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Index of reports
> Cases resulting in hospitalization (196)
> Cases with C-Reactive Protein Increased (22)
Below is the selection of adverse event reports related to Voltaren (Diclofenac) that includes cases resulting in hospitalization where reactions include c-reactive protein increased.
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 59 year old female receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-10-16
Patient: 59 year old female
Adverse reactions / side effects: Skin Exfoliation, Necrosis, Blood Albumin Decreased, Haematocrit Decreased, RED Blood Cell Count Decreased, C-Reactive Protein Increased, Gamma-Glutamyltransferase Increased, Blister, Lymphocyte Count Decreased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Toxic Epidermal Necrolysis, Blood Cholinesterase Decreased, Protein Total Decreased, Haemoglobin Decreased, Rash Erythematous, Skin Erosion
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lansoprazole
Dosage: 60 mg/day
Indication: Gastric Ulcer
Start date: 2007-07-23
End date: 2007-08-03
Lansoprazole
Dosage: 30 mg/day
Administration route: Oral
Start date: 2007-08-04
End date: 2007-08-21
Olmetec
Dosage: unk, unk
Administration route: Oral
Start date: 2007-08-08
End date: 2007-08-21
Apresolin
Dosage: 50 mg, bid
Administration route: Oral
Indication: Hypertension
Start date: 2007-07-30
End date: 2007-08-08
Voltaren
Dosage: 25 mg/day
Indication: Antipyresis
Start date: 2007-07-23
End date: 2007-08-05
Levofloxacin
Dosage: 400 mg/day
Administration route: Oral
Indication: Infection
Start date: 2007-08-08
End date: 2007-08-12
Omegacin
Dosage: 600 mg/day
Indication: Interstitial Lung Disease
Start date: 2007-07-23
End date: 2007-08-04
Dormicum
Dosage: 10 ug/day
Indication: Sedation
Start date: 2007-07-23
End date: 2007-07-28
Pentazocine Lactate
Dosage: 30 ug/day
Indication: Sedation
Start date: 2007-07-23
End date: 2007-07-28
Prodif
Dosage: 800 mg/day
Start date: 2007-07-23
End date: 2007-08-04
Prodif
Dosage: 400 mg/day
Start date: 2007-07-23
End date: 2007-08-04
Baktar
Dosage: 2 g/day
Administration route: Oral
Indication: Interstitial Lung Disease
Start date: 2007-07-24
End date: 2007-08-01
Norvasc
Dosage: 5 mg/day
Administration route: Oral
Indication: Hypertension
Start date: 2007-08-08
End date: 2007-08-21
Other drugs received by patient: Polymyxin B; Elaspol
Adverse event in male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Japan on 2007-10-12
Patient: male
Adverse reactions / side effects: Blood Urea Increased, Hyperkalaemia, Hypoglycaemia, Hyponatraemia, Acidosis, C-Reactive Protein Increased, Sepsis, Dehydration, Adrenal Insufficiency, Enteritis Infectious, Blood Creatinine Increased, Shock, Renal Failure Acute, Anuria
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in 55 year old female receiving Voltaren (Diclofenac)
Reported by a health professional (non-physician/pharmacist) from Norway on 2007-07-31
Patient: 55 year old female
Adverse reactions / side effects: Vomiting, Anaemia, Faeces Discoloured, Haematemesis, Haemoglobin Decreased, Diarrhoea, C-Reactive Protein Increased, Bacterial DNA Test Positive, Duodenal Ulcer Haemorrhage, Melaena, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren
Dosage: 50 mg, tid
Indication: Back Pain
Start date: 2007-01-01
End date: 2007-07-10
Mobic
Dosage: 15 mg, bid
Administration route: Oral
End date: 2007-07-10
Other drugs received by patient: Surmontil; Paralgin Forte; Sobril; Sumatriptan Succinate
Adverse event in 61 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Japan on 2007-07-16
Patient: 61 year old female, weighing 59.0 kg (129.8 pounds)
Adverse reactions / side effects: Blood Bilirubin Increased, Drug Eruption, Thoracic Cavity Drainage, Disseminated Intravascular Coagulation, Pyrexia, Erythema, Laboratory Test Abnormal, Gamma-Glutamyltransferase Increased, C-Reactive Protein Increased, Pleural Effusion, Blood Creatinine Increased, Lymphocyte Count Decreased, Oxygen Saturation Decreased, White Blood Cell Count Increased, Blood Urea Increased, Dyspnoea, Neutrophil Count Increased, Monocyte Count Decreased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Urine Output Decreased, Lymphocyte Stimulation Test Positive, Rash Macular, Haemoglobin Decreased, Renal Failure, Aspartate Aminotransferase Increased, Oliguria, Platelet Count Decreased, Lung Infiltration
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Voltaren
Dosage: 37.5 mg/day
Administration route: Oral
Indication: Pyrexia
Start date: 2005-11-09
End date: 2005-11-10
Loxonin
Dosage: 60 mg, tid
Administration route: Oral
Indication: Pyrexia
Start date: 2005-11-10
End date: 2005-11-13
Dacarbazine
Dosage: 180 mg/day
Indication: Malignant Melanoma
Start date: 2005-11-08
End date: 2005-11-12
Nidran
Dosage: 100 mg/day
Indication: Malignant Melanoma
Start date: 2005-11-08
End date: 2005-11-08
Oncovin
Dosage: 1 mg/day
Indication: Malignant Melanoma
Start date: 2005-11-08
End date: 2005-11-08
Feron
Dosage: 3000000 iu/day
Indication: Malignant Melanoma
Start date: 2005-11-08
End date: 2005-11-12
Other drugs received by patient: Norvasc; Towamin; Lipitor; Voglibose
Adverse event in 94 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-06-25
Patient: 94 year old female
Adverse reactions / side effects: Back Pain, Blood Alkaline Phosphatase Increased, Dysphagia, Hypotension, Blood Lactate Dehydrogenase Increased, Disorientation, Pallor, Oesophageal Varices Haemorrhage, Haematemesis, Haemoglobin Decreased, Oesophagoscopy, C-Reactive Protein Increased, Oesophageal Variceal Ligation
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Omeprazole; Vastarel; Lorazepam; Furosemide; Celectol; Prozac; Efferalgan Codeine; Delursan
Adverse event in 43 year old male receiving Voltaren (Diclofenac)
Reported by a physician from France on 2007-06-13
Patient: 43 year old male, weighing 72.0 kg (158.4 pounds)
Adverse reactions / side effects: Pancreatitis Acute, Abdominal Pain, Epigastric Discomfort, C-Reactive Protein Increased, Lipase Increased, Serum Ferritin Increased, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Alpha Amylase; Pivalone
Adverse event in 11 year old male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Japan on 2007-06-07
Patient: 11 year old male, weighing 32.0 kg (70.4 pounds)
Adverse reactions / side effects: Blood PH Increased, Disseminated Intravascular Coagulation, Blood Albumin Decreased, Petechiae, Pyrexia, Erythema, Blood Fibrinogen Decreased, Interstitial Lung Disease, C-Reactive Protein Increased, Acute Respiratory Distress Syndrome, Blood Creatinine Increased, White Blood Cell Count Increased, Cough, Renal Failure Acute, Hypertensive Encephalopathy, Dyspnoea, Blood Urea Increased, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Pancytopenia, Life Support, Rash, Protein Total Decreased, Lymphocyte Stimulation Test Positive, Aspartate Aminotransferase Increased, Platelet Count Decreased, PO2 Increased, Lung Infiltration, Calculus Ureteric
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Predonine; Bufferin; Sulpyrine; Kashilon; Cefazolin Sodium; Methylprednisolone 16mg TAB
Adverse event in 35 year old male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Japan on 2007-06-07
Patient: 35 year old male, weighing 64.0 kg (140.8 pounds)
Adverse reactions / side effects: Drug Eruption, Viral Infection, Rash Papular, Pyrexia, Eosinophil Count Increased, Erythema, Rash Pruritic, C-Reactive Protein Increased, Gamma-Glutamyltransferase Increased, Lymphocyte Count Decreased, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren
Dosage: 37.5 mg, bid
Administration route: Oral
Indication: Arthralgia
Start date: 2001-12-23
End date: 2002-02-06
Selbex
Dosage: .5 g, bid
Administration route: Oral
Indication: Prophylaxis Against Gastrointestinal Ulcer
Start date: 2001-12-23
End date: 2002-02-06
Voltaren
Administration route: Topical
Adefuronic
Indication: Hyperthermia
Start date: 2002-02-18
End date: 2002-02-18
Adverse event in 11 year old male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Japan on 2007-06-04
Patient: 11 year old male, weighing 32.0 kg (70.4 pounds)
Adverse reactions / side effects: Blood PH Increased, Disseminated Intravascular Coagulation, Petechiae, Blood Albumin Decreased, Blood Fibrinogen Decreased, C-Reactive Protein Increased, Acute Respiratory Distress Syndrome, Blood Creatinine Increased, White Blood Cell Count Increased, Renal Failure Acute, Cough, Dyspnoea, Blood Urea Increased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Pancytopenia, Protein Total Decreased, Lymphocyte Stimulation Test Positive, Rash, Aspartate Aminotransferase Increased, Platelet Count Decreased, PO2 Increased, Lung Infiltration, Calculus Ureteric
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Predonine; Bufferin; Sulpyrine; Kashilon; Cefazolin Sodium
Adverse event in 16 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-05-22
Patient: 16 year old male
Adverse reactions / side effects: Glucose-6-Phosphate Dehydrogenase Deficiency, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Protein Urine Present, Haematuria, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Pyrexia, Haemoglobin Decreased, Haematocrit Decreased, C-Reactive Protein Increased, Aspartate Aminotransferase Increased, Platelet Count Decreased, Haemolytic Anaemia, Influenza
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Onon; Clarithromycin; Selbex; PL Gran.; Pansporin; Relenza; Calonal; Alpinyl; Miltax
Adverse event in 41 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-05-11
Patient: 41 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Brain Death, Rhabdomyolysis, Blood Creatine Phosphokinase Increased, Blood Calcium Increased, Pyrexia, C-Reactive Protein Increased, Brain Oedema, Blood Creatinine Increased, White Blood Cell Count Increased, Mydriasis, Brain Stem Haemorrhage, Blood Urea Increased, Dyspnoea, Urine Output Decreased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Dependence ON Respirator, Haemodialysis, Brain Stem Syndrome, Dehydration, Aspartate Aminotransferase Increased, Platelet Count Decreased, Blood Pressure Decreased
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Adona; Transamin; Primperan INJ; Gaster; Glyceol
Adverse event in 94 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-04-30
Patient: 94 year old female
Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Back Pain, Dysphagia, Blood Lactate Dehydrogenase Increased, Hypotension, Disorientation, Pallor, Haematemesis, Haemoglobin Decreased, C-Reactive Protein Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Omeprazole; Vastarel; Temesta; Furosemide
Adverse event in 16 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-04-13
Patient: 16 year old male
Adverse reactions / side effects: Glucose-6-Phosphate Dehydrogenase Deficiency, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Protein Urine Present, Haematuria, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Pyrexia, Haemoglobin Decreased, Haematocrit Decreased, C-Reactive Protein Increased, Aspartate Aminotransferase Increased, Platelet Count Decreased, Haemolytic Anaemia, Influenza
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Onon; Clarithromycin; Selbex; PL Gran.; Pansporin; Relenza; Calonal; Alpinyl; Miltax
Adverse event in 41 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-04-06
Patient: 41 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Brain Death, Rhabdomyolysis, Blood Creatine Phosphokinase Increased, Blood Calcium Increased, Pyrexia, C-Reactive Protein Increased, Brain Oedema, Blood Creatinine Increased, White Blood Cell Count Increased, Mydriasis, Brain Stem Haemorrhage, Blood Urea Increased, Dyspnoea, Urine Output Decreased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Dependence ON Respirator, Haemodialysis, Brain Stem Syndrome, Dehydration, Aspartate Aminotransferase Increased, Platelet Count Decreased, Blood Pressure Decreased
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Adona; Transamin; Primperan INJ; Gaster; Glyceol
Adverse event in 91 year old female receiving Voltaren (Diclofenac)
Reported by a health professional (non-physician/pharmacist) from Norway on 2007-03-26
Patient: 91 year old female
Adverse reactions / side effects: Blood Calcium Increased, Drug Interaction, Platelet Count Increased, Constipation, Muscle Rigidity, Gastrointestinal Ulcer, Hypokinesia, C-Reactive Protein Increased, Methylmalonic Aciduria, Bacterial DNA Test Positive, Blood Sodium Decreased, Blood Creatinine Increased, Decreased Appetite, White Blood Cell Count Increased, Blood Iron Decreased, Endoscopy, Thyroxine Increased, Eating Disorder, Haematochezia, Blood Potassium Decreased, Mental Disorder, Tardive Dyskinesia, Alanine Aminotransferase Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren
Administration route: Oral
End date: 2007-02-01
Prednisolone
Dosage: unk, unk
Administration route: Oral
Indication: Myalgia
Start date: 2006-12-01
End date: 2007-02-01
Trilafon
Dosage: 8 mg daily
Administration route: Oral
End date: 2007-02-25
Albyl-E
Dosage: 160 mg daily
Administration route: Oral
Other drugs received by patient: Plendil; Atacand HCT; Selo-ZOK
Adverse event in 39 year old male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-03-20
Patient: 39 year old male
Adverse reactions / side effects: Pyoderma Gangrenosum, Staphylococcal Skin Infection, C-Reactive Protein Increased, Skin Ulcer, Rash Macular, Skin Nodule, Inflammation
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren
Dosage: 300 mg/day
Administration route: Oral
Indication: Spondylitis
Enbrel
Dosage: 50 mg/week
Indication: Spondylitis
Other drugs received by patient: Minocin
Adverse event in 41 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-03-16
Patient: 41 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Brain Death, Rhabdomyolysis, Blood Creatine Phosphokinase Increased, Blood Calcium Increased, Pyrexia, C-Reactive Protein Increased, Brain Oedema, Blood Creatinine Increased, White Blood Cell Count Increased, Mydriasis, Brain Stem Haemorrhage, Blood Urea Increased, Dyspnoea, Urine Output Decreased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Dependence ON Respirator, Haemodialysis, Brain Stem Syndrome, Dehydration, Aspartate Aminotransferase Increased, Platelet Count Decreased, Blood Pressure Decreased
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Adona; Transamin; Primperan INJ; Gaster; Glyceol
Adverse event in 96 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-03-14
Patient: 96 year old female, weighing 55.0 kg (121.0 pounds)
Adverse reactions / side effects: Confusional State, Pyrexia, Pallor, Microcytic Anaemia, Haematemesis, C-Reactive Protein Increased, Hypoglycaemic Coma, Melaena, Hypertonia, Blood Glucose Increased, Blood Urea Increased, Hyponatraemia, Status Epilepticus, Protein Total Decreased, Hallucination, Visual, Psychomotor Skills Impaired, Peptic Ulcer Haemorrhage, Asthenia
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Kardegic
Dosage: 75 mg, qd
Administration route: Oral
End date: 2006-11-08
Esomeprazole Magnesium
Dosage: 1 df, cont (synringe pump)
Start date: 2006-11-08
End date: 2006-11-08
Esomeprazole Magnesium
Dosage: 40 mg, bid
Start date: 2006-11-09
End date: 2006-11-13
Esomeprazole Magnesium
Dosage: 40 mg, qd
Administration route: Oral
Start date: 2006-11-13
Voltaren
Dosage: 75 mg, qd
Administration route: Oral
End date: 2006-11-08
Other drugs received by patient: Modopar; Trivastal; Daflon; Meteoxane; Movicol; Seresta
Adverse event in 96 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-03-13
Patient: 96 year old female, weighing 55.0 kg (121.0 pounds)
Adverse reactions / side effects: Confusional State, Pyrexia, Pallor, Microcytic Anaemia, Haematemesis, C-Reactive Protein Increased, Hypoglycaemic Coma, Melaena, Hypertonia, Blood Glucose Increased, Blood Urea Increased, Hyponatraemia, Status Epilepticus, Protein Total Decreased, Hallucination, Visual, Psychomotor Skills Impaired, Peptic Ulcer Haemorrhage, Asthenia
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Kardegic
Dosage: 75 mg, qd
Administration route: Oral
End date: 2006-11-08
Esomeprazole Magnesium
Dosage: 1 df, cont (synringe pump)
Start date: 2006-11-08
End date: 2006-11-08
Esomeprazole Magnesium
Dosage: 40 mg, bid
Start date: 2006-11-09
End date: 2006-11-13
Esomeprazole Magnesium
Dosage: 40 mg, qd
Administration route: Oral
Start date: 2006-11-13
Voltaren
Dosage: 75 mg, qd
Administration route: Oral
End date: 2006-11-08
Other drugs received by patient: Modopar; Trivastal; Daflon; Meteoxane; Movicol; Seresta
Adverse event in 96 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-03-10
Patient: 96 year old female, weighing 55.0 kg (121.0 pounds)
Adverse reactions / side effects: Confusional State, Pyrexia, Pallor, Microcytic Anaemia, Haematemesis, C-Reactive Protein Increased, Hypoglycaemic Coma, Melaena, Hypertonia, Blood Glucose Increased, Blood Urea Increased, Hyponatraemia, Status Epilepticus, Protein Total Decreased, Hallucination, Visual, Psychomotor Skills Impaired, Peptic Ulcer Haemorrhage, Asthenia
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Kardegic
Dosage: 75 mg, qd
Administration route: Oral
End date: 2006-11-08
Esomeprazole Magnesium
Dosage: 1 df, cont (synringe pump)
Start date: 2006-11-08
End date: 2006-11-08
Esomeprazole Magnesium
Dosage: 40 mg, bid
Start date: 2006-11-09
End date: 2006-11-13
Esomeprazole Magnesium
Dosage: 40 mg, qd
Administration route: Oral
Start date: 2006-11-13
Voltaren
Dosage: 75 mg, qd
Administration route: Oral
End date: 2006-11-08
Other drugs received by patient: Modopar; Trivastal; Daflon; Meteoxane; Movicol; Seresta
Adverse event in 96 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-02-22
Patient: 96 year old female, weighing 55.0 kg (121.0 pounds)
Adverse reactions / side effects: Confusional State, Pyrexia, Pallor, Microcytic Anaemia, Haematemesis, C-Reactive Protein Increased, Hypoglycaemic Coma, Melaena, Hypertonia, Blood Glucose Increased, Blood Urea Increased, Hyponatraemia, Status Epilepticus, Protein Total Decreased, Hallucination, Visual, Psychomotor Skills Impaired, Peptic Ulcer Haemorrhage, Asthenia
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Kardegic
Dosage: 75 mg, qd
Administration route: Oral
End date: 2006-11-08
Esomeprazole Magnesium
Dosage: 1 df, cont (synringe pump)
Start date: 2006-11-08
End date: 2006-11-08
Esomeprazole Magnesium
Dosage: 40 mg, bid
Start date: 2006-11-09
End date: 2006-11-13
Esomeprazole Magnesium
Dosage: 40 mg, qd
Administration route: Oral
Start date: 2006-11-13
Voltaren
Dosage: 75 mg, qd
Administration route: Oral
End date: 2006-11-08
Other drugs received by patient: Modopar; Trivastal; Daflon; Meteoxane; Movicol; Seresta
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