Trisenox and pyrexia Patient Reports February 13, 2012

Trisenox Side Effects Report #4816268-3
Trisenox side effect was reported by a Physician from UNITED STATES on Oct 17, 2005. Male patient, 31 years of age, weighting 128.3 lb, was diagnosed with testicular germ cell cancer and was treated with Trisenox. After drug was administered, patient experienced the following side effects: acute respiratory distress syndrome, anxiety , haemoptysis, neoplasm progression, pyrexia. Trisenox dosage: 14.55 MG/KG QD INTRAVENOUS DRIP. Patient died on 07/26/2003.

Trisenox Side Effects Report #4855372-0
Trisenox side effect was reported by a Health Professional from UNITED STATES on Apr 05, 2005. Male patient, 70 years of age, weighting 175.0 lb, was diagnosed with myelodysplastic syndrome and was treated with Trisenox. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, av dissociation, fatigue, oedema peripheral, platelet count decreased, pyrexia, rash . Trisenox dosage: unknown. Patient was hospitalized. Patient recovered.

Trisenox Side Effects Report #4887012-9
Trisenox side effect was reported by a Health Professional from UNITED STATES on Jan 06, 2006. Female patient, 60 years of age, weighting 150.0 lb, was diagnosed with myelodysplastic syndrome and was treated with Trisenox. After drug was administered, patient experienced the following side effects: asthenia, back pain , fatigue, fluid retention, herpes zoster, neutrophil count increased, pyrexia, rash . Trisenox dosage: 17.04 MG QD INTRAVENOUS DRIP. During the same period patient was treated with THALIDOMIDE, DEXAMETHASONE, FOSAMAX, FLEXERIL, LUNESTA, BACTRIM DS, ASCORBIC ACID. Patient was hospitalized. Patient recovered.

Trisenox Side Effects Report #4621604-7
Trisenox side effect was reported by a Consumer or non-health professional from on Mar 11, 2005. Male patient, 90 years of age, was diagnosed with multiple myeloma  and was treated with Trisenox. After drug was administered, patient experienced the following side effects: abdominal mass, abdominal pain , herpes zoster, neutropenia, pyrexia, white blood cell count decreased. Trisenox dosage: (0.25 MG/KG, DAILY) IVI. During the same period patient was treated with ASCORBIC ACID, MELPHALAN, ALOXI, AREDIA, KYTRIL, ARANESP, NEUPOGEN, DECADRON. Patient was hospitalized. Patient recovered.


Trisenox Side Effects Report #4635803-1
Trisenox side effect was reported by a Health Professional from on Mar 11, 2005. Male patient, 90 years of age, was diagnosed with multiple myeloma  and was treated with Trisenox. After drug was administered, patient experienced the following side effects: abdominal mass, abdominal pain , herpes zoster, neutropenia, pyrexia. Trisenox dosage: 0.25 MG/KG DAILY IVI. During the same period patient was treated with ASCORBIC ACID, MELPHALAN, ALOXI, AREDIA, KYTRIL, ARANESP, NEUPOGEN, DECADRON. Patient was hospitalized. Patient recovered.

Trisenox Side Effects Report #4712479-6
Trisenox side effect was reported by a Consumer or non-health professional from UNITED STATES on June 20, 2005. Female patient, 70 years of age, weighting 126.0 lb, was diagnosed with multiple myeloma  and was treated with Trisenox. After drug was administered, patient experienced the following side effects: asthenia, cardiac failure congestive, dyspnoea, platelet count decreased, pyrexia, rash , white blood cell count decreased. Trisenox dosage: 14 MG IVI. During the same period patient was treated with MELPHALAN, ASCORBIC ACID, OXYTROL, SANTURA, FOLIC ACID. Patient was hospitalized. Patient recovered.

Trisenox Side Effects Report #4568437-8
Trisenox side effect was reported by a Consumer or non-health professional from on Jan 11, 2005. Male patient, 67 years of age, was diagnosed with multiple myeloma  and was treated with Trisenox. After drug was administered, patient experienced the following side effects: haematocrit decreased, haemoglobin decreased, heart rate increased, infection , light chain analysis increased, oral mucosal blistering, pyrexia, rash maculo-papular, rash pruritic. Trisenox dosage: 20 MG IVI. Patient was hospitalized. Patient recovered.

Trisenox Side Effects Report #5373417-9
Trisenox side effect was reported by a Pharmacist from UNITED STATES on June 26, 2007. Female patient, weighting 194.0 lb, was diagnosed with ill-defined disorder and was treated with Trisenox. After drug was administered, patient experienced the following side effects: chills, dyspnoea, infusion related reaction, pyrexia. Trisenox dosage: 12.45 MG 5X/WEEK FOR 5 WKS IV. Patient was hospitalized. Patient recovered.

Trisenox Side Effects Report #5093427-9
Trisenox side effect was reported by a Physician from JAPAN on Aug 16, 2006. Female patient, 84 years of age, was diagnosed with acute promyelocytic leukaemia and was treated with Trisenox. After drug was administered, patient experienced the following side effects: groin pain, pain in extremity, pyrexia, white blood cell count decreased. Trisenox dosage: 5 MG 0.13MG/KG/DAY QD INTRAVENOUS DRIP. During the same period patient was treated with NICORANDIL, FUROSEMIDE, VORICONAZOLE, FAMOTIDINE. Patient recovered.


Trisenox Side Effects Report #5320876-3
Trisenox side effect was reported by a Physician from JAPAN 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 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.

Trisenox Side Effects Report #5047199-4
Trisenox side effect was reported by a Physician from JAPAN on June 23, 2006. Male patient, 54 years of age, was diagnosed with acute promyelocytic leukaemia and was treated with Trisenox. After drug was administered, patient experienced the following side effects: c-reactive protein increased, hyperglycaemia, pyrexia. Trisenox dosage: 12 MG QD INTRAVENOUS DRIP. During the same period patient was treated with PREDNISOLONE, METHYLPREDNISOLONE, DALTEPARIN, MICAFUNGIN, ACYCLOVIR, AMIKACIN SULPHATE, TAZOBACTAM PIPERACILLIN, CEFTAZIDIME. Patient was hospitalized. Patient recovered.

Trisenox Side Effects Report #4638293-8
Trisenox side effect was reported by a Physician from on Mar 14, 2005. Female patient, 52 years of age, was diagnosed with acute promyelocytic leukaemia and was treated with Trisenox. After drug was administered, patient experienced the following side effects: basophilia, electrocardiogram qt corrected interval prolonged, leukocytosis, pyrexia. Trisenox dosage: unknown. Patient was hospitalized. Patient recovered.

Trisenox Side Effects Report #4848006-2
Trisenox side effect was reported by a Physician from JAPAN on Aug 24, 2005. Female patient, 52 years of age, was diagnosed with acute promyelocytic leukaemia and was treated with Trisenox. After drug was administered, patient experienced the following side effects: basophilia, electrocardiogram qt corrected interval prolonged, leukocytosis, pyrexia. Trisenox dosage: 9.52 MG QD INTRAVENOUS DRIP. During the same period patient was treated with INSULIN, SPIRONOLACTONE, LANSOPRAZOLE, LEVOFLOXACIN, TAZOBACTAM, VANCOMYCIN HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Trisenox Side Effects Report #5084863-5
Trisenox side effect was reported by a Physician from JAPAN on July 31, 2006. Male patient, 50 years of age, was diagnosed with acute promyelocytic leukaemia and was treated with Trisenox. After drug was administered, patient experienced the following side effects: acute promyelocytic leukaemia, condition aggravated, headache , leukaemic infiltration brain, leukocytosis, myalgia, promyelocyte count increased, pyrexia, subarachnoid haemorrhage. Trisenox dosage: 11.692 MG QD INTRAVENOUS DRIP. During the same period patient was treated with IDARUBICIN. Patient recovered.


Trisenox Side Effects Report #4801211-3
Trisenox side effect was reported by a Physician from JAPAN on Sept 26, 2005. Female patient, 36 years of age, was diagnosed with acute promyelocytic leukaemia and was treated with Trisenox. After drug was administered, patient experienced the following side effects: bacterial infection , blood bilirubin increased, c-reactive protein increased, electrocardiogram qt corrected interval prolonged, electrocardiogram qt prolonged, jaundice , neutrophil count decreased, pyrexia, white blood cell count decreased. Trisenox dosage: 6.93 MG QD INTRAVENOUS DRIP. During the same period patient was treated with LACTOBACILLUS CASEI, LENOGRASTIM, CEFCAPENE PIVOXIL, GENTAMICIN, BUFEXAMAC. Patient was hospitalized. Patient recovered.

Trisenox Side Effects Report #5228030-0
Trisenox side effect was reported by a Pharmacist from UNITED STATES on May 05, 2006. Female patient, 14 years of age, weighting 61.73 lb, was diagnosed with acute promyelocytic leukaemia and was treated with Trisenox. After drug was administered, patient experienced the following side effects: pyrexia. Trisenox dosage: 10 MG DAYS 1-5 X 5 WEEKS QD INTRAVENOUS DRIP. During the same period patient was treated with ZOFRAN. Patient was hospitalized. Patient recovered.

Trisenox Side Effects Report #4622031-9
Trisenox side effect was reported by a Physician from on Mar 08, 2005. Male patient, 78 years of age, was diagnosed with acute myeloid leukaemia and was treated with Trisenox. After drug was administered, patient experienced the following side effects: aphasia , blood creatinine abnormal, coma, lung infiltration, platelet count decreased, pyrexia. Trisenox dosage: (0.25 MG/KG, 5 DOSE LOAD: 2X/WK), IVI. During the same period patient was treated with AMBIEN, CYTARABINE. Patient was hospitalized. Patient recovered.

Trisenox Side Effects Report #5473074-7
Trisenox side effect was reported by a Physician from JAPAN on Sept 19, 2007. Female patient, 28 years of age, was treated with Trisenox. After drug was administered, patient experienced the following side effects: pleurisy, pyrexia. Trisenox dosage: unknown. Patient recovered.