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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Voltaren (Diclofenac). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (391)
Cases resulting in a serious event (389)
Cases resulting in death (52)
Cases resulting in life threatening events (42)
Cases resulting in hospitalization (196)
Cases resulting in disability (17)
Cases resulting in other serious reactions (196)
Below is a sample of reports where side effects / adverse reactions may be related to Voltaren (Diclofenac). For a complete list and/or a specific selection of reports, please use the links in the index above.
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 receiving Voltaren (Diclofenac)
Reported by a physician from Turkey on 2007-10-29
Patient:
Adverse reactions / side effects: Sciatic Nerve Palsy
Adverse event resulted in: disablity
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in 62 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-10-29
Patient: 62 year old male
Adverse reactions / side effects: Anal Haemorrhage, Anal Fissure
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in receiving Voltaren (Diclofenac)
Reported by a pharmacist from Japan on 2007-10-29
Patient:
Adverse reactions / side effects: Anal Haemorrhage, Traumatic Haemorrhage
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in male receiving Voltaren (Diclofenac)
Reported by a physician from Turkey on 2007-10-29
Patient: male
Adverse reactions / side effects: Sciatic Nerve Palsy
Suspect drug(s):
Voltaren (Diclofenac)
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 male receiving Voltaren (Diclofenac)
Reported by a physician from Turkey on 2007-10-29
Patient: male
Adverse reactions / side effects: Sciatic Nerve Palsy
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in male receiving Voltaren (Diclofenac)
Reported by a physician from Turkey on 2007-10-29
Patient: male
Adverse reactions / side effects: Peripheral Nerve Lesion
Adverse event resulted in: disablity
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in 62 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-10-26
Patient: 62 year old male
Adverse reactions / side effects: Anal Haemorrhage, Anal Fissure
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in 53 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Norway on 2007-10-26
Patient: 53 year old female
Adverse reactions / side effects: Tinnitus, Deafness Unilateral
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 2007-10-25
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 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 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 56 year old female receiving Voltaren (Diclofenac)
Reported by a physician from Norway on 2007-10-24
Patient: 56 year old female
Adverse reactions / side effects: Dyspnoea, Hyponatraemia, Obstructive Airways Disorder, Generalised Oedema
Adverse event resulted in: life threatening event
Suspect drug(s):
Brexidol
Administration route: Oral
Indication: Arthralgia
Cozaar
Dosage: 1 df, qd
Administration route: Oral
Indication: Hypertension
Diural
Dosage: 40 mg, qd
Administration route: Oral
Indication: Oedema
Start date: 2007-08-28
Ibux
Indication: Arthralgia
Start date: 2007-08-01
Naproxen
Administration route: Oral
Indication: Arthralgia
Voltaren
Dosage: 50 mg, tid
Administration route: Oral
Indication: Arthralgia
Start date: 2007-08-01
Other drugs received by patient: Pinex Forte; Doxylin; Vival; Noni Juice; Pinex; Fenazon-Koffein
Adverse event in 70 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Norway on 2007-10-24
Patient: 70 year old male
Adverse reactions / side effects: Confusional State, Amnesia
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Marevan; Digoxin
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 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 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 53 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Norway on 2007-10-19
Patient: 53 year old female
Adverse reactions / side effects: Tinnitus, Deafness Unilateral
Suspect drug(s):
Voltaren (Diclofenac)
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
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