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Voltarene adverse events reported to FDA.

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Summary

FDA Adverse Reports: 4. View All

Voltarene FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 9

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Often additional risks of using a medication, such as Voltarene, 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 Voltarene users, Learn more about unwanted side effects & find ways to reduce them. Browse Voltarene Adverse Reports reported to FDA and participate in Voltarene discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Voltarene. 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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Voltarene Adverse Effect Reports (FDA)

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6108411-3 | Acidosis, Anaphylactic Shock, Asthenia, Cyanosis, Haemodynamic Instability, Liver Disorder, Loss Of Consciousness, Malaise
on Mar 04, 2009 Female patient from FRANCE , weighting 185.2 lb, was diagnosed with pain (What is pain?) and was treated with Voltarene (View Usage). Patient experienced the following unwanted or unexpected effects: acidosis, anaphylactic shock, asthenia, cyanosis, haemodynamic instability, liver disorder, loss of consciousness, malaise. Voltarene dosage: 1 Df, Qd. Patient was hospitalized.

6089595-2 | Basal Cell Carcinoma, Dermatitis Exfoliative, Eosinophil Count Increased, Hyperkeratosis, Insomnia, Pruritus, Rash Erythematous, Rash Maculo-papular, Scar Excision
Patient was taking Voltarene (View Usage). Patient had the following side effects: basal cell carcinoma, dermatitis exfoliative, eosinophil count increased, hyperkeratosis, insomnia, pruritus, rash erythematous, rash maculo-papular, scar excision on Feb 10, 2009 from FRANCE Additional patient health information: Female patient , 71 years of age, . Voltarene dosage: Unk. During the same period patient was treated with INIPOMP (Unk) (View Inipomp Review and Inipomp Label ), ALDALIX (50 Mg/20 Mg) (View Aldalix Review and Aldalix Label ), DOMPERIDONE (Unk) (View Domperidone Review and Domperidone Label ), MONO TILDIEM (Unk) (View Mono-tildiem Review and Mono-tildiem Label ), PRAVASTATIN (Unk) (View Pravastatin Review and Pravastatin Label ), BETAHISTINE (View Betahistine Review and Betahistine Label ), STABLON (View Stablon Review and Stablon Label ). Patient was hospitalized.

6089326-6 | Abdominal Pain, Chills, Ileitis, Ischaemia
Adverse event was reported on Feb 10, 2009 by a Male patient taking Voltarene (View Usage) (Dosage: 1 Df, Qd) was diagnosed with arthralgia and. Location: FRANCE , 80 years of age, After Voltarene was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), chills, ileitis, ischaemia. During the same period patient was treated with HEPARIN SODIUM (Unk) (View Heparin Sodium Review and Heparin Sodium Label ), LOVENOX (Unk) (View Lovenox Review and Lovenox Label ). Patient was hospitalized.

6054508-6 | Acute Pulmonary Oedema, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Biopsy Heart, Blood Alkaline Phosphatase, Dyspnoea, Ejection Fraction Decreased, Mitral Valve Incompetence, Myocarditis
on Jan 14, 2009 Female patient from FRANCE , 54 years of age, was treated with Voltarene (View Usage). Patient experienced the following unwanted or unexpected effects: acute pulmonary oedema, alanine aminotransferase increased, aspartate aminotransferase increased, biopsy heart, blood alkaline phosphatase, dyspnoea, ejection fraction decreased, mitral valve incompetence, myocarditis. Voltarene dosage: Unk. During the same period patient was treated with FUNGIZONE (1500 Mg/day (6 Capsules Daily)) (View Fungizone Review and Fungizone Label ), KETEK (1 Df/day) (View Ketek Review and Ketek Label ), CYCLOSPORINE (View Cyclosporine Review and Cyclosporine Label ), HEPARIN (View Heparin Review and Heparin Label ), PENTACARINAT (View Pentacarinat Review and Pentacarinat Label ), ZOVIRAX (View Zovirax Review and Zovirax Label ), ZELITREX (View Zelitrex Review and Zelitrex Label ), BACTRIM (View Bactrim Review and Bactrim Label ). Patient was hospitalized.


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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 Voltarene 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 Voltarene quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Voltarene 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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How Did You Deal with Side Effects?

If You had Voltaren side effect, You are not alone. Other patients reported side effects.

Complete Guide to Voltaren Nuro Side Effects | Male patient, 55 years of age, took Voltaren |Page 1

Complete Guide to Voltarene Lp Side Effects | Male patient, 39 years of age, weighting 185.2 |Page 1

About Voltaren : Risks and Benefits, News and Updates, Voltaren video and TV resources

Complete Guide to Voltaren Retard Side Effects | Female patient, 70 years of age, weighting 198.4 |Page 1

Post Voltaren Side Effect Reporting Your Voltaren side effect will help others recognize and deal with Voltaren side effects. Recent Reports View Voltaren reports ...

Voltaren injection Side Effect Report#5496 feet feel dead and lame after one week very painfullfor pain

Complete Guide to Voltaren Dolo Liquid Side Effects | Female patient, weighting 152.1 lb, was diagnosed with |Page 1

During the same period patient was treated with MESULID (3 Tablets) (View Mesulid Review and Mesulid Label ), VOLTAREN (View Voltaren Review and Voltaren Label ).

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Voltarene Reactions
Abdominal PainWhat is Abdominal pain?
Acidosis
Acute Pulmonary Oedema
Alanine Aminotransferase Increased
Anaphylactic Shock
Aspartate Aminotransferase Increased
Asthenia
Basal Cell Carcinoma
Biopsy Heart
Blood Alkaline Phosphatase
Chills
Cyanosis
Dermatitis Exfoliative
Dyspnoea
Ejection Fraction Decreased
Eosinophil Count Increased
Haemodynamic Instability
Hyperkeratosis
Ileitis
Insomnia
Ischaemia
Liver Disorder
Loss Of Consciousness
Malaise
Mitral Valve Incompetence
Myocarditis
Pruritus
Rash Erythematous
Rash Maculo-papular
Scar Excision
Voltarene 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 Voltarene 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!