REFUSAL OF TREATMENT BY PATIENT side effect
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Drugs associated with REFUSAL OF TREATMENT BY PATIENT
ACYCLOVIR ALEVE AMBIEN AMNESTEEM ARIXTRA ATORVASTATIN AVONEX BACITRACIN BEVACIZUMAB BROVANA BYETTA CAP CARBOPLATIN CEFTRIAXONE CEREZYME CHANTIX CISPLATIN CLARAVIS CLOZAPINE CYMBALTA CYTARABINE DEXAMETHASONE DIGOXIN DILTIAZEM ERBITUX ERLOTINIB ESCITALOPRAM EXCEGRAN FLUPHENAZINE FOSAMAX GEMCITABINE HANCE HYDROMORPHONE IMPLANON INSULIN LAMICTAL LEUPROLIDE LUNESTA METOPROLOL MINOCYCLINE MIRTAZAPINE MITOXANTRONE NAMENDA NATALIZUMAB NEUPOGEN NEXIUM NOVOSEVEN OMNISCAN ORENCIA OXYCONTIN PEGETRON PLETAL PREDNISOLONE PROPRANOLOL PROVIGIL REBIF RENAGEL REVLIMID RITUXIMAB ROGAINE SERTRALINE SIMVASTATIN SORAFENIB SUTENT TACROLIMUS TARCEVA TEMODAL TEMODAR TYSABRI ULTRAVIST VANCOMYCIN VELCADE VESICARE VICODIN VISUDYNE WARFARIN ZANTAC ZELNORM ZETIA ZYPREXACerezyme Side Effects Report #5660000-0
Physician from UNITED STATES reported CEREZYME problem on Feb 26, 2008. Female patient, 59 years of age, weighting 134.5 lb, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, splenectomy, splenic artery aneurysm, . CEREZYME dosage: unknown. Patient was hospitalized. Patient recovered.
Hance Side Effects Report #5627162-2
HANCE problem was reported by a Pharmacist from UNITED STATES on Feb 13, 2008. Female patient was treated with HANCE. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, vomiting, . HANCE dosage: 16.8 ML. Patient recovered.
Cisplatin Side Effects Report #5642802-X
Pharmacist from UNITED STATES reported CISPLATIN problem on Feb 27, 2008. Male patient, 55 years of age, weighting 154.3 lb, was diagnosed with neoplasm malignant and was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, renal failure acute, . CISPLATIN dosage: 200MG ONCE IV. Patient was hospitalized. Patient recovered.
Cerezyme Side Effects Report #5614435-2
CEREZYME problem was reported by a Physician from KOREA, REPUBLIC OF on Jan 17, 2008. Female patient, child 12 years of age, weighting 39.68 lb, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, respiratory failure, vomiting, . CEREZYME dosage: unknown. Patient died on 01/02/2008.
Fosamax Side Effects Report #5477799-9
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Oct 03, 2007. Female patient, 63 years of age, was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, . FOSAMAX dosage: unknown. Patient recovered.
Tacrolimus Side Effects Report #5483021-X
TACROLIMUS problem was reported by a Physician from JAPAN on Sept 18, 2007. Male patient, 74 years of age, was diagnosed with rheumatoid arthritis and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, renal impairment, shock, . TACROLIMUS dosage: 1.5 MG, ORAL. During the same period patient was treated with BASEN, KINEDAK, AMARYL, FUROSEMIDE, SALOBELLET, PREDNISOLONE, LOXONIN. Patient died on 02/10/2007.
Zantac Side Effects Report #5400935-7
Consumer or non-health professional from UNITED STATES reported ZANTAC problem on May 11, 2007. Female patient was treated with ZANTAC. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, . ZANTAC dosage: 1.3ML TWICE PER DAY. Patient recovered.
Zantac Side Effects Report #5400935-7
ZANTAC problem was reported by a Consumer or non-health professional from UNITED STATES on May 11, 2007. Female patient was treated with ZANTAC. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, . ZANTAC dosage: 1.3ML TWICE PER DAY. Patient recovered.
Revlimid Side Effects Report #5761788-0
Physician from UNITED STATES reported REVLIMID problem on May 23, 2008. Female patient, 85 years of age, was diagnosed with chronic lymphocytic leukaemia and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, . REVLIMID dosage: 10 MG, 1 IN 1 D, ORAL. Patient died.
Vicodin Side Effects Report #5787757-2
VICODIN problem was reported by a Consumer or non-health professional from UNITED STATES on June 24, 2008. Male patient, 69 years of age, weighting 194.0 lb, was diagnosed with pain and was treated with VICODIN. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, suicidal ideation, . VICODIN dosage: unknown. Patient recovered.
Leuprolide Side Effects Report #5377781-6
Consumer or non-health professional from JAPAN reported LEUPROLIDE ACETATE problem on June 27, 2007. Female patient was diagnosed with uterine leiomyoma and was treated with LEUPROLIDE ACETATE. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, reversible posterior leukoencephalopathy syndrome, . LEUPROLIDE ACETATE dosage: unknown. Patient was hospitalized. Patient recovered.
Rituximab Side Effects Report #5335097-8
RITUXIMAB problem was reported by a Health Professional from UNITED STATES on Jan 08, 2007. Female patient, weighting 205.0 lb, was diagnosed with rheumatoid arthritis and was treated with RITUXIMAB. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, rheumatoid arthritis, . RITUXIMAB dosage: 1000 MG, X2. During the same period patient was treated with ACETAMINOPHEN, IBUPROFEN, FOLIC ACID, METHOTREXATE, ALESSE, SLOW FE, NAPROXEN. Patient recovered.
Visudyne Side Effects Report #5306972-5
Physician from UNITED STATES reported VISUDYNE problem on Apr 03, 2007. Male patient, 81 years of age, weighting 194.0 lb, was treated with VISUDYNE. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, retinal disorder, vision blurred, visual acuity reduced, . VISUDYNE dosage: 13.2 MG DAILY IV. During the same period patient was treated with AVASTIN. Patient recovered.
Amnesteem Side Effects Report #5280892-7
AMNESTEEM problem was reported by a Health Professional from UNITED STATES on Jan 26, 2007. Female patient, 32 years of age, weighting 127.0 lb, was diagnosed with acne and was treated with AMNESTEEM. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, suicidal ideation, . AMNESTEEM dosage: 20MG, TID, PO. During the same period patient was treated with MEDROXYPROGESTERONE. Patient recovered.
Omniscan Side Effects Report #5657848-5
Consumer or non-health professional from SWEDEN reported OMNISCAN problem on Feb 25, 2008. Female patient, 48 years of age, was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: nephrogenic systemic fibrosis, refusal of treatment by patient, . OMNISCAN dosage: unknown. During the same period patient was treated with SACCHARATED IRON OXIDE, FOLACIN, POLYSTYRENE SULFONATE, CYANOCOBALAMIN, PREDNISOLONE, AMINESS, TRANDATE, ALFACALCIDOL. Patient recovered.
Ceftriaxone Side Effects Report #5679987-5
CEFTRIAXONE problem was reported by a Health Professional from UNITED STATES on Mar 25, 2008. Male patient, 74 years of age, weighting 192.0 lb, was diagnosed with osteomyelitis and was treated with CEFTRIAXONE. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, urticaria, . CEFTRIAXONE dosage: unknown. During the same period patient was treated with VANCOMYCIN. Patient recovered.
Orencia Side Effects Report #5636755-8
Physician from UNITED STATES reported ORENCIA problem on Feb 19, 2008. Female patient, 65 years of age, was diagnosed with rheumatoid arthritis and was treated with ORENCIA. After drug was administered, patient experienced the following problems/side effects: convulsion, refusal of treatment by patient, . ORENCIA dosage: unknown. During the same period patient was treated with METHOTREXATE, BONIVA. Patient recovered.
Avonex Side Effects Report #5637901-2
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 11, 2008. Male patient was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: cardiac operation, refusal of treatment by patient, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Rogaine Side Effects Report #5590324-7
Consumer or non-health professional from UNITED STATES reported ROGAINE problem on Dec 31, 2007. Male patient, 21 years of age, weighting 168.0 lb, was diagnosed with alopecia, acne and was treated with ROGAINE. After drug was administered, patient experienced the following problems/side effects: petit mal epilepsy, refusal of treatment by patient, . ROGAINE dosage: unknown. During the same period patient was treated with ACCUTANE. Patient recovered.
Rogaine Side Effects Report #5590326-0
ROGAINE problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 31, 2007. Male patient, 21 years of age, weighting 168.0 lb, was diagnosed with alopecia, acne and was treated with ROGAINE. After drug was administered, patient experienced the following problems/side effects: petit mal epilepsy, refusal of treatment by patient, . ROGAINE dosage: unknown. During the same period patient was treated with ACCUTANE. Patient recovered.
Chantix Side Effects Report #5604547-1
Pharmacist from UNITED STATES reported CHANTIX problem on Jan 24, 2008. Male patient, 70 years of age, weighting 231.5 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: chest pain, refusal of treatment by patient, suicide attempt, unresponsive to stimuli, . CHANTIX dosage: unknown. Patient was hospitalized. Patient recovered.
Natalizumab Side Effects Report #5543178-9
NATALIZUMAB problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 27, 2007. Female patient, 51 years of age, weighting 170.0 lb, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia, refusal of treatment by patient, somnolence, . NATALIZUMAB dosage: 300 MG;QM;IV. Patient was hospitalized. Patient recovered.
Novoseven Side Effects Report #5545448-7
Physician from ISRAEL reported NOVOSEVEN problem on Nov 29, 2007. Female patient was diagnosed with haemorrhage and was treated with NOVOSEVEN. After drug was administered, patient experienced the following problems/side effects: gastritis haemorrhagic, refusal of treatment by patient, . NOVOSEVEN dosage: 7.2 MG, UNK. During the same period patient was treated with BLOOD CELLS. Patient was hospitalized. Patient died on 10/18/2007.
Clozapine Side Effects Report #5554924-2
CLOZAPINE problem was reported by a Physician from UNITED STATES on Nov 26, 2007. Male patient, 31 years of age, weighting 180.0 lb, was diagnosed with schizophrenia and was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: brugada syndrome, refusal of treatment by patient, . CLOZAPINE dosage: 300 MG (300 MG, 1 IN 1 D), ORAL. During the same period patient was treated with BENZTROPINE MESYLATE, BACTRIM. Patient recovered.
Temodar Side Effects Report #5577711-8
Physician from UNITED STATES reported TEMODAR problem on Dec 20, 2007. Male patient, 53 years of age, weighting 250.0 lb, was diagnosed with glioblastoma multiforme and was treated with TEMODAR. After drug was administered, patient experienced the following problems/side effects: pulmonary embolism, refusal of treatment by patient, . TEMODAR dosage: QD; PO; 3500 MG; PO. During the same period patient was treated with DECADRON, LEXAPRO, NEXIUM, VICODIN, WELLBUTRIN, XANAX. Patient died on 12/17/2007.
Vancomycin Side Effects Report #5582920-8
VANCOMYCIN HYDROCHLORIDE problem was reported by a Pharmacist from CANADA on Dec 13, 2007. Male patient, 79 years of age, weighting 165.3 lb, was diagnosed with arterial graft, graft infection, coronary artery disease and was treated with VANCOMYCIN HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, renal failure acute, . VANCOMYCIN HYDROCHLORIDE dosage: unknown. During the same period patient was treated with VANCOMYCIN HYDROCHLORIDE, RAMIPRIL, COUMADIN, ATORVASTATIN CALCIUM, METOPROLOL TARTRATE, FUROSEMIDE, CIPRO, CLOPIDOGREL. Patient was hospitalized. Patient recovered.
Insulin Side Effects Report #5509711-8
Health Professional from LATVIA reported INSULIN GLARGINE problem on Nov 05, 2007. Female patient, 52 years of age, was diagnosed with diabetes mellitus, hypothyroidism, hypertension and was treated with INSULIN GLARGINE. After drug was administered, patient experienced the following problems/side effects: cardiac failure, refusal of treatment by patient, weight increased, . INSULIN GLARGINE dosage: unknown. During the same period patient was treated with OPTIPEN, LEVOTHYROXINE, PERINDOPRIL, AMLODIPINE, THIAZIDE, ASPIRIN, METFORMIN. Patient recovered.
Provigil Side Effects Report #5527190-1
PROVIGIL problem was reported by a Health Professional from UNITED STATES on Nov 13, 2007. Female patient, 25 years of age, was treated with PROVIGIL. After drug was administered, patient experienced the following problems/side effects: incorrect dose administered, refusal of treatment by patient, suicide attempt, . PROVIGIL dosage: 200 MG ONCE ORAL. Patient recovered.
Mirtazapine Side Effects Report #5528725-5
Health Professional from UNITED STATES reported MIRTAZAPINE problem on Nov 19, 2007. Male patient, 40 years of age, weighting 183.6 lb, was diagnosed with depression and was treated with MIRTAZAPINE. After drug was administered, patient experienced the following problems/side effects: acute myocardial infarction, refusal of treatment by patient, tricuspid valve incompetence, . MIRTAZAPINE dosage: 15 MG BW ORAL, ONCE PER 4 DAYS. Patient was hospitalized and became disabled. Patient recovered.
Cap Side Effects Report #5532344-4
CAP VORINOSTAT UNK problem was reported by a Physician from UNITED STATES on Nov 26, 2007. Female patient, 57 years of age, weighting 166.0 lb, was diagnosed with non-small cell lung cancer and was treated with CAP VORINOSTAT UNK. After drug was administered, patient experienced the following problems/side effects: dermatitis exfoliative, refusal of treatment by patient, . CAP VORINOSTAT UNK dosage: 300 MG/DAILY/PO. During the same period patient was treated with TARCEVA, BACTRIN DS, BENADRYL, COMPAZINE, FLOVENT, IMODIUM, LIPITOR, MAALOX. Patient recovered.
Digoxin Side Effects Report #5484868-6
Physician from PORTUGAL reported DIGOXIN problem on Sept 25, 2007. Male patient, 79 years of age, was treated with DIGOXIN. After drug was administered, patient experienced the following problems/side effects: intentional overdose, refusal of treatment by patient, renal failure, rhabdomyolysis, stupor, suicide attempt, therapeutic agent toxicity, . DIGOXIN dosage: 30 MG/ SINGLE DOSE. Patient was hospitalized. Patient recovered.
Atorvastatin Side Effects Report #5489890-1
ATORVASTATIN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Sept 17, 2007. Female patient, weighting 165.3 lb, was diagnosed with coronary artery disease and was treated with ATORVASTATIN. After drug was administered, patient experienced the following problems/side effects: depressed mood, refusal of treatment by patient, suicidal ideation, . ATORVASTATIN dosage: unknown. During the same period patient was treated with CARVEDILOL, FUROSEMIDE, LOSARTAN POTASSIUM, ARGININE, CITRULLINE, ADCAL, CLOPIDOGREL. Patient recovered.
Rebif Side Effects Report #5445727-8
Physician from UNITED STATES reported REBIF problem on Aug 23, 2007. Female patient, 40 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: hepatic failure, refusal of treatment by patient, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.
Renagel Side Effects Report #5448439-X
RENAGEL problem was reported by a Health Professional from UNITED STATES on Aug 22, 2007. Male patient, weighting 156.0 lb, was diagnosed with hyperphosphataemia and was treated with RENAGEL. After drug was administered, patient experienced the following problems/side effects: malignant neoplasm progression, refusal of treatment by patient, . RENAGEL dosage: unknown. Patient died on 11/30/2006.
Minocycline Side Effects Report #5413788-8
Physician from GERMANY reported MINOCYCLINE problem on July 20, 2007. Male patient, 30 years of age, was treated with MINOCYCLINE. After drug was administered, patient experienced the following problems/side effects: acute febrile neutrophilic dermatosis, refusal of treatment by patient, . MINOCYCLINE dosage: 300 MG, QD. During the same period patient was treated with TETRACYCLINE, DOXYCYCLINE. Patient recovered.
Fluphenazine Side Effects Report #5420882-4
FLUPHENAZINE problem was reported by a Pharmacist from UNITED STATES on Aug 17, 2007. Male patient, weighting 173.3 lb, was diagnosed with schizophrenia and was treated with FLUPHENAZINE. After drug was administered, patient experienced the following problems/side effects: paranoia, refusal of treatment by patient, trismus, . FLUPHENAZINE dosage: 15 MG/DAY. Patient recovered.
Warfarin Side Effects Report #5427490-X
Consumer or non-health professional from MEXICO reported WARFARIN problem on Aug 24, 2007. Female patient, 62 years of age, weighting 116.8 lb, was diagnosed with pulmonary embolism and was treated with WARFARIN. After drug was administered, patient experienced the following problems/side effects: chest pain, refusal of treatment by patient, . WARFARIN dosage: unknown. During the same period patient was treated with ENOXAPARIN, ENALAPRIL, DIGOXIN, SPIRONOLACTONE. Patient died on 07/21/2007.
Byetta Side Effects Report #5377170-4
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on June 21, 2007. Male patient, 60 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: pyrexia, refusal of treatment by patient, vomiting, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN, AMARYL, COUMADIN, DIGITEK, COREG, AVANDIA, GLIMEPIRIDE. Patient recovered.
Prednisolone Side Effects Report #5386739-2
Consumer or non-health professional from UNITED KINGDOM reported PREDNISOLONE PHOSPHATE problem on July 03, 2007. Female patient, 85 years of age, was diagnosed with anaemia haemolytic autoimmune and was treated with PREDNISOLONE PHOSPHATE. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, splenectomy, . PREDNISOLONE PHOSPHATE dosage: unknown. During the same period patient was treated with PREDNISOLONE PHOSPHATE, CYCLOPHOSPHAMIDE, RITUXIMAB, VINCRISTINE. Patient died.
Oxycontin Side Effects Report #5395585-5
OXYCONTIN problem was reported by a Consumer or non-health professional from on May 31, 2007. Male patient, weighting 220.5 lb, was diagnosed with pain management and was treated with OXYCONTIN. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, renal failure acute, . OXYCONTIN dosage: unknown. During the same period patient was treated with UNIPHYL, IMDUR, ZESTRIL, LASIX, DOPAMINE, LIDOCAINE, VALIUM, LOPRESSOR. Patient died.
Prednisolone Side Effects Report #5400485-8
Consumer or non-health professional from UNITED KINGDOM reported PREDNISOLONE PHOSPHATE problem on July 16, 2007. Female patient, 85 years of age, was diagnosed with anaemia haemolytic autoimmune and was treated with PREDNISOLONE PHOSPHATE. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, . PREDNISOLONE PHOSPHATE dosage: unknown. During the same period patient was treated with PREDNISOLONE PHOSPHATE, CYCLOPHOSPHAMIDE, RITUXIMAB, VINCRISTINE, IMMUNE GLOBULIN. Patient died.
Erlotinib Side Effects Report #5402032-3
ERLOTINIB problem was reported by a Physician from SWITZERLAND on July 12, 2007. Male patient, 63 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: refusal of treatment by patient, . ERLOTINIB dosage: 150 MG (QD), ORAL. During the same period patient was treated with BEVACIZUMAB, METFORMIN, ACETAMINOPHEN, CITALOPRAM HYDROBROMIDE. Patient died on 07/04/2007.
Byetta Side Effects Report #5377170-4
Consumer or non-health professional from UNITED STATES reported BYETTA problem on June 21, 2007. Male patient, 60 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: pyrexia, refusal of treatment by patient, vomiting, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN, AMARYL, COUMADIN, DIGITEK, COREG, AVANDIA, GLIMEPIRIDE. Patient recovered.
Prednisolone Side Effects Report #5386739-2
PREDNISOLONE PHOSPHATE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on July 03, 2007. Female patient, 85 years of age, was diagnosed with anaemia haemolytic autoimmune and was treated with PREDNISOLONE PHOSPHATE. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, splenectomy, . PREDNISOLONE PHOSPHATE dosage: unknown. During the same period patient was treated with PREDNISOLONE PHOSPHATE, CYCLOPHOSPHAMIDE, RITUXIMAB, VINCRISTINE. Patient died.
Oxycontin Side Effects Report #5395585-5
Consumer or non-health professional from reported OXYCONTIN problem on May 31, 2007. Male patient, weighting 220.5 lb, was diagnosed with pain management and was treated with OXYCONTIN. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, renal failure acute, . OXYCONTIN dosage: unknown. During the same period patient was treated with UNIPHYL, IMDUR, ZESTRIL, LASIX, DOPAMINE, LIDOCAINE, VALIUM, LOPRESSOR. Patient died.
Prednisolone Side Effects Report #5400485-8
PREDNISOLONE PHOSPHATE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on July 16, 2007. Female patient, 85 years of age, was diagnosed with anaemia haemolytic autoimmune and was treated with PREDNISOLONE PHOSPHATE. After drug was administered, patient experienced the following problems/side effects: refusal of treatment by patient, . PREDNISOLONE PHOSPHATE dosage: unknown. During the same period patient was treated with PREDNISOLONE PHOSPHATE, CYCLOPHOSPHAMIDE, RITUXIMAB, VINCRISTINE, IMMUNE GLOBULIN. Patient died.
Erlotinib Side Effects Report #5402032-3
Physician from SWITZERLAND reported ERLOTINIB problem on July 12, 2007. Male patient, 63 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: refusal of treatment by patient, . ERLOTINIB dosage: 150 MG (QD), ORAL. During the same period patient was treated with BEVACIZUMAB, METFORMIN, ACETAMINOPHEN, CITALOPRAM HYDROBROMIDE. Patient died on 07/04/2007.
Pegetron Side Effects Report #5775322-2
PEGETRON problem was reported by a Physician from CANADA on June 03, 2008. Male patient was diagnosed with hepatitis c and was treated with PEGETRON. After drug was administered, patient experienced the following problems/side effects: hypoglycaemia, refusal of treatment by patient, . PEGETRON dosage: ; SC, 1000 MG; QD; PO. Patient recovered.
Nexium Side Effects Report #5788991-8
Pharmacist from UNITED STATES reported NEXIUM problem on June 25, 2008. Female patient, 86 years of age, was diagnosed with gastrooesophageal reflux disease and was treated with NEXIUM. After drug was administered, patient experienced the following problems/side effects: liver disorder, refusal of treatment by patient, thrombocytopenia, . NEXIUM dosage: ORAL;40.0 MILLIGRAM. During the same period patient was treated with CARVEDIOLOL, ALLOPURINOL, COLACE, FUROSEMIDE, ASCORBIC ACID, FERROUS SULPHATE, BRIMONIDINE TARTRATE. Patient recovered.
Vesicare Side Effects Report #5749142-9
VESICARE problem was reported by a Physician from JAPAN on May 13, 2008. Male patient, 75 years of age, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: dizziness, refusal of treatment by patient, renal failure, . VESICARE dosage: 5 MG, UID/QD, ORAL; 2.5 MG, UID/QD, ORAL. During the same period patient was treated with FLIVAS. Patient recovered.
Bevacizumab Side Effects Report #5755242-X
Health Professional from UNITED STATES reported BEVACIZUMAB problem on May 29, 2008. Female patient, weighting 104.7 lb, was diagnosed with renal cell carcinoma and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: abdominal pain, refusal of treatment by patient, . BEVACIZUMAB dosage: 713 MG Q/ 21 DAYS IV. During the same period patient was treated with BERTOZOMIB. Patient was hospitalized. Patient recovered.