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Leflunomide Side Effects Report #5652175-4
Consumer or non-health professional from FRANCE reported LEFLUNOMIDE problem on Feb 18, 2008. Female patient, 34 years of age, was diagnosed with juvenile arthritis, therapeutic procedure and was treated with LEFLUNOMIDE. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, hepatic lesion, hepatic necrosis, hepatitis fulminant, hepatomegaly, hepatotoxicity, vitamin k deficiency, . LEFLUNOMIDE dosage: 20 MG/DAY. During the same period patient was treated with CHOLESTYRAMINE, ACETAMINOPHEN W. Patient was hospitalized. Patient recovered.

Byetta Side Effects Report #5645019-8
BYETTA problem was reported by a Physician from UNITED STATES on Feb 21, 2008. Male patient was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, portal hypertension, varices oesophageal, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN, ACTOS. Patient recovered.

Clofarabine Side Effects Report #5646790-1
Physician from UNITED KINGDOM reported CLOFARABINE problem on Feb 18, 2008. Female patient, 76 years of age, was diagnosed with acute myeloid leukaemia and was treated with CLOFARABINE. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, pneumonia, . CLOFARABINE dosage: 35 MG, QDX5, INTRAVENOUS. During the same period patient was treated with GLICLAZIDE, METFORMIN, QUINE SULPHATE, ACARBOSE, TIMOLOL MALEATE. Patient died on 01/26/2008.

Baycol Side Effects Report #5590945-1
BAYCOL problem was reported by a Physician from GERMANY on Jan 02, 2008. Female patient, 61 years of age, was diagnosed with hypercholesterolaemia and was treated with BAYCOL. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, laboratory test abnormal, muscular weakness, rash, . BAYCOL dosage: unknown. During the same period patient was treated with EXELON, TREVILON RET, GYNODIAN DEP. Patient recovered.


Isradipine Side Effects Report #5605693-9
Consumer or non-health professional from SWITZERLAND reported ISRADIPINE problem on Jan 16, 2008. Female patient, 57 years of age, was diagnosed with liver transplant and was treated with ISRADIPINE. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, hepatic steatosis, . ISRADIPINE dosage: 2.5 MG; QD; PO. During the same period patient was treated with NEORAL, COPEGUS, PEGINTERFERON ALFA, OMEPRAZOLE, POTASSIUM CHLORIDE, COZAAR, FUROSEMIDE. Patient recovered.

Cellcept Side Effects Report #5563018-1
CELLCEPT problem was reported by a Physician from GERMANY on Dec 04, 2007. Female patient was treated with CELLCEPT. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, . CELLCEPT dosage: UP TO A MAXIMUM DOSE OF 2000MG/DAY. During the same period patient was treated with IMUREK, STEROID NOS, ATGAM, ZENAPAX, INTRON A, REBETOL. Patient recovered.

Cellcept Side Effects Report #5563025-9
Physician from GERMANY reported CELLCEPT problem on Dec 04, 2007. Female patient was treated with CELLCEPT. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, . CELLCEPT dosage: UP TO A MAXIMUM DOSE OF 2000MG/DAY. During the same period patient was treated with IMUREK, STEROID NOS, ATGAM, ZENAPAX, INTRON A, REBETOL. Patient recovered.

Cellcept Side Effects Report #5563027-2
CELLCEPT problem was reported by a Physician from GERMANY on Dec 04, 2007. Female patient was treated with CELLCEPT. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, . CELLCEPT dosage: UP TO A MAXIMUM DOSE OF 2000MG/DAY. During the same period patient was treated with IMUREK, STEROID NOS, ATGAM, ZENAPAX, INTRON A, REBETOL. Patient recovered.

Cellcept Side Effects Report #5563028-4
Physician from GERMANY reported CELLCEPT problem on Dec 04, 2007. Female patient was treated with CELLCEPT. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, . CELLCEPT dosage: UP TO A MAXIMUM DOSE OF 2000MG/DAY. During the same period patient was treated with IMUREK, STEROID NOS, ATGAM, ZENAPAX, INTRON A, REBETOL. Patient recovered.


Cellcept Side Effects Report #5563033-8
CELLCEPT problem was reported by a Physician from GERMANY on Dec 04, 2007. Female patient was treated with CELLCEPT. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, . CELLCEPT dosage: UP TO A MAXIMUM DOSE OF 2000MG/DAY. During the same period patient was treated with IMUREK, STEROID NOS, ATGAM, ZENAPAX, INTRON A, REBETOL. Patient recovered.

Cellcept Side Effects Report #5563036-3
Physician from GERMANY reported CELLCEPT problem on Dec 04, 2007. Female patient was treated with CELLCEPT. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, . CELLCEPT dosage: UP TO A MAXIMUM DOSE OF 2000MG/DAY. During the same period patient was treated with IMUREK, STEROID NOS, ATGAM, ZENAPAX, INTRON A, REBETOL. Patient recovered.

Levaquin Side Effects Report #5474203-1
LEVAQUIN problem was reported by a Physician from UNITED STATES on Sept 28, 2007. Male patient, 49 years of age, was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, hepatic necrosis, hepatitis c, hepatitis c rna positive, hepatotoxicity, liver injury, suicidal ideation, . LEVAQUIN dosage: 500MG/DAY. During the same period patient was treated with LEXAPRO, XANAX, VICODIN. Patient recovered.

Gemcitabine Side Effects Report #5402347-9
Physician from UNITED STATES reported GEMCITABINE problem on July 20, 2007. Male patient, 61 years of age, was diagnosed with pancreatic carcinoma and was treated with GEMCITABINE. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, . GEMCITABINE dosage: unknown. During the same period patient was treated with OXALIPLATIN, CAPECITABINE. Patient recovered.

Aprovel Side Effects Report #5400991-6
APROVEL problem was reported by a Physician from FRANCE on July 26, 2007. Female patient, 40 years of age, was diagnosed with hypertension, hiv infection and was treated with APROVEL. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, hepatitis cholestatic, lipodystrophy acquired, lymphopenia, portal hypertension, varices oesophageal, . APROVEL dosage: unknown. During the same period patient was treated with VIDEX, EPIVIR, VIRAMUNE, VIREAD. Patient recovered.


Leuprolide Side Effects Report #5404665-7
Consumer or non-health professional from JAPAN reported LEUPROLIDE ACETATE problem on July 27, 2007. Male patient, 73 years of age, was diagnosed with prostate cancer and was treated with LEUPROLIDE ACETATE. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, hepatic steatosis, obesity, . LEUPROLIDE ACETATE dosage: 11.25 MG (11.25 MG, 1 IN 12 WK SUBCUTANEOUS. During the same period patient was treated with LEUPROLIDE ACETATE, LANSOPRAZOLE, ERBANTIL, CERNILTON, CASODEX, PRAVASTATIN, LASIX, UNIPHYL LA. Patient recovered.

Aprovel Side Effects Report #5400991-6
APROVEL problem was reported by a Physician from FRANCE on July 26, 2007. Female patient, 40 years of age, was diagnosed with hypertension, hiv infection and was treated with APROVEL. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, hepatitis cholestatic, lipodystrophy acquired, lymphopenia, portal hypertension, varices oesophageal, . APROVEL dosage: unknown. During the same period patient was treated with VIDEX, EPIVIR, VIRAMUNE, VIREAD. Patient recovered.

Leuprolide Side Effects Report #5404665-7
Consumer or non-health professional from JAPAN reported LEUPROLIDE ACETATE problem on July 27, 2007. Male patient, 73 years of age, was diagnosed with prostate cancer and was treated with LEUPROLIDE ACETATE. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, hepatic steatosis, obesity, . LEUPROLIDE ACETATE dosage: 11.25 MG (11.25 MG, 1 IN 12 WK SUBCUTANEOUS. During the same period patient was treated with LEUPROLIDE ACETATE, LANSOPRAZOLE, ERBANTIL, CERNILTON, CASODEX, PRAVASTATIN, LASIX, UNIPHYL LA. Patient recovered.

Elmiron Side Effects Report #5772197-2
ELMIRON problem was reported by a Physician from UNITED STATES on June 05, 2008. Female patient, weighting 145.0 lb, was diagnosed with cystitis interstitial and was treated with ELMIRON. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, hepatic steatosis, . ELMIRON dosage: unknown. During the same period patient was treated with VESICARE, AMITRIPTYLINE, HYDROXYZINE. Patient recovered.

Prezista Side Effects Report #5787612-8
Health Professional from CANADA reported PREZISTA problem on June 16, 2008. Male patient, weighting 142.2 lb, was diagnosed with hiv infection, hyperlipidaemia, hypertension, depression, antiviral prophylaxis and was treated with PREZISTA. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, hepatic steatosis, . PREZISTA dosage: unknown. During the same period patient was treated with LIPITOR, NIASPAM, COZAAR, HYDROCHLOROTHIAZIDE, MONITAN, EFFEXOR, FAMVIR. Patient recovered.


Glivec Side Effects Report #5792036-3
GLIVEC problem was reported by a Consumer or non-health professional from GERMANY on June 16, 2008. Male patient was diagnosed with gastrointestinal stromal tumour and was treated with GLIVEC. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, hepatic necrosis, hepatic steatosis, . GLIVEC dosage: 400 MG, QD. Patient recovered.

Prezista Side Effects Report #5793401-0
Health Professional from CANADA reported PREZISTA problem on June 16, 2008. Male patient, weighting 142.2 lb, was diagnosed with hiv infection, hyperlipidaemia, hypertension, depression, antiviral prophylaxis and was treated with PREZISTA. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, . PREZISTA dosage: unknown. During the same period patient was treated with LIPITOR, NIASPAM, COZAAR, HYDROCHLOROTHIAZIDE, MONITAN, EFFEXOR, FAMVIR. Patient recovered.

Azathioprine Side Effects Report #5798904-0
AZATHIOPRINE problem was reported by a Consumer or non-health professional from FRANCE on June 17, 2008. Female patient, 58 years of age, was diagnosed with autoimmune hepatitis and was treated with AZATHIOPRINE. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, non-hodgkin's lymphoma, . AZATHIOPRINE dosage: 50 MG; DAILY. During the same period patient was treated with CORTANCYL, BISOPROLOL FUMARATE. Patient recovered.

Cordarone Side Effects Report #5725994-3
Physician from UNITED STATES reported CORDARONE problem on May 01, 2008. Male patient, 62 years of age, was treated with CORDARONE. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, hepatic steatosis, hypotension, ill-defined disorder, ischaemic hepatitis, liver injury, multi-organ failure, therapeutic agent toxicity, . CORDARONE dosage: unknown. Patient recovered.

Lucentis Side Effects Report #5740321-3
LUCENTIS problem was reported by a Physician from SWITZERLAND on May 05, 2008. Female patient was treated with LUCENTIS. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, hepatitis toxic, . LUCENTIS dosage: unknown. Patient recovered.

Elmiron Side Effects Report #5746619-7
Physician from UNITED STATES reported ELMIRON problem on May 12, 2008. Female patient, 41 years of age, was diagnosed with cystitis interstitial, hypertonic bladder and was treated with ELMIRON. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, hepatic steatosis, . ELMIRON dosage: unknown. During the same period patient was treated with VESICARE, AMITRIPTYLINE, HYDROXYZINE. Patient recovered.

Rebif Side Effects Report #5364312-X
REBIF problem was reported by a Consumer or non-health professional from ITALY on June 06, 2007. Male patient, 38 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, hepatic steatosis, hepatomegaly, liver disorder, . REBIF dosage: unknown. Patient recovered.

Methotrexate Side Effects Report #5294432-X
Consumer or non-health professional from UNITED STATES reported METHOTREXATE problem on Apr 09, 2007. Female patient, 48 years of age, weighting 160.0 lb, was diagnosed with psoriasis and was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, hepatic pain, hepatic steatosis, . METHOTREXATE dosage: 10 MG A WEEK FOR 2 MONTH PO 7.5 MG WEEKLY FOR 4 MONTH PO. Patient recovered.

Ancaron Side Effects Report #5266003-2
ANCARON problem was reported by a Health Professional from JAPAN on Mar 14, 2007. Male patient, 70 years of age, was diagnosed with atrial fibrillation and was treated with ANCARON. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, . ANCARON dosage: unknown. Patient recovered.

Aprovel Side Effects Report #5274117-6
Physician from FRANCE reported APROVEL problem on Mar 20, 2007. Female patient, 40 years of age, was diagnosed with hypertension, hiv infection and was treated with APROVEL. After drug was administered, patient experienced the following problems/side effects: hepatic fibrosis, hepatitis cholestatic, lipodystrophy acquired, lymphopenia, portal hypertension, varices oesophageal, . APROVEL dosage: unknown. During the same period patient was treated with VIDEX, EPIVIR, VIRAMUNE, VIREAD. Patient recovered.

Allopurinol Side Effects Report #5676018-8
ALLOPURINOL problem was reported by a Physician from SPAIN on Mar 03, 2008. Female patient, 60 years of age, was diagnosed with hyperuricaemia and was treated with ALLOPURINOL. After drug was administered, patient experienced the following problems/side effects: cholestasis, hepatic fibrosis, hepatitis, hepatosplenomegaly, nephritis interstitial, renal failure chronic, vasculitis, . ALLOPURINOL dosage: 100 MG TWICE DAILY, ORAL. Patient was hospitalized. Patient recovered.

Leflunomide Side Effects Report #5676746-4
Physician from FRANCE reported LEFLUNOMIDE problem on Mar 03, 2008. Female patient, 34 years of age, was diagnosed with juvenile arthritis, therapeutic procedure and was treated with LEFLUNOMIDE. After drug was administered, patient experienced the following problems/side effects: blood fibrinogen decreased, hepatic fibrosis, hepatic necrosis, hepatitis fulminant, hepatomegaly, hepatotoxicity, prothrombin level abnormal, serum ferritin increased, vitamin k deficiency, . LEFLUNOMIDE dosage: 20 MG/DAY. During the same period patient was treated with CHOLESTYRAMINE, ACETAMINOPHEN W, PREDNISONE, NICARDECREASEINE, CANDESARTAN CILEXETIL, CALCIUM CARBONATE, CHOLECALCIFEROL. Patient was hospitalized. Patient recovered.

Campath Side Effects Report #5625705-6
CAMPATH problem was reported by a Physician from UNITED KINGDOM on Feb 07, 2008. Male patient, 61 years of age, was diagnosed with chronic lymphocytic leukaemia and was treated with CAMPATH. After drug was administered, patient experienced the following problems/side effects: autoimmune hepatitis, hepatic fibrosis, . CAMPATH dosage: unknown. During the same period patient was treated with PREDNISOLONE. Patient recovered.

Campath Side Effects Report #5635588-6
Physician from UNITED KINGDOM reported CAMPATH problem on Feb 18, 2008. Male patient, 61 years of age, was diagnosed with chronic lymphocytic leukaemia and was treated with CAMPATH. After drug was administered, patient experienced the following problems/side effects: autoimmune hepatitis, hepatic fibrosis, . CAMPATH dosage: unknown. During the same period patient was treated with PREDNISOLONE. Patient recovered.

Campath Side Effects Report #5599609-1
CAMPATH problem was reported by a Physician from UNITED KINGDOM on Jan 08, 2008. Male patient, 61 years of age, was diagnosed with chronic lymphocytic leukaemia and was treated with CAMPATH. After drug was administered, patient experienced the following problems/side effects: autoimmune hepatitis, hepatic fibrosis, . CAMPATH dosage: unknown. During the same period patient was treated with PREDNISOLONE. Patient recovered.

Campath Side Effects Report #5600912-7
Physician from UNITED KINGDOM reported CAMPATH problem on Jan 08, 2008. Male patient, 61 years of age, was diagnosed with chronic lymphocytic leukaemia and was treated with CAMPATH. After drug was administered, patient experienced the following problems/side effects: autoimmune hepatitis, hepatic fibrosis, . CAMPATH dosage: unknown. During the same period patient was treated with PREDNISOLONE. Patient recovered.

Nevirapine Side Effects Report #5564054-1
NEVIRAPINE problem was reported by a Consumer or non-health professional from on Dec 11, 2007. Male patient, 60 years of age, was diagnosed with hiv infection and was treated with NEVIRAPINE. After drug was administered, patient experienced the following problems/side effects: gastric varices, hepatic fibrosis, lipodystrophy acquired, liver function test abnormal, oesophageal varices haemorrhage, portal hypertension, splenomegaly, thrombocytopenia, . NEVIRAPINE dosage: unknown. During the same period patient was treated with LAMIVUDINE, TENOFOVIR DISOPROXIL FUMARATE, ATAZANAVIR. Patient recovered.

Nevirapine Side Effects Report #5564055-3
Consumer or non-health professional from reported NEVIRAPINE problem on Dec 11, 2007. Male patient, 35 years of age, was diagnosed with hiv infection and was treated with NEVIRAPINE. After drug was administered, patient experienced the following problems/side effects: bleeding varicose vein, hepatic fibrosis, hepatosplenomegaly, lipodystrophy acquired, liver function test abnormal, portal hypertension, thrombocytopenia, . NEVIRAPINE dosage: unknown. During the same period patient was treated with LAMIVUDINE, TENOFOVIR DISOPROXIL FUMARATE, NELFINAVIR. Patient recovered.

Nevirapine Side Effects Report #5564056-5
NEVIRAPINE problem was reported by a Consumer or non-health professional from on Dec 11, 2007. Male patient, 50 years of age, was diagnosed with hiv infection and was treated with NEVIRAPINE. After drug was administered, patient experienced the following problems/side effects: bleeding varicose vein, hepatic fibrosis, liver function test abnormal, portal hypertension, portal vein thrombosis, renal failure, sepsis, thrombocytopenia, . NEVIRAPINE dosage: unknown. During the same period patient was treated with LAMIVUDINE, TENOFOVIR DISOPROXIL FUMARATE, LOPINAVIR, FAMCICLOVIR. Patient was hospitalized. Patient recovered.

Campath Side Effects Report #5564578-7
Physician from UNITED KINGDOM reported CAMPATH problem on Dec 12, 2007. Male patient, 61 years of age, was diagnosed with chronic lymphocytic leukaemia and was treated with CAMPATH. After drug was administered, patient experienced the following problems/side effects: autoimmune hepatitis, hepatic fibrosis, . CAMPATH dosage: unknown. During the same period patient was treated with PREDNISOLONE. Patient recovered.

Fortamet Side Effects Report #5527422-X
FORTAMET problem was reported by a Health Professional from UNITED STATES on Nov 12, 2007. Male patient, 63 years of age, was treated with FORTAMET. After drug was administered, patient experienced the following problems/side effects: cholangitis, hepatic fibrosis, hepatic necrosis, hepatitis, portal triaditis, . FORTAMET dosage: 500 MG, BID X 4 WEEKS, ORAL. During the same period patient was treated with GLYBURIDE, ALLOPURINOL, ASPIRIN. Patient was hospitalized. Patient recovered.

Kaletra Side Effects Report #5475253-1
Physician from FRANCE reported KALETRA problem on Sept 25, 2007. Female patient, 52 years of age, was diagnosed with hiv infection and was treated with KALETRA. After drug was administered, patient experienced the following problems/side effects: asthenia, hepatic fibrosis, portal hypertension, . KALETRA dosage: unknown. During the same period patient was treated with DIDANOSINE, LAMIVUDINE. Patient was hospitalized. Patient recovered.

Levaquin Side Effects Report #5491588-0
LEVAQUIN problem was reported by a Physician from UNITED STATES on Oct 19, 2007. Male patient, 37 years of age, was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: dermatitis acneiform, hepatic fibrosis, hepatitis cholestatic, mobility decreased, speech disorder, weight decreased, . LEVAQUIN dosage: unknown. During the same period patient was treated with URSODIOL, ACCUPRIL. Patient recovered.

Keflex Side Effects Report #5469188-8
Physician from UNITED STATES reported KEFLEX problem on Sept 26, 2007. Female patient, 41 years of age, was treated with KEFLEX. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, hepatic fibrosis, hepatic steatosis, hepatitis, liver disorder, lymphocytic infiltration, myopathy, peripheral ischaemia, . KEFLEX dosage: unknown. During the same period patient was treated with OMNICEF. Patient recovered.

Avonex Side Effects Report #5776962-7
AVONEX problem was reported by a Consumer or non-health professional from CANADA on May 30, 2008. Female patient, child 12 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: autoimmune hepatitis, hepatic fibrosis, . AVONEX dosage: unknown. Patient recovered.

Minocycline Side Effects Report #5778113-1
Pharmacist from UNITED STATES reported MINOCYCLINE problem on June 17, 2008. Female patient, weighting 143.3 lb, was diagnosed with acne and was treated with MINOCYCLINE. After drug was administered, patient experienced the following problems/side effects: autoimmune hepatitis, hepatic fibrosis, hepatic necrosis, . MINOCYCLINE dosage: unknown. Patient was hospitalized. Patient recovered.

Ticlopidine Side Effects Report #5692681-X
TICLOPIDINE HYDROCHLORIDE problem was reported by a Consumer or non-health professional from ITALY on Mar 13, 2008. Male patient, 53 years of age, was diagnosed with prophylaxis and was treated with TICLOPIDINE HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: antinuclear antibody positive, hepatic fibrosis, hepatic necrosis, hepatitis cholestatic, immunoglobulins increased, liver transplant, renal transplant, . TICLOPIDINE HYDROCHLORIDE dosage: 250 MG; DAILY, 250 MG; DAILY. During the same period patient was treated with ERYTHROPOIETINS, CARVEDILOL, OMEPRAZOLE, CALCIUM CARBONATE. Patient was hospitalized. Patient recovered.

Augmentin Side Effects Report #5721244-2
Physician from UNITED STATES reported AUGMENTIN problem on Apr 28, 2008. Male patient, weighting 182.0 lb, was diagnosed with acute sinusitis, nasal polyps and was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: chronic hepatitis, hepatic fibrosis, hepatic necrosis, . AUGMENTIN dosage: unknown. Patient recovered.

Busulfan Side Effects Report #5348502-8
BUSULFAN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on May 22, 2007. Female patient, 45 years of age, was diagnosed with stem cell transplant and was treated with BUSULFAN. After drug was administered, patient experienced the following problems/side effects: granulomatous liver disease, hepatic fibrosis, sarcoidosis, . BUSULFAN dosage: unknown. During the same period patient was treated with FLUDARABINE PHOSPHATE, CAMPATH, ACYCLOVIR, PHENOXYMETHYL PENICILLIN. Patient recovered.

Prograf Side Effects Report #5371931-3
Consumer or non-health professional from BRAZIL reported PROGRAF problem on June 15, 2007. Female patient, 40 years of age, was diagnosed with liver transplant rejection and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, hepatic fibrosis, pruritus, . PROGRAF dosage: unknown. Patient recovered.

Levaquin Side Effects Report #5318709-4
LEVAQUIN problem was reported by a Physician from UNITED STATES on May 03, 2007. Female patient, 51 years of age, was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: abdominal pain, hepatic fibrosis, hepatitis acute, hepatitis c, liver injury, smooth muscle antibody positive, . LEVAQUIN dosage: unknown. During the same period patient was treated with ZITHROMAX, EFFEXOR, CLARITIN, FLONASE, TRAZODONE. Patient recovered.

Viraferonpeg Side Effects Report #5323663-5
Physician from UNITED KINGDOM reported VIRAFERONPEG problem on Apr 24, 2007. Female patient, 50 years of age, was diagnosed with hepatitis c and was treated with VIRAFERONPEG. After drug was administered, patient experienced the following problems/side effects: depression, hepatic fibrosis, platelet count decreased, weight decreased, . VIRAFERONPEG dosage: unknown. During the same period patient was treated with REBETOL. Patient recovered.