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Alkeran (Melphalan) - Reports of Side Effects & Adverse Reactions

 


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This is an index of adverse event reports related to Alkeran (Melphalan). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the adverse reaction. Or scroll down to view a sample of recent reports further on this page.

Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.

All cases (97)
     Pyrexia (15)Stomatitis (10)Anaemia (8)more >>

Cases resulting in a serious event (97)
     Pyrexia (15)Stomatitis (10)Anaemia (8)more >>

Cases resulting in death (14)
     Cardiac Failure (4)Blood Bilirubin Increased (2)Confusional State (2)more >>

Cases resulting in life threatening events (23)
     Pyrexia (6)Myelocytosis (5)Acute Leukaemia (4)more >>

Cases resulting in hospitalization (49)
     Pyrexia (11)Bone Marrow Failure (8)Pancytopenia (7)more >>

Cases resulting in disability (7)
     Stomatitis (4)Mechanical Ventilation (2)Pyrexia (2)more >>

Cases resulting in other serious reactions (30)
     Thrombocytopenia (4)White Blood Cell Count Decreased (3)Haemoglobin Decreased (3)more >>

Below is a sample of adverse event reports reports related to Alkeran (Melphalan). For a complete list and/or a specific selection of reports, please use the links in the index above.

Adverse event in receiving Alkeran (Melphalan)

Reported by a individual with unspecified qualification from France on 2007-10-31

Patient:

Adverse reactions / side effects: Drug Toxicity, Cardiac Failure

Adverse event resulted in: death

Suspect drug(s):
Alkeran
    Dosage: oral
    Administration route: Oral
    Indication: Multiple Myeloma

Cyclophosphamide
    Indication: Stem Cell Transplant

Dexamethasone
    Dosage: oral
    Administration route: Oral
    Indication: Multiple Myeloma

Disodium Clodronate (Formulation Unknown) (Disodium Clodronate)
    Dosage: oral
    Administration route: Oral

Doxorubicin Hydrochloride
    Dosage: intravenous infus
    Indication: Multiple Myeloma

Granulocyte Col.stim.fact (Formulation Unknown) (Granulocyte Col.stim.

Mesna
    Indication: Stem Cell Transplant

Stem Cell Transplant (Formulation Unknown) (Stem Cell Transplant)
    Indication: Multiple Myeloma

Vincristine
    Dosage: intravenous infus
    Indication: Multiple Myeloma



Adverse event in receiving Alkeran (Melphalan)

Reported by a health professional (non-physician/pharmacist) from France on 2007-10-31

Patient:

Adverse reactions / side effects: Cerebrovascular Accident

Suspect drug(s):
Alkeran
    Dosage: oral
    Administration route: Oral
    Indication: Multiple Myeloma

Thalidomide
    Indication: Multiple Myeloma

Other drugs received by patient: Prednisone; Disodium Clodronate



Adverse event in 57 year old male receiving Alkeran (Melphalan)

Reported by a consumer/non-health professional from France on 2007-10-31

Patient: 57 year old male

Adverse reactions / side effects: Hyperthermia, Lung Neoplasm, Pancytopenia, Cholestasis, Cardiac Disorder, Liver Function Test Abnormal, Bone Marrow Failure, Hepatosplenomegaly, Oxygen Saturation Decreased

Adverse event resulted in: hospitalization

Suspect drug(s):
Alkeran
    Dosage: 280mg single dose
    Start date: 2007-02-21
    End date: 2007-02-21

Bicnu
    Dosage: 600mg single dose
    Start date: 2007-02-16
    End date: 2007-02-16

Cytarabine
    Dosage: 400mg twice per day
    Start date: 2007-02-17
    End date: 2007-02-20

Etoposide
    Dosage: 400mg per day
    Start date: 2007-02-17
    End date: 2007-02-20

Kepivance
    Dosage: 8mg per day
    Start date: 2007-02-12
    End date: 2007-02-25

Mabthera
    Dosage: 500mg cumulative dose
    Start date: 2007-02-08
    End date: 2007-02-21

Zevalin
    Dosage: 890mbq single dose
    Start date: 2007-02-08
    End date: 2007-02-08

Other drugs received by patient: Heparin; Zofran; Emend; Tazocilline; Fortum; Ciflox; Flagyl; Vancomycin; Caspofungin; Voriconazole; Ambisome; Zelitrex; Zovirax; Bactrim; Amiklin; Autograft OF Peripheral Blood Stem Cells; Granocyte; Tienam



Adverse event in receiving Alkeran (Melphalan)

Reported by a individual with unspecified qualification from France on 2007-10-31

Patient:

Adverse reactions / side effects: Drug Toxicity

Adverse event resulted in: death

Suspect drug(s):
Alkeran
    Dosage: oral
    Administration route: Oral
    Indication: Multiple Myeloma

Cyclophosphamide
    Indication: Stem Cell Transplant

Dexamethasone
    Dosage: oral
    Administration route: Oral
    Indication: Multiple Myeloma

Disodium Clodronate (Formulation Unknown) (Disodium Clodronate)
    Dosage: oral
    Administration route: Oral

Doxorubicin HCL
    Dosage: intravenous infus
    Indication: Multiple Myeloma

Granulocyte Col.stim.fact (Formulation Unknown) (Granulocyte Col.stim.

Mesna
    Indication: Stem Cell Transplant

Stem Cell Transplant (Formulation Unknown) (Stem Cell Transplant)

Vincristine
    Dosage: intravenous infus
    Indication: Multiple Myeloma



Adverse event in 39 year old male receiving Alkeran (Melphalan)

Reported by a individual with unspecified qualification from Japan on 2007-10-26

Patient: 39 year old male

Adverse reactions / side effects: Mechanical Ventilation, Status Epilepticus, Pyrexia, Disorientation, Rash, Convulsion, Pruritus Generalised, Encephalitis Herpes, Human Herpes Virus 6 Serology Positive, Memory Impairment, Altered State of Consciousness

Adverse event resulted in: life threatening event, disablity

Suspect drug(s):
Alkeran
    Dosage: 135 g/d
    Start date: 2007-01-15
    End date: 2007-01-15

Fludara
    Dosage: 42 g/d
    Start date: 2007-01-10
    End date: 2007-01-14

Foscarnet

Gleevec
    Dosage: 800 mg/d
    Administration route: Oral
    Indication: Acute Lymphocytic Leukaemia
    End date: 2007-01-15

Gleevec
    Dosage: 600/d
    Administration route: Oral
    Start date: 2007-05-01

Other drugs received by patient: Diflucan; Urso 250; Zovirax; Denosine; Methotrexate; Tacrolimus



Adverse event in 39 year old male receiving Alkeran (Melphalan)

Reported by a individual with unspecified qualification from Japan on 2007-10-22

Patient: 39 year old male

Adverse reactions / side effects: Mechanical Ventilation, Encephalitis Herpes, Human Herpes Virus 6 Serology Positive, Memory Impairment, Pyrexia, Status Epilepticus, Altered State of Consciousness

Adverse event resulted in: life threatening event, disablity

Suspect drug(s):
Alkeran
    Dosage: 135 g/d
    Start date: 2007-01-15
    End date: 2007-01-15

Fludara
    Dosage: 42 g/d
    Start date: 2007-01-10
    End date: 2007-01-14

Gleevec
    Dosage: 600 /d
    Administration route: Oral
    Indication: Acute Lymphocytic Leukaemia
    End date: 2007-01-15

Gleevec
    Dosage: 600/d
    Administration route: Oral
    Start date: 2007-05-01

Other drugs received by patient: Diflucan; Urso 250; Zovirax; Denosine



Adverse event in 63 year old male receiving Alkeran (Melphalan)

Reported by a physician from France on 2007-10-22

Patient: 63 year old male, weighing 65.0 kg (143.0 pounds)

Adverse reactions / side effects: Anaemia, Lung Infection, Rales, Disorientation, Pyrexia, Fall, Nervous System Disorder, Neutropenia, Leukopenia, Cough, Infection, Inflammation

Adverse event resulted in: hospitalization

Suspect drug(s):
Alkeran
    Dosage: 8.00 mg, oral
    Administration route: Oral
    Indication: Multiple Myeloma
    Start date: 2007-05-21
    End date: 2007-09-13

Velcade
    Dosage: 0.70 mg/m2, intravenous
    Indication: Multiple Myeloma
    Start date: 2007-05-21
    End date: 2007-09-17



Adverse event in 57 year old female receiving Alkeran (Melphalan)

Reported by a physician from France on 2007-10-12

Patient: 57 year old female

Adverse reactions / side effects: Bone Marrow Failure

Adverse event resulted in: hospitalization

Suspect drug(s):
Alkeran
    Indication: Drug USE FOR Unknown Indication

CC-5013 (Lenalidomide) (Capsules)
    Dosage: 25 mg, 21 days per month, oral; 25 mg, daily, oral
    Administration route: Oral
    Indication: Multiple Myeloma
    End date: 2007-07-15

CC-5013 (Lenalidomide) (Capsules)
    Dosage: 25 mg, 21 days per month, oral; 25 mg, daily, oral
    Administration route: Oral
    Indication: Multiple Myeloma
    Start date: 2007-08-30
    End date: 2007-09-18

Other drugs received by patient: Dexamethasone TAB; Pamidronate Disodium



Adverse event in 51 year old male receiving Alkeran (Melphalan)

Reported by a physician from France on 2007-10-09

Patient: 51 year old male, weighing 73.0 kg (160.6 pounds)

Adverse reactions / side effects: C-Reactive Protein Increased, Febrile Bone Marrow Aplasia

Adverse event resulted in: hospitalization

Suspect drug(s):
Alkeran
    Indication: Multiple Myeloma
    Start date: 2006-12-06
    End date: 2006-12-06

Cisplatin
    Indication: Multiple Myeloma

Cyclophosphamide
    Indication: Multiple Myeloma

Dexamethasone
    Indication: Multiple Myeloma

Doxorubicin HCL
    Indication: Multiple Myeloma

Etoposide
    Indication: Multiple Myeloma

Velcade
    Indication: Multiple Myeloma



Adverse event in male receiving Alkeran (Melphalan)

Reported by a pharmacist from Japan on 2007-10-04

Patient: male, weighing 62.0 kg (136.4 pounds)

Adverse reactions / side effects: Interstitial Lung Disease, Angina Pectoris, Upper Respiratory Tract Inflammation, Headache, Pyrexia, Abdominal Pain Upper

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Alkeran (Melphalan)

Other drugs received by patient: Aspirin; Rabeprazole Sodium; Frandol S; Prednisolone



Adverse event in receiving Alkeran (Melphalan)

Reported by a pharmacist from United States on 2007-10-02

Patient:

Adverse reactions / side effects: Visual Disturbance

Suspect drug(s):
Alkeran (Melphalan)



Adverse event in 10 year old female receiving Alkeran (Melphalan)

Reported by a physician from Japan on 2007-07-31

Patient: 10 year old female, weighing 23.2 kg (51.0 pounds)

Adverse reactions / side effects: Photosensitivity Reaction, Bedridden, Toxic Encephalopathy, Muscular Weakness, Loss of Consciousness, Convulsion, Abdominal Pain Upper, Dysstasia, Fatigue, Vitreous Floaters, Dizziness

Adverse event resulted in: hospitalization

Suspect drug(s):
Alkeran
    Dosage: 55mg per day
    Indication: Stem Cell Transplant
    Start date: 2007-07-09
    End date: 2007-07-11

Fludarabine Phosphate
    Dosage: 20mg per day
    Indication: Stem Cell Transplant
    Start date: 2007-07-05
    End date: 2007-07-08

Hydroxyzine Pamoate
    Dosage: 20mg per day
    Indication: Sedation
    Start date: 2007-07-11
    End date: 2007-07-11

Pentazocine Lactate
    Dosage: 12mg per day
    Indication: Sedation
    Start date: 2007-07-11
    End date: 2007-07-11

Zaditen
    Dosage: .99mg three times per day
    Administration route: Oral
    Start date: 2007-06-30
    End date: 2007-07-11

Other drugs received by patient: Baktar; Diflucan; Kytril; Heparin; Gamimune N 5%; Radiation; Chemotherapy; Unknown Drug



Adverse event in 10 year old female receiving Alkeran (Melphalan)

Reported by a physician from Japan on 2007-07-20

Patient: 10 year old female

Adverse reactions / side effects: Dizziness, Convulsion

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Alkeran (Melphalan)

Other drugs received by patient: Fludarabine Phosphate; Zaditen; Baktar; Diflucan; Hydroxyzine Pamoate; Pentazocine Lactate



Adverse event in 81 year old female receiving Alkeran (Melphalan)

Reported by a physician from United States on 2007-07-13

Patient: 81 year old female, weighing 87.1 kg (191.6 pounds)

Adverse reactions / side effects: White Blood Cell Count Decreased, Fatigue, Oedema Peripheral, Platelet Count Decreased, Hypoaesthesia, Rash Maculo-Papular, Erythema, Rash Pruritic

Adverse event resulted in: hospitalization

Suspect drug(s):
Alkeran
    Indication: Multiple Myeloma
    Start date: 2007-01-01

Revlimid
    Dosage: see image
    Administration route: Oral
    Indication: Multiple Myeloma
    Start date: 2006-08-01
    End date: 2007-04-17

Revlimid
    Dosage: see image
    Administration route: Oral
    Indication: Multiple Myeloma
    Start date: 2007-04-24
    End date: 2007-05-15

Other drugs received by patient: Allopurinol; Dexamethasone TAB; Aredia



Adverse event in 79 year old male receiving Alkeran (Melphalan)

Reported by a physician from United States on 2007-07-06

Patient: 79 year old male

Adverse reactions / side effects: Myocardial Infarction

Adverse event resulted in: death

Suspect drug(s):
Alkeran
    Dosage: 2 mg, daily;
    Indication: Multiple Myeloma
    Start date: 2007-03-14

Revlimid
    Dosage: 20 mg, 2 in1 d, oral
    Administration route: Oral
    Indication: Multiple Myeloma
    Start date: 2007-03-14



Adverse event in 75 year old female receiving Alkeran (Melphalan)

Reported by a physician from Germany on 2007-07-02

Patient: 75 year old female

Adverse reactions / side effects: Tooth Loss, Primary Sequestrum, Post Procedural Haematoma, X-RAY Abnormal, Dental Operation, Oedema Mouth, Blood Creatinine Increased, Cellulitis, Osteomyelitis Chronic, Osteitis, Operative Haemorrhage, Antibiotic Prophylaxis, Histology Abnormal, Osteonecrosis, Acute Sinusitis, Swelling, Disturbance in Attention, Nasal Operation, Actinomycosis, Plastic Surgery, Purulent Discharge, Biopsy, Dental Fistula, Sequestrectomy, General Anaesthesia, Depression, Bone Disorder, Blood Immunoglobulin A Increased, Gingival Ulceration, Gingival Swelling, Odontogenic Cyst, Amnesia, Haemoglobin Decreased, Osteotomy, Fibroma, Impaired Healing, Tumour Excision, JAW Disorder, Dental Alveolar Anomaly, Leukopenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Acetylsalicylic Acid SRT
    Dosage: 100 mg/day

Alkeran
    Indication: Plasmacytoma
    Start date: 2006-05-11

Alkeran
    Start date: 2006-05-24

Alkeran
    Start date: 2005-04-27

Alkeran
    Start date: 2006-04-27

Alkeran
    Start date: 2006-06-21

Alkeran
    Start date: 2006-07-19

Cortisone Acetate

Zometa
    Indication: Osteopenia
    Start date: 2004-06-02

Zometa
    Dosage: every 8 weeks
    Start date: 2005-01-04

Zometa
    Dosage: unk, qmo
    Start date: 2005-08-16
    End date: 2006-09-20

Other drugs received by patient: Fortecortin; Fortecortin; Fortecortin; Fortecortin; Arlevert; Magnesium Sulfate; Adalat; Isoket Retard; Diclofenac; Hydrochlorothiazide; Tramadol HCL; Metronidazole; Staphylex; Melphalan; Melphalan; Melphalan; Melphalan



Adverse event in 45 year old male receiving Alkeran (Melphalan)

Reported by a consumer/non-health professional from France on 2007-06-29

Patient: 45 year old male, weighing 112.0 kg (246.4 pounds)

Adverse reactions / side effects: Creatinine Renal Clearance Decreased, Proteinuria, Glomerulonephritis Acute, Blood Creatinine Increased, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Alkeran (Melphalan)

Other drugs received by patient: Zelitrex; Zofran; Neurontin; Bactrim DS; Speciafoldine; Omeprazole; Diantalvic; Dexamethasone 0.5mg TAB; Laroxyl; Fungizone; Gentamicin; Velcade; Cyclophosphamide; Dexamethasone 0.5mg TAB



Adverse event in 10 year old male receiving Alkeran (Melphalan)

Reported by a physician from Japan on 2007-06-26

Patient: 10 year old male, weighing 25.5 kg (56.1 pounds)

Adverse reactions / side effects: Stomatitis, Diarrhoea

Adverse event resulted in: disablity

Suspect drug(s):
Alkeran
    Dosage: 70mg per day
    Indication: Stem Cell Transplant
    Start date: 2003-01-13
    End date: 2003-01-19

Thiotepa
    Dosage: 2mg per day
    Indication: Stem Cell Transplant
    Start date: 2003-01-13
    End date: 2003-01-19

Other drugs received by patient: Neutrogin; Firstcin; Carbenin; Amikacin Sulfate; Diflucan; Zovirax; Fungizone; Baktar; Polymyxin B Sulfate; Florid



Adverse event in 79 year old male receiving Alkeran (Melphalan)

Reported by a individual with unspecified qualification from United States on 2007-06-25

Patient: 79 year old male

Adverse reactions / side effects: Myocardial Infarction

Adverse event resulted in: death

Suspect drug(s):
Alkeran
    Dosage: 2 mg, daily
    Indication: Multiple Myeloma
    Start date: 2007-03-14

Revlimid
    Dosage: 10 mg, 1 in 1 d, oral
    Administration route: Oral
    Indication: Multiple Myeloma
    Start date: 2007-03-14



Adverse event in 47 year old female receiving Alkeran (Melphalan)

Reported by a consumer/non-health professional from France on 2007-06-20

Patient: 47 year old female, weighing 55.0 kg (121.0 pounds)

Adverse reactions / side effects: Atelectasis, Dyspnoea, Lung Cyst Benign, Obstructive Airways Disorder, Lung Infiltration, Pulmonary Fibrosis

Adverse event resulted in: hospitalization

Suspect drug(s):
Alkeran
    Dosage: 230mg per day
    Start date: 2001-01-26
    End date: 2001-01-30

Myleran
    Dosage: 8mg per day
    Administration route: Oral
    Start date: 2001-01-26
    End date: 2001-01-30

Other drugs received by patient: Melphalan



Adverse event in 73 year old male receiving Alkeran (Melphalan)

Reported by a physician from United States on 2007-06-15

Patient: 73 year old male

Adverse reactions / side effects: Palpitations, Angina Pectoris, Heart Rate Irregular, Myocardial Infarction

Adverse event resulted in: hospitalization

Suspect drug(s):
Alkeran
    Dosage: 25 mg
    Indication: Multiple Myeloma
    Start date: 2007-04-27

Prednisone TAB
    Dosage: 100 mg
    Indication: Multiple Myeloma
    Start date: 2007-04-27

Revlimid
    Dosage: 10 mg, 1 in 1 d, oral
    Administration route: Oral
    Indication: Multiple Myeloma
    Start date: 2007-04-27
    End date: 2007-05-06

Other drugs received by patient: Isosorbide Dinitrate



Adverse event in 72 year old male receiving Alkeran (Melphalan)

Reported by a consumer/non-health professional from Canada on 2007-06-04

Patient: 72 year old male

Adverse reactions / side effects: Blood Bilirubin Increased, Confusional State, Hepatic Function Abnormal, Acidosis, Fall, Somnolence, Hepatomegaly, Pulmonary Oedema, Hypoxia, Blood Creatinine Increased, Thrombocytopenia, Lethargy, Anaemia, Hypotension, Pancytopenia, Aggression, Cardiac Failure, Dehydration, Respiratory Arrest, Cardiac Arrest

Adverse event resulted in: death

Suspect drug(s):
Alkeran
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Prednisone TAB
    Dosage: 125mg per day

Other drugs received by patient: Adalat; Atenolol; Colace; Dapsone; Dexamethasone; Docusate; Eprex; Gemfibrozil; Imovane; Lactulose; Lasix; Loperamide HCL; M-Eslon; Morphine; MS Contin; Oxygen; Percocet; RED Blood Cells; Risperdal; Senokot; Statex; Zopiclone



Adverse event in 74 year old male receiving Alkeran (Melphalan)

Reported by a individual with unspecified qualification from France on 2007-05-30

Patient: 74 year old male, weighing 75.0 kg (165.0 pounds)

Adverse reactions / side effects: Neurotoxicity, Chromosome Analysis Abnormal, Condition Aggravated, Myeloid Leukaemia, Multiple Myeloma

Adverse event resulted in: life threatening event

Suspect drug(s):
Alkeran
    Dosage: 10.00 mg, unk, intravenous
    Indication: Multiple Myeloma
    Start date: 2004-04-01
    End date: 2004-08-01

Cyclophosphamide
    Indication: Multiple Myeloma
    Start date: 2006-04-01
    End date: 2006-06-01

Thalidomide
    Indication: Multiple Myeloma
    Start date: 2004-11-01
    End date: 2005-01-01

Velcade
    Dosage: 9.60 mg, unk, intravenous
    Indication: Multiple Myeloma
    Start date: 2005-10-10
    End date: 2006-01-13



Adverse event in 75 year old male receiving Alkeran (Melphalan)

Reported by a physician from Japan on 2007-05-24

Patient: 75 year old male, weighing 53.0 kg (116.6 pounds)

Adverse reactions / side effects: Gastrointestinal Haemorrhage, Anaemia, Cystitis Haemorrhagic, Pyrexia, Urinary Bladder Haemorrhage

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Alkeran
    Administration route: Oral
    Indication: Multiple Myeloma
    Start date: 2007-03-05
    End date: 2007-03-30

Predonine
    Administration route: Oral
    Indication: Multiple Myeloma
    Start date: 2007-03-05
    End date: 2007-03-30

Other drugs received by patient: Onealfa; Allopurinol



Adverse event in 70 year old female receiving Alkeran (Melphalan)

Reported by a pharmacist from Japan on 2007-05-24

Patient: 70 year old female

Adverse reactions / side effects: White Blood Cell Count Decreased, Blood Potassium Decreased, Muscular Weakness

Adverse event resulted in: hospitalization

Suspect drug(s):
Alkeran (Melphalan)

Other drugs received by patient: Ranimustine; Vindesine Sulfate; Prednisolone; Zometa; Potassium Replacement

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