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GRANULOCYTE COUNT DECREASED side effect

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Artist Side Effects Report #5661713-7
Physician from JAPAN reported ARTIST problem on Mar 03, 2008. Female patient, 81 years of age, was diagnosed with cardiac failure, insomnia, tachycardia and was treated with ARTIST. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . ARTIST dosage: 3.75MG TWICE PER DAY. During the same period patient was treated with VEGETAMIN, WARFARIN, LASIX, DIGOXIN. Patient was hospitalized. Patient recovered.

Lipitor Side Effects Report #5620872-2
LIPITOR problem was reported by a Physician from JAPAN on Jan 28, 2008. Male patient, 64 years of age, was diagnosed with hypercholesterolaemia and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . LIPITOR dosage: DAILY DOSE:10MG. Patient recovered.

Olanzapine Side Effects Report #5623060-9
Physician from JAPAN reported OLANZAPINE problem on Jan 31, 2008. Female patient, weighting 99.65 lb, was diagnosed with schizophrenia, schizoaffective disorder and was treated with OLANZAPINE. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, white blood cell count decreased, . OLANZAPINE dosage: 10 MG, DAILY (1/D). During the same period patient was treated with BARNETIL, SETOUS, VALERIN, PROMETHAZINE. Patient was hospitalized. Patient recovered.

Artist Side Effects Report #5624713-9
ARTIST problem was reported by a Physician from JAPAN on Feb 11, 2008. Female patient, 81 years of age, was diagnosed with cardiac failure and was treated with ARTIST. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . ARTIST dosage: 7.5MG PER DAY. During the same period patient was treated with VEGETAMIN, WARFARIN, LASIX. Patient was hospitalized. Patient recovered.


Olanzapine Side Effects Report #5636767-4
Physician from JAPAN reported OLANZAPINE problem on Feb 14, 2008. Female patient, weighting 99.65 lb, was diagnosed with schizophrenia, schizoaffective disorder and was treated with OLANZAPINE. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, white blood cell count decreased, . OLANZAPINE dosage: 10 MG, DAILY (1/D). During the same period patient was treated with BARNETIL, SETOUS, VALERIN, PROMETHAZINE. Patient was hospitalized. Patient recovered.

Revlimid Side Effects Report #5643822-1
REVLIMID problem was reported by a Physician from UNITED STATES on Oct 29, 2007. Male patient, 59 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, haemoglobin decreased, platelet count decreased, white blood cell count decreased, . REVLIMID dosage: 30 MG, QD X 21 DAYS, ORAL. Patient recovered.

Zyprexa Side Effects Report #5531475-2
Physician from JAPAN reported ZYPREXA problem on Nov 26, 2007. Female patient, 80 years of age, was diagnosed with mania and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, pyrexia, . ZYPREXA dosage: 10 MG, DAILY (1/D). During the same period patient was treated with CRAVIT, GASTER. Patient was hospitalized. Patient recovered.

Micardis Side Effects Report #5538044-9
MICARDIS problem was reported by a Physician from JAPAN on Dec 06, 2007. Female patient, weighting 103.6 lb, was diagnosed with hypertension, headache and was treated with MICARDIS. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, sepsis, . MICARDIS dosage: unknown. During the same period patient was treated with VONFENAC. Patient recovered.

Micardis Side Effects Report #5571985-5
Physician from JAPAN reported MICARDIS problem on Dec 20, 2007. Female patient, weighting 103.6 lb, was diagnosed with hypertension, headache and was treated with MICARDIS. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, sepsis, wound complication, . MICARDIS dosage: unknown. During the same period patient was treated with VONFENAC. Patient recovered.


Bayaspirin Side Effects Report #5512964-3
BAYASPIRIN problem was reported by a Physician from JAPAN on Nov 05, 2007. Female patient, 83 years of age, weighting 103.6 lb, was treated with BAYASPIRIN. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . BAYASPIRIN dosage: TOTAL DAILY DOSE: 100 MG UNIT DOSE: 100 MG. During the same period patient was treated with FLUCONAZOLE, MEROPEN. Patient was hospitalized. Patient recovered.

Aspirin Side Effects Report #5441389-4
Physician from JAPAN reported ASPIRIN problem on Aug 29, 2007. Female patient, 83 years of age, weighting 83.78 lb, was treated with ASPIRIN. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . ASPIRIN dosage: TOTAL DAILY DOSE: 100 MG UNIT DOSE: 100 MG. During the same period patient was treated with FLUCONAZOLE, MEROPEN. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5404234-9
ZYPREXA problem was reported by a Physician from JAPAN on July 26, 2007. Female patient, 41 years of age, weighting 112.4 lb, was diagnosed with schizoaffective disorder and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . ZYPREXA dosage: 10 MG, DAILY (1/D). During the same period patient was treated with DEPAKENE, LITHIUM CARBONATE, LITHIUM CARBONATE, LITHIUM CARBONATE, RISPERDAL. Patient recovered.

Aspirin Side Effects Report #5427262-6
Physician from JAPAN reported ASPIRIN problem on Aug 24, 2007. Female patient was treated with ASPIRIN. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . ASPIRIN dosage: TOTAL DAILY DOSE: 100 MG UNIT DOSE: 100 MG. Patient recovered.

Zyprexa Side Effects Report #5382493-9
ZYPREXA problem was reported by a Physician from JAPAN on July 03, 2007. Female patient, 41 years of age, weighting 112.4 lb, was diagnosed with schizoaffective disorder and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . ZYPREXA dosage: 10 MG, DAILY (1/D). During the same period patient was treated with DEPAKENE, LIMAS, RISPERDAL, AKINETON, ROHYPNOL. Patient recovered.


Taxotere Side Effects Report #5398920-7
Consumer or non-health professional from UNITED STATES reported TAXOTERE problem on July 24, 2007. Male patient, weighting 154.3 lb, was treated with TAXOTERE. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, white blood cell count decreased, . TAXOTERE dosage: 135 MG. Patient recovered.

Argatroban Side Effects Report #5400566-9
ARGATROBAN problem was reported by a Health Professional from JAPAN on July 12, 2007. Male patient, 67 years of age, was diagnosed with cerebral infarction and was treated with ARGATROBAN. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . ARGATROBAN dosage: unknown. During the same period patient was treated with RADICUT, CITICOLINE, DEXTRAN L, CHLORIDE, SOLCOSERYL. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5382493-9
Physician from JAPAN reported ZYPREXA problem on July 03, 2007. Female patient, 41 years of age, weighting 112.4 lb, was diagnosed with schizoaffective disorder and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . ZYPREXA dosage: 10 MG, DAILY (1/D). During the same period patient was treated with DEPAKENE, LIMAS, RISPERDAL, AKINETON, ROHYPNOL. Patient recovered.

Taxotere Side Effects Report #5398920-7
TAXOTERE problem was reported by a Consumer or non-health professional from UNITED STATES on July 24, 2007. Male patient, weighting 154.3 lb, was treated with TAXOTERE. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, white blood cell count decreased, . TAXOTERE dosage: 135 MG. Patient recovered.

Argatroban Side Effects Report #5400566-9
Health Professional from JAPAN reported ARGATROBAN problem on July 12, 2007. Male patient, 67 years of age, was diagnosed with cerebral infarction and was treated with ARGATROBAN. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . ARGATROBAN dosage: unknown. During the same period patient was treated with RADICUT, CITICOLINE, DEXTRAN L, CHLORIDE, SOLCOSERYL. Patient was hospitalized. Patient recovered.


Salazopyrin Side Effects Report #5761804-6
SALAZOPYRIN problem was reported by a Physician from JAPAN on May 30, 2008. Female patient, weighting 112.4 lb, was diagnosed with proctocolitis and was treated with SALAZOPYRIN. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . SALAZOPYRIN dosage: DAILY DOSE:1000MG. Patient was hospitalized. Patient recovered.

Norvasc Side Effects Report #5765892-2
Physician from JAPAN reported NORVASC problem on June 04, 2008. Male patient, weighting 129.0 lb, was diagnosed with hypertension and was treated with NORVASC. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, neutropenia, . NORVASC dosage: unknown. During the same period patient was treated with FERROMIA. Patient recovered.

Salazopyrin Side Effects Report #5772884-6
SALAZOPYRIN problem was reported by a Physician from JAPAN on June 03, 2008. Female patient, weighting 112.4 lb, was diagnosed with proctocolitis and was treated with SALAZOPYRIN. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . SALAZOPYRIN dosage: DAILY DOSE:1000MG. Patient was hospitalized. Patient recovered.

Cyclophosphamide Side Effects Report #5774907-7
Consumer or non-health professional from UNITED STATES reported CYCLOPHOSPHAMIDE problem on June 16, 2008. Male patient, weighting 193.8 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, haemoglobin decreased, white blood cell count decreased, . CYCLOPHOSPHAMIDE dosage: 1597 MG. During the same period patient was treated with DOXIL, PREDNISONE, RITUXIMAB, VINCRISTINE SULPHATE, ALTACE, LIPITOR, MAGNESIUM OXIDE, METFORMIN. Patient recovered.

Norvasc Side Effects Report #5739449-3
NORVASC problem was reported by a Physician from JAPAN on May 08, 2008. Male patient, 67 years of age, was diagnosed with hypertension and was treated with NORVASC. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . NORVASC dosage: DAILY DOSE:5MG. During the same period patient was treated with FERROUS CITRATE. Patient was hospitalized. Patient recovered.

Norvasc Side Effects Report #5744692-3
Physician from JAPAN reported NORVASC problem on May 12, 2008. Male patient, 67 years of age, was diagnosed with hypertension and was treated with NORVASC. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . NORVASC dosage: DAILY DOSE:5MG. During the same period patient was treated with FERROUS CITRATE. Patient was hospitalized. Patient recovered.

Lipitor Side Effects Report #5695035-5
LIPITOR problem was reported by a Physician from JAPAN on Mar 27, 2008. Male patient, 64 years of age, was diagnosed with hypercholesterolaemia and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . LIPITOR dosage: DAILY DOSE:10MG. Patient recovered.

Abilify Side Effects Report #5711526-2
Physician from UNITED STATES reported ABILIFY problem on Apr 18, 2008. Male patient, weighting 200.8 lb, was diagnosed with schizophrenia and was treated with ABILIFY. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, white blood cell count decreased, . ABILIFY dosage: 30MG QD PO. During the same period patient was treated with LEXAPRO. Patient recovered.

Zyprexa Side Effects Report #5344117-6
ZYPREXA problem was reported by a Physician from JAPAN on May 25, 2007. Female patient, 41 years of age, was diagnosed with bipolar i disorder and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . ZYPREXA dosage: unknown. During the same period patient was treated with DEPAKENE. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5352837-2
Physician from UNITED STATES reported ZYPREXA ZYDIS problem on May 31, 2007. Male patient, 30 years of age, was diagnosed with schizoaffective disorder and was treated with ZYPREXA ZYDIS. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, hepatitis b positive, liver function test abnormal, prescribed overdose, white blood cell count decreased, . ZYPREXA ZYDIS dosage: 30 MG, DAILY (1/D). During the same period patient was treated with ATIVAN, COGENTIN. Patient recovered.

Clozapine Side Effects Report #5360146-0
CLOZAPINE problem was reported by a Physician from CZECH REPUBLIC on June 07, 2007. Male patient, 31 years of age, was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, leukocytosis, lymphocyte count decreased, white blood cell count increased, . CLOZAPINE dosage: 600 MG, QD. During the same period patient was treated with DEPAKENE, RIVOTRIL. Patient recovered.

Zyprexa Side Effects Report #5360237-4
Physician from JAPAN reported ZYPREXA problem on June 07, 2007. Female patient, 41 years of age, weighting 112.4 lb, was diagnosed with schizoaffective disorder and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . ZYPREXA dosage: 10 MG, DAILY (1/D). During the same period patient was treated with DEPAKENE, LIMAS, RISPERDAL, AKINETON, ROHYPNOL. Patient recovered.

Novantrone Side Effects Report #5375765-5
NOVANTRONE problem was reported by a Health Professional from UNITED STATES on June 15, 2007. Male patient, 64 years of age, was diagnosed with off label use and was treated with NOVANTRONE. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, neutrophil count decreased, . NOVANTRONE dosage: 25 MG, 1 IN 1 DAYS, INTRAVENOUS (NOT OTHERWISE SPECIFIED). During the same period patient was treated with IXABEPILONE, PREDNISONE, ALDACTONE, AMITRIPTYLINE, FUROSEMIDE, LORAZEPAM, OXYCODONE, OXYCONTIN. Patient recovered.

Cetuximab Side Effects Report #5323545-9
Consumer or non-health professional from UNITED STATES reported CETUXIMAB problem on May 10, 2007. Female patient, 71 years of age, weighting 156.5 lb, was diagnosed with non-small cell lung cancer and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . CETUXIMAB dosage: unknown. During the same period patient was treated with PACLITAXEL, CARBOPLATIN, BEVACIZUMAB. Patient recovered.

Zyprexa Side Effects Report #5323746-X
ZYPREXA problem was reported by a Physician from GERMANY on May 04, 2007. Male patient, 18 years of age, was diagnosed with schizoaffective disorder and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, leukopenia, . ZYPREXA dosage: 15 MG, DAILY (1/D). Patient recovered.

Rivotril Side Effects Report #5328325-6
Physician from CZECH REPUBLIC reported RIVOTRIL problem on May 10, 2007. Female patient, 52 years of age, was treated with RIVOTRIL. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, lymphocyte count decreased, white blood cell count decreased, . RIVOTRIL dosage: unknown. During the same period patient was treated with CLOZAPINE. Patient recovered.

Gemzar Side Effects Report #5328837-5
GEMZAR problem was reported by a Physician from JAPAN on May 09, 2007. Female patient, 55 years of age, was diagnosed with small intestine leiomyosarcoma and was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, platelet count decreased, tumour haemorrhage, . GEMZAR dosage: 675 MG/M2, OTHER. During the same period patient was treated with TAXOTERE. Patient recovered.

Seroquel Side Effects Report #5296137-8
Health Professional from JAPAN reported SEROQUEL problem on Apr 10, 2007. Male patient, 77 years of age, was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, pyelonephritis acute, pyrexia, . SEROQUEL dosage: unknown. During the same period patient was treated with GASTER D, MYSLEE, GASCON, ROHYPNOL, URIEF, NELBON, RISUMIC. Patient recovered.

Erbitux Side Effects Report #5304441-X
ERBITUX problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 16, 2007. Female patient, 74 years of age, weighting 112.4 lb, was diagnosed with non-small cell lung cancer and was treated with ERBITUX. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . ERBITUX dosage: unknown. During the same period patient was treated with TAXOL, CARBOPLATIN, BEVACIZUMAB. Patient recovered.

Nexavar Side Effects Report #5321020-9
Health Professional from UNITED STATES reported NEXAVAR problem on Oct 17, 2006. Female patient, 84 years of age, was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, white blood cell count decreased, . NEXAVAR dosage: 400 MG; 200 MG : BID; ORAL. Patient recovered.

Zyprexa Side Effects Report #5266376-0
ZYPREXA problem was reported by a Consumer or non-health professional from CANADA on Mar 01, 2007. Male patient, 35 years of age, was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, . ZYPREXA dosage: unknown. Patient recovered.

Cetuximab Side Effects Report #5509017-7
Consumer or non-health professional from UNITED STATES reported CETUXIMAB problem on Nov 01, 2007. Female patient, 52 years of age, weighting 125.7 lb, was diagnosed with squamous cell carcinoma and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: dehydration, granulocyte count decreased, haemoglobin decreased, hypoalbuminaemia, hypocalcaemia, hypokalaemia, hypomagnesaemia, hyponatraemia, oral pain, . CETUXIMAB dosage: unknown. During the same period patient was treated with CISPLATIN. Patient was hospitalized. Patient recovered.

Cetuximab Side Effects Report #5347639-7
CETUXIMAB problem was reported by a Health Professional from UNITED STATES on June 05, 2007. Male patient, 63 years of age, weighting 207.2 lb, was diagnosed with non-small cell lung cancer and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: febrile neutropenia, granulocyte count decreased, . CETUXIMAB dosage: unknown. During the same period patient was treated with CARBOPLATIN, PACLITAXEL, BEVACIZUMAB. Patient was hospitalized. Patient recovered.

Gemzar Side Effects Report #5330844-3
Physician from JAPAN reported GEMZAR problem on May 09, 2007. Female patient, 55 years of age, was diagnosed with small intestine leiomyosarcoma and was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: computerised tomogram abnormal, granulocyte count decreased, platelet count decreased, tumour haemorrhage, . GEMZAR dosage: 675 MG/M2, OTHER. During the same period patient was treated with TAXOTERE. Patient recovered.

Cetuximab Side Effects Report #5333605-4
CETUXIMAB problem was reported by a Consumer or non-health professional from UNITED STATES on May 21, 2007. Female patient, 71 years of age, weighting 156.5 lb, was diagnosed with non-small cell lung cancer and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: dehydration, granulocyte count decreased, hypokalaemia, hypotension, muscular weakness, . CETUXIMAB dosage: unknown. During the same period patient was treated with PACLITAXEL, CARBOPLATIN, BEVACIZUMAB. Patient was hospitalized. Patient recovered.

Cetuximab Side Effects Report #5337091-X
Health Professional from UNITED STATES reported CETUXIMAB problem on May 24, 2007. Male patient, 69 years of age, weighting 116.8 lb, was diagnosed with neoplasm malignant and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, granulocyte count decreased, haemoglobin, hypotension, pyrexia, stomatitis, . CETUXIMAB dosage: unknown. During the same period patient was treated with CISPLATIN, COLACE, FENTANYL, OXYCONTIN, TIMENTIN. Patient recovered.

Amlodin Side Effects Report #5669929-0
AMLODIN problem was reported by a Physician from JAPAN on Mar 05, 2008. Female patient, 84 years of age, was diagnosed with hypertension, gastritis, hyperuricaemia and was treated with AMLODIN. After drug was administered, patient experienced the following problems/side effects: eosinophil count increased, granulocyte count decreased, lymphadenitis, lymphocyte stimulation test positive, neutrophil count decreased, skin exfoliation, . AMLODIN dosage: unknown. During the same period patient was treated with RANITIDINE, ALLORINE, CLARITIN, CARBON, LABETALOL, NITRODERM, FUROSEMIDE, ASPIRIN. Patient recovered.

Erbitux Side Effects Report #5682440-6
Consumer or non-health professional from UNITED STATES reported ERBITUX problem on Mar 21, 2008. Male patient, weighting 158.7 lb, was diagnosed with squamous cell carcinoma and was treated with ERBITUX. After drug was administered, patient experienced the following problems/side effects: dehydration, dysphagia, granulocyte count decreased, hyponatraemia, lymphopenia, radiation skin injury, stomatitis, white blood cell count decreased, . ERBITUX dosage: unknown. During the same period patient was treated with CISPLATIN, AVELOX, CIPRO, VANCOMYCIN, LACTULOSE, NEUPOGEN. Patient was hospitalized. Patient recovered.

Carboplatin Side Effects Report #5500418-X
CARBOPLATIN problem was reported by a Health Professional from UNITED STATES on Oct 24, 2007. Male patient, 77 years of age, weighting 216.1 lb, was diagnosed with non-small cell lung cancer and was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: dehydration, diarrhoea, granulocyte count decreased, nausea, . CARBOPLATIN dosage: unknown. During the same period patient was treated with ALIMTA, IPRATROPIUM, CLONIDINE, CODEINE, CYANOCOBALAMIN, DEXAMETHASONE, FOLIC ACID. Patient was hospitalized. Patient recovered.

Bevacizumab Side Effects Report #5793499-X
Physician from JAPAN reported BEVACIZUMAB problem on June 13, 2008. Male patient was diagnosed with rectal cancer recurrent and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: cholecystitis acute, enterocolitis, granulocyte count decreased, hepatic function abnormal, pharyngitis, white blood cell count decreased, . BEVACIZUMAB dosage: 5 MG/KG, 1 PER 1 DAY. During the same period patient was treated with FLUOROURACIL, IRINOTECAN, ISOVORIN, MAGMITT. Patient recovered.

Erbitux Side Effects Report #5692316-6
ERBITUX problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 21, 2008. Male patient, weighting 158.7 lb, was diagnosed with squamous cell carcinoma and was treated with ERBITUX. After drug was administered, patient experienced the following problems/side effects: dehydration, dysphagia, granulocyte count decreased, hyponatraemia, lymphopenia, radiation skin injury, stomatitis, white blood cell count decreased, . ERBITUX dosage: unknown. During the same period patient was treated with CISPLATIN, AVELOX, CIPRO, VANCOMYCIN, LACTULOSE, NEUPOGEN. Patient was hospitalized. Patient recovered.

Cyclophosphamide Side Effects Report #5329896-6
Consumer or non-health professional from UNITED STATES reported CYCLOPHOSPHAMIDE problem on May 17, 2007. Female patient, weighting 133.3 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: fatigue, febrile neutropenia, granulocyte count decreased, platelet count decreased, white blood cell count decreased, . CYCLOPHOSPHAMIDE dosage: 966 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE. Patient was hospitalized. Patient recovered.