Menu

• Ask a Health Expert about ACUTE PROMYELOCYTIC LEUKAEMIA
• Post Your Side Effect related to ACUTE PROMYELOCYTIC LEUKAEMIA
• ACUTE PROMYELOCYTIC LEUKAEMIA and FDA Warnings
• ACUTE PROMYELOCYTIC LEUKAEMIA in Patients Wiki
• Report ACUTE PROMYELOCYTIC LEUKAEMIA in Drug Side Effect Survey

ACUTE PROMYELOCYTIC LEUKAEMIA side effect

What is ACUTE PROMYELOCYTIC LEUKAEMIA ?

A Health Expert wants to answer your question. Please provide details below.

Type your question here

 letters left

Januvia Side Effects Report #5653351-7
Physician from UNITED STATES reported JANUVIA problem on Feb 29, 2008. Male patient, 75 years of age, weighting 227.1 lb, was diagnosed with type 2 diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . JANUVIA dosage: unknown. During the same period patient was treated with ATENOLOL, ASPIRIN, ACTOS, ZOCOR. Patient was hospitalized and became disabled. Patient recovered.

Novantrone Side Effects Report #5661645-4
NOVANTRONE problem was reported by a Consumer or non-health professional from ITALY on Feb 21, 2008. Male patient, 55 years of age, was diagnosed with multiple sclerosis and was treated with NOVANTRONE. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, cerebral haemorrhage, treatment related secondary malignancy, . NOVANTRONE dosage: unknown. Patient was hospitalized. Patient died on 01/01/2004.

Novantrone Side Effects Report #5661747-2
Consumer or non-health professional from ITALY reported NOVANTRONE problem on Feb 21, 2008. Male patient, 27 years of age, was diagnosed with multiple sclerosis and was treated with NOVANTRONE. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, cerebral haemorrhage, treatment related secondary malignancy, . NOVANTRONE dosage: 80 MG/M2, 1 IN 1 MONTHS. Patient was hospitalized. Patient died on 01/01/2006.

Gemcitabine Side Effects Report #5628130-7
GEMCITABINE problem was reported by a Physician from JAPAN on Feb 07, 2008. Female patient, weighting 101.4 lb, was diagnosed with gallbladder cancer stage iv, anorexia, prophylaxis of nausea and vomiting and was treated with GEMCITABINE. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . GEMCITABINE dosage: 800 MG, OTHER. During the same period patient was treated with DECADRON, KYTRIL. Patient recovered.


Januvia Side Effects Report #5645387-7
Physician from UNITED STATES reported JANUVIA problem on Feb 26, 2008. Male patient, 75 years of age, weighting 227.1 lb, was diagnosed with type 2 diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . JANUVIA dosage: unknown. Patient recovered.

Sandostatin Side Effects Report #5582626-5
SANDOSTATIN LAR problem was reported by a Consumer or non-health professional from ISRAEL on Dec 30, 2007. Female patient, 41 years of age, was diagnosed with carcinoid syndrome and was treated with SANDOSTATIN LAR. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . SANDOSTATIN LAR dosage: 30 MG, QMO. Patient was hospitalized. Patient recovered.

Gemcitabine Side Effects Report #5591938-0
Physician from JAPAN reported GEMCITABINE problem on Jan 07, 2008. Female patient, weighting 101.4 lb, was diagnosed with gallbladder cancer stage iv, anorexia, prophylaxis of nausea and vomiting and was treated with GEMCITABINE. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . GEMCITABINE dosage: 800 MG, OTHER. During the same period patient was treated with DECADRON, KYTRIL. Patient recovered.

Gemcitabine Side Effects Report #5545615-2
GEMCITABINE problem was reported by a Physician from JAPAN on Nov 27, 2007. Female patient was diagnosed with gallbladder cancer and was treated with GEMCITABINE. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . GEMCITABINE dosage: unknown. Patient recovered.

Colchicum Side Effects Report #5550531-6
Physician from UNITED STATES reported COLCHICUM JTL LIQ problem on Nov 26, 2007. Male patient, 34 years of age, was diagnosed with behcet's syndrome and was treated with COLCHICUM JTL LIQ. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, anaemia, aphthous stomatitis, ecchymosis, exercise tolerance decreased, haematuria, haemorrhagic diathesis, leukopenia, rash pustular, . COLCHICUM JTL LIQ dosage: 1 MG/DAY. Patient was hospitalized. Patient recovered.


Tretinoin Side Effects Report #5565309-7
TRETINOIN problem was reported by a Pharmacist from CANADA on Feb 05, 2003. Male patient, 69 years of age, was diagnosed with acute promyelocytic leukaemia and was treated with TRETINOIN. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, haemorrhage intracranial, . TRETINOIN dosage: unknown. During the same period patient was treated with DAUNORUBICIN, CYTARABINE, METHOTREXATE. Patient was hospitalized. Patient died.

Gleevec Side Effects Report #5512192-1
Physician from SPAIN reported GLEEVEC problem on Nov 02, 2007. Male patient, 70 years of age, was diagnosed with gastrointestinal stromal tumour and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . GLEEVEC dosage: 400 MG/D. Patient recovered.

Betaseron Side Effects Report #5520086-0
BETASERON problem was reported by a Health Professional from UNITED STATES on Nov 08, 2007. Female patient, 67 years of age, was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . BETASERON dosage: unknown. Patient died on 03/13/2007.

Gleevec Side Effects Report #5520456-0
Physician from SPAIN reported GLEEVEC problem on Nov 09, 2007. Male patient, 70 years of age, was diagnosed with gastrointestinal stromal tumour and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, pancytopenia, . GLEEVEC dosage: 400 MG/D. Patient recovered.

Pegasys Side Effects Report #5525372-6
PEGASYS problem was reported by a Physician from JAPAN on Nov 12, 2007. Female patient, 59 years of age, was diagnosed with hepatitis c and was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . PEGASYS dosage: unknown. During the same period patient was treated with NORVASC, ENALAPRIL MALEATE, HALCION, VOLTAREN. Patient was hospitalized. Patient recovered.


Novantrone Side Effects Report #5485571-9
Physician from FRANCE reported NOVANTRONE problem on Sept 28, 2007. Female patient, 28 years of age, was diagnosed with multiple sclerosis and was treated with NOVANTRONE. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . NOVANTRONE dosage: 120 MG. During the same period patient was treated with METHOTREXATE. Patient recovered.

Fluorouracil Side Effects Report #5491445-X
FLUOROURACIL problem was reported by a Consumer or non-health professional from SPAIN on Oct 09, 2007. Male patient, 52 years of age, was diagnosed with colon cancer and was treated with FLUOROURACIL. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, septic shock, . FLUOROURACIL dosage: TOTAL CUMULATIVE DOSE 6,600MG/M2. Patient died on 01/01/2003.

Roaccutan Side Effects Report #5497288-5
Consumer or non-health professional from ARGENTINA reported ROACCUTAN problem on Oct 17, 2007. Male patient, 19 years of age, was diagnosed with acne and was treated with ROACCUTAN. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, epistaxis, mouth haemorrhage, platelet count decreased, . ROACCUTAN dosage: unknown. Patient was hospitalized. Patient recovered.

Colchicum Side Effects Report #5473163-7
COLCHICUM JTL LIQ problem was reported by a Health Professional from TURKEY on Sept 20, 2007. Male patient, 34 years of age, was diagnosed with behcet's syndrome and was treated with COLCHICUM JTL LIQ. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . COLCHICUM JTL LIQ dosage: 1 MG, DAILY. Patient was hospitalized. Patient recovered.

Hysron Side Effects Report #5406569-2
Consumer or non-health professional from JAPAN reported HYSRON problem on July 20, 2007. Female patient, 40 years of age, was diagnosed with breast cancer recurrent and was treated with HYSRON. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . HYSRON dosage: unknown. During the same period patient was treated with ZOLADEX, TAMOXIFEN CITRATE. Patient was hospitalized. Patient recovered.


Epirubicin Side Effects Report #5420224-4
EPIRUBICIN problem was reported by a Physician from FINLAND on Aug 06, 2007. Female patient, 35 years of age, was diagnosed with malignant histiocytosis and was treated with EPIRUBICIN. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . EPIRUBICIN dosage: unknown. During the same period patient was treated with ETOPOSIDE, CYCLOPHOSPHAMIDE, PREDNISOLONE. Patient died.

Seroquel Side Effects Report #5421180-5
Physician from UNITED KINGDOM reported SEROQUEL problem on Aug 17, 2007. Female patient, 40 years of age, was diagnosed with schizophrenia and was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . SEROQUEL dosage: 350 MG MANE, 400 MG NOCTE. Patient died.

Prednisone Side Effects Report #5762150-7
PREDNISONE problem was reported by a Consumer or non-health professional from KOREA, REPUBLIC OF on May 23, 2008. Male patient, 62 years of age, was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . PREDNISONE dosage: unknown. During the same period patient was treated with TACROLIMUS. Patient was hospitalized. Patient recovered.

Solage Side Effects Report #5779755-X
Consumer or non-health professional from INDIA reported SOLAGE problem on June 04, 2008. Male patient, 19 years of age, was treated with SOLAGE. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, hypotension, hypoxia, ileal perforation, peritonitis, retinoic acid syndrome, somnolence, tachycardia, tachypnoea, . SOLAGE dosage: unknown. Patient was hospitalized. Patient died.

Mitoxantrone Side Effects Report #5751458-7
MITOXANTRONE problem was reported by a Health Professional from UNITED STATES on May 15, 2008. Female patient, 48 years of age, was diagnosed with multiple sclerosis and was treated with MITOXANTRONE. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, marrow hyperplasia, pancytopenia, . MITOXANTRONE dosage: 12 MG/M2OTH. Patient recovered.

Mitoxantrone Side Effects Report #5751459-9
Physician from UNITED STATES reported MITOXANTRONE problem on May 15, 2008. Male patient, 51 years of age, was diagnosed with multiple sclerosis and was treated with MITOXANTRONE. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, cellulitis, marrow hyperplasia, pancytopenia, . MITOXANTRONE dosage: unknown. Patient recovered.

Novantrone Side Effects Report #5757134-9
NOVANTRONE problem was reported by a Health Professional from UNITED STATES on May 13, 2008. Male patient, 58 years of age, was treated with NOVANTRONE. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, disseminated intravascular coagulation, leukocytosis, . NOVANTRONE dosage: unknown. Patient recovered.

Trisenox Side Effects Report #5320876-3
Physician from JAPAN reported TRISENOX problem on Apr 24, 2007. Male patient, 73 years of age, was diagnosed with acute promyelocytic leukaemia and was treated with TRISENOX. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, cerebral haemorrhage, cheilitis, chills, condition aggravated, disseminated intravascular coagulation, hyperhidrosis, pyrexia, rash, . TRISENOX dosage: 9.075 MG QD INTRAVENOUS DRIP. During the same period patient was treated with FAMOTIDINE, CANDESARTAN CILEXETIL, MEROPENEM TRIHYDRATE, LENOGRASTIM. Patient was hospitalized. Patient died on 03/22/2007.

Novantrone Side Effects Report #5330106-4
NOVANTRONE problem was reported by a Physician from UNITED STATES on May 02, 2007. Female patient was diagnosed with multiple sclerosis and was treated with NOVANTRONE. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, pancytopenia, . NOVANTRONE dosage: 5 MG/M2, 3 IN 1 MONTHS, INTRAVENOUS. During the same period patient was treated with REBIF, CELLCEPT. Patient was hospitalized. Patient recovered.

Trisenox Side Effects Report #5292474-1
Physician from JAPAN reported TRISENOX problem on Mar 20, 2007. Male patient, 51 years of age, was diagnosed with acute promyelocytic leukaemia and was treated with TRISENOX. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, blood alkaline phosphatase increased, blood potassium decreased, blood urea increased, electrocardiogram qt prolonged, malaise, malignant neoplasm progression, renal impairment, sepsis, . TRISENOX dosage: 9.165 MG QD INTRAVENOUS DRIP. During the same period patient was treated with AMPHOTERICIN N, CEFTAZIDIME, MICAFUNGIN, IDARUBICIN, CYTARABINE, DALTEPARIN, ISEPAMICIN SULPHATE. Patient was hospitalized. Patient died on 04/18/2006.

Novantrone Side Effects Report #5293777-7
NOVANTRONE problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 21, 2007. Female patient, weighting 138.9 lb, was treated with NOVANTRONE. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . NOVANTRONE dosage: unknown. During the same period patient was treated with OXYBUTYNIN CHLORIDE, CARBAMAZEPINE. Patient was hospitalized. Patient recovered.

Pegasys Side Effects Report #5264993-5
Physician from JAPAN reported PEGASYS problem on Mar 05, 2007. Female patient, 59 years of age, was diagnosed with hepatitis c and was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . PEGASYS dosage: unknown. During the same period patient was treated with NORVASC, RENIVACE, HALCION, VOLTAREN. Patient was hospitalized. Patient recovered.

Novantrone Side Effects Report #5278308-X
NOVANTRONE problem was reported by a Physician from UNITED STATES on Mar 08, 2007. Female patient, 54 years of age, was diagnosed with multiple sclerosis and was treated with NOVANTRONE. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, anaemia, pancytopenia, subdural haematoma, . NOVANTRONE dosage: unknown. Patient was hospitalized. Patient recovered.

Novantrone Side Effects Report #5278309-1
Health Professional from UNITED STATES reported NOVANTRONE problem on Mar 15, 2007. Female patient, 66 years of age, was diagnosed with multiple sclerosis and was treated with NOVANTRONE. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, cardiac failure congestive, cytomegalovirus infection, gastritis, pancytopenia, sepsis, . NOVANTRONE dosage: unknown. Patient was hospitalized. Patient died on 03/13/2007.

Betaseron Side Effects Report #5280906-4
BETASERON problem was reported by a Health Professional from UNITED STATES on Mar 14, 2007. Female patient, 67 years of age, was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: acute promyelocytic leukaemia, . BETASERON dosage: unknown. Patient died on 03/13/2007.

Trisenox Side Effects Report #5680028-4
Physician from JAPAN reported TRISENOX problem on Mar 12, 2008. Male patient, 63 years of age, was diagnosed with acute promyelocytic leukaemia and was treated with TRISENOX. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, acute promyelocytic leukaemia, alanine aminotransferase increased, aspartate aminotransferase increased, blood albumin decreased, blood alkaline phosphatase increased, blood bilirubin increased, blood calcium decreased, blood lactate dehydrogenase increased, . TRISENOX dosage: K9.75 MG QD; INTRAVENOUS. During the same period patient was treated with ARBEKACIN SULPHATE, MEROPENEM, MEXILETINE HYDROCHLORIDE, DALTEPARIN, HYDROCORTISONE SUCCINATE, RANITIDINE HYDROCHLORIDE, ALLOPURINOL. Patient was hospitalized. Patient died on 05/10/2007.

Zetia Side Effects Report #5572173-9
ZETIA problem was reported by a Pharmacist from UNITED KINGDOM on Dec 18, 2007. Male patient, 54 years of age, weighting 262.4 lb, was diagnosed with blood cholesterol increased, myocardial infarction, hypertension, epilepsy, diabetes mellitus and was treated with ZETIA. After drug was administered, patient experienced the following problems/side effects: acute myeloid leukaemia, acute promyelocytic leukaemia, . ZETIA dosage: unknown. During the same period patient was treated with ATENOLOL, CARBAMAZEPINE, ATORVASTATIN, GLICLAZIDE, METFORMIN. Patient was hospitalized. Patient recovered.

Trisenox Side Effects Report #5701452-7
Physician from JAPAN reported TRISENOX problem on Mar 24, 2008. Male patient, 63 years of age, was diagnosed with acute promyelocytic leukaemia and was treated with TRISENOX. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, acute promyelocytic leukaemia, alanine aminotransferase increased, aspartate aminotransferase increased, blood albumin decreased, blood alkaline phosphatase increased, blood bilirubin increased, blood calcium decreased, blood creatinine increased, . TRISENOX dosage: 9.75 MG, QD; INTRAVENOUS. During the same period patient was treated with ARBEKACIN SULPHATE, MEROPENEM TRIHYDRATE, MEROPENEM TRIHYDRATE, MEXILETINE HYDROCHLORIDE, DALTEPARIN, HYDROCORTISONE SUCCINATE, RANITIDINE HYDROCHLORIDE. Patient was hospitalized. Patient died on 05/08/2007.