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Lamictal Side Effects Report #5672912-2
Consumer or non-health professional from UNITED STATES reported LAMICTAL problem on Mar 12, 2008. Male patient, 16 years of age, was diagnosed with epilepsy and was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: haemoglobin increased, . LAMICTAL dosage: unknown. Patient was hospitalized. Patient recovered.

Procrit Side Effects Report #5615210-5
PROCRIT problem was reported by a Pharmacist from UNITED STATES on Feb 05, 2008. Female patient, 74 years of age, weighting 100.3 lb, was diagnosed with anaemia macrocytic and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: haemoglobin increased, therapeutic response unexpected, . PROCRIT dosage: unknown. Patient recovered.

Velcade Side Effects Report #5585637-9
Physician from AUSTRALIA reported VELCADE problem on Dec 24, 2007. Male patient, 62 years of age, weighting 205.0 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: haemoglobin increased, platelet count decreased, . VELCADE dosage: 2.80 MG, 2.20 MG. During the same period patient was treated with DEXAMETHASONE, METFORMIN, GLYBURIDE. Patient recovered.

Remicade Side Effects Report #5592977-6
REMICADE problem was reported by a Physician from GERMANY on Jan 07, 2008. Male patient, 66 years of age, was diagnosed with psoriasis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: haemoglobin increased, . REMICADE dosage: unknown. Patient recovered.


Clozapine Side Effects Report #5566760-1
Pharmacist from UNITED STATES reported CLOZAPINE problem on Dec 18, 2007. Male patient, 37 years of age, weighting 292.0 lb, was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: haemoglobin increased, platelet count decreased, pyrexia, sedation, stupor, tachycardia, . CLOZAPINE dosage: 250MG PO. During the same period patient was treated with DEPAKOTE, COGENTIN, GEODON, WELLBUTRIN, ABILIFY. Patient recovered.

Tekturna Side Effects Report #5488210-6
TEKTURNA problem was reported by a Consumer or non-health professional from UNITED STATES on July 31, 2007. Female patient was treated with TEKTURNA. After drug was administered, patient experienced the following problems/side effects: haemoglobin increased, . TEKTURNA dosage: unknown. Patient recovered.

Humatrope Side Effects Report #5763032-7
Physician from SWEDEN reported HUMATROPE problem on May 28, 2008. Male patient, weighting 171.1 lb, was diagnosed with growth hormone deficiency, hypothyroidism, adrenal insufficiency and was treated with HUMATROPE. After drug was administered, patient experienced the following problems/side effects: haemoglobin increased, . HUMATROPE dosage: 0.4 MG, DAILY (1/D). During the same period patient was treated with LEVOTHYROXINE, CORTISONACETAT. Patient recovered.

Humatrope Side Effects Report #5732169-0
HUMATROPE problem was reported by a Physician from SWEDEN on Apr 24, 2008. Male patient, weighting 171.1 lb, was diagnosed with growth hormone deficiency, hypothyroidism, adrenal insufficiency and was treated with HUMATROPE. After drug was administered, patient experienced the following problems/side effects: haemoglobin increased, . HUMATROPE dosage: 0.4 MG, DAILY (1/D). During the same period patient was treated with LEVOTHYROXINE, CORTISONACETAT. Patient recovered.

Prilosec Side Effects Report #5345615-1
Consumer or non-health professional from UNITED STATES reported PRILOSEC problem on July 06, 2006. Female patient, 62 years of age, weighting 125.7 lb, was diagnosed with dyspepsia and was treated with PRILOSEC. After drug was administered, patient experienced the following problems/side effects: haemoglobin increased, . PRILOSEC dosage: unknown. During the same period patient was treated with PREVACID. Patient recovered.


Procrit Side Effects Report #5314455-1
PROCRIT problem was reported by a Physician from UNITED STATES on Apr 18, 2007. Male patient, weighting 139.1 lb, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: haemoglobin increased, thrombosis, . PROCRIT dosage: unknown. During the same period patient was treated with RIBAVIRIN. Patient was hospitalized. Patient recovered.

Epoetin Side Effects Report #5321373-1
Pharmacist from UNITED STATES reported EPOETIN ALFA problem on May 07, 2007. Male patient, 80 years of age, was diagnosed with anaemia and was treated with EPOETIN ALFA. After drug was administered, patient experienced the following problems/side effects: haemoglobin increased, headache, hypertension, . EPOETIN ALFA dosage: unknown. Patient was hospitalized. Patient recovered.

Procrit Side Effects Report #5325428-7
PROCRIT problem was reported by a Physician from UNITED STATES on May 07, 2007. Male patient, weighting 139.1 lb, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: haemoglobin increased, thrombosis, . PROCRIT dosage: unknown. During the same period patient was treated with RIBAVIRIN. Patient was hospitalized. Patient recovered.

Sensipar Side Effects Report #5300998-3
Consumer or non-health professional from UNITED STATES reported SENSIPAR problem on Jan 16, 2007. Male patient, 49 years of age, was diagnosed with hyperparathyroidism secondary and was treated with SENSIPAR. After drug was administered, patient experienced the following problems/side effects: haemoglobin increased, . SENSIPAR dosage: unknown. During the same period patient was treated with PHOSLO, HEPARIN, CHLORIDE. Patient recovered.

Iressa Side Effects Report #5268854-7
IRESSA problem was reported by a Pharmacist from UNITED STATES on Oct 23, 2003. Female patient was diagnosed with non-small cell lung cancer and was treated with IRESSA. After drug was administered, patient experienced the following problems/side effects: haemoglobin increased, . IRESSA dosage: 250 MG QD PO. During the same period patient was treated with LOTENSIN, DECADRON, COUMADIN, ZANTAC. Patient recovered.


Aranesp Side Effects Report #5630474-X
Health Professional from AUSTRALIA reported ARANESP problem on Feb 06, 2008. Male patient, weighting 165.3 lb, was diagnosed with dialysis, renal failure chronic and was treated with ARANESP. After drug was administered, patient experienced the following problems/side effects: central line infection, haemoglobin increased, lymphopenia, neutrophilia, . ARANESP dosage: unknown. During the same period patient was treated with OMEPRAZOLE, CALTRATE, CALCITRIOL, MYLANTA, SENSIPAR. Patient was hospitalized. Patient recovered.

Trimethoprim Side Effects Report #5648237-8
TRIMETHOPRIM problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Feb 21, 2008. Male patient was diagnosed with urinary tract infection and was treated with TRIMETHOPRIM. After drug was administered, patient experienced the following problems/side effects: blood disorder, haemoglobin increased, haemoglobin s decreased, mouth ulceration, renal impairment, . TRIMETHOPRIM dosage: 200 MG, BID, ORAL. During the same period patient was treated with BECLOMETASONE, BENDROFLUAZIDE, MOVICOL, TERBUTALINE SULPHATE, TRAMADOL. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5553912-X
Consumer or non-health professional from UNITED STATES reported REBIF problem on Nov 30, 2007. Female patient, 45 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: basedow's disease, haemoglobin increased, . REBIF dosage: unknown. During the same period patient was treated with IBUPROFEN. Patient recovered.

Avandamet Side Effects Report #5512415-9
AVANDAMET problem was reported by a Consumer or non-health professional from UNITED STATES on May 21, 2007. Male patient, 52 years of age, was treated with AVANDAMET. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, haemoglobin increased, oedema peripheral, . AVANDAMET dosage: unknown. During the same period patient was treated with DIOVAN, PRILOSEC, LORAZEPAM. Patient recovered.

Nexavar Side Effects Report #5519128-8
Pharmacist from UNITED STATES reported NEXAVAR problem on Nov 14, 2007. Male patient, 70 years of age, weighting 159.0 lb, was diagnosed with hepatic neoplasm malignant, atrial fibrillation and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, haemoglobin increased, haemorrhage, international normalised ratio decreased, international normalised ratio increased, occult blood positive, pain in extremity, prothrombin time prolonged, . NEXAVAR dosage: unknown. During the same period patient was treated with COUMADIN. Patient was hospitalized. Patient recovered.


Rebif Side Effects Report #5527429-2
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 14, 2007. Female patient, 45 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: basedow's disease, haemoglobin increased, . REBIF dosage: unknown. During the same period patient was treated with IBUPROFEN. Patient recovered.

Norvasc Side Effects Report #5409975-5
Physician from JAPAN reported NORVASC problem on July 31, 2007. Male patient, 57 years of age, was treated with NORVASC. After drug was administered, patient experienced the following problems/side effects: haematocrit increased, haemoglobin increased, red blood cell count increased, . NORVASC dosage: DAILY DOSE:10MG. During the same period patient was treated with AMARYL, MICARDIS, OMEPRAZOLE, MUCOSTA, WARFARIN, ANPLAG. Patient recovered.

Norvasc Side Effects Report #5401703-2
NORVASC problem was reported by a Pharmacist from JAPAN on July 19, 2007. Male patient, 57 years of age, was treated with NORVASC. After drug was administered, patient experienced the following problems/side effects: haematocrit increased, haemoglobin increased, red blood cell count increased, . NORVASC dosage: DAILY DOSE:10MG. During the same period patient was treated with AMARYL, MICARDIS, WARFARIN, OMEPRAZOLE, ANPLAG, MUCOSTA. Patient recovered.

Norvasc Side Effects Report #5401703-2
Pharmacist from JAPAN reported NORVASC problem on July 19, 2007. Male patient, 57 years of age, was treated with NORVASC. After drug was administered, patient experienced the following problems/side effects: haematocrit increased, haemoglobin increased, red blood cell count increased, . NORVASC dosage: DAILY DOSE:10MG. During the same period patient was treated with AMARYL, MICARDIS, WARFARIN, OMEPRAZOLE, ANPLAG, MUCOSTA. Patient recovered.

Seroquel Side Effects Report #5740567-4
SEROQUEL problem was reported by a Physician from UNITED STATES on May 09, 2008. Male patient, 56 years of age, was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: blood triglycerides increased, haemoglobin increased, . SEROQUEL dosage: unknown. Patient recovered.

Byetta Side Effects Report #5364771-2
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Jan 23, 2007. Male patient, 58 years of age, was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, haemoglobin increased, hyperglycaemia, . BYETTA dosage: unknown. Patient recovered.

Bevacizumab Side Effects Report #5309051-6
BEVACIZUMAB problem was reported by a Health Professional from UNITED STATES on Apr 17, 2007. Female patient, weighting 93.98 lb, was diagnosed with colon cancer metastatic and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: carcinoembryonic antigen increased, haemoglobin increased, hyponatraemia, pancreatitis, . BEVACIZUMAB dosage: 5 MG/KG, 2/MONTH. During the same period patient was treated with CAPECITABINE. Patient was hospitalized. Patient recovered.

Lyrica Side Effects Report #5255760-7
Health Professional from UNITED STATES reported LYRICA problem on Feb 21, 2007. Female patient, weighting 170.0 lb, was diagnosed with fibromyalgia and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: haematocrit increased, haemoglobin increased, orthostatic hypotension, . LYRICA dosage: unknown. During the same period patient was treated with CELEBREX, MORPHINE SULPHATE, ARTHROTEC, CYMBALTA, ZYRTEC, ASCORBIC ACID, CALCIUM. Patient recovered.

Roaccutane Side Effects Report #5645290-2
ROACCUTANE problem was reported by a Physician from BELGIUM on Feb 19, 2008. Male patient, 16 years of age, was diagnosed with acne and was treated with ROACCUTANE. After drug was administered, patient experienced the following problems/side effects: blood cholesterol increased, haematocrit increased, haemoglobin increased, . ROACCUTANE dosage: unknown. Patient recovered.

Nicorette Side Effects Report #5601221-2
Consumer or non-health professional from UNITED STATES reported NICORETTE problem on Jan 23, 2008. Male patient, 47 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, dependence, haemoglobin increased, . NICORETTE dosage: unknown. During the same period patient was treated with NEXIUM, ROBINULTE, SERTRALINE. Patient recovered.

Aranesp Side Effects Report #5605855-0
ARANESP problem was reported by a Physician from AUSTRALIA on Jan 15, 2008. Male patient, weighting 121.3 lb, was treated with ARANESP. After drug was administered, patient experienced the following problems/side effects: calciphylaxis, gangrene, haemoglobin increased, ischaemia, . ARANESP dosage: unknown. During the same period patient was treated with CALTRATE. Patient was hospitalized. Patient recovered.

Nicorette Side Effects Report #5541634-0
Consumer or non-health professional from UNITED STATES reported NICORETTE problem on Dec 06, 2007. Male patient, 47 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, dependence, haemoglobin increased, . NICORETTE dosage: unknown. During the same period patient was treated with NEXIUM, ROBINULTE, SERTRALINE. Patient recovered.

Emtricitabine Side Effects Report #5554951-5
EMTRICITABINE problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 05, 2007. Female patient, 39 years of age, weighting 79.37 lb, was diagnosed with hiv infection and was treated with EMTRICITABINE. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, gastroenteritis, haemoglobin increased, hypotension, interstitial lung disease, . EMTRICITABINE dosage: unknown. During the same period patient was treated with NEVIRAPINE, COTRIM. Patient was hospitalized. Patient recovered.

Aranesp Side Effects Report #5562772-2
Physician from AUSTRALIA reported ARANESP problem on Dec 05, 2007. Male patient, weighting 121.3 lb, was treated with ARANESP. After drug was administered, patient experienced the following problems/side effects: calciphylaxis, finger amputation, haemoglobin increased, ischaemia, . ARANESP dosage: unknown. Patient was hospitalized. Patient recovered.

Equasym Side Effects Report #5524933-8
EQUASYM problem was reported by a Physician from GERMANY on Oct 31, 2007. Male patient, child 10 years of age, was treated with EQUASYM. After drug was administered, patient experienced the following problems/side effects: electrocardiogram qrs complex prolonged, electrocardiogram st segment elevation, haemoglobin increased, mean cell volume increased, sinus arrhythmia, . EQUASYM dosage: 30 MG /D. During the same period patient was treated with RITALIN. Patient recovered.

Equasym Side Effects Report #5527543-1
Consumer or non-health professional from GERMANY reported EQUASYM problem on Nov 06, 2007. Male patient, child 10 years of age, was treated with EQUASYM. After drug was administered, patient experienced the following problems/side effects: electrocardiogram qrs complex prolonged, electrocardiogram st segment elevation, haemoglobin increased, mean cell volume increased, sinus arrhythmia, . EQUASYM dosage: 30 MG /D. During the same period patient was treated with RITALIN. Patient recovered.

Floxuridine Side Effects Report #5445732-1
FLOXURIDINE problem was reported by a Physician from UNITED STATES on Aug 23, 2007. Female patient, 73 years of age, was diagnosed with metastases to lung and was treated with FLOXURIDINE. After drug was administered, patient experienced the following problems/side effects: dyspnoea, haematocrit increased, haemoglobin increased, pulmonary arteriovenous fistula, tachycardia, . FLOXURIDINE dosage: unknown. During the same period patient was treated with FLUOROURACIL, ALPHA, GEMCITABINE, CAPECITABINE. Patient recovered.

Revlimid Side Effects Report #5449448-7
Physician from CANADA reported REVLIMID problem on Aug 30, 2007. Female patient, 77 years of age, was diagnosed with 5q-syndrome and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: abdominal pain, febrile neutropenia, haemoglobin increased, platelet count decreased, white blood cell count decreased, . REVLIMID dosage: 5 MG, 1 IN 1 D, ORAL; 2.5 MG, 1 IN 2 D, ORAL. During the same period patient was treated with FENOFIBRATE, INDAPAMIDE, GLYBURIDE, ASPIRIN, MECLIZINE, DILTIAZEM, ALLOPURINOL. Patient was hospitalized. Patient recovered.

Avastin Side Effects Report #5416676-6
AVASTIN problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 07, 2007. Female patient, weighting 170.0 lb, was diagnosed with non-small cell lung cancer and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, blood pressure increased, haemoglobin increased, . AVASTIN dosage: 25 MG/ML, Q3W. During the same period patient was treated with CARBOPLATIN, PACLITAXEL, ARANESP, CLONIDINE, FLAGYL, TOPROL, LOTREL, HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.

Prialt Side Effects Report #5397039-9
Health Professional from UNITED STATES reported PRIALT problem on July 06, 2007. Female patient, 53 years of age, was diagnosed with bone pain and was treated with PRIALT. After drug was administered, patient experienced the following problems/side effects: conjunctival haemorrhage, haematocrit increased, haemoglobin increased, international normalised ratio decreased, petechiae, red blood cell count increased, . PRIALT dosage: unknown. Patient recovered.

Prialt Side Effects Report #5397039-9
PRIALT problem was reported by a Health Professional from UNITED STATES on July 06, 2007. Female patient, 53 years of age, was diagnosed with bone pain and was treated with PRIALT. After drug was administered, patient experienced the following problems/side effects: conjunctival haemorrhage, haematocrit increased, haemoglobin increased, international normalised ratio decreased, petechiae, red blood cell count increased, . PRIALT dosage: unknown. Patient recovered.

Erlotinib Side Effects Report #5776185-1
Physician from AUSTRALIA reported ERLOTINIB problem on May 29, 2008. Male patient, 75 years of age, was diagnosed with non-small cell lung cancer and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: confusional state, diarrhoea, haemoglobin increased, hypomagnesaemia, neutropenia, somnolence, thrombocytopenia, . ERLOTINIB dosage: (150 MG, QD), ORAL. During the same period patient was treated with ASPIRIN, METFORMIN, MELIZIDE, PERINDOPRIL ERBUMINE, SIMVASTATIN, LOPERAMIDE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5735581-9
SUTENT problem was reported by a Physician from UNITED KINGDOM on Apr 30, 2008. Male patient, weighting 187.4 lb, was diagnosed with renal cancer metastatic, splenectomy and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: blood erythropoietin increased, haematocrit increased, haemoglobin increased, macrocytosis, volume blood decreased, . SUTENT dosage: unknown. During the same period patient was treated with PENICILLIN, LANSOPRAZOLE. Patient recovered.

Sutent Side Effects Report #5711779-0
Physician from UNITED KINGDOM reported SUTENT problem on Apr 09, 2008. Male patient, weighting 187.4 lb, was diagnosed with renal cancer metastatic, splenectomy and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: blood erythropoietin increased, haematocrit increased, haemoglobin increased, macrocytosis, volume blood decreased, . SUTENT dosage: unknown. During the same period patient was treated with PENICILLIN, LANSOPRAZOLE. Patient recovered.

Denileukin Side Effects Report #5358549-3
DENILEUKIN DIFTITOX SERAGEN problem was reported by a Physician from UNITED STATES on June 13, 2007. Male patient, weighting 214.0 lb, was diagnosed with mycosis fungoides and was treated with DENILEUKIN DIFTITOX SERAGEN. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, capillary leak syndrome, haemoglobin increased, orthostatic hypotension, syncope vasovagal, . DENILEUKIN DIFTITOX SERAGEN dosage: unknown. During the same period patient was treated with NAPROXEN. Patient died on 04/23/2007.

Prialt Side Effects Report #5363025-8
Health Professional from UNITED STATES reported PRIALT problem on June 01, 2007. Female patient, 53 years of age, was diagnosed with pain and was treated with PRIALT. After drug was administered, patient experienced the following problems/side effects: erythema, haematocrit increased, haemoglobin increased, international normalised ratio decreased, ocular hyperaemia, red blood cell count increased, . PRIALT dosage: unknown. Patient recovered.