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Prograf Side Effects Report #5670353-5
Health Professional from UNITED STATES reported PROGRAF problem on Mar 03, 2008. Female patient, 60 years of age, was diagnosed with liver transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, . PROGRAF dosage: 5 MG. During the same period patient was treated with MYCOPHENOLATE MOFETIL, PREDNISOLONE ACETATE, BACTRIM, ASPIRIN. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5678757-1
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 11, 2008. Female patient, 53 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, gastrointestinal motility disorder, hypertrophy, intestinal obstruction, pancreatic disorder, procedural complication, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5628431-2
Physician from CANADA reported HUMIRA problem on Feb 05, 2008. Female patient, 36 years of age, was diagnosed with ankylosing spondylitis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, bleeding time prolonged, leukopenia, . HUMIRA dosage: unknown. Patient recovered.

Soriatane Side Effects Report #5583876-4
SORIATANE problem was reported by a Physician from UNITED STATES on Dec 26, 2007. Male patient was diagnosed with transient acantholytic dermatosis and was treated with SORIATANE. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, hepatic steatosis, pancreatitis chronic, . SORIATANE dosage: 25 MG;QD;PO. During the same period patient was treated with DIOVAN, FLURAZEPAM, NEXIUM, ZANTAC, FLOMAX, ANDROGEL, LAMISIL. Patient recovered.


Ambisome Side Effects Report #5605741-6
Health Professional from AUSTRALIA reported AMBISOME problem on Jan 16, 2008. Male patient, 59 years of age, weighting 260.1 lb, was diagnosed with acute myeloid leukaemia and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, hepatic encephalopathy, hepatitis acute, hepatorenal failure, injury, nephritis interstitial, sepsis, . AMBISOME dosage: 30 MG, UID/QD, IV DRIP. During the same period patient was treated with IDARUBICIN, ETOPOSIDE, CYTARABINE, VANCOMYCIN HYDROCHLORIDE, MEROPENEM, AZITHROMYCIN. Patient was hospitalized and became disabled. Patient recovered.

Harnal Side Effects Report #5575392-0
HARNAL problem was reported by a Physician from JAPAN on Dec 20, 2007. Male patient, weighting 145.5 lb, was diagnosed with benign prostatic hyperplasia, cerebral infarction, hypertension, constipation, diabetes mellitus and was treated with HARNAL. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, liver disorder, . HARNAL dosage: unknown. During the same period patient was treated with BUFFERIN, RENIVEZE, OZAGREL, SENNOSIDE, CETILO, INSULINECTION. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5509483-7
Health Professional from UNITED STATES reported PROGRAF problem on Oct 26, 2007. Female patient, 60 years of age, was diagnosed with liver transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, . PROGRAF dosage: 5 MG, ORAL. During the same period patient was treated with MYCOPHENOLATE MOFETIL, PREDNISONE, BACTRIM, ASPIRIN. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5517529-5
FORTEO problem was reported by a Consumer or non-health professional from SPAIN on Oct 31, 2007. Female patient, 71 years of age, was diagnosed with osteoporosis, pain and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, . FORTEO dosage: unknown. During the same period patient was treated with PARACETAMOL, NOLOTIL. Patient was hospitalized. Patient recovered.

Thymoglobulin Side Effects Report #5484982-5
Physician from UNITED STATES reported THYMOGLOBULIN problem on Sept 18, 2007. Male patient, 59 years of age, weighting 170.2 lb, was diagnosed with liver transplant and was treated with THYMOGLOBULIN. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, hepatitis, hepatitis c virus, oedema, . THYMOGLOBULIN dosage: 110 MG DAILY IV. During the same period patient was treated with CALCIUM SUPPLEMENT, CELLCEPT, NEURONTIN, BACTRIM DS, FLORNINEF, VORICONAZOLE. Patient was hospitalized. Patient recovered.


Atorvastatin Side Effects Report #5487435-3
ATORVASTATIN CALCIUM problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 05, 2007. Male patient, weighting 216.5 lb, was diagnosed with coronary artery disease and was treated with ATORVASTATIN CALCIUM. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, cholecystitis, hypoxia, . ATORVASTATIN CALCIUM dosage: DAILY DOSE:20MG. During the same period patient was treated with ATORVASTATIN CALCIUM, AMLODIPINE, SILDENAFIL, VITAMIN CAP, ASPIRIN, IBUPROFEN, PIMECROLIMUS, TRAZODONE. Patient was hospitalized. Patient recovered.

Zoloft Side Effects Report #5498035-3
Consumer or non-health professional from SWEDEN reported ZOLOFT problem on Oct 15, 2007. Male patient, 65 years of age, was diagnosed with depression and was treated with ZOLOFT. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, memory impairment, pancreatic neoplasm, . ZOLOFT dosage: unknown. During the same period patient was treated with ZOPICLONE, PROPAVAN. Patient was hospitalized. Patient recovered.

Byetta Side Effects Report #5499570-4
BYETTA problem was reported by a Physician from UNITED STATES on Oct 18, 2007. Male patient, weighting 210.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, blood glucose decreased, blood glucose increased, malaise, post procedural bile leak, vomiting, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN, GLYBURIDE. Patient was hospitalized. Patient recovered.

Ambisome Side Effects Report #5449654-1
Health Professional from AUSTRALIA reported AMBISOME problem on Aug 27, 2007. Male patient, 59 years of age, weighting 260.1 lb, was diagnosed with acute myeloid leukaemia and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, blood creatinine increased, hepatic encephalopathy, hepatic function abnormal, hepatitis acute, nephritis interstitial, pyrexia, renal impairment, . AMBISOME dosage: 30 MG, UID/QD, IV DRIP. During the same period patient was treated with IDARUBICIN, ETOPOSIDE, CYTARABINE, VANCOMYCIN HYDROCHLORIDE, MEROPENEM, AZITHROMYCIN. Patient was hospitalized. Patient recovered.

Atorvastatin Side Effects Report #5467309-4
ATORVASTATIN CALCIUM problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 17, 2007. Male patient, weighting 216.5 lb, was diagnosed with coronary artery disease and was treated with ATORVASTATIN CALCIUM. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, cholecystitis, hypoxia, . ATORVASTATIN CALCIUM dosage: DAILY DOSE:20MG. During the same period patient was treated with ATORVASTATIN CALCIUM, AMLODIPINE, SILDENAFIL, VITAMIN CAP, ASPIRIN, IBUPROFEN, PIMECROLIMUS, TRAZODONE. Patient was hospitalized. 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.

Ambisome Side Effects Report #5421591-8
AMBISOME problem was reported by a Health Professional from AUSTRALIA on July 30, 2007. Male patient, 59 years of age, was diagnosed with acute myeloid leukaemia and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, blood creatinine increased, hepatic encephalopathy, hepatic function abnormal, hepatitis, hepatitis acute, nephritis interstitial, pyrexia, . AMBISOME dosage: 30 MG, UID/QD, IV DRIP. During the same period patient was treated with IDARUBICIN, ETOPOSIDE, CYTARABINE, VANCOMYCIN HYDROCHLORIDE, MEROPENEM, AZITHROMYCIN. Patient was hospitalized. Patient recovered.

Topamax Side Effects Report #5385294-0
Health Professional from PORTUGAL reported TOPAMAX problem on July 02, 2007. Female patient, 50 years of age, was diagnosed with weight loss diet, migraine prophylaxis and was treated with TOPAMAX. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, gamma-glutamyltransferase increased, . TOPAMAX dosage: unknown. Patient recovered.

Lexapro Side Effects Report #5391831-2
LEXAPRO problem was reported by a Health Professional from UNITED STATES on July 06, 2007. Female patient was treated with LEXAPRO. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, congenital anomaly, cyst, foetal disorder, . LEXAPRO dosage: 20 MG QD TRANSPLACENTAL. During the same period patient was treated with PRENATAL VITAMINS. Patient recovered.

Topamax Side Effects Report #5395268-1
Health Professional from PORTUGAL reported TOPAMAX problem on July 17, 2007. Female patient, 50 years of age, was diagnosed with weight loss diet, migraine prophylaxis and was treated with TOPAMAX. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, gamma-glutamyltransferase increased, . TOPAMAX dosage: unknown. Patient recovered.


Topamax Side Effects Report #5385294-0
TOPAMAX problem was reported by a Health Professional from PORTUGAL on July 02, 2007. Female patient, 50 years of age, was diagnosed with weight loss diet, migraine prophylaxis and was treated with TOPAMAX. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, gamma-glutamyltransferase increased, . TOPAMAX dosage: unknown. Patient recovered.

Lexapro Side Effects Report #5391831-2
Health Professional from UNITED STATES reported LEXAPRO problem on July 06, 2007. Female patient was treated with LEXAPRO. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, congenital anomaly, cyst, foetal disorder, . LEXAPRO dosage: 20 MG QD TRANSPLACENTAL. During the same period patient was treated with PRENATAL VITAMINS. Patient recovered.

Topamax Side Effects Report #5395268-1
TOPAMAX problem was reported by a Health Professional from PORTUGAL on July 17, 2007. Female patient, 50 years of age, was diagnosed with weight loss diet, migraine prophylaxis and was treated with TOPAMAX. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, gamma-glutamyltransferase increased, . TOPAMAX dosage: unknown. Patient recovered.

Actos Side Effects Report #5732486-4
Health Professional from FRANCE reported ACTOS problem on Apr 29, 2008. Female patient, 47 years of age, was diagnosed with diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, hepatitis cholestatic, . ACTOS dosage: 30 MG (30 MG, 1 IN 1 D) ORAL. Patient was hospitalized. Patient recovered.

Vfend Side Effects Report #5744752-7
VFEND problem was reported by a Pharmacist from UNITED KINGDOM on May 08, 2008. Female patient, weighting 110.2 lb, was diagnosed with cerebral aspergillosis and was treated with VFEND. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, liver function test abnormal, transplant rejection, . VFEND dosage: unknown. During the same period patient was treated with TACROLIMUS, PREDNISOLONE, OMEPRAZOLE. Patient recovered.

Arixtra Side Effects Report #5702769-2
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Apr 04, 2008. Male patient, 72 years of age, was diagnosed with portal vein thrombosis, back pain and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, feeling abnormal, gastrointestinal haemorrhage, haematemesis, melaena, varices oesophageal, . ARIXTRA dosage: unknown. During the same period patient was treated with NAPROXEN, NOLVADEX, ELISOR, LASILIX, BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE, AVLOCARDYL, SPIRONOLACTONE, GLUCOPHAGE. Patient was hospitalized. Patient recovered.

Kivexa Side Effects Report #5708176-0
KIVEXA problem was reported by a Consumer or non-health professional from FRANCE on Apr 14, 2008. Male patient, 34 years of age, was diagnosed with hiv infection and was treated with KIVEXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, hepatitis b, hepatocellular injury, hepatotoxicity, hyperbilirubinaemia, microlithiasis, treatment noncompliance, . KIVEXA dosage: unknown. During the same period patient was treated with SUSTIVA, TRUVADA, CANNABIS. Patient was hospitalized. Patient recovered.

Chantix Side Effects Report #5711680-2
Physician from UNITED STATES reported CHANTIX problem on Apr 09, 2008. Female patient, weighting 160.1 lb, was diagnosed with smoker and was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, liver function test abnormal, . CHANTIX dosage: unknown. During the same period patient was treated with LIPITOR. Patient recovered.

Ibuprofen Side Effects Report #5724204-0
IBUPROFEN ORAL USP problem was reported by a Health Professional from FRANCE on Apr 15, 2008. Female patient, 37 years of age, was diagnosed with conjunctivitis, pharyngitis, pyrexia and was treated with IBUPROFEN ORAL USP. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, hepatitis cholestatic, stevens-johnson syndrome, thrombosis, . IBUPROFEN ORAL USP dosage: unknown. During the same period patient was treated with IBUPROFEN ORAL USP, IBUPROFEN ORAL USP, AMOXICILLIN. Patient was hospitalized. Patient recovered.

Enbrel Side Effects Report #5352951-1
Physician from ARGENTINA reported ENBREL problem on May 30, 2007. Male patient, 66 years of age, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, jaundice, lung neoplasm, . ENBREL dosage: unknown. Patient recovered.

Zelnorm Side Effects Report #5364806-7
ZELNORM problem was reported by a Consumer or non-health professional from UNITED STATES on June 11, 2007. Female patient, 72 years of age, was diagnosed with diarrhoea and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, diarrhoea, hepatitis, malaise, . ZELNORM dosage: 6 MG, BID. During the same period patient was treated with ANALGESICS, ANTIEMETICS, ANTIDEPRESSANTS. Patient recovered.

Zyprexa Side Effects Report #5373941-9
Consumer or non-health professional from UNITED STATES reported ZYPREXA problem on June 18, 2007. Female patient, 61 years of age, weighting 196.0 lb, was diagnosed with depression and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, candidiasis, cholecystectomy, depression, diabetes mellitus, hyperlipidaemia, hypertension, metabolic disorder, obesity, . ZYPREXA dosage: 5 MG, UNK. During the same period patient was treated with ARIPIPRAZOLE, QUETIAPINE, ZIPRASIDONE, BUPROPION HYDROCHLORIDE, FLUOXETINE, SERTRALINE, PREDNISONE. Patient was hospitalized. Patient recovered.

Humalog Side Effects Report #5382338-7
HUMALOG problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 26, 2007. Male patient was diagnosed with diabetes mellitus non-insulin-dependent and was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, dialysis, gallbladder operation, hepatic failure, liver operation, renal failure, . HUMALOG dosage: unknown. During the same period patient was treated with HUMALOG PEN. Patient was hospitalized. Patient died on 02/06/2005.

Zyprexa Side Effects Report #5356500-3
Consumer or non-health professional from UNITED STATES reported ZYPREXA problem on Oct 23, 2006. Female patient, 24 years of age, weighting 267.0 lb, was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, blood triglycerides increased, diabetes mellitus, diabetic ketoacidosis, hypertension, metabolic disorder, obesity, . ZYPREXA dosage: unknown. During the same period patient was treated with CLOZAPINE, SEROQUEL, RISPERDAL, THORAZINE, REMERON, ZOLOFT. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5356725-7
ZYPREXA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 13, 2006. Female patient, 58 years of age, weighting 214.1 lb, was diagnosed with depression and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, diabetes mellitus, hyperglycaemia, hypertension, metabolic disorder, mumps, obesity, pancreatitis, . ZYPREXA dosage: unknown. Patient recovered.

Zyprexa Side Effects Report #5358112-4
Consumer or non-health professional from UNITED STATES reported ZYPREXA problem on Oct 03, 2006. Female patient, 61 years of age, weighting 145.9 lb, was diagnosed with depression and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, blood cholesterol increased, blood triglycerides increased, cerebrovascular accident, diabetes mellitus, hyperglycaemia, vision blurred, weight decreased, . ZYPREXA dosage: 20 MG. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5358142-2
ZYPREXA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 27, 2006. Female patient, 35 years of age, weighting 196.9 lb, was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, lactic acidosis, pancreatitis, vision blurred, weight decreased, . ZYPREXA dosage: 5 MG. During the same period patient was treated with QUETIAPINE FUMARATE, CHLORPROMAZINE, BUPROPION, DOXEPIN, PREDNISOLONE. Patient recovered.

Zyprexa Side Effects Report #5358164-1
Consumer or non-health professional from UNITED STATES reported ZYPREXA problem on Nov 01, 2006. Male patient, 46 years of age, weighting 330.0 lb, was diagnosed with bipolar disorder and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, blood cholesterol increased, blood triglycerides increased, diabetes mellitus, diabetic coma, hypertension, metabolic disorder, pancreatitis, . ZYPREXA dosage: 20 MG. During the same period patient was treated with SEROQUEL, RISPERIDONE. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5358170-7
ZYPREXA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 19, 2006. Male patient, 44 years of age, weighting 418.0 lb, was diagnosed with schizophrenia and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, diabetes mellitus, hypertension, metabolic disorder, obesity, . ZYPREXA dosage: 20 MG. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5358222-1
Consumer or non-health professional from UNITED STATES reported ZYPREXA problem on Oct 18, 2006. Female patient, 44 years of age, weighting 160.1 lb, was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, pancreatitis, . ZYPREXA dosage: 20 MG. During the same period patient was treated with BUPROPION. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5358241-5
ZYPREXA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 16, 2006. Female patient, 55 years of age, weighting 155.0 lb, was diagnosed with bipolar i disorder and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, blood cholesterol, blood triglycerides abnormal, convulsion, diabetes mellitus, insulin resistance, metabolic disorder, obesity, weight decreased, . ZYPREXA dosage: 2.5 MG. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5358274-9
Consumer or non-health professional from UNITED STATES reported ZYPREXA problem on Oct 27, 2006. Female patient, 75 years of age, weighting 201.9 lb, was diagnosed with depression and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, blood cholesterol increased, blood triglycerides increased, cerebrovascular disorder, diabetes mellitus, diabetic ketoacidosis, glycosuria, hyperglycaemia, hyperglycaemic hyperosmolar nonketotic syndrome, . ZYPREXA dosage: 5 MG, ORAL. During the same period patient was treated with METOPROLOL TARTRATE, ROSIGLITAZONE, ACTOS, INSULIN. Patient recovered.

Zyprexa Side Effects Report #5359597-X
ZYPREXA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 19, 2006. Male patient, 65 years of age, weighting 226.9 lb, was diagnosed with depression and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, diabetes mellitus, pancreatitis, . ZYPREXA dosage: 5 MG,. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5309937-2
Consumer or non-health professional from SPAIN reported FORTEO problem on Apr 18, 2007. Female patient, 71 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, jaundice, pain, pyrexia, . FORTEO dosage: unknown. During the same period patient was treated with ENALAPRIL MALEATE, TRANSDERM PATCH. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5216583-8
ZYPREXA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 14, 2006. Male patient, 45 years of age, weighting 340.0 lb, was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, blood cholesterol abnormal, blood triglycerides increased, diabetes mellitus, glucose tolerance impaired, hyperglycaemic hyperosmolar nonketotic syndrome, hypertension, mumps, obesity, . ZYPREXA dosage: 30 MG. During the same period patient was treated with WELLBUTRIN, GEODON. Patient recovered.

Zyprexa Side Effects Report #5216624-8
Consumer or non-health professional from UNITED STATES reported ZYPREXA problem on May 01, 2006. Female patient, weighting 147.9 lb, was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, blood triglycerides increased, diabetes mellitus, glucose tolerance impaired, hyperglycaemia, hyperinsulinism, hypertension, hypoglycaemia, pancreatitis acute, . ZYPREXA dosage: 2.5 MG, ORAL. During the same period patient was treated with PAXIL. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5216660-1
ZYPREXA problem was reported by a Consumer or non-health professional from UNITED STATES on May 31, 2006. Female patient, 42 years of age, weighting 222.9 lb, was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, blood cholesterol abnormal, diabetes mellitus, hyperglycaemia, hypertension, obesity, polyuria, . ZYPREXA dosage: 10 MG. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5217769-9
Consumer or non-health professional from UNITED STATES reported ZYPREXA problem on Oct 03, 2006. Female patient, 61 years of age, weighting 145.9 lb, was diagnosed with depression and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, blood cholesterol increased, blood triglycerides increased, cerebrovascular accident, diabetes mellitus, hyperglycaemia, vision blurred, weight decreased, . ZYPREXA dosage: 20 MG. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5217909-1
ZYPREXA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 15, 2006. Female patient, 48 years of age, weighting 185.0 lb, was diagnosed with psychotic disorder and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, blood triglycerides increased, diabetes mellitus, metabolic disorder, pancreatitis, . ZYPREXA dosage: 20 MG. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5218215-1
Consumer or non-health professional from UNITED STATES reported ZYPREXA problem on Aug 07, 2006. Female patient, 21 years of age, weighting 203.0 lb, was diagnosed with mood swings and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, blood cholesterol abnormal, blood disorder, blood triglycerides increased, diabetes mellitus non-insulin-dependent, hypertension, metabolic disorder, obesity, polycystic ovaries, . ZYPREXA dosage: 20 MG, ORAL. During the same period patient was treated with ABILIFY. Patient recovered.

Zyprexa Side Effects Report #5218599-4
ZYPREXA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 22, 2006. Female patient, 43 years of age, was diagnosed with bipolar disorder and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, blood cholesterol abnormal, diabetes mellitus, obesity, . ZYPREXA dosage: 15 MG, ORAL. Patient recovered.

Humalog Side Effects Report #5256657-9
Consumer or non-health professional from UNITED STATES reported HUMALOG problem on Feb 26, 2007. Male patient was diagnosed with diabetes mellitus non-insulin-dependent and was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, dialysis, gallbladder operation, hepatic failure, liver operation, renal failure, . HUMALOG dosage: unknown. Patient was hospitalized. Patient died on 02/06/2005.