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Elisor adverse events reported to FDA.

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Summary

FDA Adverse Reports: 36. View All

Elisor FDA safety alerts: No

Reported deaths: 7

Reported hospitalizations: 73

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

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6640621-9 | Blood Creatine Phosphokinase Increased, Chest Pain, Decreased Appetite, Myalgia, Weight Decreased
on Mar 09, 2010 Female patient from FRANCE , 43 years of age, was treated with Elisor (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatine phosphokinase increased, chest pain (What is chest pain?), decreased appetite, myalgia, weight decreased. Elisor dosage: 1 Intake. During the same period patient was treated with CRESTOR (1 Intake) (View Crestor Review and Crestor Label ). Patient was hospitalized.

6500539-9 | Interstitial Lung Disease
Patient was taking Elisor (View Usage). Patient had the following side effects: interstitial lung disease on Dec 09, 2009 from FRANCE Additional patient health information: Male patient , 85 years of age, . Elisor dosage: . During the same period patient was treated with ZESTORETIC (View Zestoretic Review and Zestoretic Label ), ZYLORIC (View Zyloric Review and Zyloric Label ), FELDENE (View Feldene Review and Feldene Label ), LASILIX (View Lasilix Review and Lasilix Label ).

6461612-7 | Hypertension, Peripheral Sensorimotor Neuropathy, Renal Failure
Adverse event was reported on Nov 24, 2009 by a Female patient taking Elisor (View Usage) (Dosage: ) was diagnosed with hypercholesterolaemia, essential thrombocythaemia and. Location: FRANCE , 76 years of age, After Elisor was administered, patient had the following side effects: hypertension, peripheral sensorimotor neuropathy, renal failure. During the same period patient was treated with XAGRID (2006-28oct09:3mg 29oct09-ong:2.5mg (dose Reduced) Caps) (View Xagrid Review and Xagrid Label ).

6245365-3 | Inflammation
on Jun 23, 2009 Male patient from FRANCE , 68 years of age, weighting 163.1 lb, was diagnosed with hypercholesterolaemia, diabetes mellitus, type 1 diabetes mellitus and was treated with Elisor (View Usage). Patient experienced the following unwanted or unexpected effects: inflammation. Elisor dosage: 1 Df- 1 Tab/d. During the same period patient was treated with INSULIN (View Insulin Review and Insulin Label ).


6183048-9 | Inflammation
on May 04, 2009 Male patient from FRANCE , 68 years of age, was diagnosed with diabetes mellitus and was treated with Elisor (View Usage). Patient had the following side effects: inflammation. Elisor dosage: . During the same period patient was treated with INSULIN (View Insulin Review and Insulin Label ).

5982895-3 | Haemorrhagic Disorder, Hepatitis Fulminant, Hypercreatininaemia, Rhabdomyolysis
Patient was taking Elisor (View Usage). After Elisor was administered, patient had the following side effects: haemorrhagic disorder, hepatitis fulminant, hypercreatininaemia, rhabdomyolysis on Dec 03, 2008 from FRANCE Additional patient health information: Female patient , 89 years of age, was diagnosed with hypercholesterolaemia, depression (What is depression?) and. Elisor dosage: . During the same period patient was treated with NORSET (View Norset Review and Norset Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), CO TAREG (View Co-tareg Review and Co-tareg Label ). Patient was hospitalized.

5815127-7 | Respiratory Tract Congestion, Rhabdomyolysis
Adverse event was reported on Jul 16, 2008 by a Female patient taking Elisor (View Usage) (Dosage: ) . Location: FRANCE , 73 years of age, Patient experienced the following unwanted or unexpected effects: respiratory tract congestion, rhabdomyolysis. During the same period patient was treated with SUSTIVA (View Sustiva Review and Sustiva Label ), TELZIR (View Telzir Review and Telzir Label ), NORVIR (View Norvir Review and Norvir Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), LASIX (View Lasix Review and Lasix Label ), UN ALFA (View Un-alfa Review and Un-alfa Label ), SODIUM BICARBONATE (View Sodium Bicarbonate Review and Sodium Bicarbonate Label ), STABLON (View Stablon Review and Stablon Label ).

5767440-X | Abdominal Pain, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Asthenia, Blood Alkaline Phosphatase Increased, Blood Creatine Phosphokinase Increased, Blood Lactate Dehydrogenase Increased, Myalgia, Vomiting
on Jun 10, 2008 Female patient from FRANCE , 47 years of age, weighting 238.1 lb, was diagnosed with dyslipidaemia, obesity (What is obesity?), infertility (What is infertility?), hypothyroidism, anaemia, hypopituitarism and was treated with Elisor (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), alanine aminotransferase increased, aspartate aminotransferase increased, asthenia, blood alkaline phosphatase increased, blood creatine phosphokinase increased, blood lactate dehydrogenase increased, myalgia, vomiting. Elisor dosage: 1dosage Form= 1tablet. During the same period patient was treated with GLUCOPHAGE (View Glucophage Review and Glucophage Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), HYDROCORTISONE (View Hydrocortisone Review and Hydrocortisone Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), FERRO SANOL (1 Dosage Form = 1 Capsule) (View Ferro Sanol Review and Ferro Sanol Label ), NUTROPIN (View Nutropin Review and Nutropin Label ). Patient was hospitalized.

5678481-5 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Creatine Phosphokinase Increased, Blood Lactate Dehydrogenase Increased, Myalgia
on Mar 17, 2008 Female patient from FRANCE , 47 years of age, was diagnosed with dyslipidaemia and was treated with Elisor (View Usage). After Elisor was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood creatine phosphokinase increased, blood lactate dehydrogenase increased, myalgia. Elisor dosage: . During the same period patient was treated with GLUCOPHAGE (1 Dosage Form = 1 Tab) (View Glucophage Review and Glucophage Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), HYDROCORTISONE (View Hydrocortisone Review and Hydrocortisone Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), FERRO SANOL (1 Dosage Form = 1 Cap) (View Ferro Sanol Review and Ferro Sanol Label ).

5677605-3 | Cerebral Haemorrhage, Subdural Haematoma, Tonic Clonic Movements
Patient was taking Elisor (View Usage). Patient experienced the following unwanted or unexpected effects: cerebral haemorrhage, subdural haematoma, tonic clonic movements on Mar 19, 2008 from FRANCE Additional patient health information: Female patient , 87 years of age, . Elisor dosage: . During the same period patient was treated with PREVISCAN (1 Dosage Form = 1/4 On Even Day And 1/2 On Odd Day.) (View Previscan Review and Previscan Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), CARDENSIEL (View Cardensiel Review and Cardensiel Label ), TOPALGIC (View Topalgic Review and Topalgic Label ), ZOLOFT (View Zoloft Review and Zoloft Label ), SOLUPRED (View Solupred Review and Solupred Label ), LASILIX (View Lasilix Review and Lasilix Label ), FORLAX (View Forlax Review and Forlax Label ).

5602754-5 | Intraventricular Haemorrhage
Adverse event was reported on Jan 22, 2008 by a Male patient taking Elisor (View Usage) (Dosage: ) . Location: FRANCE , 69 years of age, Patient had the following side effects: intraventricular haemorrhage. During the same period patient was treated with PRAVADUAL (View Pravadual Review and Pravadual Label ), PLAVIX (View Plavix Review and Plavix Label ), KARDEGIC (Kardegic Powder.) (View Kardegic Review and Kardegic Label ), TRILEPTAL (View Trileptal Review and Trileptal Label ). Patient was hospitalized.

5599792-8 | Intraventricular Haemorrhage
on Jan 22, 2008 Male patient from FRANCE , 69 years of age, was treated with Elisor (View Usage). After Elisor was administered, patient had the following side effects: intraventricular haemorrhage. Elisor dosage: . During the same period patient was treated with PRAVADUAL (View Pravadual Review and Pravadual Label ), PLAVIX (View Plavix Review and Plavix Label ), KARDEGIC (Kardegic Powder.) (View Kardegic Review and Kardegic Label ), TRILEPTAL (View Trileptal Review and Trileptal Label ). Patient was hospitalized.

5551072-2 | Fall, Subdural Haematoma
on Dec 10, 2007 Male patient from FRANCE , 89 years of age, was treated with Elisor (View Usage). Patient experienced the following unwanted or unexpected effects: fall (What is fall?), subdural haematoma. Elisor dosage: . During the same period patient was treated with POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), ASPEGIC 1000 (View Aspegic 1000 Review and Aspegic 1000 Label ), NITRODERM (View Nitroderm Review and Nitroderm Label ), BURINEX (View Burinex Review and Burinex Label ), MOPRAL (View Mopral Review and Mopral Label ), IKOREL (View Ikorel Review and Ikorel Label ). Patient was hospitalized.

5542473-7 | Porphyria Non-acute
Patient was taking Elisor (View Usage). Patient had the following side effects: porphyria non-acute on Nov 28, 2007 from FRANCE Additional patient health information: Male patient , 65 years of age, was diagnosed with dyslipidaemia and. Elisor dosage: . During the same period patient was treated with PLAVIX (Unk) (View Plavix Review and Plavix Label ). Patient was hospitalized.

5530819-5 | Porphyria Non-acute
Adverse event was reported on Nov 28, 2007 by a Male patient taking Elisor (View Usage) (Dosage: ) . Location: FRANCE , 65 years of age, After Elisor was administered, patient had the following side effects: porphyria non-acute. During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ). Patient was hospitalized.

5496188-4 | Atrial Fibrillation, Ischaemic Stroke, Thrombocytopenia
on Oct 22, 2007 Male patient from FRANCE , 75 years of age, was treated with Elisor (View Usage). Patient experienced the following unwanted or unexpected effects: atrial fibrillation (What is atrial fibrillation?), ischaemic stroke, thrombocytopenia. Elisor dosage: . During the same period patient was treated with HEPARIN (View Heparin Review and Heparin Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), CORDARONE (View Cordarone Review and Cordarone Label ), LASIX (View Lasix Review and Lasix Label ). Patient was hospitalized.

5479276-8 | Purpura, Spontaneous Haematoma, Thrombocytopenia
on Oct 01, 2007 Female patient from FRANCE , 84 years of age, was treated with Elisor (View Usage). Patient had the following side effects: purpura, spontaneous haematoma, thrombocytopenia. Elisor dosage: . During the same period patient was treated with FUCIDINE (View Fucidine Review and Fucidine Label ), ALDACTAZIDE (View Aldactazide Review and Aldactazide Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), INEXIUM (View Inexium Review and Inexium Label ), TANGANIL (View Tanganil Review and Tanganil Label ), STABLON (View Stablon Review and Stablon Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), FORLAX (View Forlax Review and Forlax Label ). Patient was hospitalized.

5468558-1 | Rectal Haemorrhage
Patient was taking Elisor (View Usage). After Elisor was administered, patient had the following side effects: rectal haemorrhage on Sep 25, 2007 from FRANCE Additional patient health information: Male patient , 59 years of age, was diagnosed with hypercholesterolaemia, cardiac failure, thrombosis, hypertension and. Elisor dosage: . During the same period patient was treated with ALDACTONE (View Aldactone Review and Aldactone Label ), PREVISCAN (View Previscan Review and Previscan Label ), TRIATEC (View Triatec Review and Triatec Label ), LASIX (View Lasix Review and Lasix Label ). Patient was hospitalized.

5411360-7 | Bronchospasm, Tongue Oedema, Urticaria
Adverse event was reported on Aug 06, 2007 by a Female patient taking Elisor (View Usage) (Dosage: ) was diagnosed with hypercholesterolaemia, osteoporosis (What is osteoporosis?), hypertension and. Location: FRANCE , 77 years of age, weighting 136.7 lb, Patient experienced the following unwanted or unexpected effects: bronchospasm, tongue oedema, urticaria. During the same period patient was treated with BONIVA (View Boniva Review and Boniva Label ), COTAREG (View Cotareg Review and Cotareg Label ).

5331104-7 | Bone Marrow Failure
on May 18, 2007 Male patient from FRANCE , 60 years of age, was treated with Elisor (View Usage). Patient had the following side effects: bone marrow failure. Elisor dosage: . During the same period patient was treated with COAPROVEL (View Coaprovel Review and Coaprovel Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), AMARYL (View Amaryl Review and Amaryl Label ), VIRAFERONPEG (View Viraferonpeg Review and Viraferonpeg Label ).

5312524-3 | Cardiac Arrest, Hypoxia, Interstitial Lung Disease, Pneumothorax, Pulmonary Alveolar Haemorrhage, Renal Failure
on Apr 24, 2007 Female patient from FRANCE , 69 years of age, was diagnosed with hypercholesterolaemia and was treated with Elisor (View Usage). After Elisor was administered, patient had the following side effects: cardiac arrest (What is cardiac arrest?), hypoxia, interstitial lung disease, pneumothorax, pulmonary alveolar haemorrhage, renal failure. Elisor dosage: . During the same period patient was treated with EUTHYRAL (View Euthyral Review and Euthyral Label ). Patient was hospitalized.

5299424-2 | Biliary Cyst, Blood Amylase Increased, Gastrointestinal Disorder, Lipase Increased
Patient was taking Elisor (View Usage). Patient experienced the following unwanted or unexpected effects: biliary cyst, blood amylase increased, gastrointestinal disorder, lipase increased on Apr 13, 2007 from FRANCE Additional patient health information: Female patient , 56 years of age, weighting 110.2 lb, was diagnosed with hypercholesterolaemia, dyskinesia, phlebitis and. Elisor dosage: 10mg Per Day From 04-dec-2003, Increased To 20mg Per Day On 06-sep-2005. During the same period patient was treated with EFFEXOR XR (View Effexor Xr Review and Effexor Xr Label ), XENAZINE (View Xenazine Review and Xenazine Label ), PREVISCAN (View Previscan Review and Previscan Label ), DAFLON (View Daflon Review and Daflon Label ), ACTONEL (View Actonel Review and Actonel Label ), STILNOX (View Stilnox Review and Stilnox Label ), ABUFENE (View Abufene Review and Abufene Label ), AGREAL (View Agreal Review and Agreal Label ).

5289738-4 | Ligament Rupture, Muscle Atrophy, Muscular Weakness
Adverse event was reported on Apr 04, 2007 by a Female patient taking Elisor (View Usage) (Dosage: One Year Prior To This 40mg Daily Dose, The Patient Took 20 Mg Daily For One Year.) was diagnosed with hypercholesterolaemia and. Location: FRANCE , 64 years of age, Patient had the following side effects: ligament rupture, muscle atrophy, muscular weakness. During the same period patient was treated with KARDEGIC (View Kardegic Review and Kardegic Label ), FOSAMAX (View Fosamax Review and Fosamax Label ).

4912008-8 | Pseudo Lymphoma
on Feb 09, 2006 Male patient from FRANCE , 75 years of age, was diagnosed with hypercholesterolaemia, arrhythmia (What is arrhythmia?), oesophagitis, arthralgia and was treated with Elisor (View Usage). After Elisor was administered, patient had the following side effects: pseudo lymphoma. Elisor dosage: . During the same period patient was treated with SOTALEX TABS (View Sotalex Tabs Review and Sotalex Tabs Label ), MOPRAL (View Mopral Review and Mopral Label ), PLAVIX (View Plavix Review and Plavix Label ), DIALGIREX (View Dialgirex Review and Dialgirex Label ). Patient was hospitalized.

4869291-7 | Hyponatraemia
on Dec 20, 2005 Female patient from FRANCE , 55 years of age, was treated with Elisor (View Usage). Patient experienced the following unwanted or unexpected effects: hyponatraemia. Elisor dosage: . During the same period patient was treated with LEXOMIL (View Lexomil Review and Lexomil Label ), TRIMETAZIDINE (View Trimetazidine Review and Trimetazidine Label ), EQUANIL (View Equanil Review and Equanil Label ), DAFLON (View Daflon Review and Daflon Label ), HAWTHORN (View Hawthorn Review and Hawthorn Label ), SPASFON (View Spasfon Review and Spasfon Label ), AMLOR (View Amlor Review and Amlor Label ), TIAPRIDAL (View Tiapridal Review and Tiapridal Label ). Patient was hospitalized.

4865001-8 | Acute Coronary Syndrome, Bundle Branch Block Left, Neutropenia, Stent Placement
Patient was taking Elisor (View Usage). Patient had the following side effects: acute coronary syndrome, bundle branch block left, neutropenia, stent placement on Dec 13, 2005 from FRANCE Additional patient health information: Female patient , 55 years of age, was diagnosed with depression (What is depression?) and. Elisor dosage: 40 Mg/day. During the same period patient was treated with CORVASAL (1 Tab/day) (View Corvasal Review and Corvasal Label ), PLAVIX (1 Tab/day) (View Plavix Review and Plavix Label ), KARDEGIC (75 Mg/day) (View Kardegic Review and Kardegic Label ), SECTRAL (200 Mg/day) (View Sectral Review and Sectral Label ), LUDIOMIL (View Ludiomil Review and Ludiomil Label ). Patient was hospitalized.

4844647-7 | Gamma-glutamyltransferase Increased, Pleural Effusion, Pneumonia
Adverse event was reported on Mar 22, 2005 by a Female patient taking Elisor (View Usage) (Dosage: ) was diagnosed with hypercholesterolaemia and. Location: FRANCE , 67 years of age, After Elisor was administered, patient had the following side effects: gamma-glutamyltransferase increased, pleural effusion, pneumonia (What is pneumonia?). Patient was hospitalized.

4834120-4 | Abdominal Pain Upper, Blood Creatine Phosphokinase Increased, Helicobacter Infection, Myalgia
on Nov 15, 2005 Male patient from FRANCE , 41 years of age, was diagnosed with myocardial infarction and was treated with Elisor (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, blood creatine phosphokinase increased, helicobacter infection, myalgia. Elisor dosage: .

4767623-1 | Arthralgia, Back Pain, Muscle Spasms, Pain In Extremity, Tendonitis
on Sep 01, 2005 Female patient from FRANCE , 77 years of age, was treated with Elisor (View Usage). Patient had the following side effects: arthralgia, back pain (What is back pain?), muscle spasms, pain in extremity, tendonitis. Elisor dosage: . During the same period patient was treated with SOLU MEDROL (View Solu-medrol Review and Solu-medrol Label ), NOVATREX (View Novatrex Review and Novatrex Label ), VIOXX (View Vioxx Review and Vioxx Label ), VOLTAREN (View Voltaren Review and Voltaren Label ). Patient was hospitalized.

4765720-8 | Arteriospasm Coronary, Myocardial Infarction
Patient was taking Elisor (View Usage). After Elisor was administered, patient had the following side effects: arteriospasm coronary, myocardial infarction on Mar 09, 2005 from FRANCE Additional patient health information: Male patient , 68 years of age, was diagnosed with prostate cancer (What is prostate cancer?) and. Elisor dosage: . During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ), FONZYLANE (View Fonzylane Review and Fonzylane Label ), KREDEX (View Kredex Review and Kredex Label ), XATRAL (View Xatral Review and Xatral Label ), ZOLADEX (Implant) (View Zoladex Review and Zoladex Label ), ASPEGIC 325 (View Aspegic 325 Review and Aspegic 325 Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), LIBRAX (View Librax Review and Librax Label ). Patient was hospitalized.

4680932-X | Muscle Disorder, Muscular Weakness, Myalgia
Adverse event was reported on Apr 06, 2005 by a Female patient taking Elisor (View Usage) (Dosage: ) was diagnosed with hypercholesterolaemia and. Location: , 53 years of age, weighting 194.0 lb, Patient experienced the following unwanted or unexpected effects: muscle disorder (What is muscle disorder?), muscular weakness, myalgia. During the same period patient was treated with AMARYL (View Amaryl Review and Amaryl Label ), IMODIUM (View Imodium Review and Imodium Label ), TAREG (View Tareg Review and Tareg Label ), DIFFU K (View Diffu-k Review and Diffu-k Label ), DEBRIDAT (View Debridat Review and Debridat Label ), DICETEL (View Dicetel Review and Dicetel Label ), METEOSPASMYL (View Meteospasmyl Review and Meteospasmyl Label ), EUPANTOL (View Eupantol Review and Eupantol Label ).

4635911-5 | Blood Creatine Phosphokinase Increased, Tendonitis
on Oct 05, 2004 Male patient from , 42 years of age, was diagnosed with myocardial infarction and was treated with Elisor (View Usage). Patient had the following side effects: blood creatine phosphokinase increased, tendonitis. Elisor dosage: . During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ), TENORMIN (View Tenormin Review and Tenormin Label ), KARDEGIC (View Kardegic Review and Kardegic Label ).

4625041-0 | Gamma-glutamyltransferase Increased, Pleural Effusion, Pneumonia
on Mar 22, 2005 Female patient from , 67 years of age, was diagnosed with hypercholesterolaemia and was treated with Elisor (View Usage). After Elisor was administered, patient had the following side effects: gamma-glutamyltransferase increased, pleural effusion, pneumonia (What is pneumonia?). Elisor dosage: . Patient was hospitalized.

4619039-6 | Blood Alkaline Phosphatase Increased, Gamma-glutamyltransferase Increased, Hepatic Enzyme Increased
Patient was taking Elisor (View Usage). Patient experienced the following unwanted or unexpected effects: blood alkaline phosphatase increased, gamma-glutamyltransferase increased, hepatic enzyme increased on Mar 15, 2005 from Additional patient health information: Female patient , 53 years of age, weighting 130.1 lb, was diagnosed with hypercholesterolaemia and. Elisor dosage: . During the same period patient was treated with PREVISCAN (View Previscan Review and Previscan Label ), COVERSYL (View Coversyl Review and Coversyl Label ), PARACETAMOL (View Paracetamol Review and Paracetamol Label ), CELECTOL (View Celectol Review and Celectol Label ), OESTRODOSE (View Oestrodose Review and Oestrodose Label ), LUTENYL (View Lutenyl Review and Lutenyl Label ), FRAXIPARINE (View Fraxiparine Review and Fraxiparine Label ). Patient was hospitalized.

4613476-1 | Arteriospasm Coronary, Myocardial Infarction
Adverse event was reported on Mar 09, 2005 by a Male patient taking Elisor (View Usage) (Dosage: ) was diagnosed with prostate cancer (What is prostate cancer?) and. Location: , 68 years of age, Patient had the following side effects: arteriospasm coronary, myocardial infarction. During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ), FONZYLANE (View Fonzylane Review and Fonzylane Label ), KREDEX (View Kredex Review and Kredex Label ), XATRAL (View Xatral Review and Xatral Label ), ZOLADEX (View Zoladex Review and Zoladex Label ), ASPEGIC 1000 (View Aspegic 1000 Review and Aspegic 1000 Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), LIBRAX (View Librax Review and Librax Label ). Patient was hospitalized.

4612672-7 | Blood Creatine Phosphokinase Increased, Complex Regional Pain Syndrome, Fracture, Joint Dislocation
on May 25, 2004 Male patient from , 49 years of age, weighting 180.8 lb, was diagnosed with hypercholesterolaemia, coronary artery insufficiency and was treated with Elisor (View Usage). After Elisor was administered, patient had the following side effects: blood creatine phosphokinase increased, complex regional pain syndrome (What is complex regional pain syndrome?), fracture (What is fracture?), joint dislocation. Elisor dosage: . During the same period patient was treated with KARDEGIC (View Kardegic Review and Kardegic Label ), SECTRAL (View Sectral Review and Sectral Label ), ISOCARD (View Isocard Review and Isocard 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 Elisor 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 Elisor quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Elisor 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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Elisor Reactions
Abdominal PainWhat is Abdominal pain?
Abdominal Pain Upper
Acute Coronary Syndrome
Alanine Aminotransferase Increased
Arteriospasm Coronary
Arthralgia
Aspartate Aminotransferase Increased
Asthenia
Atrial FibrillationWhat is Atrial fibrillation?
Back PainWhat is Back pain?
Biliary Cyst
Blood Alkaline Phosphatase Increased
Blood Amylase Increased
Blood Creatine Phosphokinase Increased
Blood Lactate Dehydrogenase Increased
Gamma-glutamyltransferase Increased
Inflammation
Interstitial Lung Disease
Intraventricular Haemorrhage
Muscular Weakness
Myalgia
Myocardial Infarction
Pleural Effusion
PneumoniaWhat is Pneumonia?
Porphyria Non-acute
Renal Failure
Rhabdomyolysis
Subdural Haematoma
Tendonitis
Thrombocytopenia
Elisor 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 Elisor 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!