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Voltaren (Diclofenac) - Adverse Event Reports - Hospitalization

 



Index of reports > Cases resulting in hospitalization (196)

     Haemoglobin Decreased (28)Blood Creatinine Increased (24)C-Reactive Protein Increased (22)Blood Urea Increased (21)Alanine Aminotransferase Increased (21)Pyrexia (21)Aspartate Aminotransferase Increased (21)White Blood Cell Count Increased (21)Renal Failure Acute (21)Dyspnoea (20)

Below is the selection of adverse event reports related to Voltaren (Diclofenac) that includes cases resulting in hospitalization.

 Reports 1 - 25 of 196   Next >>

Adverse event in 23 year old male receiving Voltaren (Diclofenac)

Reported by a individual with unspecified qualification from France on 2007-10-31

Patient: 23 year old male

Adverse reactions / side effects: Abdominal Pain, Pancreatitis Acute, Lymphadenopathy, Acute Abdomen, Pyrexia, Lymphoma

Adverse event resulted in: hospitalization

Suspect drug(s):
Acetaminophen
    Administration route: Oral
    Start date: 2007-07-01
    End date: 2007-07-18

Voltaren
    Administration route: Oral
    Start date: 2007-07-11
    End date: 2007-07-18



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):
Apresoline
    Administration route: Oral
    Indication: Hypertension

Baktar
    Administration route: Oral
    Indication: Interstitial Lung Disease

Cravit
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Dormicum
    Indication: Sedation

Lansoprazole
    Indication: Gastric Ulcer

Lansoprazole
    Administration route: Oral

Norvasc
    Administration route: Oral
    Indication: Hypertension

Olmetec
    Administration route: Oral
    Indication: Hypertension

Omegacin
    Indication: Interstitial Lung Disease

Pentazocine Lactate
    Indication: Sedation

Prodif
    Indication: Interstitial Lung Disease

Voltaren
    Indication: Hyperthermia

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 female receiving Voltaren (Diclofenac)

Reported by a physician from Japan on 2007-10-25

Patient: female

Adverse reactions / side effects: Pneumocystis Jiroveci Pneumonia

Adverse event resulted in: hospitalization

Suspect drug(s):
Bonalon
    Administration route: Oral
    Indication: Osteoporosis

Foliamin
    Administration route: Oral
    Indication: Prophylaxis

Prednisolone
    Administration route: Oral

Prednisolone
    Administration route: Oral
    Indication: Rheumatoid Arthritis

Prograf
    Administration route: Oral
    Indication: Rheumatoid Arthritis

Remicade

Remicade
    Dosage: 5 infusions

Remicade
    Indication: Rheumatoid Arthritis

Rheumatrex
    Administration route: Oral
    Indication: Rheumatoid Arthritis

Voltaren
    Administration route: Oral
    Indication: Rheumatoid Arthritis



Adverse event in 59 year old female receiving Voltaren (Diclofenac)

Reported by a individual with unspecified qualification from Japan on 2007-10-25

Patient: 59 year old female

Adverse reactions / side effects: Toxic Epidermal Necrolysis

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Apresoline
    Dosage: 100 mg (50 mg, 2 in 1 d), per oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-07-23
    End date: 2007-08-03

Baktar (Sulfamethoxazole, Trimethoprim) (Sulfamethoxazole, Trimethopri
    Dosage: 2 gm (1 gm, 2 in 1 d), per oral
    Administration route: Oral
    Indication: Interstitial Lung Disease
    Start date: 2007-07-25
    End date: 2007-08-01

Cravit (Levofloxacin) (Tablet) (Levofloxacin)
    Dosage: 400 mg (200 mg, 1 in 1 d), per oral
    Administration route: Oral
    Indication: Toxic Epidermal Necrolysis
    Start date: 2007-08-08
    End date: 2007-08-12

Dormicum (Midazolam Hydrohloride) (Injection) (Midazolam Hydrochloride
    Dosage: continuous intravenous (not otherwise specified)
    Indication: Sedation
    Start date: 2007-07-23
    End date: 2007-07-28

Norvasc
    Dosage: 5 mg ( 5 mg, 1 in 1 d) per oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-08-08
    End date: 2007-08-21

Olmesartan Medoxomil
    Dosage: 20 mg (20 mg, 1 in 1 d), per oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-08-08
    End date: 2007-08-21

Omegacin (Biapenem) (Injection) (Biapenem)
    Dosage: 600 mg (300 mg, 2 in 1 d), intravenous drip
    Indication: Interstitial Lung Disease
    Start date: 2007-07-23
    End date: 2007-08-04

Prodif (Injection)
    Dosage: 800 mg, 400 mg (2 in 1 d), intavenous (not otherwise specified)
    Indication: Interstitial Lung Disease
    Start date: 2007-07-23
    End date: 2007-08-04

Sosegon (Pentazocine) (Injection) (Pentazocine)
    Dosage: continuous intravenous (not otherwise specified)
    Indication: Sedation
    Start date: 2007-07-23
    End date: 2007-07-28

Takepron (Lansoprazole) (Injection) (Lansoprazole)
    Dosage: 60 mg (30 mg, 2 in 1 d), intravenous drip; 30 mg (30 mg, 1 in 1 d), per oral
    Administration route: Oral
    Indication: Gastric Ulcer
    Start date: 2007-07-23
    End date: 2007-08-03

Takepron (Lansoprazole) (Injection) (Lansoprazole)
    Dosage: 60 mg (30 mg, 2 in 1 d), intravenous drip; 30 mg (30 mg, 1 in 1 d), per oral
    Administration route: Oral
    Indication: Gastric Ulcer
    Start date: 2007-08-04
    End date: 2007-08-21

Voltaren
    Dosage: continuous intravenous ( otherwise not specified)
    Indication: Hyperthermia
    Start date: 2007-07-23
    End date: 2007-08-05



Adverse event in 77 year old male receiving Voltaren (Diclofenac)

Reported by a consumer/non-health professional from Japan on 2007-10-25

Patient: 77 year old male

Adverse reactions / side effects: Epistaxis

Adverse event resulted in: hospitalization

Suspect drug(s):
Voltaren
    Dosage: 50 mg, bid
    Indication: Thoracic Vertebral Fracture
    Start date: 2007-01-15
    End date: 2007-01-01

Voltaren
    Dosage: 50 mg, qd
    Start date: 2007-02-01
    End date: 2007-04-01



Adverse event in female receiving Voltaren (Diclofenac)

Reported by a physician from Japan on 2007-10-24

Patient: female

Adverse reactions / side effects: Toxic Epidermal Necrolysis, Hypertension

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Apresoline
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-07-30
    End date: 2007-08-07

Baktar
    Administration route: Oral
    Start date: 2007-07-25
    End date: 2007-08-01

Biapenem
    Indication: Interstitial Lung Disease
    Start date: 2007-07-23
    End date: 2007-08-08

Dormicum FOR Injection
    Indication: Sedation
    Start date: 2007-07-23
    End date: 2007-07-28

Elaspol

Lansoprazole
    Indication: Gastric Ulcer
    Start date: 2007-07-23
    End date: 2007-08-03

Lansoprazole
    Dosage: daily dose:30mg
    Administration route: Oral
    Start date: 2007-08-04
    End date: 2007-08-21

Levofloxacin
    Administration route: Oral
    Start date: 2007-08-08
    End date: 2007-08-12

Norvasc
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-08-08
    End date: 2007-08-27

Olmetec
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-08-08
    End date: 2007-08-21

Pentazocine Lactate
    Start date: 2007-07-23
    End date: 2007-07-28

Prodif
    Indication: Fungal Infection
    Start date: 2007-07-23
    End date: 2007-08-04

Voltaren
    Dosage: daily dose:25mg-freq:frequency: prn
    Indication: Pyrexia
    Start date: 2007-07-23
    End date: 2007-08-05

Other drugs received by patient: Flumetholon; Prednisolone



Adverse event in 79 year old female receiving Voltaren (Diclofenac)

Reported by a individual with unspecified qualification from France on 2007-10-23

Patient: 79 year old female

Adverse reactions / side effects: Confusional State, Vomiting, Blood Urea Increased, Nausea, Hypotension, Hypoglycaemia, Somnolence, Blood Creatinine Increased, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Actiskenan
    Dosage: 10 mg/day
    Administration route: Oral
    Indication: Skin Ulcer
    Start date: 2007-07-17
    End date: 2007-07-18

Amaryl
    Dosage: 1 mg/day
    Administration route: Oral
    Indication: Type 2 Diabetes Mellitus
    Start date: 2006-11-01
    End date: 2007-07-18

Lasix
    Administration route: Oral

Voltaren
    Dosage: 75 mg/day
    Administration route: Oral
    Indication: Pain
    End date: 2007-07-18

Zofenil
    Dosage: 30 mg/day
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-11-01
    End date: 2007-07-18

Other drugs received by patient: Levothyrox; Ginkor; Pyostacine; Acetaminophen; Forlax; Diffu K; Vitamin B-12; Sterogyl; Rivotril; Topalgic



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):
Kineret
    Indication: Rheumatoid Arthritis
    Start date: 2003-04-01
    End date: 2003-05-01

Prednisolone

Voltaren
    Indication: Rheumatoid Arthritis

Other drugs received by patient: Methotrexate; Plasmapheresis; Hydroxychloroquine Sulfate; Metoprolol Succinate; Furosemide; Levothyroxine Sodium; Esomeprazole Magnesium



Adverse event in 77 year old female receiving Voltaren (Diclofenac)

Reported by a physician from Finland on 2007-10-22

Patient: 77 year old female

Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Gamma-Glutamyltransferase Increased, Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased, Cholestasis, Hepatic Enzyme Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Voltaren (Diclofenac)

Other drugs received by patient: Optinate; Calcichew; Magnesium Sulfate



Adverse event in female receiving Voltaren (Diclofenac)

Reported by a health professional (non-physician/pharmacist) from Switzerland on 2007-10-22

Patient: female

Adverse reactions / side effects: Emphysema, Dyspnoea, Rales, Cardiomegaly, Lung Disorder, Cardiac Failure, Chest Pain, Aortic Arteriosclerosis, Pleural Effusion, Lung Infiltration, Sinus Rhythm, Atrioventricular Block First Degree

Adverse event resulted in: hospitalization

Suspect drug(s):
Voltaren (Diclofenac)

Other drugs received by patient: Nitroderm; Prednisone; Plavix; Dilatrend; Eltroxin; Rohypnol; Zyloric; Torsemide; Digoxin; Rocaltrol



Adverse event in 51 year old female receiving Voltaren (Diclofenac)

Reported by a physician from Japan on 2007-10-19

Patient: 51 year old female, weighing 63.1 kg (138.8 pounds)

Adverse reactions / side effects: Vomiting, Nausea, Dehydration, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Valtrex
    Administration route: Oral
    Indication: Herpes Zoster
    Start date: 2007-09-14
    End date: 2007-09-18

Voltaren
    Indication: Facet Joint Syndrome
    Start date: 2007-08-23
    End date: 2007-09-18

Other drugs received by patient: Celestamine TAB; Methycobal; Mucosta



Adverse event in 39 year old female receiving Voltaren (Diclofenac)

Reported by a individual with unspecified qualification from Japan on 2007-10-17

Patient: 39 year old female

Adverse reactions / side effects: Large Intestinal Ulcer Haemorrhage, Appendicitis

Adverse event resulted in: hospitalization

Suspect drug(s):
Voltaren (Diclofenac)



Adverse event in 79 year old female receiving Voltaren (Diclofenac)

Reported by a individual with unspecified qualification on 2007-10-17

Patient: 79 year old female

Adverse reactions / side effects: Confusional State, Vomiting, Nausea, Drug Intolerance, Hypoglycaemia, Hypotension, Somnolence, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Actiskenan
    Administration route: Oral
    Start date: 2007-07-17
    End date: 2007-07-18

Amaryl
    Administration route: Oral
    Start date: 2006-11-01
    End date: 2007-07-18

Voltaren
    Administration route: Oral
    End date: 2007-07-18

Zofenil
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-11-01
    End date: 2007-07-18

Other drugs received by patient: Levothyrox; Ginkor; Pyostacine; Efferalgan / 00020001 /; Lasix; Forlax; Diffu K; Vitamin B-12; Sterogyl / 00765501 /; Rivotril; Topalgic



Adverse event in female receiving Voltaren (Diclofenac)

Reported by a physician from Japan on 2007-10-17

Patient: female

Adverse reactions / side effects: Toxic Epidermal Necrolysis

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Apresoline
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-07-30
    End date: 2007-08-07

Baktar
    Administration route: Oral
    Start date: 2007-07-25
    End date: 2007-08-01

Biapenem
    Indication: Interstitial Lung Disease
    Start date: 2007-07-23
    End date: 2007-08-08

Dormicum FOR Injection
    Indication: Sedation
    Start date: 2007-07-23
    End date: 2007-07-28

Elaspol

Lansoprazole
    Indication: Gastric Ulcer
    Start date: 2007-07-23
    End date: 2007-08-03

Lansoprazole
    Dosage: daily dose:30mg
    Administration route: Oral
    Start date: 2007-08-04
    End date: 2007-08-21

Levofloxacin
    Administration route: Oral
    Start date: 2007-08-08
    End date: 2007-08-12

Norvasc
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-08-08
    End date: 2007-08-27

Olmetec
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-08-08
    End date: 2007-08-21

Prodif
    Indication: Fungal Infection
    Start date: 2007-07-23
    End date: 2007-08-04

Voltaren
    Dosage: daily dose:25mg-freq:frequency: prn
    Indication: Pyrexia
    Start date: 2007-07-23
    End date: 2007-08-05

Other drugs received by patient: Flumetholon; Prednisolone; Pentazocine Lactate



Adverse event in male receiving Voltaren (Diclofenac)

Reported by a consumer/non-health professional from Australia on 2007-10-16

Patient: male

Adverse reactions / side effects: Hypersensitivity, Dysstasia, Blood Pressure Decreased

Adverse event resulted in: hospitalization

Suspect drug(s):
Voltaren (Diclofenac)



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):
Apresolin
    Dosage: 50 mg, bid
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-07-30
    End date: 2007-08-08

Baktar
    Dosage: 2 g/day
    Administration route: Oral
    Indication: Interstitial Lung Disease
    Start date: 2007-07-24
    End date: 2007-08-01

Dormicum
    Dosage: 10 ug/day
    Indication: Sedation
    Start date: 2007-07-23
    End date: 2007-07-28

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

Levofloxacin
    Dosage: 400 mg/day
    Administration route: Oral
    Indication: Infection
    Start date: 2007-08-08
    End date: 2007-08-12

Norvasc
    Dosage: 5 mg/day
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-08-08
    End date: 2007-08-21

Olmetec
    Dosage: unk, unk
    Administration route: Oral
    Start date: 2007-08-08
    End date: 2007-08-21

Omegacin
    Dosage: 600 mg/day
    Indication: Interstitial Lung Disease
    Start date: 2007-07-23
    End date: 2007-08-04

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

Voltaren
    Dosage: 25 mg/day
    Indication: Antipyresis
    Start date: 2007-07-23
    End date: 2007-08-05

Other drugs received by patient: Polymyxin B; Elaspol



Adverse event in 94 year old female receiving Voltaren (Diclofenac)

Reported by a health professional (non-physician/pharmacist) from Italy on 2007-10-16

Patient: 94 year old female

Adverse reactions / side effects: Renal Failure, Blood Potassium Increased, Bundle Branch Block Left, Blood Creatinine Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Acarbose

Bactrim DS
    End date: 2007-07-02

Dafalgan Codeine

DI-Antalvic
    End date: 2007-07-02

Discortrine (Glyceryl Trinitrate)

Duragesic-100

Fenofibrate

Flector EP Gel (Diclofenac Epolaminum)

Iperten(manidipne Hydrochloride)

Irbesartan
    Dosage: 150 mg po
    Administration route: Oral

Lansoyl (Parrafin, Liquid)
    End date: 2007-07-02

Lasix
    Dosage: 20 mg

Mediatensyl (Urapidil)

Monuril(fosfomycin Trometamol)
    Dosage: 3 g po
    Administration route: Oral
    End date: 2007-07-02

Motilyo (Domperidone)

Pantoprazole Sodium
    Dosage: 20 mg po
    Administration route: Oral
    End date: 2007-07-02

Plavix

Preterax
    End date: 2007-07-02

Temerit (Nebivolol)

Vastarel (Trimetazidine)
    Dosage: 35 mg qd po
    Administration route: Oral
    End date: 2007-07-02

Voltaren



Adverse event in female receiving Voltaren (Diclofenac)

Reported by a consumer/non-health professional from United Kingdom on 2007-10-12

Patient: female, weighing 36.0 kg (79.2 pounds)

Adverse reactions / side effects: White Blood Cell Count Decreased, Weight Decreased, Anaemia

Adverse event resulted in: hospitalization

Suspect drug(s):
Bevacizumab
    Dosage: 4.8 mg/kg, unk
    Indication: Colorectal Cancer Metastatic
    Start date: 2007-06-21

Fluorouracil
    Dosage: 393 mg/m2, unk
    Indication: Colorectal Cancer Metastatic
    Start date: 2007-06-21

Irinotecan HCL
    Dosage: 149 mg/m2, unk
    Indication: Colorectal Cancer Metastatic
    Start date: 2007-06-21

Isovorin
    Dosage: 188 mg/m2, unk
    Indication: Colorectal Cancer Metastatic
    Start date: 2007-06-21

Voltaren
    Indication: Drug USE FOR Unknown Indication
    End date: 2007-06-21

Other drugs received by patient: Halcion; Fosamax; Nasea (Japan); Chinese Medicine; Selbex



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 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 51 year old female receiving Voltaren (Diclofenac)

Reported by a physician from Japan on 2007-10-11

Patient: 51 year old female, weighing 63.1 kg (138.8 pounds)

Adverse reactions / side effects: Vomiting, Nausea, Dehydration, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Valtrex
    Administration route: Oral
    Indication: Herpes Zoster
    Start date: 2007-09-14
    End date: 2007-09-18

Voltaren
    Indication: Facet Joint Syndrome
    Start date: 2007-08-23
    End date: 2007-09-18

Other drugs received by patient: Celestamine TAB; Methycobal; Mucosta



Adverse event in 74 year old male receiving Voltaren (Diclofenac)

Reported by a physician from Guatemala on 2007-10-09

Patient: 74 year old male

Adverse reactions / side effects: Dyspnoea, Cardiac Pacemaker Insertion, Heart Rate Increased, Chest Pain, Atrial Fibrillation, Atrioventricular Block, Electrocardiogram ST Segment Elevation

Adverse event resulted in: hospitalization

Suspect drug(s):
Voltaren (Diclofenac)

Other drugs received by patient: Ioversol; Hydrochlorothiazide; Hyperlipen; Allopurinol



Adverse event in male receiving Voltaren (Diclofenac)

Reported by a individual with unspecified qualification from Japan on 2007-10-05

Patient: male

Adverse reactions / side effects: Dehydration, Sepsis, Adrenal Insufficiency, Enteritis Infectious, Shock, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Voltaren (Diclofenac)



Adverse event in 73 year old male receiving Voltaren (Diclofenac)

Reported by a health professional (non-physician/pharmacist) from Italy on 2007-10-04

Patient: 73 year old male

Adverse reactions / side effects: Erythema, Loss of Consciousness

Adverse event resulted in: hospitalization

Suspect drug(s):
Voltaren (Diclofenac)



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