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Leukeran adverse events reported to FDA.

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Summary

FDA Adverse Reports: 63. View All

Leukeran FDA safety alerts: No

Reported deaths: 8

Reported hospitalizations: 25

Leukeran Dosage, Warnings, Usage.

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

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Showing 1-50 of 63  Next Page  >

6970844-0 |
on Sep 01, 2010 Female patient from UNITED STATES , 64 years of age, was treated with Leukeran (View Usage). . Leukeran dosage: .

6749678-8 | Cold Sweat, Insomnia, Pneumonia
Patient was taking Leukeran (View Usage). Patient had the following side effects: cold sweat, insomnia, pneumonia (What is pneumonia?) on May 24, 2010 from AUSTRALIA Additional patient health information: Female patient , 83 years of age, . Leukeran dosage: . During the same period patient was treated with MICARDIS (View Micardis Review and Micardis Label ), MONODUR (View Monodur Review and Monodur Label ), LIPITOR (View Lipitor Review and Lipitor Label ), ACIMAX (View Acimax Review and Acimax Label ).

6735918-8 | Pruritus, Rash
Adverse event was reported on Nov 20, 2009 by a Male patient taking Leukeran (View Usage) (Dosage: ) . Location: RUSSIAN FEDERATION , 60 years of age, After Leukeran was administered, patient had the following side effects: pruritus, rash (What is rash?). During the same period patient was treated with AMLODIPINE (View Amlodipine Review and Amlodipine Label ), LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (View Losartan Potassium And Hydrochlorothiazide Review and Losartan Potassium And Hydrochlorothiazide Label ).

6713659-0 | Progressive Multifocal Leukoencephalopathy
on Apr 29, 2010 Female patient from NETHERLANDS , weighting 110.2 lb, was diagnosed with non-hodgkin's lymphoma and was treated with Leukeran (View Usage). Patient experienced the following unwanted or unexpected effects: progressive multifocal leukoencephalopathy. Leukeran dosage: . During the same period patient was treated with PREDNISOLON (View Prednisolon Review and Prednisolon Label ), MABTHERA (View Mabthera Review and Mabthera Label ), FLUDARA (View Fludara Review and Fludara Label ), ENDOXAN (View Endoxan Review and Endoxan Label ), VINCRISTINE (View Vincristine Review and Vincristine Label ), DEXAMETHASONE TAB (20mg Five Times Per Day) (View Dexamethasone Tab Review and Dexamethasone Tab Label ).


6683370-3 | Adverse Event, Night Sweats
on Oct 06, 2009 Male patient from UNITED STATES , 92 years of age, was diagnosed with b-cell lymphoma and was treated with Leukeran (View Usage). Patient had the following side effects: adverse event, night sweats. Leukeran dosage: 3tab Twice Per Day. During the same period patient was treated with PREDNISONE (View Prednisone Review and Prednisone Label ), TYLENOL 500 (View Tylenol-500 Review and Tylenol-500 Label ).

6683364-8 | Diarrhoea
Patient was taking Leukeran (View Usage). After Leukeran was administered, patient had the following side effects: diarrhoea on Apr 02, 2009 from UNITED STATES Additional patient health information: Female patient , 87 years of age, . Leukeran dosage: 2mg Every 3 Days.

6661197-6 | Pleurisy
Adverse event was reported on Mar 25, 2010 by a Female patient taking Leukeran (View Usage) (Dosage: 2mg Per Day) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: SPAIN , 67 years of age, weighting 145.5 lb, Patient experienced the following unwanted or unexpected effects: pleurisy. During the same period patient was treated with REMICADE (3mgk Per Day) (View Remicade Review and Remicade Label ). Patient was hospitalized.

6649147-X | Brain Oedema, Dizziness, Eye Swelling, Infection, Local Swelling, Meningitis Cryptococcal, Nasopharyngitis, Nausea
on Mar 19, 2010 Male patient from UNITED STATES , 57 years of age, weighting 199.5 lb, was diagnosed with migraine (What is migraine?) and was treated with Leukeran (View Usage). Patient had the following side effects: brain oedema, dizziness (What is dizziness?), eye swelling, infection (What is infection?), local swelling, meningitis cryptococcal, nasopharyngitis, nausea (What is nausea?). Leukeran dosage: . During the same period patient was treated with TREXIMET (1tab As Required) (View Treximet Review and Treximet Label ), VICODIN (View Vicodin Review and Vicodin Label ). Patient was hospitalized.

6498208-7 | Dyspnoea
on Dec 10, 2009 Male patient from UNITED STATES , 73 years of age, was treated with Leukeran (View Usage). After Leukeran was administered, patient had the following side effects: dyspnoea. Leukeran dosage: 2mg Per Day. During the same period patient was treated with FLOMAX (View Flomax Review and Flomax Label ), FINASTERIDE (View Finasteride Review and Finasteride Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), AZT (View Azt Review and Azt Label ). Patient was hospitalized.

6484212-1 | Brain Oedema, Dizziness, Eye Swelling, Infection, Local Swelling, Meningitis, Nasopharyngitis, Nausea
Patient was taking Leukeran (View Usage). Patient experienced the following unwanted or unexpected effects: brain oedema, dizziness (What is dizziness?), eye swelling, infection (What is infection?), local swelling, meningitis (What is meningitis?), nasopharyngitis, nausea (What is nausea?) on Dec 02, 2009 from UNITED STATES Additional patient health information: Male patient , 57 years of age, was diagnosed with migraine (What is migraine?) and. Leukeran dosage: . During the same period patient was treated with TREXIMET (1tab As Required) (View Treximet Review and Treximet Label ), VICODIN (View Vicodin Review and Vicodin Label ). Patient was hospitalized.

6444783-8 | Pruritus, Rash
Adverse event was reported on Nov 12, 2009 by a Male patient taking Leukeran (View Usage) (Dosage: ) . Location: RUSSIAN FEDERATION , 60 years of age, Patient had the following side effects: pruritus, rash (What is rash?). During the same period patient was treated with AMLODIPINE (View Amlodipine Review and Amlodipine Label ), LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (View Losartan Potassium And Hydrochlorothiazide Review and Losartan Potassium And Hydrochlorothiazide Label ).

6439614-6 | Chronic Obstructive Pulmonary Disease, Pulmonary Fibrosis
on Nov 09, 2009 Male patient from GERMANY , 74 years of age, weighting 132.3 lb, was treated with Leukeran (View Usage). After Leukeran was administered, patient had the following side effects: chronic obstructive pulmonary disease, pulmonary fibrosis (What is pulmonary fibrosis?). Leukeran dosage: 50mg Every Two Weeks. During the same period patient was treated with MABCAMPATH (View Mabcampath Review and Mabcampath Label ). Patient was hospitalized.

6405682-0 | Gamma-glutamyltransferase Increased, Hepatic Necrosis, Hepatotoxicity, Prothrombin Time Prolonged, Yellow Skin
on Oct 16, 2009 Male patient from GERMANY , 62 years of age, was diagnosed with chronic lymphocytic leukaemia and was treated with Leukeran (View Usage). Patient experienced the following unwanted or unexpected effects: gamma-glutamyltransferase increased, hepatic necrosis, hepatotoxicity, prothrombin time prolonged, yellow skin. Leukeran dosage: . During the same period patient was treated with URBASON (40mg Per Day) (View Urbason Review and Urbason Label ).

6398498-5 | Gamma-glutamyltransferase Increased, Hepatic Necrosis, Hepatotoxicity, Prothrombin Time Prolonged, Yellow Skin
Patient was taking Leukeran (View Usage). Patient had the following side effects: gamma-glutamyltransferase increased, hepatic necrosis, hepatotoxicity, prothrombin time prolonged, yellow skin on Oct 12, 2009 from GERMANY Additional patient health information: Male patient , 62 years of age, . Leukeran dosage: . During the same period patient was treated with URBASON (40mg Per Day) (View Urbason Review and Urbason Label ).

6283112-X | Condition Aggravated, Nodule, Product Quality Issue
Adverse event was reported on Jul 16, 2009 by a Male patient taking Leukeran (View Usage) (Dosage: ) . Location: BRAZIL , weighting 165.3 lb, After Leukeran was administered, patient had the following side effects: condition aggravated, nodule, product quality issue. Patient was hospitalized.

6164852-X | White Blood Cell Count Increased
on Feb 10, 2009 Female patient from UNITED STATES , 74 years of age, was treated with Leukeran (View Usage). Patient experienced the following unwanted or unexpected effects: white blood cell count increased. Leukeran dosage: 1tab Per Day. During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), MOBIC (View Mobic Review and Mobic Label ), FLECAINIDE ACETATE (View Flecainide Acetate Review and Flecainide Acetate Label ), PREVACID (View Prevacid Review and Prevacid Label ).

6160260-6 | Hearing Impaired, Hypoacusis, Tinnitus, White Blood Cell Count Decreased
on Apr 13, 2009 Male patient from CHINA , 51 years of age, was diagnosed with chronic lymphocytic leukaemia and was treated with Leukeran (View Usage). Patient had the following side effects: hearing impaired, hypoacusis, tinnitus (What is tinnitus?), white blood cell count decreased. Leukeran dosage: 2mg Three Times Per Day.

6037287-8 | Erythema Multiforme, Skin Lesion
Patient was taking Leukeran (View Usage). After Leukeran was administered, patient had the following side effects: erythema multiforme, skin lesion on Jan 09, 2009 from NETHERLANDS Additional patient health information: Male patient , 77 years of age, . Leukeran dosage: 4mg Per Day. During the same period patient was treated with LOSEC MUPS (View Losec Mups Review and Losec Mups Label ).

5990635-7 | Hypoaesthesia, Vertigo
Adverse event was reported on Dec 09, 2008 by a Female patient taking Leukeran (View Usage) (Dosage: 5.2mg Per Day) was diagnosed with arthritis (What is arthritis?) and. Location: GERMANY , 65 years of age, weighting 119.0 lb, Patient experienced the following unwanted or unexpected effects: hypoaesthesia, vertigo. During the same period patient was treated with DICLO (View Diclo Review and Diclo Label ). Patient was hospitalized.

5920492-6 | Abdominal Distension, Anorexia, Depression, Splenomegaly, Vomiting
on Oct 14, 2008 Female patient from BRAZIL , 56 years of age, weighting 132.3 lb, was treated with Leukeran (View Usage). Patient had the following side effects: abdominal distension, anorexia, depression (What is depression?), splenomegaly, vomiting. Leukeran dosage: 2tab Cyclic. During the same period patient was treated with RIVOTRIL (View Rivotril Review and Rivotril Label ), AMITRIPTYLINE HCL (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ), DOMPERIDONE (View Domperidone Review and Domperidone Label ), PLASIL (View Plasil Review and Plasil Label ).

5912273-4 | Anaemia Haemolytic Autoimmune
on Sep 29, 2008 Male patient from GERMANY , weighting 172.0 lb, was treated with Leukeran (View Usage). After Leukeran was administered, patient had the following side effects: anaemia haemolytic autoimmune. Leukeran dosage: 8mg Per Day. During the same period patient was treated with PANTOZOL (40mg Per Day) (View Pantozol Review and Pantozol Label ), PREDNI H TABLINEN (20mg Per Day) (View Predni-h-tablinen Review and Predni-h-tablinen Label ), TAMSULOSIN HCL (400mcg Per Day) (View Tamsulosin Hcl Review and Tamsulosin Hcl Label ), PREDNISOLON (View Prednisolon Review and Prednisolon Label ). Patient was hospitalized.

5892959-0 | Dyspnoea
Patient was taking Leukeran (View Usage). Patient experienced the following unwanted or unexpected effects: dyspnoea on Sep 22, 2008 from UNITED STATES Additional patient health information: Male patient , 66 years of age, weighting 196.0 lb, was diagnosed with renal disorder and. Leukeran dosage: . Patient was hospitalized.

5796520-8 | Dyspnoea
Adverse event was reported on Jun 27, 2008 by a Male patient taking Leukeran (View Usage) (Dosage: ) . Location: NETHERLANDS , 58 years of age, Patient had the following side effects: dyspnoea. During the same period patient was treated with PLAVIX (75mg Per Day) (View Plavix Review and Plavix Label ), PANTOPRAZOLE SODIUM (40mg Per Day) (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ), ASCAL (100mg Per Day) (View Ascal Review and Ascal Label ), CRESTOR (5mg Per Day) (View Crestor Review and Crestor Label ), METOPROLOL SUCCINATE (50mg Per Day) (View Metoprolol Succinate Review and Metoprolol Succinate Label ), PROMOCARD (90mg Per Day) (View Promocard Review and Promocard Label ). Patient was hospitalized.

5718004-5 | Anorexia, Asthenia, Condition Aggravated, Confusional State, Contraindication To Medical Treatment, Cough, Dysphagia, Liver Disorder, Respiratory Distress
on Apr 22, 2008 Female patient from EGYPT , 75 years of age, was diagnosed with non-hodgkin's lymphoma and was treated with Leukeran (View Usage). After Leukeran was administered, patient had the following side effects: anorexia, asthenia, condition aggravated, confusional state, contraindication to medical treatment, cough, dysphagia, liver disorder, respiratory distress. Leukeran dosage: 2mg Twice Per Day. During the same period patient was treated with LIVER SUPPORTING AGENT (View Liver Supporting Agent Review and Liver Supporting Agent Label ), FAT FREE (View Fat Free Review and Fat Free Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ).

5714440-1 | Accidental Exposure
on Oct 24, 2007 Male patient from UNITED STATES , 47 years of age, was treated with Leukeran (View Usage). Patient experienced the following unwanted or unexpected effects: accidental exposure. Leukeran dosage: 2mg Single Dose.

5714438-3 | Rash
Patient was taking Leukeran (View Usage). Patient had the following side effects: rash (What is rash?) on Apr 26, 2007 from UNITED STATES Additional patient health information: Male patient , 80 years of age, . Leukeran dosage: 2mg Three Times Per Day. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), VITAMINS (View Vitamins Review and Vitamins Label ).

5705745-9 | Anorexia, Asthenia, Condition Aggravated, Confusional State, Contraindication To Medical Treatment, Cough, Dysphagia, Liver Disorder, Respiratory Distress
Adverse event was reported on Apr 10, 2008 by a Female patient taking Leukeran (View Usage) (Dosage: 2mg Twice Per Day) was diagnosed with non-hodgkin's lymphoma and. Location: EGYPT , 75 years of age, After Leukeran was administered, patient had the following side effects: anorexia, asthenia, condition aggravated, confusional state, contraindication to medical treatment, cough, dysphagia, liver disorder, respiratory distress. During the same period patient was treated with LIVER SUPPORTING AGENT (View Liver Supporting Agent Review and Liver Supporting Agent Label ), FAT FREE (View Fat Free Review and Fat Free Label ), CORTICOSTEROID (View Corticosteroid Review and Corticosteroid Label ).

5655286-2 | Hypertension, Paraesthesia
on Mar 05, 2008 Female patient from RUSSIAN FEDERATION , 70 years of age, was treated with Leukeran (View Usage). Patient experienced the following unwanted or unexpected effects: hypertension, paraesthesia. Leukeran dosage: 10mg Twice Per Day.

5525583-X | Hypomagnesaemia
on Nov 16, 2007 Male patient from NETHERLANDS , 80 years of age, was diagnosed with diabetes mellitus and was treated with Leukeran (View Usage). Patient had the following side effects: hypomagnesaemia. Leukeran dosage: 4mg Per Day. During the same period patient was treated with ACTOS (30mg Per Day) (View Actos Review and Actos Label ), GLICLAZIDE (80mg Twice Per Day) (View Gliclazide Review and Gliclazide Label ), SIMVASTATIN (40mg Per Day) (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

5446343-4 | Pyoderma Gangrenosum, Skin Lesion, Urticaria
Patient was taking Leukeran (View Usage). After Leukeran was administered, patient had the following side effects: pyoderma gangrenosum, skin lesion, urticaria on Aug 30, 2007 from UNITED STATES Additional patient health information: Female patient , 62 years of age, was diagnosed with lymphoma (What is lymphoma?) and. Leukeran dosage: 12mg Cyclic. During the same period patient was treated with BENAZEPRIL HYDROCHLORIDE (View Benazepril Hydrochloride Review and Benazepril Hydrochloride Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), COUMADIN (View Coumadin Review and Coumadin Label ), LOVASTATIN (View Lovastatin Review and Lovastatin Label ), ZYRTEC (View Zyrtec Review and Zyrtec Label ), HYDROXYZINE (View Hydroxyzine Review and Hydroxyzine Label ), BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ).

5386587-3 | Hypersensitivity, Renal Disorder
Adverse event was reported on Jul 10, 2007 by a Male patient taking Leukeran (View Usage) (Dosage: ) . Location: SWEDEN , 26 years of age, Patient experienced the following unwanted or unexpected effects: hypersensitivity, renal disorder.

5381967-4 | Night Sweats
on Jul 03, 2007 Male patient from UNITED STATES , 65 years of age, was treated with Leukeran (View Usage). Patient had the following side effects: night sweats. Leukeran dosage: 4mg Per Day. During the same period patient was treated with INSULIN (View Insulin Review and Insulin Label ), SYNTHROID (View Synthroid Review and Synthroid Label ).

5358939-9 | Agranulocytosis
on Jun 08, 2007 Female patient from SPAIN , 76 years of age, was diagnosed with glomerulonephritis proliferative, nephrotic syndrome and was treated with Leukeran (View Usage). After Leukeran was administered, patient had the following side effects: agranulocytosis. Leukeran dosage: 8mg Per Day. Patient was hospitalized.

5273642-1 | Initial Insomnia, Restlessness
Patient was taking Leukeran (View Usage). Patient experienced the following unwanted or unexpected effects: initial insomnia, restlessness on Nov 02, 2006 from UNITED STATES Additional patient health information: Male patient , 75 years of age, . Leukeran dosage: 8mg Per Day. During the same period patient was treated with GLYBURIDE (View Glyburide Review and Glyburide Label ), HYZAAR (View Hyzaar Review and Hyzaar Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), VITAMINS (View Vitamins Review and Vitamins Label ).

5273640-8 | Paraesthesia, Pollakiuria
Adverse event was reported on Aug 03, 2006 by a Male patient taking Leukeran (View Usage) (Dosage: 2mg Per Day) . Location: UNITED STATES , 73 years of age, Patient had the following side effects: paraesthesia, pollakiuria.

5273638-X | Rash
on Aug 11, 2006 Male patient from UNITED STATES , 54 years of age, was treated with Leukeran (View Usage). After Leukeran was administered, patient had the following side effects: rash (What is rash?). Leukeran dosage: 2mg Three Times Per Day. During the same period patient was treated with EFFEXOR (View Effexor Review and Effexor Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), PROVIGIL (View Provigil Review and Provigil Label ), NEURONTIN (View Neurontin Review and Neurontin Label ).

5273637-8 | Folliculitis, Inflammation, Pruritus, Rash Papular, Staphylococcal Infection, Urticaria
on Jul 25, 2006 Female patient from UNITED STATES , 63 years of age, was treated with Leukeran (View Usage). Patient experienced the following unwanted or unexpected effects: folliculitis, inflammation, pruritus, rash papular, staphylococcal infection (What is staphylococcal infection?), urticaria. Leukeran dosage: 10mg Per Day.

5273636-6 | Alopecia
Patient was taking Leukeran (View Usage). Patient had the following side effects: alopecia on Jun 21, 2006 from UNITED STATES Additional patient health information: Female patient , 71 years of age, weighting 100.3 lb, was diagnosed with non-hodgkin's lymphoma and. Leukeran dosage: 20mg Cyclic. During the same period patient was treated with LIPITOR (20mg Per Day) (View Lipitor Review and Lipitor Label ), FOSAMAX (70mg Weekly) (View Fosamax Review and Fosamax Label ), PREDNISONE (5mg Cyclic) (View Prednisone Review and Prednisone Label ), MULTIPLE VITAMIN (View Multiple Vitamin Review and Multiple Vitamin Label ), ROGAINE (View Rogaine Review and Rogaine Label ).

5252114-4 | Autoimmune Neutropenia
Adverse event was reported on Feb 06, 2007 by a Male patient taking Leukeran (View Usage) (Dosage: 10 Mg/m2) . Location: UNITED KINGDOM , 63 years of age, After Leukeran was administered, patient had the following side effects: autoimmune neutropenia.

5242280-9 | Rash
on Feb 16, 2007 Female patient from UNITED STATES , 54 years of age, weighting 190.0 lb, was diagnosed with haemolytic anaemia, non-hodgkin's lymphoma and was treated with Leukeran (View Usage). Patient experienced the following unwanted or unexpected effects: rash (What is rash?). Leukeran dosage: 20 Tablets Once Po.

5188300-1 | Neuropathy, Walking Disability
on Dec 05, 2006 Male patient from GERMANY , 54 years of age, weighting 235.9 lb, was diagnosed with nephrotic syndrome and was treated with Leukeran (View Usage). Patient had the following side effects: neuropathy, walking disability. Leukeran dosage: 2g Per Day. During the same period patient was treated with CORTISONE ACETATE (View Cortisone Acetate Review and Cortisone Acetate Label ).

5121339-0 | Grand Mal Convulsion
Patient was taking Leukeran (View Usage). After Leukeran was administered, patient had the following side effects: grand mal convulsion on Sep 19, 2006 from HONG KONG Additional patient health information: Male patient , 70 years of age, was diagnosed with non-hodgkin's lymphoma and. Leukeran dosage: 24 Mg / Per Day / Oral.

5093002-6 | Thrombocytopenia, Vessel Puncture Site Haemorrhage
Adverse event was reported on Jul 26, 2006 by a Male patient taking Leukeran (View Usage) (Dosage: ) . Location: GERMANY , 66 years of age, weighting 198.4 lb, Patient experienced the following unwanted or unexpected effects: thrombocytopenia, vessel puncture site haemorrhage. During the same period patient was treated with GINGIUM (1tab In The Morning) (View Gingium Review and Gingium Label ), VALORON (54mg Twice Per Day) (View Valoron Review and Valoron Label ), CEFUROXIME (500mg Twice Per Day) (View Cefuroxime Review and Cefuroxime Label ), NOVALGIN (200mg Four Times Per Day) (View Novalgin Review and Novalgin Label ). Patient was hospitalized.

4976769-4 | Aplastic Anaemia, Arthralgia, Headache, Malaise, Neutropenic Sepsis, Night Sweats, Purpura, Rash
on Feb 08, 2006 Male patient from UNITED KINGDOM , 70 years of age, was diagnosed with deep vein thrombosis (What is deep vein thrombosis?) and was treated with Leukeran (View Usage). Patient had the following side effects: aplastic anaemia, arthralgia, headache (What is headache?), malaise, neutropenic sepsis, night sweats, purpura, rash (What is rash?). Leukeran dosage: . During the same period patient was treated with ZYLORIC (300mg Per Day) (View Zyloric Review and Zyloric Label ), WARFARIN SODIUM (4mg Per Day) (View Warfarin Sodium Review and Warfarin Sodium Label ), AMLODIPINE (5mg Per Day) (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized and became disabled.

4898785-3 | Erythema, Pruritus
on Dec 08, 2005 Male patient from GERMANY , 73 years of age, weighting 154.3 lb, was diagnosed with chronic lymphocytic leukaemia, blood testosterone decreased and was treated with Leukeran (View Usage). After Leukeran was administered, patient had the following side effects: erythema, pruritus. Leukeran dosage: Daily Dose: 2 Milligram(s). During the same period patient was treated with ANDROTOP GEL 50 MG (View Androtop Gel 50 Mg Review and Androtop Gel 50 Mg Label ).

4881536-6 | Cough, Interstitial Lung Disease, Pneumonitis, Pneumothorax, Pyrexia
Patient was taking Leukeran (View Usage). Patient experienced the following unwanted or unexpected effects: cough, interstitial lung disease, pneumonitis, pneumothorax, pyrexia on Jan 02, 2006 from SWEDEN Additional patient health information: Male patient , 83 years of age, was diagnosed with lymphocytic leukaemia and. Leukeran dosage: 2mg Per Day. During the same period patient was treated with SELOKEN (View Seloken Review and Seloken Label ), ALVEDON (View Alvedon Review and Alvedon Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), AMILORID (View Amilorid Review and Amilorid Label ), IMOVANE (View Imovane Review and Imovane Label ), METFORMIN (View Metformin Review and Metformin Label ), KAVEPENIN (View Kavepenin Review and Kavepenin Label ). Patient was hospitalized.

4879782-0 | Cough, Dyspnoea, Interstitial Lung Disease, Lower Respiratory Tract Inflammation, Mediastinal Disorder, Pneumonitis, Pneumothorax, Pulmonary Fibrosis, Pyrexia
Adverse event was reported on Jan 02, 2006 by a Male patient taking Leukeran (View Usage) (Dosage: 2mg Per Day) . Location: SWEDEN , 83 years of age, Patient had the following side effects: cough, dyspnoea, interstitial lung disease, lower respiratory tract inflammation, mediastinal disorder, pneumonitis, pneumothorax, pulmonary fibrosis (What is pulmonary fibrosis?), pyrexia. During the same period patient was treated with SELOKEN (View Seloken Review and Seloken Label ), ALVEDON (View Alvedon Review and Alvedon Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), AMILORID (View Amilorid Review and Amilorid Label ), IMOVANE (View Imovane Review and Imovane Label ), METFORMIN (View Metformin Review and Metformin Label ), KAVEPENIN (View Kavepenin Review and Kavepenin Label ). Patient was hospitalized.

4878847-7 | Cough, Dyspnoea, Interstitial Lung Disease, Lower Respiratory Tract Inflammation, Mediastinal Disorder, Pneumonitis, Pneumothorax, Pulmonary Fibrosis, Pyrexia
on Jan 02, 2006 Male patient from SWEDEN , 83 years of age, was diagnosed with lymphocytic leukaemia and was treated with Leukeran (View Usage). After Leukeran was administered, patient had the following side effects: cough, dyspnoea, interstitial lung disease, lower respiratory tract inflammation, mediastinal disorder, pneumonitis, pneumothorax, pulmonary fibrosis (What is pulmonary fibrosis?), pyrexia. Leukeran dosage: 2mg Per Day. During the same period patient was treated with SELOKEN (View Seloken Review and Seloken Label ), ALVEDON (View Alvedon Review and Alvedon Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), AMILORID (View Amilorid Review and Amilorid Label ), IMOVANE (View Imovane Review and Imovane Label ), METFORMIN (View Metformin Review and Metformin Label ), KAVEPENIN (View Kavepenin Review and Kavepenin Label ). Patient was hospitalized.

4869721-0 | Cough, Dyspnoea, Karyotype Analysis Abnormal, Myelodysplastic Syndrome
on Dec 12, 2005 Male patient from KOREA, REPUBLIC OF , 65 years of age, was diagnosed with waldenstrom's macroglobulinaemia and was treated with Leukeran (View Usage). Patient experienced the following unwanted or unexpected effects: cough, dyspnoea, karyotype analysis abnormal, myelodysplastic syndrome. Leukeran dosage: Cyclic / Oral. During the same period patient was treated with FLUDARABINE PHOSPHATE (Cyclic) (View Fludarabine Phosphate Review and Fludarabine Phosphate Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ).

4864163-6 | Anaemia, Aplasia Pure Red Cell
Patient was taking Leukeran (View Usage). Patient had the following side effects: anaemia, aplasia pure red cell on Dec 21, 2005 from FINLAND Additional patient health information: Male patient , 73 years of age, was diagnosed with chronic lymphocytic leukaemia and. Leukeran dosage: 4mg Per Day. During the same period patient was treated with SPIRIVA (View Spiriva Review and Spiriva Label ), SERETIDE (View Seretide Review and Seretide Label ), BUVENTOL (View Buventol Review and Buventol 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 Leukeran 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 Leukeran quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Leukeran 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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During the same period patient was treated with LEUKERAN (View Leukeran Review and Leukeran Label ). 6159103-6 | Ocular Hypertension Patient was taking Omnic . Patient ...

Report a Drug Side Effect. ... This anonymous Drug Side Effect Survey has 13 questions and takes less than 2 minutes to complete.

leukeran Episodes: 2: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: levitra Episodes: 5: Diagnosed with major depression.Side ...

During the same period patient was treated with LEUKERAN (View Leukeran Review and Leukeran Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), ...

During the same period patient was treated with LEUKERAN, PREDNISOLONE, LOVASTATIN, ACTIFFERIN. Patient died on 02/03/2008. Candesartan Side Effects Report: 5657354-8 ...

During the same period patient was treated with FLUDARA (View Fludara Review and Fludara Label ), LEUKERAN (View Leukeran Review and Leukeran Label ), CYTOXAN (View Cytoxan ...

Leukeran Side Effects During the same period patient was treated with ANDROTOP GEL 50 MG (View Androtop Gel 50 Mg Review and Androtop Gel 50 Mg Label ). 4881536-6 | Cough, ...

leukeran Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: levetiracetam Episodes: 3: Diagnosed with major depression ...

leukeran Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: leuprorelin Episodes: 1: Diagnosed with major depression ...

Leukeran Side Effects... (30mg Per Day) (View Actos Review and Actos Label ), GLICLAZIDE ... (View Benazepril Hydrochloride Review and ... Complete Guide to Benazepril ...

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Leukeran Reactions
Anaemia
Anorexia
Asthenia
Bone Marrow Depression
Brain Oedema
Condition Aggravated
Confusional State
Contraindication To Medical Treatment
Cough
DizzinessWhat is Dizziness?
Dysphagia
Dyspnoea
Eye Swelling
Gamma-glutamyltransferase Increased
Hepatic Necrosis
Hepatotoxicity
InfectionWhat is Infection?
Interstitial Lung Disease
Liver Disorder
Local Swelling
NauseaWhat is Nausea?
Night Sweats
PneumoniaWhat is Pneumonia?
Pneumonitis
Pneumothorax
Pruritus
Pulmonary FibrosisWhat is Pulmonary fibrosis?
Pyrexia
RashWhat is Rash?
Vomiting
Leukeran 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 Leukeran 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!