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It seems as though after I have applied the Voltaren to my hands and ...Keep Reading

I am 37yrfemale I had a back ache and the doctor prescribed MuscoRil 4mg ...Keep Reading

My wife died of a pulmonary embolism 5 weeks ago when we were on ...Keep Reading

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El ano pasado estuve invalida por 2 meses poruna hernias inflamadas. Fue una ...Keep Reading

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Cleamine (1)
Death (1)
Diabetics (1)
In 2004 Had Crush Injury To Distal Aspect Upper Ar (1)
In 2004 Had Crush Injury To Distal Aspect Upper Ar (1)
PAIN RELIEF!!! (1)
Pursennide (1)
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Common Voltaren Side Effects

top 5 Voltaren|Cleamine|Death|Diabetics|In 2004 ha|In 2004 ha|PAIN RELIE|Pursennide adverse effects>>See All Voltaren Side Effects

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Voltaren adverse events reported to FDA.

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Summary

FDA Adverse Reports: 1692. View All

Voltaren FDA safety alerts: 2009

Reported deaths: 163

Reported hospitalizations: 848

Voltaren Dosage, Warnings, Usage.

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Most Reported
1Death
2Pursennide
3Cleamine
4Diabetics
5PAIN RELIEF!!!
6Ulcer
7In 2004 Had Crush Injury To Distal Aspect Upper Arm. Large Haematoma Present 4 Weeks Later. Gp Ordered Voltaren For Pain. Ended Up With Compartment Syndrome. Half Cup Bloodclot Fell Out In Operating Theatre. Surgeon Said Rebleed Had Been Caused By The Voltaren, Taken At The Normal Prescribed Dosage.
8In 2004 Had Crush Injury To Distal Aspect Upper Arm. Large Haematoma Present 4 Weeks Later. Gp Ordered Voltaren For Pain. Ended Up With Compartment Syndrome. Half Cup Bloodclot Fell Out In Operating Theatre. Surgeon Said Rebleed Had Been Caused By The Voltaren
9Taken At The Normal Prescribed Dosage.
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feet feel dead and lame after one

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Often additional risks of using a medication, such as Voltaren, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Voltaren users, Learn more about unwanted side effects & find ways to reduce them. Browse Voltaren Adverse Reports reported to FDA and participate in Voltaren discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Voltaren. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Voltaren Adverse Effect Reports (FDA)

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6888502-X | Blood Creatinine Increased, Fatigue, Hypertension, Oedema, Polydipsia, Polyuria, Renal Failure, Tubulointerstitial Nephritis
on Jul 19, 2010 Female patient from DENMARK , weighting 106.0 lb, was diagnosed with pain (What is pain?), anaesthesia and was treated with Voltaren (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatinine increased, fatigue, hypertension, oedema, polydipsia, polyuria, renal failure, tubulointerstitial nephritis. Voltaren dosage: 50 Mg, Tid. During the same period patient was treated with THIOPENTAL SODIUM (Unk) (View Thiopental Sodium Review and Thiopental Sodium Label ), PROPOFOL (View Propofol Review and Propofol Label ), ULTIVA (Unk) (View Ultiva Review and Ultiva Label ). Patient was hospitalized.

6888491-8 | Back Pain, Haematoma, Intervertebral Disc Compression, Lumbar Spinal Stenosis, Motor Dysfunction, Neurological Symptom, Paraesthesia, Paraplegia
Patient was taking Voltaren (View Usage). Patient had the following side effects: back pain (What is back pain?), haematoma, intervertebral disc compression, lumbar spinal stenosis, motor dysfunction, neurological symptom, paraesthesia, paraplegia on Jul 19, 2010 from FRANCE Additional patient health information: Male patient , 68 years of age, was diagnosed with musculoskeletal pain, osteoarthritis (What is osteoarthritis?), coronary artery disease (What is coronary artery disease?) and. Voltaren dosage: Unk. During the same period patient was treated with ARCOXIA (Unk) (View Arcoxia Review and Arcoxia Label ), PLAVIX (Unk) (View Plavix Review and Plavix Label ), KARDEGIC (Unk) (View Kardegic Review and Kardegic Label ), ALTIM (Unk) (View Altim Review and Altim Label ), CRESTOR (Unk) (View Crestor Review and Crestor Label ), COAPROVEL (Unk) (View Coaprovel Review and Coaprovel Label ), DIAMICRON (Unk) (View Diamicron Review and Diamicron Label ). Patient was hospitalized.

6888470-0 | Blister, Haematoma, Paraplegia, Skin Exfoliation, Toxic Epidermal Necrolysis
Adverse event was reported on Jul 19, 2010 by a Male patient taking Voltaren (View Usage) (Dosage: Unk) was diagnosed with musculoskeletal pain, osteoarthritis (What is osteoarthritis?) and. Location: FRANCE , 68 years of age, After Voltaren was administered, patient had the following side effects: blister, haematoma, paraplegia, skin exfoliation, toxic epidermal necrolysis. During the same period patient was treated with ARCOXIA (Unk) (View Arcoxia Review and Arcoxia Label ), ALTIM (Unk) (View Altim Review and Altim Label ), CRESTOR (View Crestor Review and Crestor Label ), COAPROVEL (View Coaprovel Review and Coaprovel Label ), PLAVIX (View Plavix Review and Plavix Label ), DIAMICRON (View Diamicron Review and Diamicron Label ), STAGID (View Stagid Review and Stagid Label ), OMEPRAZOLE (Unk) (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

6888272-5 | Blood Glucose Decreased, Blood Glucose Increased
on Jul 27, 2010 Female patient from UNITED STATES , 73 years of age, weighting 174.0 lb, was diagnosed with osteoarthritis (What is osteoarthritis?), back pain (What is back pain?) and was treated with Voltaren (View Usage). Patient experienced the following unwanted or unexpected effects: blood glucose decreased, blood glucose increased. Voltaren dosage: 4 G, Qid. During the same period patient was treated with TORADOL (Unk) (View Toradol Review and Toradol Label ).


6879991-5 | Malaise, Road Traffic Accident, Somnolence, Syncope
on Jul 16, 2010 Female patient from UNITED KINGDOM , weighting 140.0 lb, was diagnosed with oedema peripheral, depression (What is depression?) and was treated with Voltaren (View Usage). Patient had the following side effects: malaise, road traffic accident, somnolence, syncope. Voltaren dosage: 2 X 25 Mg. During the same period patient was treated with FLUOXETINE (20 Mg) (View Fluoxetine Review and Fluoxetine Label ).

6878808-2 | Blood Glucose Decreased, Blood Glucose Increased
Patient was taking Voltaren (View Usage). After Voltaren was administered, patient had the following side effects: blood glucose decreased, blood glucose increased on Jul 21, 2010 from UNITED STATES Additional patient health information: Female patient , 73 years of age, weighting 174.0 lb, was diagnosed with osteoarthritis (What is osteoarthritis?), back pain (What is back pain?) and. Voltaren dosage: 4 G, Qid. During the same period patient was treated with TORADOL (Unk) (View Toradol Review and Toradol Label ).

6866359-0 | Blood Creatine Phosphokinase Increased, Blood Pressure Increased, Cardiac Murmur Functional, Dehydration, Dyspnoea, Fall, Musculoskeletal Pain, Renal Failure Acute, Rhabdomyolysis
Adverse event was reported on Jul 09, 2010 by a Male patient taking Voltaren (View Usage) (Dosage: One Tablet Daily) was diagnosed with back pain (What is back pain?) and. Location: FRANCE , weighting 205.0 lb, Patient experienced the following unwanted or unexpected effects: blood creatine phosphokinase increased, blood pressure increased, cardiac murmur functional, dehydration, dyspnoea, fall (What is fall?), musculoskeletal pain, renal failure acute, rhabdomyolysis. During the same period patient was treated with DOLIPRANE (View Doliprane Review and Doliprane Label ). Patient was hospitalized.

6856162-X | Acquired Haemophilia, Condition Aggravated, Factor Viii Deficiency, Platelet Count Decreased, Rash
on Jul 07, 2010 Male patient from JAPAN , 45 years of age, was diagnosed with pyrexia, hypertension, depression (What is depression?) and was treated with Voltaren (View Usage). Patient had the following side effects: acquired haemophilia, condition aggravated, factor viii deficiency, platelet count decreased, rash (What is rash?). Voltaren dosage: 25 Mg, Qd. During the same period patient was treated with NORVASC (5 Mg) (View Norvasc Review and Norvasc Label ), PAXIL (20 Mg) (View Paxil Review and Paxil Label ). Patient was hospitalized.

6847768-2 | Interstitial Lung Disease
on Jul 14, 2010 Male patient from JAPAN , 67 years of age, was treated with Voltaren (View Usage). After Voltaren was administered, patient had the following side effects: interstitial lung disease. Voltaren dosage: Unk.

6847763-3 | Bladder Irrigation, Concomitant Disease Progression, Cystitis, Hyperhidrosis, Renal Failure, Urine Output Decreased
Patient was taking Voltaren (View Usage). Patient experienced the following unwanted or unexpected effects: bladder irrigation, concomitant disease progression, cystitis, hyperhidrosis, renal failure, urine output decreased on Jul 14, 2010 from GERMANY Additional patient health information: Male patient , 89 years of age, . Voltaren dosage: Unk.

6843858-9 | Acute Febrile Neutrophilic Dermatosis, Arthralgia, Inflammation, Pyrexia, Rash, Rash Papular
Adverse event was reported on Jul 05, 2010 by a Female patient taking Voltaren (View Usage) (Dosage: Unk) was diagnosed with pain (What is pain?), joint sprain and. Location: FRANCE , 52 years of age, Patient had the following side effects: acute febrile neutrophilic dermatosis, arthralgia, inflammation, pyrexia, rash (What is rash?), rash papular. During the same period patient was treated with BI PROFENID (150 Mg) (View Bi-profenid Review and Bi-profenid Label ). Patient was hospitalized.

6836665-4 | Abdominal Pain, Abdominal Tenderness, Blood Albumin Decreased, C-reactive Protein Increased, Colitis Ischaemic, Decreased Appetite, Diarrhoea, Haemoglobin Decreased, Hypertrophy
on Jun 29, 2010 Male patient from JAPAN , weighting 97.00 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), folate deficiency and was treated with Voltaren (View Usage). After Voltaren was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), abdominal tenderness, blood albumin decreased, c-reactive protein increased, colitis ischaemic, decreased appetite, diarrhoea, haemoglobin decreased, hypertrophy. Voltaren dosage: Unk. During the same period patient was treated with PREDONINE (5 Mg) (View Predonine Review and Predonine Label ), AZULFIDINE (1000 Mg) (View Azulfidine Review and Azulfidine Label ), FOLIAMIN (15 Mg) (View Foliamin Review and Foliamin Label ).

6836637-X | Bladder Irrigation, Concomitant Disease Progression, Cystitis, Hyperhidrosis, Renal Failure, Urine Output Decreased
on Jul 10, 2010 Male patient from GERMANY , 89 years of age, was treated with Voltaren (View Usage). Patient experienced the following unwanted or unexpected effects: bladder irrigation, concomitant disease progression, cystitis, hyperhidrosis, renal failure, urine output decreased. Voltaren dosage: Unk.

6836634-4 | Blood Pressure Decreased, Erythema, Shock
Patient was taking Voltaren (View Usage). Patient had the following side effects: blood pressure decreased, erythema, shock on Jul 08, 2010 from JAPAN Additional patient health information: Female patient , 81 years of age, was diagnosed with pain (What is pain?) and. Voltaren dosage: 100 Mg. During the same period patient was treated with NORVASC (Unk) (View Norvasc Review and Norvasc Label ), LIPITOR (Unk) (View Lipitor Review and Lipitor Label ), LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (Unk) (View Losartan Potassium And Hydrochlorothiazide Review and Losartan Potassium And Hydrochlorothiazide Label ), PREMINANT (View Preminant Review and Preminant Label ).

6835408-8 | Application Site Rash, Application Site Swelling, Rash Erythematous, Rash Pruritic
Adverse event was reported on Jul 12, 2010 by a Female patient taking Voltaren (View Usage) (Dosage: About 2 Grams Once A Day Rub On Areas) was diagnosed with arthritis (What is arthritis?) and. Location: UNITED STATES , weighting 125.0 lb, After Voltaren was administered, patient had the following side effects: application site rash, application site swelling, rash erythematous, rash pruritic.

6833319-5 | Mallory-weiss Syndrome
on Jun 18, 2010 Male patient from JAPAN , 57 years of age, was treated with Voltaren (View Usage). Patient experienced the following unwanted or unexpected effects: mallory-weiss syndrome. Voltaren dosage: Unk.

6832266-2 | Atrial Fibrillation, Off Label Use
on Jul 02, 2010 Female patient from UNITED STATES , 78 years of age, weighting 145.0 lb, was diagnosed with rash (What is rash?) and was treated with Voltaren (View Usage). Patient had the following side effects: atrial fibrillation (What is atrial fibrillation?), off label use. Voltaren dosage: Unk. Patient was hospitalized.

6831591-9 | Intestinal Obstruction, Intestinal Operation, Metastasis, Overdose, Proctalgia
Patient was taking Voltaren (View Usage). After Voltaren was administered, patient had the following side effects: intestinal obstruction, intestinal operation, metastasis, overdose, proctalgia on Jun 30, 2010 from JAPAN Additional patient health information: Male patient , 38 years of age, . Voltaren dosage: Unk. During the same period patient was treated with BUPRENORPHINE HCL (View Buprenorphine Hcl Review and Buprenorphine Hcl Label ). Patient was hospitalized.

6831536-1 | Blister, Diplegia, Dysuria, Herpes Zoster Infection Neurological, Muscular Weakness, Pyelonephritis, Pyrexia, Urinary Retention
Adverse event was reported on Jun 28, 2010 by a Female patient taking Voltaren (View Usage) (Dosage: ) was diagnosed with pain (What is pain?), herpes zoster and. Location: JAPAN , 73 years of age, Patient experienced the following unwanted or unexpected effects: blister, diplegia, dysuria, herpes zoster infection neurological, muscular weakness, pyelonephritis, pyrexia, urinary retention. During the same period patient was treated with ACYCLOVIR (750 Mg) (View Acyclovir Review and Acyclovir Label ), PENTAZOCINE (Unk) (View Pentazocine Review and Pentazocine Label ), KETOPROFEN (Unk) (View Ketoprofen Review and Ketoprofen Label ), LIDOCAINE HYDROCHLORIDE (Unk) (View Lidocaine Hydrochloride Review and Lidocaine Hydrochloride Label ), LOXOPROFEN SODIUM (Unk) (View Loxoprofen Sodium Review and Loxoprofen Sodium Label ), GABAPENTIN (Unk) (View Gabapentin Review and Gabapentin Label ), AMITRIPTYLINE HYDROCHLORIDE (Unk) (View Amitriptyline Hydrochloride Review and Amitriptyline Hydrochloride Label ).

6831520-8 | Agranulocytosis, Asthenia, Blood Phosphorus Decreased, Bone Marrow Failure, Ear Pain, Neutrophil Count Decreased, Odynophagia, Pyrexia, Tonsillitis
on Jun 28, 2010 Female patient from FRANCE , weighting 132.3 lb, was treated with Voltaren (View Usage). Patient had the following side effects: agranulocytosis, asthenia, blood phosphorus decreased, bone marrow failure, ear pain, neutrophil count decreased, odynophagia, pyrexia, tonsillitis. Voltaren dosage: Unk. During the same period patient was treated with ADVIL LIQUI GELS (Unk) (View Advil Liqui-gels Review and Advil Liqui-gels Label ), RHINADVIL (Unk) (View Rhinadvil Review and Rhinadvil Label ), AUGMENTIN '125' (1 G, Bid) (View Augmentin '125' Review and Augmentin '125' Label ), AURICULARUM (Unk) (View Auricularum Review and Auricularum Label ), AMOXICILLIN (Unk) (View Amoxicillin Review and Amoxicillin Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ). Patient was hospitalized.

6826548-8 | Alanine Aminotransferase Increased, Basedow's Disease, Blood Alkaline Phosphatase Increased, Blood Thyroid Stimulating Hormone Decreased, Concomitant Disease Aggravated, Dysphagia, Dyspnoea, Goitre, Neck Pain
on Jun 29, 2010 Female patient from JAPAN , weighting 114.6 lb, was diagnosed with periarthritis, hyperthyroidism and was treated with Voltaren (View Usage). After Voltaren was administered, patient had the following side effects: alanine aminotransferase increased, basedow's disease, blood alkaline phosphatase increased, blood thyroid stimulating hormone decreased, concomitant disease aggravated, dysphagia, dyspnoea, goitre, neck pain. Voltaren dosage: 25 Mg Daily. During the same period patient was treated with MERCAZOLE (15 Mg, Unk) (View Mercazole Review and Mercazole Label ).

6822417-8 | Abdominal Distension, Ascites, Haematochezia, Haemorrhoids, Intestinal Haemorrhage, Intestinal Obstruction, Pain
Patient was taking Voltaren (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal distension, ascites, haematochezia, haemorrhoids, intestinal haemorrhage, intestinal obstruction, pain (What is pain?) on Jul 05, 2010 from JAPAN Additional patient health information: Male patient , 77 years of age, . Voltaren dosage: 50 Mg Daily. During the same period patient was treated with LENDORMIN (Unk) (View Lendormin Review and Lendormin Label ), GASCON (Unk) (View Gascon Review and Gascon Label ), PARIET (Unk) (View Pariet Review and Pariet Label ), MINOCYCLINE HYDROCHLORIDE (Unk) (View Minocycline Hydrochloride Review and Minocycline Hydrochloride Label ), SODIUM ALGINATE (Unk) (View Sodium Alginate Review and Sodium Alginate Label ), ALFAROL (Unk) (View Alfarol Review and Alfarol Label ), SODIUM PICOSULFATE (Unk) (View Sodium Picosulfate Review and Sodium Picosulfate Label ).

6819802-7 | Abdominal Pain, Abdominal Tenderness, Ileal Operation, Ileal Perforation, Ileal Stenosis, Ileal Ulcer
Adverse event was reported on Jun 24, 2010 by a Male patient taking Voltaren (View Usage) (Dosage: Unk) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: JAPAN , 73 years of age, Patient had the following side effects: abdominal pain (What is abdominal pain?), abdominal tenderness, ileal operation, ileal perforation, ileal stenosis, ileal ulcer. During the same period patient was treated with PREDONINE (Unk) (View Predonine Review and Predonine Label ). Patient was hospitalized.

6817118-6 | Altered State Of Consciousness, Rash, Shock
on Jun 24, 2010 Female patient from JAPAN , 75 years of age, was diagnosed with arthralgia and was treated with Voltaren (View Usage). After Voltaren was administered, patient had the following side effects: altered state of consciousness, rash (What is rash?), shock. Voltaren dosage: 50 Mg.

6809536-7 | Blood Pressure Decreased, Erythema, Shock
on Jun 17, 2010 Female patient from JAPAN , 81 years of age, was diagnosed with pain (What is pain?) and was treated with Voltaren (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure decreased, erythema, shock. Voltaren dosage: 100 Mg. During the same period patient was treated with NORVASC (Unk) (View Norvasc Review and Norvasc Label ), LIPITOR (Unk) (View Lipitor Review and Lipitor Label ), LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (Unk) (View Losartan Potassium And Hydrochlorothiazide Review and Losartan Potassium And Hydrochlorothiazide Label ), PREMINANT (View Preminant Review and Preminant Label ).

6803882-9 | Amnesia, Dizziness, Dysarthria, Fall, Headache, Hemiparesis, Hot Flush, Loss Of Consciousness
Patient was taking Voltaren (View Usage). Patient had the following side effects: amnesia, dizziness (What is dizziness?), dysarthria, fall (What is fall?), headache (What is headache?), hemiparesis, hot flush, loss of consciousness on Jun 17, 2010 from UNITED STATES Additional patient health information: Female patient , 44 years of age, weighting 164.0 lb, was diagnosed with oedema peripheral, prophylaxis, migraine (What is migraine?), nervousness and. Voltaren dosage: 2 G, Tid. During the same period patient was treated with IBUPROFEN (NGX) (Unk, Unk) (View Ibuprofen (ngx) Review and Ibuprofen (ngx) Label ), WATER PILLS (Unk, Unk) (View Water Pills Review and Water Pills Label ), MS CONTIN (View Ms Contin Review and Ms Contin Label ), XANAX (View Xanax Review and Xanax Label ), IMITREX ^GLAXO^ (View Imitrex ^glaxo^ Review and Imitrex ^glaxo^ Label ). Patient was hospitalized.

6794965-0 | Anxiety, Confusional State, Nervousness, Self-injurious Ideation
Adverse event was reported on Jun 24, 2010 by a Male patient taking Voltaren (View Usage) (Dosage: 4mm Strand 3 X Day Other) was diagnosed with arthritis (What is arthritis?) and. Location: UNITED STATES , 57 years of age, weighting 210.0 lb, After Voltaren was administered, patient had the following side effects: anxiety (What is anxiety?), confusional state, nervousness, self-injurious ideation.

6790598-0 | Amenorrhoea
on Jun 18, 2010 Female patient from CHINA , 27 years of age, was diagnosed with ankylosing spondylitis (What is ankylosing spondylitis?) and was treated with Voltaren (View Usage). Patient experienced the following unwanted or unexpected effects: amenorrhoea. Voltaren dosage: 50 Mg, Tid. During the same period patient was treated with SULFASALAZINE (Unk) (View Sulfasalazine Review and Sulfasalazine Label ), TRIPTERYGIUM (Unk) (View Tripterygium Review and Tripterygium Label ).

6790502-5 | Loss Of Consciousness
on Jun 17, 2010 Male patient from JAPAN , 80 years of age, was diagnosed with back pain (What is back pain?) and was treated with Voltaren (View Usage). Patient had the following side effects: loss of consciousness. Voltaren dosage: 75 Mg.

6790362-2 | Anaphylactic Shock, Blood Cholesterol Increased, Hypersensitivity, Oral Discomfort, Pain In Extremity, Paraesthesia, Respiratory Arrest, Syncope
Patient was taking Voltaren (View Usage). After Voltaren was administered, patient had the following side effects: anaphylactic shock, blood cholesterol increased, hypersensitivity, oral discomfort, pain in extremity, paraesthesia, respiratory arrest, syncope on Jun 11, 2010 from BRAZIL Additional patient health information: Female patient , 74 years of age, was diagnosed with pain (What is pain?), osteoporosis (What is osteoporosis?), hypercholesterolaemia and. Voltaren dosage: Unk. During the same period patient was treated with CATAFLAM (Unk) (View Cataflam Review and Cataflam Label ), CALCIUM CARBONATE (1 Mg, 1 Envelop Daily) (View Calcium Carbonate Review and Calcium Carbonate Label ), TYLENOL (View Tylenol Review and Tylenol Label ), SIMVASTATIN (Unk) (View Simvastatin Review and Simvastatin Label ), VYTORIN (View Vytorin Review and Vytorin Label ), OXYGEN (View Oxygen Review and Oxygen Label ), CARDIZEM (30 Mg, Tid) (View Cardizem Review and Cardizem Label ).

6786342-3 | Ileal Stenosis
Adverse event was reported on Jun 16, 2010 by a Male patient taking Voltaren (View Usage) (Dosage: Unk) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: JAPAN , 73 years of age, Patient experienced the following unwanted or unexpected effects: ileal stenosis. During the same period patient was treated with PREDONINE (Unk) (View Predonine Review and Predonine Label ).

6784963-5 | Blood Test Abnormal, Muscle Spasms, Off Label Use, Therapeutic Response Unexpected
on Jun 16, 2010 Female patient from UNITED STATES , 38 years of age, weighting 110.0 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Voltaren (View Usage). Patient had the following side effects: blood test abnormal, muscle spasms, off label use, therapeutic response unexpected. Voltaren dosage: Unk, 6 Times Per Day Every 4 Hours.

6783584-8 | Mallory-weiss Syndrome
on Jun 14, 2010 Male patient from JAPAN , 57 years of age, was treated with Voltaren (View Usage). After Voltaren was administered, patient had the following side effects: mallory-weiss syndrome. Voltaren dosage: Unk.

6781839-4 | Arrhythmia, Blood Pressure Decreased, Heart Rate Decreased
Patient was taking Voltaren (View Usage). Patient experienced the following unwanted or unexpected effects: arrhythmia (What is arrhythmia?), blood pressure decreased, heart rate decreased on Jun 09, 2010 from GERMANY Additional patient health information: Female patient , 89 years of age, was diagnosed with back pain (What is back pain?) and. Voltaren dosage: 1 Df, Prn. During the same period patient was treated with ATACAND (Unk) (View Atacand Review and Atacand Label ), ISCOVER (Unk) (View Iscover Review and Iscover Label ), MUSARIL (Unk) (View Musaril Review and Musaril Label ).

6781828-X | Blood Pressure Decreased, Erythema, Shock
Adverse event was reported on Jun 07, 2010 by a Female patient taking Voltaren (View Usage) (Dosage: 100 Mg) was diagnosed with pain (What is pain?) and. Location: JAPAN , 81 years of age, Patient had the following side effects: blood pressure decreased, erythema, shock. During the same period patient was treated with NORVASC (Unk) (View Norvasc Review and Norvasc Label ), LIPITOR (Unk) (View Lipitor Review and Lipitor Label ), LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (Unk) (View Losartan Potassium And Hydrochlorothiazide Review and Losartan Potassium And Hydrochlorothiazide Label ).

6781358-5 | Blood Creatinine Increased, Blood Potassium Increased, Blood Urea Increased, Dialysis, Meningitis Staphylococcal, Renal Failure Acute, Skin Necrosis
on Jun 17, 2010 Male patient from FRANCE , 97 years of age, was diagnosed with back pain (What is back pain?) and was treated with Voltaren (View Usage). After Voltaren was administered, patient had the following side effects: blood creatinine increased, blood potassium increased, blood urea increased, dialysis (What is dialysis?), meningitis staphylococcal, renal failure acute, skin necrosis. Voltaren dosage: Unk. During the same period patient was treated with ZESTORETIC (1 Df, Qd,20 Mg/12.5mg) (View Zestoretic Review and Zestoretic Label ), FUROSEMIDE (100 Mg, Qd) (View Furosemide Review and Furosemide Label ). Patient was hospitalized.

6779399-7 | Blood Creatinine Increased, Blood Potassium Increased, Blood Urea Increased, Dialysis, Meningitis Staphylococcal, Renal Failure Acute, Skin Necrosis
on Jun 14, 2010 Male patient from FRANCE , 97 years of age, was diagnosed with back pain (What is back pain?) and was treated with Voltaren (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatinine increased, blood potassium increased, blood urea increased, dialysis (What is dialysis?), meningitis staphylococcal, renal failure acute, skin necrosis. Voltaren dosage: Unk. During the same period patient was treated with ZESTORETIC (1 Df, Qd,20 Mg/12.5mg) (View Zestoretic Review and Zestoretic Label ), FUROSEMIDE (100 Mg, Qd) (View Furosemide Review and Furosemide Label ). Patient was hospitalized.

6775482-0 | Fibromyalgia, Hepatic Enzyme Increased, Local Swelling, Pain In Extremity, Surgery
Patient was taking Voltaren (View Usage). Patient had the following side effects: fibromyalgia, hepatic enzyme increased, local swelling, pain in extremity, surgery (What is surgery?) on May 21, 2010 from UNITED STATES Additional patient health information: Female patient , 54 years of age, weighting 183.0 lb, was diagnosed with myalgia, blood cholesterol, pain in extremity and. Voltaren dosage: . During the same period patient was treated with LIPITOR (20 Mg Daily) (View Lipitor Review and Lipitor Label ), NEURONTIN (Two To Three Times Daily) (View Neurontin Review and Neurontin Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), DARVOCET N 100 (View Darvocet-n 100 Review and Darvocet-n 100 Label ), MOBIC (View Mobic Review and Mobic Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), STEROIDS NOS (View Steroids Nos Review and Steroids Nos Label ).

6774835-4 | Blood Triglycerides Increased, Hyperlipidaemia, Hypertension, Intermediate Density Lipoprotein Increased, Remnant Hyperlipidaemia
Adverse event was reported on Jun 04, 2010 by a Male patient taking Voltaren (View Usage) (Dosage: 25-50 Mg Daily) was diagnosed with headache (What is headache?) and. Location: JAPAN , 47 years of age, After Voltaren was administered, patient had the following side effects: blood triglycerides increased, hyperlipidaemia, hypertension, intermediate density lipoprotein increased, remnant hyperlipidaemia.

6760419-0 | Blood Lactate Dehydrogenase Increased, Dialysis, Haemoglobin Decreased, Malaise, Platelet Count Increased, Pyrexia, Red Blood Cell Count Decreased, Tubulointerstitial Nephritis
on May 26, 2010 Male patient from JAPAN , weighting 165.3 lb, was diagnosed with pyrexia, hypertension, hyperlipidaemia and was treated with Voltaren (View Usage). Patient experienced the following unwanted or unexpected effects: blood lactate dehydrogenase increased, dialysis (What is dialysis?), haemoglobin decreased, malaise, platelet count increased, pyrexia, red blood cell count decreased, tubulointerstitial nephritis. Voltaren dosage: 25 Mg, Once/single. During the same period patient was treated with DIOVAN (80 Mg) (View Diovan Review and Diovan Label ), BEZATOL SLOW RELEASE (400 Mg) (View Bezatol - Slow Release Review and Bezatol - Slow Release Label ). Patient was hospitalized.

6759853-4 | Abdominal Pain, Abdominal Rebound Tenderness, Acute Abdomen, Enterocolitis Infectious, Gastrointestinal Inflammation, Peritoneal Disorder, Pyrexia
on May 28, 2010 Female patient from UNITED STATES , 39 years of age, weighting 116.0 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Voltaren (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), abdominal rebound tenderness, acute abdomen, enterocolitis infectious, gastrointestinal inflammation, peritoneal disorder, pyrexia. Voltaren dosage: 3x/day. During the same period patient was treated with METHOTREXATE (Week) (View Methotrexate Review and Methotrexate Label ), PREDNISOLONE (Day) (View Prednisolone Review and Prednisolone Label ), MUCOSTA (View Mucosta Review and Mucosta Label ), FOLIAMIN (View Foliamin Review and Foliamin Label ), ISCOTIN (View Iscotin Review and Iscotin Label ). Patient was hospitalized.

6759118-0 | Gastric Ulcer, Malaise
Patient was taking Voltaren (View Usage). After Voltaren was administered, patient had the following side effects: gastric ulcer, malaise on Jun 02, 2010 from UNITED STATES Additional patient health information: Female patient , 48 years of age, weighting 152.0 lb, . Voltaren dosage: Unk, Unk. Patient was hospitalized.

6758896-4 | Blood Creatinine Decreased, Eosinophil Percentage Increased, Haematocrit Decreased, Haemoglobin Decreased, Hepatitis Acute, Liver Disorder, Malaise, Monocyte Percentage Increased
Adverse event was reported on May 27, 2010 by a Male patient taking Voltaren (View Usage) (Dosage: 50 Mg, Unk) was diagnosed with pyrexia, hypertension and. Location: JAPAN , weighting 127.9 lb, Patient experienced the following unwanted or unexpected effects: blood creatinine decreased, eosinophil percentage increased, haematocrit decreased, haemoglobin decreased, hepatitis acute, liver disorder, malaise, monocyte percentage increased. During the same period patient was treated with CALBLOCK (16 Mg, Unk) (View Calblock Review and Calblock Label ), CANDESARTAN CILEXETIL (8 Mg, Unk) (View Candesartan Cilexetil Review and Candesartan Cilexetil Label ). Patient was hospitalized.

6758894-0 | Alanine Aminotransferase Increased, Basedow's Disease, Blood Alkaline Phosphatase Increased, Blood Thyroid Stimulating Hormone Decreased, Concomitant Disease Aggravated, Dysphagia, Dyspnoea, Goitre, Oedema Peripheral
on May 26, 2010 Female patient from JAPAN , weighting 114.6 lb, was diagnosed with periarthritis, hyperthyroidism and was treated with Voltaren (View Usage). Patient had the following side effects: alanine aminotransferase increased, basedow's disease, blood alkaline phosphatase increased, blood thyroid stimulating hormone decreased, concomitant disease aggravated, dysphagia, dyspnoea, goitre, oedema peripheral. Voltaren dosage: 25 Mg Daily. During the same period patient was treated with MERCAZOLE (15 Mg, Unk) (View Mercazole Review and Mercazole Label ).

6758893-9 | Back Pain, Fall, Limb Injury
on May 25, 2010 Female patient from BRAZIL , 85 years of age, weighting 160.9 lb, was diagnosed with back pain (What is back pain?), hypertension and was treated with Voltaren (View Usage). After Voltaren was administered, patient had the following side effects: back pain (What is back pain?), fall (What is fall?), limb injury. Voltaren dosage: . During the same period patient was treated with ATENSINA (One Tablet In The Morning) (View Atensina Review and Atensina Label ), HYDROCHLOROTHIAZIDE (1 Tablet Twice Daily) (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ).

6758873-3 | Heat Illness, Neurosis, Photosensitivity Reaction, Pruritus, Pyrexia, Rash, Sympathetic Nerve Injury
Patient was taking Voltaren (View Usage). Patient experienced the following unwanted or unexpected effects: heat illness (What is heat illness?), neurosis, photosensitivity reaction, pruritus, pyrexia, rash (What is rash?), sympathetic nerve injury on May 27, 2010 from JAPAN Additional patient health information: Male patient , 73 years of age, was diagnosed with nasopharyngitis and. Voltaren dosage: Unk. During the same period patient was treated with OMEPRAZOLE (Unk) (View Omeprazole Review and Omeprazole Label ), ITRACONAZOLE (Unk) (View Itraconazole Review and Itraconazole Label ). Patient was hospitalized.

6756182-X | Hyperlipidaemia, Hypertension
Adverse event was reported on May 26, 2010 by a Male patient taking Voltaren (View Usage) (Dosage: 25-50 Mg Daily) was diagnosed with headache (What is headache?) and. Location: JAPAN , 47 years of age, Patient had the following side effects: hyperlipidaemia, hypertension.

6749093-7 | Dizziness, Hyperhidrosis, Off Label Use, Skeletal Injury, Syncope
on May 25, 2010 Female patient from UNITED STATES , 56 years of age, was diagnosed with neck pain, back pain (What is back pain?), musculoskeletal pain and was treated with Voltaren (View Usage). After Voltaren was administered, patient had the following side effects: dizziness (What is dizziness?), hyperhidrosis, off label use, skeletal injury, syncope. Voltaren dosage: 1 Gram On Hip; 1.5 Grams On Shoulder, Bid.

6749092-5 | Amnesia, Chest Pain, Hallucination, Heart Rate Increased, Hypersensitivity, Off Label Use, Palpitations, Tachycardia
on May 25, 2010 Female patient from UNITED STATES , 50 years of age, weighting 180.0 lb, was diagnosed with back pain (What is back pain?) and was treated with Voltaren (View Usage). Patient experienced the following unwanted or unexpected effects: amnesia, chest pain (What is chest pain?), hallucination, heart rate increased, hypersensitivity, off label use, palpitations, tachycardia. Voltaren dosage: 2 G, Once/single.

6748809-3 | Aphagia, Back Pain, Brain Stem Infarction, Dehydration, Dyslalia, Genital Erosion, Genital Pain, Nutritional Condition Abnormal
Patient was taking Voltaren (View Usage). Patient had the following side effects: aphagia, back pain (What is back pain?), brain stem infarction, dehydration, dyslalia, genital erosion, genital pain, nutritional condition abnormal on May 21, 2010 from JAPAN Additional patient health information: Male patient , 73 years of age, weighting 130.1 lb, was diagnosed with back pain (What is back pain?) and. Voltaren dosage: 50 Mg. During the same period patient was treated with SERENAL (Unk) (View Serenal Review and Serenal Label ), TAKEPRON (Unk) (View Takepron Review and Takepron Label ), TAMIFLU (Unk) (View Tamiflu Review and Tamiflu Label ), CELTECT (Unk) (View Celtect Review and Celtect Label ).

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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Voltaren risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Voltaren quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Voltaren use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Voltaren Reactions
Abdominal PainWhat is Abdominal pain?
Alanine Aminotransferase Increased
Anaemia
Anaphylactic Shock
Aspartate Aminotransferase Increased
Blood Alkaline Phosphatase Increased
Blood Bilirubin Increased
Blood Creatine Phosphokinase Increased
Blood Creatinine Increased
Blood Lactate Dehydrogenase Increased
Blood Pressure Decreased
Blood Urea Increased
C-reactive Protein Increased
Depressed Level Of Consciousness
Diarrhoea
DizzinessWhat is Dizziness?
Dyspnoea
Erythema
Gastric Ulcer
Haemoglobin Decreased
Hypotension
Loss Of Consciousness
Malaise
NauseaWhat is Nausea?
Oedema Peripheral
PainWhat is Pain?
Pyrexia
RashWhat is Rash?
Renal Failure Acute
Shock
Voltaren Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Voltaren adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!