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Index of reports
> Cases resulting in hospitalization (196)
> Cases with Haemoglobin Decreased (28)
Below is the selection of adverse event reports related to Voltaren (Diclofenac) that includes cases resulting in hospitalization where reactions include haemoglobin decreased.
Reports 1 - 25 of 28 Next >>
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 59 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Japan on 2007-10-11
Patient: 59 year old female
Adverse reactions / side effects: Abdominal Pain, Vomiting, Small Intestine Ulcer, Endoscopy, Gastrointestinal Carcinoma, Occult Blood Positive, Haemoglobin Decreased, Jejunal Stenosis, Intestinal Operation
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren
Indication: Pain
Start date: 2004-01-01
End date: 2004-01-01
Voltaren
Indication: Pain
Start date: 2004-01-01
End date: 2004-01-01
Other drugs received by patient: Predonine; Mobic; Pentasa
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 49 year old male receiving Voltaren (Diclofenac)
Reported by a physician from United States on 2007-07-31
Patient: 49 year old male, weighing 73.9 kg (162.6 pounds)
Adverse reactions / side effects: Muscle Rigidity, Abdominal Tenderness, Abdominal Discomfort, Lymphocyte Count Decreased, Back Pain, Restlessness, Drug Withdrawal Syndrome, Respiratory Distress, Delirium, Tremor, Aggression, Respiratory Rate Decreased, Mental Disorder, Neutrophil Count Decreased, Drug Ineffective, Rectal Haemorrhage, Therapeutic Agent Toxicity, Drug Interaction, Mental Status Changes, Hepatomegaly, Frequent Bowel Movements, Fatigue, Overdose, Neck Pain, RED Blood Cell Count Decreased, Thrombocytopenia, Blood Pressure Increased, Haemoglobin Decreased, Anxiety, Haematochezia, Heart Rate Increased, Sinus Tachycardia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Celexa
Indication: Depression
Pegasys
Dosage: 90 mcg sc
Indication: Hepatitis C
Start date: 2006-06-15
End date: 2007-03-01
Pegasys
Dosage: 45 mcg qd sc
Indication: Hepatitis C
Start date: 2007-03-01
Effexor
End date: 2007-04-15
Baclofen
Start date: 2007-04-17
Opiate (Nos)
Wellbutrin
Dosage: 150 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Voltaren
Indication: Pain
Other drugs received by patient: Azithromycin; Hydrochlorothiazide; Toprol-XL
Adverse event in 49 year old male receiving Voltaren (Diclofenac)
Reported by a consumer/non-health professional from United States on 2007-07-24
Patient: 49 year old male
Adverse reactions / side effects: Agitation, Movement Disorder, Rectal Haemorrhage, Mental Status Changes, Drug Interaction, Muscle Rigidity, Abdominal Tenderness, Abdominal Discomfort, Fatigue, Hepatomegaly, Neck Pain, RED Blood Cell Count Decreased, Thrombocytopenia, Back Pain, Restlessness, Delirium, Respiratory Distress, Tremor, Aggression, Haematochezia, Anxiety, Haemoglobin Decreased, Diarrhoea, Mental Disorder, Sinus Tachycardia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Wellbutrin
Dosage: 150mg per day
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Pegasys
Dosage: 45mg per day
Indication: Hepatitis C
Start date: 2006-10-15
End date: 2007-05-11
Effexor
Indication: Drug USE FOR Unknown Indication
Start date: 2006-10-01
End date: 2007-04-15
Celexa
Indication: Depression
Opiate
Baclofen
Indication: Drug USE FOR Unknown Indication
Start date: 2007-04-17
Voltaren
Other drugs received by patient: Zithromax; Hydrochlorothiazide; Toprol-XL; Antibiotic
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 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 male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Switzerland on 2007-07-16
Patient: male
Adverse reactions / side effects: Microcytosis, Mucosal Hyperaemia, Polyp, Supraventricular Extrasystoles, Metaplasia, Diverticulitis, Pallor, Haemoglobin Decreased, Iron Deficiency Anaemia, RED Blood Cell Hypochromic Morphology Present, Serum Ferritin Decreased, Gastritis Atrophic, Inflammation
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Blopress Plus; Zocor; Imovane
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 49 year old male receiving Voltaren (Diclofenac)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-06
Patient: 49 year old male, weighing 73.9 kg (162.6 pounds)
Adverse reactions / side effects: Back Pain, Rectal Haemorrhage, Mental Status Changes, Abdominal Pain Upper, Haemoglobin Decreased, Haematochezia, Abdominal Discomfort, Hepatomegaly, Fatigue, Diarrhoea, Neck Pain, RED Blood Cell Count Decreased, Thrombocytopenia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Pegasys
Indication: Hepatitis C
Start date: 2006-06-01
End date: 2007-03-01
Pegasys
Start date: 2007-03-01
End date: 2007-05-11
Effexor
Indication: Drug USE FOR Unknown Indication
End date: 2007-04-01
Celexa
Indication: Depression
Baclofen
Indication: Drug USE FOR Unknown Indication
Opiate NOS
Indication: Drug USE FOR Unknown Indication
Wellbutrin
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Voltaren
Other drugs received by patient: Zithromax; Hydrochlorothiazide; Toprol-XL; Ativan; Benadryl; Cogentin; Parafon
Adverse event in 73 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-06-25
Patient: 73 year old female, weighing 111.0 kg (244.2 pounds)
Adverse reactions / side effects: Blood PH Increased, Rales, PO2 Decreased, Haematocrit Decreased, RED Blood Cell Count Decreased, Interstitial Lung Disease, Cyanosis, Pulmonary Oedema, Hypoxia, Knee Arthroplasty, Oxygen Supplementation, Oxygen Saturation Decreased, White Blood Cell Count Increased, Eosinophilia, Haemoglobin Decreased, Postoperative Respiratory Distress, Bronchoalveolar Lavage
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren
Dosage: unk, prn
Administration route: Oral
Indication: Osteoarthritis
Start date: 1999-12-01
End date: 2006-08-01
Feldene
Dosage: unk, prn (total of 1 pack)
Administration route: Oral
Indication: Osteoarthritis
Start date: 2005-12-01
End date: 2005-12-01
Feldene
Dosage: unk, prn (total of 1 pack)
Administration route: Oral
Start date: 2006-01-01
End date: 2006-01-01
Feldene
Dosage: 1 df, prn (total of 1 pack)
Administration route: Oral
Start date: 2005-03-01
End date: 2005-03-01
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 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 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 22 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from China on 2007-04-16
Patient: 22 year old female
Adverse reactions / side effects: Blood Bilirubin Increased, RED Blood Cell Abnormality, Chills, Pyrexia, Bone Marrow Disorder, RED Blood Cell Count Decreased, Electrophoresis, Dizziness, White Blood Cell Count Increased, Back Pain, Cardiac Murmur, Urobilin Urine Present, Pain in Extremity, Haemoglobin Decreased, Reticulocyte Count Increased, Haemolytic Anaemia, Haptoglobin Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in 61 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from China on 2007-04-16
Patient: 61 year old female
Adverse reactions / side effects: White Blood Cell Count Decreased, Monocyte Count Decreased, Anaemia, Platelet Count Increased, Muscular Weakness, Reticulocyte Count Decreased, Bone Marrow Disorder, Haemoglobin Decreased, Dyspepsia, Aplasia Pure RED Cell, Megakaryocytes Decreased, Neutrophil Count Decreased, Lymphocyte Count Decreased, Decreased Appetite
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
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 81 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-03-27
Patient: 81 year old female
Adverse reactions / side effects: Colonic Polyp, Haemoglobin Decreased, Large Intestinal Ulcer, Rectal Haemorrhage, Anaemia, Diverticulum Intestinal, Oesophageal Ulcer
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Lipanthyl; Orocal; Acetaminophen; Becotide; Ercefuryl
Adverse event in 81 year old male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Norway on 2007-03-20
Patient: 81 year old male
Adverse reactions / side effects: Anaemia, Gastric Ulcer Haemorrhage, Helicobacter Infection, Faeces Discoloured, Haematochezia, Haemoglobin Decreased, Fatigue, Helicobacter Pylori Identification Test Positive, Dizziness, Melaena
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren
Dosage: 50 mg, tid
Administration route: Oral
Indication: Myalgia
Start date: 2007-02-01
End date: 2007-02-22
Albyl-E
Dosage: 160 mg, qd
Administration route: Oral
End date: 2007-02-22
Other drugs received by patient: Norvasc; Simvastatin; Atenolol
Adverse event in 84 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-02-23
Patient: 84 year old female, weighing 66.0 kg (145.2 pounds)
Adverse reactions / side effects: Hyperkalaemia, Rales, Hypochromasia, Walking AID User, Activated Partial Thromboplastin Time Prolonged, Impaired Self-Care, Blood Creatinine Increased, Renal Failure Acute, Prothrombin Time Ratio Increased, Cataract, Blood Urea Increased, General Physical Health Deterioration, Haemoglobin Decreased, Electrocardiogram T Wave Amplitude Increased, Anxiety, Hallucination, Visual, Charles Bonnet Syndrome, Gait Disturbance, Atrioventricular Block First Degree
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient possibly interacting with the suspect drug:
Triatec
Dosage: 5 mg, qd
Administration route: Oral
Indication: Essential Hypertension
End date: 2006-12-21
Other drugs received by patient: Allopurinol Sodium; Inipomp; Acetaminophen; Torental; Furosemide; Efferalgan Codeine; Soprol; Haldol
Adverse event in 84 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-02-22
Patient: 84 year old female, weighing 66.0 kg (145.2 pounds)
Adverse reactions / side effects: Hyperkalaemia, Rales, Hypochromasia, Walking AID User, Activated Partial Thromboplastin Time Prolonged, Impaired Self-Care, Blood Creatinine Increased, Renal Failure Acute, Prothrombin Time Ratio Increased, Cataract, Blood Urea Increased, General Physical Health Deterioration, Haemoglobin Decreased, Electrocardiogram T Wave Amplitude Increased, Anxiety, Hallucination, Visual, Charles Bonnet Syndrome, Gait Disturbance, Atrioventricular Block First Degree
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient possibly interacting with the suspect drug:
Triatec
Dosage: 5 mg, qd
Administration route: Oral
Indication: Essential Hypertension
End date: 2006-12-21
Other drugs received by patient: Allopurinol Sodium; Inipomp; Acetaminophen; Torental; Furosemide; Efferalgan Codeine; Soprol; Haldol
Adverse event in 81 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-02-16
Patient: 81 year old female
Adverse reactions / side effects: Colonic Polyp, Haemoglobin Decreased, Large Intestinal Ulcer, Rectal Haemorrhage, Anaemia, Diverticulum Intestinal, Oesophageal Ulcer
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
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