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Arranon FDA adverse reports: 93. View All Arranon FDA Adverse Reports

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Reported deaths: 15

Reported hospitalizations: 34

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< Previous Arranon Side Effects Page  Showing 81-120 of 93 Next Arranon Side Effects Page>

Arranon Side Effects Report: 6044087-1,Aldolase Increased, Blood Creatine Phosphokinase Increased, Rhabdomyolysis
on Jan 08, 2009 Male patient from JAPAN , child 2 years of age, weighting 27.34 lb, was diagnosed with prophylaxis, antifungal prophylaxis, central nervous system neoplasm, neoplasm malignant and was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: aldolase increased, blood creatine phosphokinase increased, rhabdomyolysis. Arranon dosage: 650mgm2 Per Day. During the same period patient was treated with ZYLORIC (99mg Per Day) (View Zyloric Side Effects and Zyloric Label ), COTRIM (.6g Per Day) (View Cotrim Side Effects and Cotrim Label ), HYDROCORTISONE 10MG TAB (20mg Per Day) (View Hydrocortisone 10mg Tab Side Effects and Hydrocortisone 10mg Tab Label ), CYLOCIDE (View Cylocide Side Effects and Cylocide Label ), NEO MINOPHAGEN C (20mg Per Day) (View Neo-minophagen-c Side Effects and Neo-minophagen-c Label ), ZOFRAN (View Zofran Side Effects and Zofran Label ), FLUDARA (View Fludara Side Effects and Fludara Label ).

Arranon Side Effects Report: 5972519-3,Bone Marrow Tumour Cell Infiltration, Thrombocytopenia
Patient was taking Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: bone marrow tumour cell infiltration, thrombocytopenia on Nov 28, 2008 from JAPAN Additional patient health information: Female patient , 23 years of age, weighting 136.7 lb, was diagnosed with neoplasm malignant, prophylaxis of nausea and vomiting, infection prophylaxis and. Arranon dosage: 1500mgm2 Per Day. During the same period patient was treated with CYTARABINE (View Cytarabine Side Effects and Cytarabine Label ), METHOTREXATE (View Methotrexate Side Effects and Methotrexate Label ), PREDNISOLONE (View Prednisolone Side Effects and Prednisolone Label ), NASEA (View Nasea Side Effects and Nasea Label ), ZYLORIC (View Zyloric Side Effects and Zyloric Label ), DIFLUCAN (View Diflucan Side Effects and Diflucan Label ), TAKEPRON (View Takepron Side Effects and Takepron Label ), COTRIM (View Cotrim Side Effects and Cotrim Label ).

Arranon Side Effects Report: 5965744-9,Liver Disorder
Adverse event was reported on Nov 21, 2008 by a Male patient taking Arranon (Arranon Label) (Dosage: 2175mg Per Day) was diagnosed with infection prophylaxis, gastrointestinal ulcer and. Location: JAPAN , 27 years of age, After Arranon was administered, patient had the following side effects: liver disorder. During the same period patient was treated with PREDONINE (View Predonine Side Effects and Predonine Label ), FLUCONAZOLE (10mg Per Day) (View Fluconazole Side Effects and Fluconazole Label ), RABEPRAZOLE SODIUM (10mg Per Day) (View Rabeprazole Sodium Side Effects and Rabeprazole Sodium Label ).

Arranon Side Effects Report: 5961042-8,Ill-defined Disorder, Pain In Extremity, Rash
on Sep 23, 2008 Female patient from UNITED STATES , child 3 years of age, was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: ill-defined disorder, pain in extremity, rash (What is rash?). Arranon dosage: .


Arranon Side Effects Report: 5961041-6,Hypoaesthesia, Neuropathy Peripheral
on Aug 15, 2008 Female patient from UNITED STATES , 42 years of age, was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: hypoaesthesia, neuropathy peripheral. Arranon dosage: 1500mgm2 Variable Dose. During the same period patient was treated with METHOTREXATE (View Methotrexate Side Effects and Methotrexate Label ), CYTARABINE (View Cytarabine Side Effects and Cytarabine Label ), HYDROCORTISONE (View Hydrocortisone Side Effects and Hydrocortisone Label ), LEVOFLOXACIN (View Levofloxacin Side Effects and Levofloxacin Label ).

Arranon Side Effects Report: 5958085-7,Aldolase Increased, Blood Creatine Phosphokinase Increased, Rhabdomyolysis
Patient was taking Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: aldolase increased, blood creatine phosphokinase increased, rhabdomyolysis on Nov 14, 2008 from JAPAN Additional patient health information: Male patient , child 2 years of age, was diagnosed with prophylaxis, antifungal prophylaxis, central nervous system neoplasm and. Arranon dosage: 70ml Per Day. During the same period patient was treated with ZYLORIC (99mg Per Day) (View Zyloric Side Effects and Zyloric Label ), COTRIM (.6g Per Day) (View Cotrim Side Effects and Cotrim Label ), HYDROCORTISONE 10MG TAB (20mg Per Day) (View Hydrocortisone 10mg Tab Side Effects and Hydrocortisone 10mg Tab Label ), CYLOCIDE (25mg Per Day) (View Cylocide Side Effects and Cylocide Label ), NEO MINOPHAGEN C (20mg Per Day) (View Neo-minophagen-c Side Effects and Neo-minophagen-c Label ), FUNGUARD (50mg Per Day) (View Funguard Side Effects and Funguard Label ).

Arranon Side Effects Report: 5948502-0,Rhabdomyolysis
Adverse event was reported on Nov 06, 2008 by a Male patient taking Arranon (Arranon Label) (Dosage: 350mg Per Day) . Location: JAPAN , child 2 years of age, After Arranon was administered, patient had the following side effects: rhabdomyolysis. During the same period patient was treated with ZYLORIC (View Zyloric Side Effects and Zyloric Label ), COTRIM (View Cotrim Side Effects and Cotrim Label ), HYDROCORTISONE 10MG TAB (View Hydrocortisone 10mg Tab Side Effects and Hydrocortisone 10mg Tab Label ), CYLOCIDE (View Cylocide Side Effects and Cylocide Label ), NEO MINOPHAGEN C (View Neo-minophagen-c Side Effects and Neo-minophagen-c Label ), FUNGUARD (View Funguard Side Effects and Funguard Label ).

Arranon Side Effects Report: 5946530-2,Liver Function Test Abnormal
on Oct 31, 2008 Male patient from JAPAN , 27 years of age, was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: liver function test abnormal. Arranon dosage: 2250mg Per Day. During the same period patient was treated with PREDONINE (View Predonine Side Effects and Predonine Label ).

Arranon Side Effects Report: 5913882-9,Memory Impairment
on Oct 03, 2008 Male patient from JAPAN , 68 years of age, weighting 165.3 lb, was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: memory impairment. Arranon dosage: 1500mgm2 Cyclic. During the same period patient was treated with MITOXANTRONE (View Mitoxantrone Side Effects and Mitoxantrone Label ), ETOPOSIDE (View Etoposide Side Effects and Etoposide Label ), CYLOCIDE (View Cylocide Side Effects and Cylocide Label ).

Arranon Side Effects Report: 5913836-2,Adverse Event, Eye Disorder, Eye Haemorrhage, Neutropenia, Ocular Cancer Metastatic, Pyrexia, Vision Blurred
Patient was taking Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: adverse event, eye disorder, eye haemorrhage, neutropenia, ocular cancer metastatic, pyrexia, vision blurred on Oct 06, 2008 from UNITED STATES Additional patient health information: Male patient , 17 years of age, weighting 160.1 lb, . Arranon dosage: . Patient was hospitalized.

Arranon Side Effects Report: 5908693-4,Adverse Event, Eye Disorder, Eye Haemorrhage, Neutropenia, Ocular Cancer Metastatic, Optic Ischaemic Neuropathy, Pyrexia, Vision Blurred
Adverse event was reported on Sep 30, 2008 by a Male patient taking Arranon (Arranon Label) (Dosage: ) was diagnosed with t-cell type acute leukaemia and. Location: UNITED STATES , 17 years of age, weighting 160.1 lb, After Arranon was administered, patient had the following side effects: adverse event, eye disorder, eye haemorrhage, neutropenia, ocular cancer metastatic, optic ischaemic neuropathy, pyrexia, vision blurred. Patient was hospitalized.

Arranon Side Effects Report: 5905825-9,Mobility Decreased, Vertigo
on Sep 29, 2008 Male patient from JAPAN , 38 years of age, was diagnosed with t-cell type acute leukaemia, prophylaxis of nausea and vomiting and was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: mobility decreased, vertigo. Arranon dosage: 2600mg Per Day. During the same period patient was treated with KYTRIL (3mg Twice Per Day) (View Kytril Side Effects and Kytril Label ), SEISHOKU (View Seishoku Side Effects and Seishoku Label ), MEYLON (View Meylon Side Effects and Meylon Label ), GLUCOSE (View Glucose Side Effects and Glucose Label ), LANSOPRAZOLE (30mg Per Day) (View Lansoprazole Side Effects and Lansoprazole Label ), MAGMITT (330mg Three Times Per Day) (View Magmitt Side Effects and Magmitt Label ), ITRIZOLE (100mg Twice Per Day) (View Itrizole Side Effects and Itrizole Label ).

Arranon Side Effects Report: 5905802-8,Mobility Decreased, Pyrexia, Vertigo
on Sep 29, 2008 Male patient from JAPAN , 38 years of age, was diagnosed with prophylaxis of nausea and vomiting and was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: mobility decreased, pyrexia, vertigo. Arranon dosage: 2600mg Per Day. During the same period patient was treated with KYTRIL (6mg Per Day) (View Kytril Side Effects and Kytril Label ), SEISHOKU (View Seishoku Side Effects and Seishoku Label ), MEYLON (View Meylon Side Effects and Meylon Label ), GLUCOSE (View Glucose Side Effects and Glucose Label ), LANSOPRAZOLE (30mg Per Day) (View Lansoprazole Side Effects and Lansoprazole Label ), MAGMITT (990mg Per Day) (View Magmitt Side Effects and Magmitt Label ), ITRIZOLE (200mg Per Day) (View Itrizole Side Effects and Itrizole Label ).

Arranon Side Effects Report: 5903286-7,Adverse Event, Eye Disorder, Eye Haemorrhage, Neutropenia, Ocular Cancer Metastatic, Pyrexia, Vision Blurred
Patient was taking Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: adverse event, eye disorder, eye haemorrhage, neutropenia, ocular cancer metastatic, pyrexia, vision blurred on Sep 30, 2008 from UNITED STATES Additional patient health information: Male patient , 17 years of age, . Arranon dosage: . Patient was hospitalized.

Arranon Side Effects Report: 5901680-1,Adverse Event, Eye Disorder, Eye Haemorrhage, Neutropenia, Pyrexia, Vision Blurred
Adverse event was reported on Sep 26, 2008 by a Male patient taking Arranon (Arranon Label) (Dosage: ) . Location: UNITED STATES , 17 years of age, After Arranon was administered, patient had the following side effects: adverse event, eye disorder, eye haemorrhage, neutropenia, pyrexia, vision blurred. Patient was hospitalized.

Arranon Side Effects Report: 5899957-1,Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Liver Disorder
on Sep 22, 2008 Male patient from JAPAN , 38 years of age, weighting 130.1 lb, was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, liver disorder. Arranon dosage: 2500mg Per Day. During the same period patient was treated with PROGRAF (View Prograf Side Effects and Prograf Label ), ITRIZOLE (View Itrizole Side Effects and Itrizole Label ), CRAVIT (View Cravit Side Effects and Cravit Label ), FAMOTIDINE (View Famotidine Side Effects and Famotidine Label ), MUCOSTA (View Mucosta Side Effects and Mucosta Label ), ENTOMOL (View Entomol Side Effects and Entomol Label ), URSO 250 (View Urso 250 Side Effects and Urso 250 Label ).

Arranon Side Effects Report: 5893309-6,Memory Impairment
on Sep 19, 2008 Male patient from JAPAN , 68 years of age, weighting 165.3 lb, was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: memory impairment. Arranon dosage: 1500mgm2 Cyclic.

Arranon Side Effects Report: 5886311-1,Eye Disorder, Eye Haemorrhage, Neutropenia, Pyrexia, Vision Blurred
Patient was taking Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: eye disorder, eye haemorrhage, neutropenia, pyrexia, vision blurred on Sep 11, 2008 from UNITED STATES Additional patient health information: Male patient , 17 years of age, . Arranon dosage: . Patient was hospitalized.

Arranon Side Effects Report: 5873691-6,Memory Impairment
Adverse event was reported on Sep 03, 2008 by a Male patient taking Arranon (Arranon Label) (Dosage: 1500mgm2 Alternate Days) . Location: JAPAN , 68 years of age, weighting 165.3 lb, After Arranon was administered, patient had the following side effects: memory impairment.

Arranon Side Effects Report: 5867082-1,Memory Impairment
on Aug 29, 2008 Male patient from JAPAN , 68 years of age, weighting 165.3 lb, was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: memory impairment. Arranon dosage: 1500mgm2 Alternate Days.

Arranon Side Effects Report: 5867060-2,Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Liver Disorder
on Aug 26, 2008 Male patient from JAPAN , 38 years of age, was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, liver disorder. Arranon dosage: 2500mg Per Day.

Arranon Side Effects Report: 5867042-0,Supraventricular Tachycardia
Patient was taking Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: supraventricular tachycardia on Aug 29, 2008 from JAPAN Additional patient health information: Male patient , 34 years of age, weighting 172.0 lb, was diagnosed with neoplasm malignant and. Arranon dosage: 1500mgm2 Per Day. During the same period patient was treated with CYTARABINE (View Cytarabine Side Effects and Cytarabine Label ), ETOPOSIDE (View Etoposide Side Effects and Etoposide Label ), ENDOXAN (View Endoxan Side Effects and Endoxan Label ), ADRIACIN (View Adriacin Side Effects and Adriacin Label ), ONCOVIN (View Oncovin Side Effects and Oncovin Label ), PREDONINE (View Predonine Side Effects and Predonine Label ). Patient was hospitalized.

Arranon Side Effects Report: 5858302-8,Alanine Aminotransferase Increased, Blood Bilirubin Increased, Hepatic Function Abnormal
Adverse event was reported on Aug 22, 2008 by a Male patient taking Arranon (Arranon Label) (Dosage: 1500mgm2 Per Day) . Location: JAPAN , 41 years of age, After Arranon was administered, patient had the following side effects: alanine aminotransferase increased, blood bilirubin increased, hepatic function abnormal. Patient was hospitalized.

Arranon Side Effects Report: 5840088-4,Alanine Aminotransferase Increased, Blood Bilirubin Increased
on Aug 08, 2008 Male patient from JAPAN , 41 years of age, was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: alanine aminotransferase increased, blood bilirubin increased. Arranon dosage: 250mg Three Times Per Day. Patient was hospitalized.

Arranon Side Effects Report: 5824443-4,Disorientation, Haematocrit Decreased, Haemoglobin Decreased, Platelet Count Decreased, Productive Cough, Pulmonary Haemorrhage, Red Blood Cell Count Decreased, Respiratory Arrest, Restlessness
on Jul 18, 2008 Male patient from JAPAN , 63 years of age, was diagnosed with pneumonia (What is pneumonia?), disseminated intravascular coagulation and was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: disorientation, haematocrit decreased, haemoglobin decreased, platelet count decreased, productive cough, pulmonary haemorrhage, red blood cell count decreased, respiratory arrest, restlessness. Arranon dosage: 2000mg Per Day. During the same period patient was treated with PENTCILLIN (4g Per Day) (View Pentcillin Side Effects and Pentcillin Label ), ITRIZOLE (200mg Per Day) (View Itrizole Side Effects and Itrizole Label ), MAXIPIME (4g Per Day) (View Maxipime Side Effects and Maxipime Label ), TARGOCID (400mg Per Day) (View Targocid Side Effects and Targocid Label ), FUNGIZONE (5mg Per Day) (View Fungizone Side Effects and Fungizone Label ), LEVOFLOXACIN (400mg Per Day) (View Levofloxacin Side Effects and Levofloxacin Label ), TAZOCIN (5g Per Day) (View Tazocin Side Effects and Tazocin Label ).

Arranon Side Effects Report: 5811727-9,Alanine Aminotransferase Increased, Anaemia, Febrile Neutropenia, Hyperbilirubinaemia, Hypoaesthesia, Muscular Weakness, Platelet Count Decreased, Stomatitis
Patient was taking Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: alanine aminotransferase increased, anaemia, febrile neutropenia, hyperbilirubinaemia, hypoaesthesia, muscular weakness, platelet count decreased, stomatitis on Jul 11, 2008 from JAPAN Additional patient health information: Male patient , 19 years of age, weighting 110.2 lb, was diagnosed with neoplasm malignant and. Arranon dosage: 1500mg Per Day. During the same period patient was treated with MITOXANTRONE HYDROCHLORIDE (807mg Per Day) (View Mitoxantrone Hydrochloride Side Effects and Mitoxantrone Hydrochloride Label ), ETOPOSIDE (110mg Per Day) (View Etoposide Side Effects and Etoposide Label ), CYTARABINE (110mg Per Day) (View Cytarabine Side Effects and Cytarabine Label ), METHOTREXATE (View Methotrexate Side Effects and Methotrexate Label ), CYLOCIDE (View Cylocide Side Effects and Cylocide Label ), ONCOVIN (View Oncovin Side Effects and Oncovin Label ). Patient was hospitalized and became disabled.

Arranon Side Effects Report: 5808826-4,Pulmonary Haemorrhage
Adverse event was reported on Jul 09, 2008 by a Male patient taking Arranon (Arranon Label) (Dosage: 2000mg Per Day) . Location: JAPAN , 63 years of age, After Arranon was administered, patient had the following side effects: pulmonary haemorrhage.

Arranon Side Effects Report: 5808810-0,Alanine Aminotransferase Increased, Blood Bilirubin Increased
on Jul 07, 2008 Male patient from JAPAN , 41 years of age, was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: alanine aminotransferase increased, blood bilirubin increased. Arranon dosage: 250mg Three Times Per Day. Patient was hospitalized.

Arranon Side Effects Report: 5793347-8,Supraventricular Tachycardia
on Jun 26, 2008 Male patient from JAPAN , 34 years of age, weighting 172.0 lb, was diagnosed with neoplasm malignant and was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: supraventricular tachycardia. Arranon dosage: 1500mgm2 Per Day. During the same period patient was treated with CYTARABINE (View Cytarabine Side Effects and Cytarabine Label ), ETOPOSIDE (View Etoposide Side Effects and Etoposide Label ), ENDOXAN (View Endoxan Side Effects and Endoxan Label ). Patient was hospitalized.

Arranon Side Effects Report: 5758590-2,Mobility Decreased, Pyrexia, Vertigo
Patient was taking Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: mobility decreased, pyrexia, vertigo on May 27, 2008 from JAPAN Additional patient health information: Male patient , 38 years of age, was diagnosed with prophylaxis of nausea and vomiting and. Arranon dosage: 2600mg Per Day. During the same period patient was treated with KYTRIL (6mg Per Day) (View Kytril Side Effects and Kytril Label ), SEISHOKU (View Seishoku Side Effects and Seishoku Label ), MEYLON (View Meylon Side Effects and Meylon Label ), GLUCOSE (View Glucose Side Effects and Glucose Label ), LANSOPRAZOLE (30mg Per Day) (View Lansoprazole Side Effects and Lansoprazole Label ), MAGMITT (990mg Per Day) (View Magmitt Side Effects and Magmitt Label ), ITRIZOLE (200mg Per Day) (View Itrizole Side Effects and Itrizole Label ).

Arranon Side Effects Report: 5736432-9,Mobility Decreased, Pyrexia, Vertigo
Adverse event was reported on May 08, 2008 by a Male patient taking Arranon (Arranon Label) (Dosage: 2600mg Per Day) . Location: JAPAN , 38 years of age, After Arranon was administered, patient had the following side effects: mobility decreased, pyrexia, vertigo.

Arranon Side Effects Report: 5723578-4,Pyrexia, Vertigo
on Apr 28, 2008 Male patient from JAPAN , 38 years of age, was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: pyrexia, vertigo. Arranon dosage: .

Arranon Side Effects Report: 5719601-3,Acute Hepatic Failure, Cardio-respiratory Arrest, Disseminated Intravascular Coagulation, Loss Of Consciousness
on Apr 22, 2008 Male patient from JAPAN , 27 years of age, weighting 138.9 lb, was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: acute hepatic failure, cardio-respiratory arrest, disseminated intravascular coagulation, loss of consciousness. Arranon dosage: . During the same period patient was treated with KYTRIL (3mg Per Day) (View Kytril Side Effects and Kytril Label ), FUROSEMIDE (View Furosemide Side Effects and Furosemide Label ), MAXIPIME (4g Per Day) (View Maxipime Side Effects and Maxipime Label ), REMINARON (2000mg Per Day) (View Reminaron Side Effects and Reminaron Label ), CALCICOL (10ml Per Day) (View Calcicol Side Effects and Calcicol Label ), PRIMPERAN INJ (10mg Per Day) (View Primperan Inj Side Effects and Primperan Inj Label ), OXYCONTIN (5mg Per Day) (View Oxycontin Side Effects and Oxycontin Label ), NOVAMIN (10mg Per Day) (View Novamin Side Effects and Novamin Label ). Patient was hospitalized.

Arranon Side Effects Report: 5700941-9,Supraventricular Tachycardia
Patient was taking Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: supraventricular tachycardia on Apr 09, 2008 from JAPAN Additional patient health information: Male patient , 34 years of age, . Arranon dosage: 2250mg Per Day.

Arranon Side Effects Report: 5696090-9,Hepatic Failure
Adverse event was reported on Apr 04, 2008 by a Male patient taking Arranon (Arranon Label) (Dosage: 2625mg Per Day) . Location: JAPAN , 27 years of age, After Arranon was administered, patient had the following side effects: hepatic failure.

Arranon Side Effects Report: 5684344-1,Alanine Aminotransferase Increased, Blood Bilirubin Increased
on Mar 25, 2008 Male patient from JAPAN , 41 years of age, was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: alanine aminotransferase increased, blood bilirubin increased. Arranon dosage: 250mg Three Times Per Day. Patient was hospitalized.

Arranon Side Effects Report: 5672921-3,Peripheral Sensory Neuropathy, Renal Failure Acute, Tumour Lysis Syndrome
on Mar 13, 2008 Male patient from UNITED STATES , 30 years of age, was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: peripheral sensory neuropathy, renal failure acute, tumour lysis syndrome. Arranon dosage: . Patient was hospitalized and became disabled.

Arranon Side Effects Report: 5664498-3,Alanine Aminotransferase Increased, Blood Bilirubin Increased
Patient was taking Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: alanine aminotransferase increased, blood bilirubin increased on Mar 12, 2008 from JAPAN Additional patient health information: Male patient , 41 years of age, . Arranon dosage: 250mg Per Day.

Arranon Side Effects Report: 5655283-7,Alanine Aminotransferase Increased
Adverse event was reported on Mar 06, 2008 by a Male patient taking Arranon (Arranon Label) (Dosage: 250mg Per Day) . Location: JAPAN , 41 years of age, After Arranon was administered, patient had the following side effects: alanine aminotransferase increased.

Arranon Side Effects Report: 5629386-7,Dementia, Dizziness
on Feb 14, 2008 Male patient from JAPAN , 67 years of age, was treated with Arranon (Arranon Label). After Arranon was administered, patient had the following side effects: dementia (What is dementia?), dizziness (What is dizziness?). Arranon dosage: 2500mg Per Day.

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Arranon Side Effects
Arranon and Abasia
Arranon and Adverse Event
Arranon and Alanine Aminotransferase Increased
Arranon and Aldolase Increased
Arranon and Areflexia
Arranon and Aspartate Aminotransferase Increased
Arranon and Asthenia
Arranon and Blood Bilirubin Increased
Arranon and Blood Creatine Phosphokinase Increased
Arranon and Burning Sensation
Arranon and Disorientation
Arranon and Dysarthria
Arranon and Eye Disorder
Arranon and Eye Haemorrhage
Arranon and Facial Paresis
Arranon and Febrile Neutropenia
Arranon and Haematocrit Decreased
Arranon and Haemoglobin Decreased
Arranon and Hypoaesthesia
Arranon and Liver Disorder
Arranon and Memory Impairment
Arranon and Mobility Decreased
Arranon and Neutropenia
Arranon and Platelet Count Decreased
Arranon and Pyrexia
Arranon and Restlessness
Arranon and Rhabdomyolysis
Arranon and Somnolence
Arranon and Vertigo
Arranon and Vision Blurred
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Thank you for visiting Patientsville.com and viewing information about Arranon Side Effects: ARRANON and aldolase increased,ARRANON and blood creatine phosphokinase increased,ARRANON and rhabdomyolysis,ARRANON and bone marrow tumour cell infiltration,ARRANON and thrombocytopenia,ARRANON and liver disorder,ARRANON and ill-defined disorder,ARRANON and pain in extremity,ARRANON and rash,ARRANON and hypoaesthesia,ARRANON and neuropathy peripheral,ARRANON and liver function test abnormal,ARRANON and memory impairment,ARRANON and adverse event,ARRANON and eye disorder,ARRANON and eye haemorrhage,ARRANON and neutropenia,ARRANON and ocular cancer metastatic,ARRANON and pyrexia,ARRANON and vision blurred,ARRANON and optic ischaemic neuropathy,ARRANON and mobility decreased,ARRANON and vertigo,ARRANON and alanine aminotransferase increased,ARRANON and aspartate aminotransferase increased,ARRANON and supraventricular tachycardia,ARRANON and blood bilirubin increased,ARRANON and hepatic function abnormal,ARRANON and disorientation,ARRANON and haematocrit decreased,ARRANON and haemoglobin decreased,ARRANON and platelet count decreased,ARRANON and productive cough,ARRANON and pulmonary haemorrhage,ARRANON and red blood cell count decreased,ARRANON and respiratory arrest,ARRANON and restlessness,ARRANON and anaemia,ARRANON and febrile neutropenia,ARRANON and hyperbilirubinaemia,ARRANON and muscular weakness,ARRANON and stomatitis,ARRANON and acute hepatic failure,ARRANON and cardio-respiratory arrest,ARRANON and disseminated intravascular coagulation,ARRANON and loss of consciousness,ARRANON and peripheral sensory neuropathy,ARRANON and renal failure acute,ARRANON and tumour lysis syndrome,ARRANON and dementia,ARRANON and dizziness