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Casodex Side Effects Report #5581744-5
Physician from UNITED KINGDOM reported CASODEX problem on Dec 24, 2007. Male patient, 78 years of age, was diagnosed with prostate cancer and was treated with CASODEX. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, liver function test abnormal, . CASODEX dosage: unknown. Patient recovered.

Humira Side Effects Report #5585811-1
HUMIRA problem was reported by a Consumer or non-health professional from GERMANY on Jan 03, 2008. Female patient, weighting 194.0 lb, was diagnosed with rheumatoid arthritis, colitis ulcerative and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, c-reactive protein increased, cholestasis, hepatic enzyme increased, jaundice, . HUMIRA dosage: unknown. During the same period patient was treated with MESALAZIN, MELOXICAM, URSODIOL, AMINOSALICYLIC ACID, THIAMAZOLE. Patient was hospitalized and became disabled. Patient recovered.

Zetia Side Effects Report #5604022-4
Consumer or non-health professional from UNITED STATES reported ZETIA problem on Jan 23, 2008. Male patient, 63 years of age, weighting 187.0 lb, was treated with ZETIA. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, carotid artery occlusion, polyp, . ZETIA dosage: unknown. During the same period patient was treated with LIPITOR. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5576784-6
HUMIRA problem was reported by a Consumer or non-health professional from GERMANY on Dec 21, 2007. Female patient, weighting 194.0 lb, was diagnosed with rheumatoid arthritis, colitis ulcerative and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, c-reactive protein increased, cholestasis, hepatic enzyme increased, jaundice, . HUMIRA dosage: unknown. During the same period patient was treated with MESALAZIN, MELOXICAM, URSODIOL, AMINOSALICYLIC ACID, THIAMAZOLE. Patient was hospitalized and became disabled. Patient recovered.


Casodex Side Effects Report #5528276-8
Physician from UNITED KINGDOM reported CASODEX problem on Nov 16, 2007. Male patient, 78 years of age, was diagnosed with prostate cancer and was treated with CASODEX. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, liver function test abnormal, . CASODEX dosage: unknown. Patient recovered.

Tracleer Side Effects Report #5500089-2
TRACLEER problem was reported by a Physician from SPAIN on Oct 09, 2007. Female patient was diagnosed with skin ulcer and was treated with TRACLEER. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, cholestasis, cytolytic hepatitis, . TRACLEER dosage: 125 MG, BID, ORAL; 62.5 MG, BID, ORAL. Patient was hospitalized. Patient recovered.

Intron Side Effects Report #5465315-7
Consumer or non-health professional from UNITED STATES reported INTRON A problem on Sept 14, 2007. Female patient, 51 years of age, was diagnosed with malignant melanoma and was treated with INTRON A. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, . INTRON A dosage: unknown. Patient recovered.

Humira Side Effects Report #5406512-6
HUMIRA problem was reported by a Consumer or non-health professional from GERMANY on July 27, 2007. Female patient, weighting 194.0 lb, was diagnosed with rheumatoid arthritis, colitis ulcerative and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, c-reactive protein increased, cholestasis, hepatic enzyme increased, jaundice, . HUMIRA dosage: unknown. During the same period patient was treated with MESALAZIN, MELOXICAM. Patient was hospitalized and became disabled. Patient recovered.

Lipitor Side Effects Report #5443241-7
Consumer or non-health professional from UNITED STATES reported LIPITOR problem on Aug 31, 2007. Male patient, 63 years of age, weighting 188.0 lb, was diagnosed with coronary artery disease and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, hepatic enzyme increased, . LIPITOR dosage: NOW ONE 10 MG TABLET DAILY. Patient recovered.


Primaxin Side Effects Report #5382409-5
PRIMAXIN problem was reported by a Physician from JAPAN on June 29, 2007. Female patient, 83 years of age, was treated with PRIMAXIN. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, perianal abscess, pneumonia, white blood cell disorder, . PRIMAXIN dosage: unknown. During the same period patient was treated with URSODIOL. Patient was hospitalized. Patient died on 03/15/2004.

Humira Side Effects Report #5388669-9
Consumer or non-health professional from GERMANY reported HUMIRA problem on July 06, 2007. Female patient, weighting 194.0 lb, was diagnosed with rheumatoid arthritis, colitis ulcerative and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, c-reactive protein increased, cholestasis, hepatic enzyme increased, jaundice, . HUMIRA dosage: unknown. During the same period patient was treated with MESALAZIN, MELOXICAM. Patient was hospitalized and became disabled. Patient recovered.

Primaxin Side Effects Report #5382409-5
PRIMAXIN problem was reported by a Physician from JAPAN on June 29, 2007. Female patient, 83 years of age, was treated with PRIMAXIN. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, perianal abscess, pneumonia, white blood cell disorder, . PRIMAXIN dosage: unknown. During the same period patient was treated with URSODIOL. Patient was hospitalized. Patient died on 03/15/2004.

Humira Side Effects Report #5388669-9
Consumer or non-health professional from GERMANY reported HUMIRA problem on July 06, 2007. Female patient, weighting 194.0 lb, was diagnosed with rheumatoid arthritis, colitis ulcerative and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, c-reactive protein increased, cholestasis, hepatic enzyme increased, jaundice, . HUMIRA dosage: unknown. During the same period patient was treated with MESALAZIN, MELOXICAM. Patient was hospitalized and became disabled. Patient recovered.

Remicade Side Effects Report #5755062-6
REMICADE problem was reported by a Physician from UNITED STATES on May 22, 2008. Female patient, weighting 142.0 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, . REMICADE dosage: unknown. Patient recovered.


Pegasys Side Effects Report #5780435-5
Consumer or non-health professional from UNITED STATES reported PEGASYS problem on June 11, 2008. Female patient, weighting 100.1 lb, was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, blood alkaline phosphatase increased, cellulitis, cough, fatigue, gamma-glutamyltransferase increased, haemoglobin decreased, nausea, . PEGASYS dosage: unknown. During the same period patient was treated with RIBAVIRIN. Patient was hospitalized. Patient recovered.

Cymbalta Side Effects Report #5740819-8
CYMBALTA problem was reported by a Physician from GERMANY on May 06, 2008. Female patient was diagnosed with depression, sleep disorder, agitation, hypothyroidism and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, . CYMBALTA dosage: 30 MG, DAILY (1/D). During the same period patient was treated with NOVANOX, ZOLPIDEM. Patient was hospitalized. Patient recovered.

Rebetol Side Effects Report #5757740-1
Consumer or non-health professional from JAPAN reported REBETOL problem on May 21, 2008. Female patient, 60 years of age, weighting 145.5 lb, was diagnosed with hepatitis c and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, . REBETOL dosage: 800 MG; BID; PO. During the same period patient was treated with INTRON A, INTRON A. Patient recovered.

Dacarbazine Side Effects Report #5706953-3
DACARBAZINE problem was reported by a Health Professional from JAPAN on Apr 01, 2008. Male patient, 64 years of age, was diagnosed with hodgkin's disease and was treated with DACARBAZINE. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, . DACARBAZINE dosage: unknown. During the same period patient was treated with ADRIAMYCIN PFS, BLEOMYCIN SULPHATE, VINBLASTINE SULPHATE. Patient was hospitalized. Patient recovered.

Dacarbazine Side Effects Report #5707702-5
Health Professional from JAPAN reported DACARBAZINE problem on Apr 01, 2008. Male patient, 64 years of age, was diagnosed with hodgkin's disease and was treated with DACARBAZINE. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, . DACARBAZINE dosage: unknown. During the same period patient was treated with ADRIAMYCIN, BLEOMYCIN SULPHATE, VINBLASTINE SULPHATE. Patient was hospitalized. Patient recovered.


Remicade Side Effects Report #5717609-5
REMICADE problem was reported by a Physician from JAPAN on Apr 16, 2008. Female patient, 48 years of age, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, . REMICADE dosage: unknown. Patient recovered.

Fosamax Side Effects Report #5718937-X
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Apr 14, 2008. Female patient, 66 years of age, was diagnosed with osteoporosis, cardiac disorder, thyroid disorder, postmenopause and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, blood cholesterol increased, hypertension, osteomyelitis, osteonecrosis, pancreatitis, rheumatoid arthritis, . FOSAMAX dosage: unknown. During the same period patient was treated with ISORDIL, SYNTHROID, CLIMARA. Patient recovered.

Primaxin Side Effects Report #5357869-6
PRIMAXIN problem was reported by a Physician from JAPAN on June 01, 2007. Female patient, 83 years of age, was treated with PRIMAXIN. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, perianal abscess, pneumonia, white blood cell disorder, . PRIMAXIN dosage: unknown. During the same period patient was treated with URSODIOL. Patient was hospitalized. Patient died on 03/15/2004.

Cyclosporine Side Effects Report #5363191-4
Consumer or non-health professional from BRAZIL reported CYCLOSPORINE problem on June 13, 2007. Female patient, 64 years of age, weighting 101.4 lb, was diagnosed with liver transplant and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, biliary tract operation, blood pressure increased, disease recurrence, gastrointestinal infection, hepatic artery occlusion, herpes virus infection, immunodeficiency, oedema, . CYCLOSPORINE dosage: unknown. During the same period patient was treated with AMLODIPINE, MONOCORDIL, HYDROXYZINE HYDROCHLORIDE, FUROSEMIDE, ATENOLOL, OMEPRAZOLE, TACROLIMUS, BACTRIM. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5371931-3
PROGRAF problem was reported by a Consumer or non-health professional from BRAZIL 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.

Rebif Side Effects Report #5320103-7
Consumer or non-health professional from UNITED STATES reported REBIF problem on Apr 24, 2007. Female patient, 52 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, . REBIF dosage: unknown. During the same period patient was treated with ANTIBIOTICS, RELIV, BACLOFEN, NEURONTIN, CYMBALTA, LASIX, KLONOPIN. Patient recovered.

Remicade Side Effects Report #5336855-6
REMICADE problem was reported by a Physician from JAPAN on May 18, 2007. Female patient, weighting 110.2 lb, was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, . REMICADE dosage: unknown. Patient recovered.

Clarithromycin Side Effects Report #5296697-7
Physician from JAPAN reported CLARITHROMYCIN problem on Apr 06, 2007. Female patient, 43 years of age, weighting 92.59 lb, was diagnosed with pharyngitis, bronchitis and was treated with CLARITHROMYCIN. After drug was administered, patient experienced the following problems/side effects: biliary cirrhosis primary, hepatitis, liver disorder, . CLARITHROMYCIN dosage: unknown. During the same period patient was treated with COCARL, COUGHCODE. Patient was hospitalized. Patient recovered.

Cymbalta Side Effects Report #5664891-9
CYMBALTA problem was reported by a Physician from GERMANY on Mar 03, 2008. Female patient was diagnosed with depression and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: abdominal discomfort, biliary cirrhosis primary, . CYMBALTA dosage: 30 MG, DAILY (1/D). During the same period patient was treated with NOVANOX, ZOLPIDEM. Patient was hospitalized. Patient recovered.

Ketek Side Effects Report #5678935-1
Physician from UNITED STATES reported KETEK problem 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.

Accutane Side Effects Report #5608208-4
ACCUTANE problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 18, 2008. Female patient, 27 years of age, weighting 130.1 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: anaemia, biliary cirrhosis primary, chronic hepatic failure, colitis ulcerative, gastrooesophageal reflux disease, haematochezia, hepatic enzyme increased, inflammatory bowel disease, oedema, . ACCUTANE dosage: unknown. Patient was hospitalized. Patient recovered.

Ambisome Side Effects Report #5613191-1
Health Professional from FRANCE reported AMBISOME problem on Jan 11, 2008. Female patient, 33 years of age, was diagnosed with cerebral aspergillosis and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, biliary cirrhosis primary, caesarean section, cerebral aspergillosis, cytolytic hepatitis, haemolysis, hepatic encephalopathy, . AMBISOME dosage: unknown. During the same period patient was treated with VFEND, BACTRIM, KETAMINE, MEROPEN, COLISTIN SULPHATE. Patient was hospitalized. Patient died.

Tracleer Side Effects Report #5515896-X
TRACLEER problem was reported by a Physician from SPAIN on Oct 25, 2007. Female patient was diagnosed with skin ulcer and was treated with TRACLEER. After drug was administered, patient experienced the following problems/side effects: asthenia, biliary cirrhosis primary, cholestasis, cytolytic hepatitis, . TRACLEER dosage: 125 MG, BID, ORAL. Patient was hospitalized. Patient recovered.

Accutane Side Effects Report #5766541-X
Consumer or non-health professional from UNITED STATES reported ACCUTANE problem on May 30, 2008. Female patient, weighting 130.1 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: anaemia, biliary cirrhosis primary, chronic hepatic failure, colitis ulcerative, gastrooesophageal reflux disease, haematochezia, hepatic enzyme increased, hiatus hernia, inflammatory bowel disease, . ACCUTANE dosage: unknown. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5777899-X
FOSAMAX problem was reported by a Physician from UNITED STATES on June 11, 2008. Female patient, 66 years of age, was diagnosed with osteoporosis, cardiac disorder, thyroid disorder, postmenopause and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: arteriosclerosis coronary artery, biliary cirrhosis primary, blood cholesterol increased, essential hypertension, hypothyroidism, osteoarthritis, osteomyelitis, osteonecrosis, . FOSAMAX dosage: unknown. During the same period patient was treated with ISORDIL, SYNTHROID, CLIMARA. Patient recovered.

Fosamax Side Effects Report #5785333-9
Physician from UNITED STATES reported FOSAMAX problem on June 13, 2008. Female patient, 66 years of age, was diagnosed with osteoporosis, cardiac disorder, thyroid disorder, postmenopause and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: arteriosclerosis coronary artery, biliary cirrhosis primary, blood cholesterol increased, essential hypertension, hypothyroidism, oral disorder, osteoarthritis, osteomyelitis, . FOSAMAX dosage: unknown. During the same period patient was treated with ISORDIL, SYNTHROID, CLIMARA. Patient recovered.

Ketek Side Effects Report #5696170-8
KETEK problem was reported by a Physician from UNITED STATES on Mar 27, 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, erosive oesophagitis, faeces pale, gastrooesophageal reflux disease, iron deficiency anaemia, liver disorder, . KETEK dosage: unknown. During the same period patient was treated with ERYTHROMYCIN, HYDROCODONE, TEQUIN. Patient was hospitalized. Patient recovered.

Adalat Side Effects Report #5696241-6
Health Professional from FRANCE reported ADALAT problem on Mar 26, 2008. Female patient, weighting 105.8 lb, was diagnosed with systemic lupus erythematosus and was treated with ADALAT. After drug was administered, patient experienced the following problems/side effects: bile duct stenosis, biliary cirrhosis primary, cholangitis sclerosing, cholestasis, hepatitis, rash, . ADALAT dosage: unknown. During the same period patient was treated with CORTANCYL, PLAQUENIL. Patient was hospitalized. Patient recovered.

Arimidex Side Effects Report #5700765-2
ARIMIDEX problem was reported by a Consumer or non-health professional from BRAZIL on Apr 03, 2008. Female patient, 65 years of age, weighting 114.6 lb, was diagnosed with breast cancer and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: arthritis, biliary cirrhosis primary, osteopenia, vaginal polyp, . ARIMIDEX dosage: unknown. During the same period patient was treated with NOLVADEX. Patient recovered.

Arimidex Side Effects Report #5722428-X
Consumer or non-health professional from BRAZIL reported ARIMIDEX problem on Apr 23, 2008. Female patient, 65 years of age, weighting 114.6 lb, was diagnosed with breast cancer and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: arthritis, biliary cirrhosis primary, osteopenia, vaginal polyp, . ARIMIDEX dosage: unknown. During the same period patient was treated with NOLVADEX. Patient recovered.

Fosamax Side Effects Report #5729604-0
FOSAMAX problem was reported by a Physician from UNITED STATES on May 01, 2008. Male patient, 56 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anxiety, arthralgia, biliary cirrhosis primary, blood cholesterol increased, depression, hypertension, liver disorder, movement disorder, oral infection, . FOSAMAX dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Fosamax Side Effects Report #5711462-1
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Apr 11, 2008. Male patient, 56 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anxiety, arthralgia, biliary cirrhosis primary, blood cholesterol increased, depression, hypertension, liver disorder, movement disorder, oral infection, . FOSAMAX dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.