
Pazufloxacin Mesilate
Dosage: drug reported as pasil.
Indication: Infection
Start date: 2006-09-20
End date: 2006-09-20
Tegretol
Administration route: Oral
Start date: 2006-09-22
End date: 2006-09-23
Polaramine
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-23
Selbex
Administration route: Oral
Indication: Gastritis
Start date: 2006-09-24
End date: 2006-09-24
Aminofluid
Indication: Fluid Replacement
Start date: 2006-09-25
End date: 2006-09-26
Adverse event in male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-07-17
Patient: male, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Shock
Adverse event resulted in: death
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in 20 year old male receiving Voltaren (Diclofenac)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-07-16
Patient: 20 year old male, weighing 55.0 kg (121.0 pounds)
Adverse reactions / side effects: Blood Bilirubin Increased, Drug Eruption, Disseminated Intravascular Coagulation, Pyrexia, Haematocrit Decreased, RED Blood Cell Count Decreased, Gamma-Glutamyltransferase Increased, Dermatitis Bullous, Blood Creatinine Increased, Melaena, Blister, Stevens-Johnson Syndrome, White Blood Cell Count Increased, Blood Pressure Increased, Pneumonia, Histiocytosis Haematophagic, Blood Urea Increased, Alanine Aminotransferase Increased, Life Support, Pulmonary Haemorrhage, Mucosal Erosion, Haemoglobin Decreased, Aspartate Aminotransferase Increased, Platelet Count Decreased, Skin Erosion
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Voltaren
Dosage: unk, unk
Administration route: Oral
Indication: Pyrexia
Voltaren
Dosage: 25 mg/day
Start date: 2007-03-22
End date: 2007-03-29
Loxoprofen
Dosage: 60 mg/day
Administration route: Oral
Indication: Headache
Start date: 2007-03-28
End date: 2007-04-03
Meropen
Dosage: 1.5 g/day
Indication: Infection
Start date: 2007-03-23
End date: 2007-03-28
Other drugs received by patient: Minocycline HCL; Rocephin; Zyvox; Amikacin; Funguard
Adverse event in 20 year old male receiving Voltaren (Diclofenac)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-07-16
Patient: 20 year old male, weighing 55.0 kg (121.0 pounds)
Adverse reactions / side effects: Blood Bilirubin Increased, Drug Eruption, Disseminated Intravascular Coagulation, Pyrexia, Haematocrit Decreased, RED Blood Cell Count Decreased, Gamma-Glutamyltransferase Increased, Dermatitis Bullous, Blood Creatinine Increased, Melaena, Blister, Stevens-Johnson Syndrome, White Blood Cell Count Increased, Blood Pressure Increased, Pneumonia, Histiocytosis Haematophagic, Blood Urea Increased, Alanine Aminotransferase Increased, Life Support, Pulmonary Haemorrhage, Mucosal Erosion, Haemoglobin Decreased, Aspartate Aminotransferase Increased, Platelet Count Decreased, Skin Erosion
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Voltaren
Dosage: unk, unk
Administration route: Oral
Indication: Pyrexia
Voltaren
Dosage: 25 mg/day
Start date: 2007-03-22
End date: 2007-03-29
Loxoprofen
Dosage: 60 mg/day
Administration route: Oral
Indication: Headache
Start date: 2007-03-28
End date: 2007-04-03
Meropen
Dosage: 1.5 g/day
Indication: Infection
Start date: 2007-03-23
End date: 2007-03-28
Other drugs received by patient: Minocycline HCL; Rocephin; Zyvox; Amikacin; Funguard
Adverse event in 70 year old female receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-07-13
Patient: 70 year old female, weighing 36.0 kg (79.2 pounds)
Adverse reactions / side effects: Hyperhidrosis, Cardiac Massage, Blood Creatinine Increased, White Blood Cell Count Increased, Metabolic Acidosis, Urine Output Decreased, Blood Lactate Dehydrogenase Increased, Hypotension, Haemodialysis, Respiratory Rate Decreased, Heart Rate Decreased, Aspartate Aminotransferase Increased, Depressed Level of Consciousness, Intubation, Anaphylactic Shock, Pallor, Haematocrit Decreased, RED Blood Cell Count Decreased, Tachypnoea, Oxygen Supplementation, Hepatitis Fulminant, Oxygen Saturation Decreased, Blood Urea Increased, Mydriasis, Alanine Aminotransferase Increased, Drug Hypersensitivity, Life Support, Hepatic Enzyme Increased, Haemoglobin Decreased, Blood Glucose Decreased, Catheterisation Cardiac, Feeling Abnormal, Electrocardiogram ST Segment Elevation
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Loxonin; Pentagin; Aspirin; Ticlopidine HCL; Sigmart; Lansoprazole; Artist; Ferromia
Adverse event in 70 year old female receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-07-13
Patient: 70 year old female, weighing 36.0 kg (79.2 pounds)
Adverse reactions / side effects: Hyperhidrosis, Cardiac Massage, Blood Creatinine Increased, White Blood Cell Count Increased, Metabolic Acidosis, Blood Lactate Dehydrogenase Increased, Hypotension, Urine Output Decreased, Haemodialysis, Respiratory Rate Decreased, Heart Rate Decreased, Aspartate Aminotransferase Increased, Depressed Level of Consciousness, Anaphylactic Shock, Pallor, Haematocrit Decreased, RED Blood Cell Count Decreased, Tachypnoea, Oxygen Supplementation, Hepatitis Fulminant, Oxygen Saturation Decreased, Blood Urea Increased, Mydriasis, Drug Hypersensitivity, Alanine Aminotransferase Increased, Life Support, Hepatic Enzyme Increased, Haemoglobin Decreased, Blood Glucose Decreased, Catheterisation Cardiac, Feeling Abnormal, Electrocardiogram ST Segment Elevation
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Loxonin; Pentagin; Aspirin; Ticlopidine HCL; Sigmart; Lansoprazole; Artist; Ferromia
Adverse event in 70 year old female receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-07-12
Patient: 70 year old female
Adverse reactions / side effects: Anaphylactic Shock, Hyperhidrosis, Pallor, Cardiac Massage, Tachypnoea, Oxygen Supplementation, Oxygen Saturation Decreased, Hepatitis Fulminant, Metabolic Acidosis, Mydriasis, Urine Output Decreased, Hypotension, Drug Hypersensitivity, Life Support, Haemodialysis, Hepatic Enzyme Increased, Respiratory Rate Decreased, Blood Glucose Decreased, Heart Rate Decreased, Catheterisation Cardiac, Depressed Level of Consciousness, Electrocardiogram ST Segment Elevation, Feeling Abnormal
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Loxonin; Pentagin
Adverse event in 70 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-07-05
Patient: 70 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Pneumonia, Post Procedural Complication, Pleurisy, Hepatitis, Staphylococcal Sepsis, Haemodialysis, Liver Disorder, Cerebral Infarction, Granulocytopenia, NO Therapeutic Response, Sepsis, Pleural Effusion, Cardiac Arrest, Stevens-Johnson Syndrome, Shock
Adverse event resulted in: death
Suspect drug(s):
Aspirin
Dosage: total daily dose: 100 mg unit dose: 100 mg
Administration route: Oral
Indication: Cerebrovascular Accident Prophylaxis
Start date: 2006-08-30
End date: 2006-09-30
Magmitt
Dosage: total daily dose: 990 mg unit dose: 330 mg
Administration route: Oral
Indication: Constipation
Start date: 2006-08-29
End date: 2006-09-26
Cercine
Dosage: total daily dose: 2 mg unit dose: 2 mg
Administration route: Oral
Indication: Convulsion Prophylaxis
Start date: 2006-09-24
End date: 2006-09-26
Phenobarbital TAB
Dosage: total daily dose: 100 mg unit dose: 100 mg
Administration route: Oral
Indication: Convulsion Prophylaxis
Start date: 2006-08-28
End date: 2006-09-23
Amoban
Dosage: total daily dose: 7.5 mg unit dose: 7.5 mg
Administration route: Oral
Indication: Insomnia
Start date: 2006-09-20
End date: 2006-09-20
Amoban
Dosage: total daily dose: 7.5 mg unit dose: 7.5 mg
Administration route: Oral
Start date: 2006-09-22
End date: 2006-09-23
Amoban
Dosage: total daily dose: 7.5 mg unit dose: 7.5 mg
Administration route: Oral
Start date: 2006-09-25
End date: 2006-09-25
Rohypnol
Dosage: total daily dose: 1 mg unit dose: 1 mg
Administration route: Oral
Indication: Insomnia
Start date: 2006-09-18
End date: 2006-09-19
Rohypnol
Dosage: total daily dose: 1 mg unit dose: 1 mg
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-26
Rohypnol
Dosage: total daily dose: 1 mg unit dose: 1 mg
Administration route: Oral
Start date: 2006-09-13
End date: 2006-09-15
Rohypnol
Dosage: total daily dose: 1 mg unit dose: 1 mg
Administration route: Oral
Start date: 2006-09-21
End date: 2006-09-21
Ubretid
Dosage: total daily dose: 10 mg unit dose: 5 mg
Administration route: Oral
Indication: Neurogenic Bladder
Start date: 2006-09-08
End date: 2006-09-29
Spelear
Dosage: total daily dose: 1200 mg unit dose: 200 mg
Indication: Sputum Retention
Start date: 2006-09-14
End date: 2006-09-24
Takepron
Dosage: total daily dose: 30 mg unit dose: 15 mg
Administration route: Oral
Indication: Gastric Ulcer
Start date: 2006-08-24
End date: 2006-08-24
Takepron
Dosage: total daily dose: 30 mg unit dose: 15 mg
Administration route: Oral
Start date: 2006-09-06
End date: 2006-09-29
Naproxen
Dosage: total daily dose: 300 mg unit dose: 100 mg
Administration route: Oral
Indication: Pyrexia
Start date: 2006-09-20
End date: 2006-09-26
Loxonin
Dosage: total daily dose: 180 mg unit dose: 60 mg
Administration route: Oral
Indication: Intercostal Neuralgia
Start date: 2006-09-23
End date: 2006-09-24
Loxonin
Dosage: total daily dose: 180 mg unit dose: 60 mg
Administration route: Oral
Start date: 2006-09-18
End date: 2006-09-20
Voltaren
Dosage: total daily dose: 25 mg unit dose: 25 mg
Indication: Wound Complication
Start date: 2006-08-24
End date: 2006-08-24
Voltaren
Dosage: total daily dose: 50 mg unit dose: 50 mg
Start date: 2006-09-20
End date: 2006-09-22
Voltaren
Dosage: total daily dose: 50 mg unit dose: 50 mg
Start date: 2006-09-17
End date: 2006-09-17
Voltaren
Dosage: total daily dose: 25 mg unit dose: 25 mg
Start date: 2006-09-04
End date: 2006-09-23
Wakobital
Dosage: total daily dose: 200 mg unit dose: 100 mg
Indication: Convulsion Prophylaxis
Start date: 2006-08-25
End date: 2006-08-28
Potacol-R
Dosage: total daily dose: 500 ml unit dose: 500 ml
Indication: Fluid Replacement
Start date: 2006-08-24
End date: 2006-08-24
Potacol-R
Dosage: total daily dose: 500 ml unit dose: 500 ml
Start date: 2006-08-31
End date: 2006-09-11
Radicut
Dosage: total daily dose: 60 mg unit dose: 30 mg
Indication: Cerebral Infarction
Start date: 2006-08-24
End date: 2006-09-03
Zolpidem
Dosage: total daily dose: 5 mg unit dose: 5 mg
Administration route: Oral
Indication: Insomnia
Start date: 2006-08-22
End date: 2006-08-22
Zolpidem
Dosage: total daily dose: 5 mg unit dose: 5 mg
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-23
Zolpidem
Dosage: total daily dose: 5 mg unit dose: 5 mg
Administration route: Oral
Start date: 2006-08-31
End date: 2006-08-31
Tegretol
Dosage: total daily dose: 100 mg unit dose: 100 mg
Administration route: Oral
Indication: Wound Complication
Start date: 2006-09-22
End date: 2006-09-23
Flumarin
Dosage: total daily dose: 2 g unit dose: 1 g
Indication: Infection
Start date: 2006-09-17
End date: 2006-09-17
Other drugs received by patient: Selbex; Sennoside; Polaramine; Mobic; Mohrus Tape; Laxoberon; Rinderon-VG; Albumin (Human); Humulin 70 / 30; Naropin; Aminotripa No.1; Aminotripa No.2; Aminofluid; Omepral; Cataclot; Solu-Medrol; Soldem 3A; Multivitamin Additive; Novo Heparin; Pasil; Pansporin; Finibax; Perdipine; LOW-Molecular Dextran; Bisolvon; Bisolvon
Adverse event in 70 year old male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Japan on 2007-07-02
Patient: 70 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Blood Bilirubin Increased, Productive Cough, Pruritus, Erythema Annulare, Pyrexia, Dermatitis, C-Reactive Protein Increased, White Blood Cell Count Increased, Pleurisy, Blood Lactate Dehydrogenase Increased, LIP Ulceration, Staphylococcal Infection, Cerebral Infarction, Aspartate Aminotransferase Increased, Insomnia, Depressed Level of Consciousness, Platelet Count Decreased, Hemiplegia, Drug Eruption, Oculomucocutaneous Syndrome, Post Procedural Complication, Culture Urine Positive, Liver Disorder, Lung Neoplasm Malignant, Pleural Effusion, White Blood Cell Count Decreased, Intercostal Neuralgia, Alanine Aminotransferase Increased, Haemorrhoids, Muscular Weakness, Rash, LIP Pain, Haematochezia, Agranulocytosis, Sepsis, Sputum Retention, Cardiac Arrest, Shock, Infection
Adverse event resulted in: death
Suspect drug(s):
Voltaren
Dosage: 25 mg/day
Indication: Wound Complication
Start date: 2006-08-24
End date: 2006-08-24
Voltaren
Dosage: 25 mg/day
Start date: 2006-09-04
End date: 2006-09-23
Voltaren
Dosage: 50 mg/day
Start date: 2006-09-17
End date: 2006-09-17
Voltaren
Dosage: 50 mg/day
Start date: 2006-09-20
End date: 2006-09-20
Voltaren
Dosage: 50 mg/day
Start date: 2006-09-21
End date: 2006-09-21
Voltaren
Dosage: 50 mg/day
Start date: 2006-09-22
End date: 2006-09-22
Tegretol
Dosage: 100 mg/day
Administration route: Oral
Indication: Wound Complication
Start date: 2006-09-22
End date: 2006-09-23
Other drugs received by patient: Amoban; Zolpidem; Rohypnol; Ubretid; Spelear; Selbex; Sennoside; Takepron; Naproxen; Aspirin; Polaramine; Aminofluid; Omepral; Cataclot; Solu-Medrol; Soldem 3A; Multivitamin Additive; Heparin Sodium; Pacil; Pansporin; Finibax; Flumarin; Perdipine; Potacol-R; Radicut; NEO-Minophagen C; LOW Molecular Dextran L; Bisolvon; Magmitt Kenei; Cercine; Phenobarbital TAB; Mobic; Loxonin; Distilled Water; Ketoprofen; Laxoberon; Rinderon-VG; Wakobital; Serum Albumin Human; Humulin 70 / 30; Ropivacaine; Aminotripa 1; Aminotripa 2
Adverse event in 2 year old male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Japan on 2007-07-02
Patient: 2 year old male, weighing 13.0 kg (28.6 pounds)
Adverse reactions / side effects: Blood Bilirubin Increased, Myoglobinuria, Blood Creatine Phosphokinase Increased, Hepatic Necrosis, Rhabdomyolysis, Hepatic Failure, Resuscitation, Hypoxia, Myoglobin Blood Increased, Blood Creatinine Increased, Blood Urea Increased, Metabolic Acidosis, Alanine Aminotransferase Increased, Haemodialysis, Hepatic Steatosis, Renal Failure, Aspartate Aminotransferase Increased, Depressed Level of Consciousness, Prothrombin Time Shortened, Retroperitoneal Neoplasm, Bradycardia, Obstructive Airways Disorder, Venous Occlusion
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Voltaren
Nitrous Oxide W / Oxygen
Vecuronium Bromide
Fentanyl
Adverse event in 2 year old male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Japan on 2007-06-25
Patient: 2 year old male, weighing 13.0 kg (28.6 pounds)
Adverse reactions / side effects: Multi-Organ Failure, Rhabdomyolysis, Hepatic Failure
Adverse event resulted in: death
Suspect drug(s):
Voltaren
Nitrous Oxide W / Oxygen
Vecuronium Bromide
Fentanyl
Adverse event in 82 year old male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Italy on 2007-06-25
Patient: 82 year old male
Adverse reactions / side effects: Blood Bilirubin Increased, Jaundice, Hepatic Neoplasm Malignant, Antibody Test Abnormal, Hepatic Failure, Neoplasm, Hepatomegaly, Pulmonary Oedema, Small Intestinal Haemorrhage, Thrombocytopenia, Endoscopy Abnormal, Hepatitis Fulminant, Alanine Aminotransferase Increased, Duodenal Ulcer, Coagulation Time Shortened, Gastric Haemorrhage, Renal Failure, Aspartate Aminotransferase Increased
Adverse event resulted in: death
Suspect drug(s):
Glibomet
Dosage: 400 glibe - 2.5 metf mg/day
Administration route: Oral
Indication: Diabetes Mellitus non-Insulin-Dependent
Start date: 2006-12-03
End date: 2007-05-03
Voltaren
Dosage: 75 mg/day
Indication: Bone Pain
Start date: 2007-04-30
End date: 2007-05-02
Adverse event in 70 year old male receiving Voltaren (Diclofenac)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-06-21
Patient: 70 year old male
Adverse reactions / side effects: Oculomucocutaneous Syndrome, Sepsis, Liver Disorder
Adverse event resulted in: death
Suspect drug(s):
Voltaren
Dosage: 25 mg/day
Start date: 2006-08-01
End date: 2006-09-01
Voltaren
Dosage: 50 mg/day
Start date: 2006-09-01
End date: 2006-09-01
Tegretol
Dosage: 100 mg/day
Administration route: Oral
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