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ASCITES side effect

What is ASCITES ?
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Drugs associated with ASCITES

ABRAXANE  ACCUTANE  ACETAMINOPHEN  ACIPHEX  ACTOS  ADEFOVIR  ALDACTONE  ALDURAZYME  ALEMTUZUMAB  ALIMTA  ALKERAN  ALOXI  AMBISOME  AMEVIVE  AMIODARONE  AMLODIPINE  AMOXICILLIN  ARANESP  ARAVA  AREDIA  ARICEPT  ARIMIDEX  ARIXTRA  AROMASIN  AROPAX  ASPIRIN  ATAZANAVIR  AUGMENTIN  AVANDAMET  AVANDIA  AVASTIN  AVELOX  AVONEX  AZATHIOPRINE  BARACLUDE  BASILIXIMAB  BELOC  BENDAMUSTINE  BETAMETHASONE  BETASERON  BEVACIZUMAB  BISOPROLOL  BLEOMYCIN  BORTEZOMIB  BUSULFAN  BUSULFEX  BUSULPHAN  BYETTA  CAELYX  CAMPATH  CAMPRAL  CAMPTOSAR  CANCIDAS  CAP  CAPECITABINE  CARBAMAZEPINE  CARBATROL  CARBOPLATIN  CEREZYME  CETROTIDE  CETUXIMAB  CHANTIX  CHORIONIC  CILOSTAZOL  CISPLATIN  CLAFORAN  CLINORIL  CLOFARABINE  CLOLAR  CLOMIPHENE  CLOZAPINE  COMBIVIR  CORDARONE  COREG  CRESTOR  CRIXIVAN  CUBICIN  CYCLOPHOSPHAMIDE CYCLOSPORINE  CYMBALTA  CYTARABINE  CYTOVENE  DACLIZUMAB  DASATINIB  DAUNOMYCIN  DECADRON  DECITABINE  DEXAMETHASONE  DIANEAL  DICLOFENAC  DIDANOSINE  DIGOXIN  DIOVAN  DOCETAXEL  DOXORUBICIN  DROSPIRENONE  EFAVIRENZ  ELISOR  EMANTONE  EMSELEX  EMTRICITABINE  ENALAPRIL  ENANTONE  ENBREL  ENTECAVIR  EPIVIR  EPZICOM  ERBITUX  ERGENYL  ERLOTINIB  EVISTA  EXJADE  EXTRANEAL  FEMARA  FERTINORM  FLAGYL  FLUDARA  FLUDARABINE  FLUOROURACIL  FOLLICLE  FOLLITROPIN  FORTEO  FOSAMAX  GABAPEN  GABAPENTIN  GEMCITABINE  GEMZAR  GLEEVEC  GLIVEC  GLYBURIDE  GONAL  GOODYS  HEPARIN  HEPSERA  HUMIRA  HUMULIN  HYCAMTIN  HYDREA  IBUPROFEN  IMATINIB  INDOMETHACIN  INJ  INTRON  IRBESARTAN  IRESSA  IRINOTECAN  ISENTRESS  ISONIAZID  ISOPTIN  ISOVUE  ITRACONAZOLE  IXEMPRA  JANUVIA  KALETRA  KETEK  KIVEXA  LAMIVUDINE  LANSAP  LANTUS  LANVIS  LAPATINIB  LASIX  LENALIDOMIDE  LETAIRIS  LEUPROLIDE  LEVAQUIN  LEVEMIR  LIDOCAINE  LIORESAL  LISINOPRIL  LISPRO  LITHIUM  LOGYNON  LOPERAMIDE  LOPINAVIR  LUVOX  MABTHERA  MAGNEVIST  MALARONE  MEGACE  MELPHALAN  MENOTROPHIN  MENOTROPINS  MEROPENEM  METHADONE  METHOTREXATE  METOPROLOL  MIFEPRISTONE  MINOCYCLINE  MIRENA  MODACIN  MYCOPHENOLATE  MYLANTA  MYLOTARG  MYOZYME  NAMENDA  NAPROSYN  NATEGLINIDE  NELFINAVIR  NEORAL  NEULASTA  NEURONTIN  NEVIRAPINE  NEXAVAR  NILOTINIB  NITRIC  NOLVADEX  NORVIR  OCTREOTIDE  OLANZAPINE  ORFADIN  ORTHOCLONE  OVIDREL  OXALIPLATIN  OXANDRIN  OXYCODONE  OXYCONTIN  PAXIL  PEGASYS  PENTOSTATIN  PERINDOPRIL  PERMAX  PHENYTOIN  PHYTONADIONE  PLETAL  PRAVIDEL  PREDNISOLONE  PREDNISONE  PREDONINE  PRIMAXIN  PROBENECID  PROGRAF  PROTONIX  RAPAMUNE  REGLAN  REMICADE  RENAGEL  REVLIMID  REYATAZ  RIBASPHERE  RIBAVIRIN  RITONAVIR  RITUXAN  ROCEPHIN  ROFERON  SANDIMMUNE  SANDOSTATIN  SEBIVO  SEGURIL  SEREVENT  SEVORANE  SILDENAFIL  SIMETHICONE  SIROLIMUS  SORAFENIB  SPIRONOLACTONE  SULFAMETHOXAZOLE SUSTIVA  SUTENT  SYMLIN  TACROLIMUS  TARCEVA  TAXOL  TAXOTERE  TEGRETOL  TELBIVUDINE  TEMODAL  TEMODAR  THALIDOMIDE  THALOMID  THIOGUANINE  THYMOGLOBULIN  TIPRANAVIR  TOPAMAX  TOPOTECAN  TOPROL  TOREM  TRACLEER  TRELSTAR  TRISENOX  TRUVADA  TYKERB  VALCYTE  VALTREX  VELCADE  VESICARE  VIDEX  VINCRISTINE  VIRACEPT  VIRAFERONPEG  VIRAMUNE  VISIPAQUE  VORINOSTAT  WINRHO  XELODA  XYREM  ZEFIX  ZELNORM  ZEVALIN  ZOLEDRONIC  ZOMETA  ZONISAMIDE  ZOVIRAX  ZYBAN  


Aromasin Side Effects Report #5649572-X
Physician from GERMANY reported AROMASIN problem on Feb 21, 2008. Female patient, weighting 125.7 lb, was diagnosed with breast cancer metastatic, bone pain and was treated with AROMASIN. After drug was administered, patient experienced the following problems/side effects: ascites, hepatic failure, nasopharyngitis, neoplasm progression, . AROMASIN dosage: unknown. During the same period patient was treated with KATADOLON, PAMIDRONATE DI, ZOMETA, ARIMIDEX. Patient was hospitalized. Patient died.

Arimidex Side Effects Report #5653615-7
ARIMIDEX problem was reported by a Consumer or non-health professional from BRAZIL on Feb 27, 2008. Female patient, 36 years of age, weighting 136.7 lb, was diagnosed with breast cancer, bone density decreased and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: ascites, chest pain, dyspnoea, pericardial effusion, . ARIMIDEX dosage: unknown. During the same period patient was treated with XELODA, AREDIA. Patient recovered.

Gleevec Side Effects Report #5654685-2
Health Professional from UNITED KINGDOM reported GLEEVEC problem on Feb 22, 2008. Female patient, 43 years of age, was diagnosed with fluid retention, analgesia and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: ascites, blood potassium decreased, diarrhoea, disease progression, haematemesis, neutropenia, oedema, vomiting, . GLEEVEC dosage: unknown. During the same period patient was treated with SUNITINIB MALATE, FRUSEMIDE, OXYNORM, SPIRONOLACTONE. Patient was hospitalized. Patient recovered.

Avastin Side Effects Report #5661452-2
AVASTIN problem was reported by a Physician from UNITED KINGDOM on Feb 27, 2008. Male patient, weighting 132.3 lb, was diagnosed with colon cancer metastatic and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: ascites, gastrointestinal perforation, neoplasm progression, oedema, . AVASTIN dosage: unknown. During the same period patient was treated with CAPECITABINE, OXALIPLATIN. Patient was hospitalized. Patient recovered.


Prograf Side Effects Report #5661589-8
Physician from SWITZERLAND reported PROGRAF problem on Mar 07, 2008. Female patient, child 8 years of age, was diagnosed with liver transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: ascites, blood pressure fluctuation, capillary leak syndrome, cardiac arrest, haemodialysis, haemodynamic instability, hypertension, pericardial drainage, . PROGRAF dosage: unknown. During the same period patient was treated with PROSTIN E, HEPARIN, ZINACEF, GARAMYCIN, AMPHO, MORPHINE ELIXIR, CYMEVENE, NIPRIDE. Patient died on 08/09/2007.

Cisplatin Side Effects Report #5661664-8
CISPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 10, 2008. Male patient, 52 years of age, was diagnosed with gastric cancer, nausea, vomiting, pain and was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: ascites, blood creatinine increased, dehydration, respiratory failure, respiratory tract infection, sepsis, . CISPLATIN dosage: unknown. During the same period patient was treated with GRAVOL, KETOROLAC TROMETHAMINE, DEXAMETHASONE. Patient was hospitalized. Patient died on 07/16/2006.

Crestor Side Effects Report #5661761-7
Physician from JAPAN reported CRESTOR problem on Mar 06, 2008. Female patient, 58 years of age, was diagnosed with hypercholesterolaemia and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: ascites, oedema, pleural effusion, . CRESTOR dosage: unknown. Patient recovered.

Velcade Side Effects Report #5663660-3
VELCADE problem was reported by a Physician from NETHERLANDS on Feb 27, 2008. Male patient, 64 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: ascites, atelectasis, gastroenteritis, glomerulonephritis rapidly progressive, pleural effusion, . VELCADE dosage: 2.60 MG, INTRAVENOUS. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5664036-5
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on Mar 12, 2008. Male patient, 52 years of age, was diagnosed with gastric cancer, nausea, vomiting, pain and was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: ascites, blood creatinine increased, dehydration, respiratory failure, respiratory tract infection, sepsis, . CISPLATIN dosage: unknown. During the same period patient was treated with GRAVOL, KETOROLAC TROMETHAMINE, DEXAMETHASONE. Patient was hospitalized. Patient died on 07/16/2006.


Tacrolimus Side Effects Report #5671561-X
TACROLIMUS problem was reported by a Physician from TURKEY on Feb 07, 2008. Male patient, 48 years of age, was diagnosed with liver transplant and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: ascites, blood bilirubin increased, coagulopathy, coma, jaundice, kaposi's sarcoma, multi-organ failure, oedema peripheral, pleural effusion, . TACROLIMUS dosage: unknown. During the same period patient was treated with PREDNISOLONE, HEPATITIS B IMMUNE GLOBULIN, LAMIVUDINE. Patient died.

Extraneal Side Effects Report #5671763-2
Physician from FRANCE reported EXTRANEAL problem on Mar 12, 2008. Female patient, 60 years of age, was diagnosed with peritoneal dialysis and was treated with EXTRANEAL. After drug was administered, patient experienced the following problems/side effects: ascites, cytomegalovirus infection, diarrhoea, dyspepsia, intestinal obstruction, nausea, sclerosing encapsulating peritonitis, vomiting, weight decreased, . EXTRANEAL dosage: unknown. During the same period patient was treated with DIANEAL, PHYSIOSOL IN PLASTIC CONTAINER. Patient was hospitalized. Patient recovered.

Emselex Side Effects Report #5672638-5
EMSELEX EXTENDED RELEASE problem was reported by a Pharmacist from CYPRUS on Mar 13, 2008. Male patient was diagnosed with urinary incontinence and was treated with EMSELEX EXTENDED RELEASE. After drug was administered, patient experienced the following problems/side effects: ascites, constipation, urinary retention, . EMSELEX EXTENDED RELEASE dosage: 15MG. Patient was hospitalized. Patient recovered.

Emselex Side Effects Report #5673530-2
Pharmacist from CYPRUS reported EMSELEX EXTENDED RELEASE problem on Mar 13, 2008. Male patient was diagnosed with urinary incontinence and was treated with EMSELEX EXTENDED RELEASE. After drug was administered, patient experienced the following problems/side effects: ascites, constipation, urinary retention, . EMSELEX EXTENDED RELEASE dosage: 15MG. Patient was hospitalized. Patient recovered.

Bevacizumab Side Effects Report #5673798-2
BEVACIZUMAB problem was reported by a Physician from UNITED STATES on Mar 11, 2008. Female patient, 81 years of age, was diagnosed with colon cancer and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: ascites, portal hypertension, . BEVACIZUMAB dosage: 5 MG/KG, Q2W. During the same period patient was treated with PEGFILGRASTIM, FOLINIC ACID, FLUOROURACIL, OXALIPLATIN, CETUXIMAB. Patient recovered.


Emselex Side Effects Report #5674151-8
Pharmacist from CYPRUS reported EMSELEX EXTENDED RELEASE problem on Mar 13, 2008. Male patient was diagnosed with urinary incontinence and was treated with EMSELEX EXTENDED RELEASE. After drug was administered, patient experienced the following problems/side effects: ascites, constipation, urinary retention, . EMSELEX EXTENDED RELEASE dosage: 15MG. Patient was hospitalized. Patient recovered.

Neoral Side Effects Report #5674174-9
NEORAL problem was reported by a Physician from SPAIN on Mar 13, 2008. Female patient, 64 years of age, weighting 165.3 lb, was diagnosed with liver transplant and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: ascites, asthenia, autoantibody positive, cholestasis, disease progression, encephalopathy, fibrosis, graft dysfunction, . NEORAL dosage: 300 MG, BID. During the same period patient was treated with INTERFERON GAMMA. Patient was hospitalized. Patient recovered.

Toprol Side Effects Report #5674784-9
Physician from UNITED STATES reported TOPROL problem on Mar 18, 2008. Female patient, 63 years of age, weighting 232.6 lb, was diagnosed with arteriosclerosis and was treated with TOPROL. After drug was administered, patient experienced the following problems/side effects: ascites, . TOPROL dosage: unknown. During the same period patient was treated with ISOSORBIDE DINITRATE, LASIX, SPIRONOLACTONE, MAGOXIDE, DIGOXIN, ZOCOR, COUMADIN, ESTROPIPATE. Patient recovered.

Sildenafil Side Effects Report #5676216-3
SILDENAFIL problem was reported by a Consumer or non-health professional from FRANCE on Mar 10, 2008. Female patient, weighting 119.0 lb, was diagnosed with pulmonary hypertension and was treated with SILDENAFIL. After drug was administered, patient experienced the following problems/side effects: ascites, dyspnoea, . SILDENAFIL dosage: unknown. Patient was hospitalized. Patient recovered.

Methotrexate Side Effects Report #5676271-0
Consumer or non-health professional from reported METHOTREXATE problem on Mar 18, 2008. Female patient, 62 years of age, was diagnosed with systemic lupus erythematosus and was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: ascites, epstein-barr virus test positive, hepatitis acute, . METHOTREXATE dosage: unknown. During the same period patient was treated with PREDNISOLONE, FOLATES. Patient was hospitalized. Patient recovered.


Acetaminophen Side Effects Report #5678682-6
ACETAMINOPHEN AND CODEINE PHOSPHATE problem was reported by a Health Professional from FRANCE on Mar 10, 2008. Male patient, 60 years of age, was diagnosed with pain and was treated with ACETAMINOPHEN AND CODEINE PHOSPHATE. After drug was administered, patient experienced the following problems/side effects: ascites, hepatic cirrhosis, hepatotoxicity, incorrect dose administered, portal hypertension, prothrombin time prolonged, thrombocytopenia, . ACETAMINOPHEN AND CODEINE PHOSPHATE dosage: unknown. Patient recovered.

Ketek Side Effects Report #5678931-4
Consumer or non-health professional from UNITED STATES reported KETEK problem on Mar 11, 2008. Female patient was diagnosed with pneumonia and was treated with KETEK. After drug was administered, patient experienced the following problems/side effects: ascites, aspartate aminotransferase increased, injury, . KETEK dosage: unknown. Patient died.

Ketek Side Effects Report #5678935-1
KETEK problem was reported by a Physician from UNITED STATES on Mar 11, 2008. Female patient was diagnosed with upper respiratory tract infection, bronchitis, cough, nasopharyngitis and was treated with KETEK. After drug was administered, patient experienced the following problems/side effects: ascites, biliary cirrhosis primary, blood albumin decreased, eosinophil count increased, iron deficiency anaemia, liver disorder, pleural effusion, splenomegaly, . KETEK dosage: unknown. During the same period patient was treated with ERYTHROMYCIN, METHORPHAN, HYDROCODONE, TEQUIN. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5679844-4
Physician from SWITZERLAND reported PROGRAF problem on Mar 07, 2008. Female patient, child 8 years of age, was diagnosed with liver transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: ascites, capillary leak syndrome, cardiac arrest, cardiovascular disorder, haemodialysis, myocardial ischaemia, pericardial effusion, pleural effusion, . PROGRAF dosage: 2 MG, ORAL. During the same period patient was treated with SIMULECT, PROSTIN E, HEPARIN, ZINACEF, GARAMYCIN, AMPHO MORONAL, MORPHINE, GANCICLOVIR. Patient died on 08/09/2007.

Drospirenone Side Effects Report #5680304-5
DROSPIRENONE AND ETHINYL ESTRADIOL problem was reported by a Health Professional from GERMANY on Mar 13, 2008. Female patient, 16 years of age, was diagnosed with oral contraception and was treated with DROSPIRENONE AND ETHINYL ESTRADIOL. After drug was administered, patient experienced the following problems/side effects: ascites, . DROSPIRENONE AND ETHINYL ESTRADIOL dosage: unknown. Patient was hospitalized. Patient recovered.

Lidocaine Side Effects Report #5683526-2
Consumer or non-health professional from GERMANY reported LIDOCAINE problem on Mar 20, 2008. Female patient, 82 years of age, weighting 143.3 lb, was diagnosed with post herpetic neuralgia and was treated with LIDOCAINE. After drug was administered, patient experienced the following problems/side effects: ascites, atrial fibrillation, carbohydrate antigen 125 increased, cardiac failure, colonic polyp, haemorrhoids, hepatic enzyme increased, ovarian neoplasm, rectal polyp, . LIDOCAINE dosage: unknown. During the same period patient was treated with PREGABALIN, MARIVARIN, ULTOP, LANITOP, LEKADOL. Patient was hospitalized. Patient recovered.

Orfadin Side Effects Report #5683820-5
ORFADIN problem was reported by a Health Professional from KOREA, REPUBLIC OF on Mar 11, 2008. Female patient, weighting 14.33 lb, was diagnosed with tyrosinaemia and was treated with ORFADIN. After drug was administered, patient experienced the following problems/side effects: ascites, disseminated intravascular coagulation, gastrointestinal haemorrhage, hypoalbuminaemia, hypovolaemic shock, peritonitis bacterial, sepsis, . ORFADIN dosage: 8 MILLIGRAM A DAY ORAL. During the same period patient was treated with AMPICILLIN, FUROSEMIDE, CEFOTAXIME. Patient died.

Symlin Side Effects Report #5685105-X
Pharmacist from UNITED STATES reported SYMLIN problem on Mar 14, 2008. Female patient, weighting 300.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with SYMLIN. After drug was administered, patient experienced the following problems/side effects: ascites, livedo reticularis, right ventricular failure, weight increased, . SYMLIN dosage: unknown. During the same period patient was treated with ACTOS. Patient was hospitalized. Patient recovered.

Truvada Side Effects Report #5685363-1
TRUVADA problem was reported by a Pharmacist from FRANCE on Mar 25, 2008. Male patient, 42 years of age, weighting 88.18 lb, was diagnosed with hiv infection and was treated with TRUVADA. After drug was administered, patient experienced the following problems/side effects: ascites, cardiac failure, jaundice, oedema peripheral, pulmonary oedema, weight increased, . TRUVADA dosage: unknown. During the same period patient was treated with LOPINAVIR. Patient was hospitalized. Patient recovered.

Revlimid Side Effects Report #5688056-X
Health Professional from UNITED STATES reported REVLIMID problem on Mar 18, 2008. Female patient, 72 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: ascites, constipation, fatigue, haematocrit decreased, haemoglobin decreased, peritoneal haemorrhage, splenic haemorrhage, splenomegaly, vomiting, . REVLIMID dosage: 5 MG, 1 IN 2 D, ORAL. During the same period patient was treated with FOSAMAX, VALTREX, PRILOSEC, LOMOTIL. Patient was hospitalized. Patient recovered.

Ixempra Side Effects Report #5688801-3
IXEMPRA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 25, 2008. Female patient, 63 years of age, was diagnosed with breast cancer metastatic and was treated with IXEMPRA. After drug was administered, patient experienced the following problems/side effects: ascites, dehydration, diarrhoea, febrile neutropenia, ileus, pancytopenia, sepsis, stomatitis, . IXEMPRA dosage: unknown. During the same period patient was treated with ZANTAC, BENADRYL, DECADRON. Patient was hospitalized. Patient recovered.

Revlimid Side Effects Report #5689353-4
Physician from UNITED STATES reported REVLIMID problem on Mar 19, 2008. Male patient, 57 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: ascites, brain natriuretic peptide increased, cardiac failure high output, disease recurrence, liver disorder, oedema peripheral, plasmacytoma, right ventricular systolic pressure increased, tricuspid valve incompetence, . REVLIMID dosage: unknown. During the same period patient was treated with DEXAMETHASONE. Patient recovered.

Erlotinib Side Effects Report #5691937-4
ERLOTINIB problem was reported by a Health Professional from JAPAN on Feb 12, 2008. Male patient was diagnosed with pancreatic carcinoma and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: ascites, . ERLOTINIB dosage: (100 MG,QD),ORAL. During the same period patient was treated with GEMCITABINE. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5615323-8
Physician from JAPAN reported ARIXTRA problem on Feb 01, 2008. Female patient was diagnosed with fracture and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: ascites, pleural effusion, . ARIXTRA dosage: 2.5MG PER DAY. Patient recovered.

Gleevec Side Effects Report #5621818-3
GLEEVEC problem was reported by a Health Professional from UNITED KINGDOM on Jan 31, 2008. Female patient, 43 years of age, was diagnosed with fluid retention and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: ascites, blood potassium decreased, diarrhoea, haematemesis, neutropenia, oedema, vomiting, . GLEEVEC dosage: unknown. During the same period patient was treated with SUNITINIB MALATE, FUROSEMIDE, OXYNORM, SPIRONOLACTONE. Patient was hospitalized. Patient recovered.

Actos Side Effects Report #5622181-4
Consumer or non-health professional from UNITED KINGDOM reported ACTOS problem on Jan 23, 2008. Female patient, 63 years of age, was diagnosed with glycosylated haemoglobin increased and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: ascites, cardiac failure, crepitations, dyspnoea, fluid retention, hepatomegaly, oedema peripheral, rash, weight increased, . ACTOS dosage: 30 MG. During the same period patient was treated with INSULIN HUMALOG, LEVEMIR. Patient recovered.

Intron Side Effects Report #5623892-7
INTRON A problem was reported by a Physician from JAPAN on Jan 30, 2008. Female patient, 26 years of age, weighting 94.80 lb, was diagnosed with renal cell carcinoma and was treated with INTRON A. After drug was administered, patient experienced the following problems/side effects: ascites, aspiration pleural cavity abnormal, atelectasis, back pain, bile duct obstruction, disease progression, gastroenteritis radiation, jaundice cholestatic, malignant neoplasm progression, . INTRON A dosage: unknown. During the same period patient was treated with INTRON A, INTRON A, INTRON A, INTRON A, SORAFENIB. Patient was hospitalized. Patient recovered.

Avastin Side Effects Report #5624913-8
Physician from UNITED STATES reported AVASTIN problem on Feb 06, 2008. Female patient was diagnosed with breast cancer metastatic and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: ascites, . AVASTIN dosage: 10 MG/KG, Q2W. During the same period patient was treated with ABRAXANE. Patient recovered.

Arixtra Side Effects Report #5625760-3
ARIXTRA problem was reported by a Physician from JAPAN on Feb 05, 2008. Female patient was diagnosed with fracture and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: ascites, pleural effusion, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with INSULIN. Patient recovered.

Basiliximab Side Effects Report #5626009-8
Health Professional from FRANCE reported BASILIXIMAB problem on Feb 06, 2008. Male patient, 63 years of age, was diagnosed with renal transplant and was treated with BASILIXIMAB. After drug was administered, patient experienced the following problems/side effects: ascites, cardiac tamponade, chronic allograft nephropathy, complications of transplanted kidney, kidney transplant rejection, pericarditis, pleural effusion, primary effusion lymphoma, renal impairment, . BASILIXIMAB dosage: unknown. During the same period patient was treated with MYCOPHENOLATE MOFETIL, PREDNISONE, RAPAMYCIN, CYCLOSPORINE. Patient was hospitalized. Patient died.

Gleevec Side Effects Report #5626032-3
GLEEVEC problem was reported by a Physician from UNITED STATES on Feb 04, 2008. Female patient, weighting 116.0 lb, was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: ascites, atelectasis, dyspnoea, pericardial effusion, pleural effusion, pleurisy, . GLEEVEC dosage: 800 MG, QD. Patient recovered.

Heparin Side Effects Report #5627507-3
Consumer or non-health professional from UNITED STATES reported HEPARIN problem on Feb 15, 2008. Female patient, 52 years of age, weighting 168.0 lb, was diagnosed with coagulopathy and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: ascites, blood pressure increased, contusion, dyspnoea, electrocardiogram abnormal, heart rate abnormal, hypersensitivity, injection site bruising, oedema, . HEPARIN dosage: unknown. Patient was hospitalized. Patient recovered.

Intron Side Effects Report #5629916-5
INTRON A problem was reported by a Physician from JAPAN on Feb 07, 2008. Female patient, 26 years of age, weighting 94.80 lb, was diagnosed with renal cell carcinoma and was treated with INTRON A. After drug was administered, patient experienced the following problems/side effects: ascites, atelectasis, cholelithiasis, disease progression, gastroenteritis radiation, gastrointestinal hypermotility, jaundice cholestatic, melaena, metastases to lymph nodes, . INTRON A dosage: unknown. During the same period patient was treated with INTRON A, INTRON A, INTRON A, INTRON A, SORAFENIB. Patient was hospitalized. Patient recovered.

Arimidex Side Effects Report #5630763-9
Consumer or non-health professional from BRAZIL reported ARIMIDEX problem on Feb 13, 2008. Female patient, 36 years of age, weighting 136.7 lb, was diagnosed with breast cancer, bone density decreased and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: ascites, chest pain, dyspnoea, metastases to spine, pericardial effusion, pericardial effusion malignant, . ARIMIDEX dosage: unknown. During the same period patient was treated with XELODA, AREDIA. Patient recovered.

Amiodarone Side Effects Report #5631728-3
AMIODARONE problem was reported by a Consumer or non-health professional from TAIWAN, PROVINCE OF CHINA on Feb 08, 2008. Female patient, 72 years of age, was diagnosed with atrial fibrillation and was treated with AMIODARONE. After drug was administered, patient experienced the following problems/side effects: ascites, cerebral infarction, coma hepatic, hepatotoxicity, loss of consciousness, pyelonephritis acute, renal failure acute, . AMIODARONE dosage: unknown. During the same period patient was treated with VERA. Patient was hospitalized. Patient died.

Imatinib Side Effects Report #5631789-1
Physician from AUSTRALIA reported IMATINIB MESYLATE problem on Feb 11, 2008. Male patient, 62 years of age, was diagnosed with gastrointestinal stromal tumour and was treated with IMATINIB MESYLATE. After drug was administered, patient experienced the following problems/side effects: ascites, atelectasis, incisional drainage, lung consolidation, nausea, peritonitis, pleural effusion, vomiting, . IMATINIB MESYLATE dosage: 800MG. During the same period patient was treated with OXYCONTIN, MAXOLON, COLOXYL WITH SENNA, SUNITINIB MALATE, PERINDOPRIL, MOVICOL, HALOPERIDOL, OXYCODONE. Patient was hospitalized. Patient recovered.

Toprol Side Effects Report #5634518-0
TOPROL problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 14, 2008. Female patient, 63 years of age, weighting 179.9 lb, was treated with TOPROL. After drug was administered, patient experienced the following problems/side effects: ascites, . TOPROL dosage: unknown. During the same period patient was treated with ISOSORBIDE DINITRATE, FUROSEMIDE, SPIRONOLACTONE, MAGOXIDE, DIGOXIN, ZOCOR, COUMADIN. Patient recovered.

Cerezyme Side Effects Report #5635688-0
Physician from MEXICO reported CEREZYME problem on Feb 07, 2008. Male patient, 16 years of age, weighting 88.18 lb, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: ascites, aspiration pleural cavity, hepatocellular injury, hypoalbuminaemia, pericardial effusion, pleural effusion, . CEREZYME dosage: unknown. Patient was hospitalized. Patient died on 02/09/2008.

Velcade Side Effects Report #5635817-9
VELCADE problem was reported by a Physician from FRANCE on Feb 12, 2008. Male patient, 58 years of age, weighting 138.9 lb, was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: ascites, confusional state, diarrhoea, escherichia infection, febrile bone marrow aplasia, gastroenteritis proteus, rectal haemorrhage, septic shock, thrombocytopenia, . VELCADE dosage: 2.50 MG. During the same period patient was treated with CYCLOPHOSPHAMIDE, DOXORUBICIN, ELDISINE, BLEOMYCIN, METHOTREXATE, ISOPTIN. Patient was hospitalized. Patient recovered.

Aricept Side Effects Report #5636139-2
Physician from JAPAN reported ARICEPT problem on Feb 14, 2008. Female patient, 78 years of age, weighting 93.48 lb, was diagnosed with dementia alzheimer's type and was treated with ARICEPT. After drug was administered, patient experienced the following problems/side effects: ascites, blood creatine phosphokinase increased, blood glucose increased, chronic hepatitis, coagulopathy, dehydration, depressed level of consciousness, disease progression, feeling abnormal, . ARICEPT dosage: 5 MG, 1 IN 1 D, ORAL. During the same period patient was treated with SINEMET, METHYCOBAL, OLMETEC. Patient was hospitalized. Patient died on 12/31/2007.

Revlimid Side Effects Report #5637352-0
REVLIMID problem was reported by a Physician from UNITED STATES on Feb 08, 2008. Male patient, 65 years of age, was diagnosed with amyloidosis and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: ascites, atelectasis, gastrointestinal haemorrhage, ileus, intestinal ischaemia, intestinal perforation, mesenteric vein thrombosis, pericardial effusion, . REVLIMID dosage: 25 MG, 1 IN 1, ORAL. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5637570-1
Consumer or non-health professional from UNITED KINGDOM reported HUMIRA problem on Feb 15, 2008. Male patient, weighting 227.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: ascites, lung neoplasm malignant, metastases to liver, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISOLONE, AMLODIPINE, BEZAFIBRATE, FRUMIL, GLICLAZIDE, WARFARIN. Patient was hospitalized. Patient died on 10/28/2007.

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