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BLOOD CHOLESTEROL DECREASED side effect

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Candesartan Side Effects Report #5564242-4
Consumer or non-health professional from JAPAN reported CANDESARTAN CILEXETIL problem on Dec 03, 2007. Female patient, 69 years of age, was diagnosed with essential hypertension, type 2 diabetes mellitus and was treated with CANDESARTAN CILEXETIL. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, rhinorrhoea, thyroxine free increased, . CANDESARTAN CILEXETIL dosage: 8 MG (8 MG,1 IN 1 D), PER ORAL. During the same period patient was treated with CANDESARTAN CILEXETIL, ACTOS, AMARYL, NORVASC, GLYBURIDE, ADALAT, FAMOTIDINE, MERCAZOLE. Patient died.

Prograf Side Effects Report #5574538-8
PROGRAF problem was reported by a Physician from UNITED STATES on Dec 07, 2007. Male patient, 45 years of age, was diagnosed with immunosuppression and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, chronic inflammatory demyelinating polyradiculoneuropathy, cytomegalovirus antibody positive, demyelinating polyneuropathy, diarrhoea, fatigue, headache, liver transplant rejection, . PROGRAF dosage: 7 MG, BID, ORAL; 5 MG, BID, ORAL; 4 MG, BID, ORAL; 3 MG, BID, ORAL. During the same period patient was treated with CORTICOSTEROID NOS. Patient recovered.

Lipitor Side Effects Report #5551428-8
Consumer or non-health professional from UNITED STATES reported LIPITOR problem on Apr 25, 2007. Male patient, 66 years of age, weighting 160.3 lb, was diagnosed with low density lipoprotein increased and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, hepatocellular damage, high density lipoprotein abnormal, high density lipoprotein decreased, low density lipoprotein abnormal, . LIPITOR dosage: unknown. During the same period patient was treated with TORPOL. Patient recovered.

Exenatide Side Effects Report #5552147-4
EXENATIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 27, 2007. Male patient, 53 years of age, weighting 194.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with EXENATIDE. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood pressure decreased, decreased appetite, dizziness, weight decreased, . EXENATIDE dosage: unknown. During the same period patient was treated with METFORMIN, ZETIA, DIOVAN. Patient recovered.


Exenatide Side Effects Report #5556144-4
Consumer or non-health professional from UNITED STATES reported EXENATIDE problem on July 06, 2007. Female patient, 60 years of age, weighting 218.9 lb, was diagnosed with type 2 diabetes mellitus and was treated with EXENATIDE. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood glucose decreased, blood glucose increased, blood triglycerides decreased, constipation, decreased appetite, dyspepsia, flatulence, gastrooesophageal reflux disease, . EXENATIDE dosage: unknown. Patient recovered.

Exenatide Side Effects Report #5556765-9
EXENATIDE problem was reported by a Consumer or non-health professional from UNITED STATES on July 23, 2007. Male patient, 46 years of age, weighting 250.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with EXENATIDE. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, injection site bruising, injection site irritation, weight decreased, . EXENATIDE dosage: unknown. During the same period patient was treated with METFORMIN, JANUVIA, AVANDAMET. Patient recovered.

Byetta Side Effects Report #5576881-5
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Sept 25, 2007. Female patient, 58 years of age, weighting 190.0 lb, was diagnosed with weight decreased and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood triglycerides decreased, fatigue, glycosylated haemoglobin increased, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN, GLYBURIDE. Patient recovered.

Seroquel Side Effects Report #5460324-6
SEROQUEL problem was reported by a Consumer or non-health professional from UNITED STATES on June 11, 2007. Male patient, 32 years of age, weighting 153.0 lb, was diagnosed with mood swings, bipolar disorder, blood pressure management and was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, weight decreased, . SEROQUEL dosage: unknown. During the same period patient was treated with BENICAR. Patient recovered.

Omacor Side Effects Report #5486545-4
Consumer or non-health professional from UNITED STATES reported OMACOR problem on May 21, 2007. Female patient, 68 years of age, weighting 106.0 lb, was diagnosed with blood cholesterol increased and was treated with OMACOR. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, high density lipoprotein decreased, hot flush, off label use, therapeutic response unexpected, . OMACOR dosage: unknown. During the same period patient was treated with RED YEAST RICE, RED YEAST RICE, RED YEAST RICE, VITAMINS NOS. Patient recovered.


Neurontin Side Effects Report #5403263-9
NEURONTIN problem was reported by a Consumer or non-health professional from UNITED STATES on July 20, 2007. Male patient, weighting 250.0 lb, was diagnosed with neuropathy and was treated with NEURONTIN. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, neuropathy, pain, . NEURONTIN dosage: unknown. During the same period patient was treated with LYRICA, ATENOLOL, ACCUPRIL, PROCARDIA. Patient recovered.

Nexium Side Effects Report #5413565-8
Consumer or non-health professional from UNITED STATES reported NEXIUM problem on Aug 10, 2007. Female patient, 43 years of age, weighting 210.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with NEXIUM. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood pressure decreased, myocardial infarction, . NEXIUM dosage: unknown. During the same period patient was treated with TYLENOL. Patient recovered.

Byetta Side Effects Report #5424330-X
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on June 01, 2007. Female patient, 57 years of age, weighting 136.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, decreased appetite, nausea, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE, METFORMIN. Patient recovered.

Exenatide Side Effects Report #5426630-6
Consumer or non-health professional from UNITED STATES reported EXENATIDE problem on Apr 01, 2007. Female patient, 57 years of age, weighting 164.9 lb, was diagnosed with type 2 diabetes mellitus and was treated with EXENATIDE. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood glucose increased, influenza like illness, nausea, weight decreased, . EXENATIDE dosage: unknown. During the same period patient was treated with METFORMIN, LIPITOR, TRICOR, ASPIRIN. Patient recovered.

Exenatide Side Effects Report #5426665-3
EXENATIDE problem was reported by a Consumer or non-health professional from UNITED STATES on May 14, 2007. Female patient, 60 years of age, weighting 218.9 lb, was diagnosed with type 2 diabetes mellitus and was treated with EXENATIDE. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood glucose decreased, blood glucose increased, blood triglycerides decreased, constipation, decreased appetite, dyspepsia, flatulence, gastrooesophageal reflux disease, . EXENATIDE dosage: unknown. During the same period patient was treated with GLUCOVANCE, GLUCOPHAGE. Patient recovered.


Byetta Side Effects Report #5427022-6
Consumer or non-health professional from UNITED STATES reported BYETTA problem on May 02, 2007. Male patient, 62 years of age, weighting 187.0 lb, was diagnosed with diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, nausea, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with AVANDIA, GLUCOTROL, METFORMIN. Patient recovered.

Byetta Side Effects Report #5429696-2
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on May 03, 2007. Male patient, 63 years of age, weighting 190.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood pressure decreased, decreased appetite, energy increased, increased appetite, weight fluctuation, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE, AMARYL. Patient recovered.

Byetta Side Effects Report #5431801-9
Consumer or non-health professional from UNITED STATES reported BYETTA problem on June 11, 2007. Female patient, 57 years of age, weighting 179.9 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood glucose decreased, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE PEN, GLUCOPHAGE, ZOCOR. Patient recovered.

Byetta Side Effects Report #5431809-3
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on June 11, 2007. Male patient, 74 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood pressure decreased, oedema peripheral, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE PEN, LANTUS, ATENOLOL, SIMVASTATIN, HYDROCHLOROTHIAZIDE, FELODIPINE, ACTOS. Patient recovered.

Byetta Side Effects Report #5441038-5
Consumer or non-health professional from UNITED STATES reported BYETTA problem on May 02, 2007. Female patient, 61 years of age, weighting 145.1 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, decreased appetite, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE. Patient recovered.


Byetta Side Effects Report #5424330-X
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on June 01, 2007. Female patient, 57 years of age, weighting 136.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, decreased appetite, nausea, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE, METFORMIN. Patient recovered.

Exenatide Side Effects Report #5426630-6
Consumer or non-health professional from UNITED STATES reported EXENATIDE problem on Apr 01, 2007. Female patient, 57 years of age, weighting 164.9 lb, was diagnosed with type 2 diabetes mellitus and was treated with EXENATIDE. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood glucose increased, influenza like illness, nausea, weight decreased, . EXENATIDE dosage: unknown. During the same period patient was treated with METFORMIN, LIPITOR, TRICOR, ASPIRIN. Patient recovered.

Exenatide Side Effects Report #5426665-3
EXENATIDE problem was reported by a Consumer or non-health professional from UNITED STATES on May 14, 2007. Female patient, 60 years of age, weighting 218.9 lb, was diagnosed with type 2 diabetes mellitus and was treated with EXENATIDE. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood glucose decreased, blood glucose increased, blood triglycerides decreased, constipation, decreased appetite, dyspepsia, flatulence, gastrooesophageal reflux disease, . EXENATIDE dosage: unknown. During the same period patient was treated with GLUCOVANCE, GLUCOPHAGE. Patient recovered.

Byetta Side Effects Report #5427022-6
Consumer or non-health professional from UNITED STATES reported BYETTA problem on May 02, 2007. Male patient, 62 years of age, weighting 187.0 lb, was diagnosed with diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, nausea, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with AVANDIA, GLUCOTROL, METFORMIN. Patient recovered.

Byetta Side Effects Report #5429696-2
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on May 03, 2007. Male patient, 63 years of age, weighting 190.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood pressure decreased, decreased appetite, energy increased, increased appetite, weight fluctuation, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE, AMARYL. Patient recovered.

Byetta Side Effects Report #5431801-9
Consumer or non-health professional from UNITED STATES reported BYETTA problem on June 11, 2007. Female patient, 57 years of age, weighting 179.9 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood glucose decreased, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE PEN, GLUCOPHAGE, ZOCOR. Patient recovered.

Byetta Side Effects Report #5431809-3
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on June 11, 2007. Male patient, 74 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood pressure decreased, oedema peripheral, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE PEN, LANTUS, ATENOLOL, SIMVASTATIN, HYDROCHLOROTHIAZIDE, FELODIPINE, ACTOS. Patient recovered.

Byetta Side Effects Report #5441038-5
Consumer or non-health professional from UNITED STATES reported BYETTA problem on May 02, 2007. Female patient, 61 years of age, weighting 145.1 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, decreased appetite, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE. Patient recovered.

Byetta Side Effects Report #5772351-X
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 28, 2008. Male patient was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood glucose increased, hypoglycaemia, nausea, . BYETTA dosage: unknown. During the same period patient was treated with GLYBURIDE, AVANDIA, VYTORIN, ZOCOR, ZETIA. Patient recovered.

Byetta Side Effects Report #5773446-7
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Mar 24, 2008. Female patient, 57 years of age, weighting 136.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, decreased appetite, nausea, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN. Patient recovered.

Miglitol Side Effects Report #5738890-2
MIGLITOL problem was reported by a Consumer or non-health professional from on May 07, 2008. Male patient, 69 years of age, was treated with MIGLITOL. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood pressure decreased, dizziness, . MIGLITOL dosage: unknown. During the same period patient was treated with LOCHOL. Patient recovered.

Excedrin Side Effects Report #5712695-0
Consumer or non-health professional from UNITED STATES reported EXCEDRIN problem on Apr 14, 2008. Female patient, 65 years of age, weighting 130.1 lb, was diagnosed with headache and was treated with EXCEDRIN. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, . EXCEDRIN dosage: unknown. During the same period patient was treated with ATENOLOL, LISINOPRIL. Patient recovered.

Vytorin Side Effects Report #5355174-5
VYTORIN problem was reported by a Health Professional from UNITED STATES on Jan 25, 2007. Female patient, 61 years of age, was diagnosed with blood cholesterol increased and was treated with VYTORIN. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, muscular weakness, myalgia, . VYTORIN dosage: 10-40 MG/DAILY/PO. During the same period patient was treated with LANTUS, INSULIN. Patient recovered.

Byetta Side Effects Report #5360733-X
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Feb 11, 2007. Female patient, 57 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood pressure increased, sensation of heaviness, speech disorder, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with COZAAR, METFORMIN, LIPITOR. Patient recovered.

Byetta Side Effects Report #5360863-2
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 08, 2007. Female patient, 42 years of age, weighting 252.5 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood triglycerides decreased, decreased appetite, high density lipoprotein decreased, nausea, total cholesterol/hdl ratio abnormal, very low density lipoprotein decreased, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN. Patient recovered.

Byetta Side Effects Report #5380624-8
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Mar 01, 2007. Male patient, 46 years of age, weighting 268.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood glucose decreased, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOTROL, METFORMIN. Patient recovered.

Eurodin Side Effects Report #5150958-0
EURODIN problem was reported by a Consumer or non-health professional from JAPAN on Nov 02, 2006. Male patient, weighting 134.9 lb, was diagnosed with insomnia, alcoholic psychosis and was treated with EURODIN. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, pulmonary embolism, . EURODIN dosage: unknown. During the same period patient was treated with VEGETAMIN, LODOPIN, LULLAN, ETHYL LOFLAZEPATE, ZOPICLONE, HALOPERIDOL, FLUNITRAZEPAM, TRAZODONE. Patient was hospitalized. Patient recovered.

Byetta Side Effects Report #5231479-3
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Sept 14, 2006. Female patient, 45 years of age, weighting 288.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, dyspepsia, energy increased, nausea, therapeutic response unexpected, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with PRECOSE. Patient recovered.

Crestor Side Effects Report #5240227-2
CRESTOR problem was reported by a Consumer or non-health professional from UNITED STATES on May 15, 2006. Female patient, 70 years of age, weighting 165.8 lb, was diagnosed with blood cholesterol increased and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, haemoglobin decreased, high density lipoprotein decreased, . CRESTOR dosage: 10 MG QD PO. During the same period patient was treated with NEXIUM ORAL, CLARINEX, HYDROCHLOROTHIAZIDE, SINGULAIR. Patient recovered.

Byetta Side Effects Report #5240929-8
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Aug 05, 2006. Male patient, 60 years of age, weighting 205.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood glucose increased, . BYETTA dosage: unknown. During the same period patient was treated with AMARYL, METFORMIN. Patient recovered.

Byetta Side Effects Report #5242789-8
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 17, 2006. Female patient, 60 years of age, weighting 229.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood glucose decreased, blood glucose increased, blood triglycerides decreased, decreased appetite, dyspepsia, gastrooesophageal reflux disease, hunger, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOVANCE, GLUCOPHAGE. Patient recovered.

Byetta Side Effects Report #5248932-9
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Aug 23, 2006. Male patient, 59 years of age, weighting 120.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood glucose decreased, blood glucose increased, blood triglycerides decreased, change of bowel habit, dizziness, dyspepsia, injection site bruising, injection site pain, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN, GLUCOPHAGE, GLYBURIDE, AVANDIA, CHOLESTYRAMINE, ACTOS. Patient recovered.

Byetta Side Effects Report #5253235-2
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on July 31, 2006. Female patient, 54 years of age, weighting 250.0 lb, was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood glucose fluctuation, blood pressure decreased, weight decreased, . BYETTA dosage: unknown. Patient recovered.

Byetta Side Effects Report #5255529-3
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Aug 31, 2006. Female patient, 44 years of age, weighting 192.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, blood pressure decreased, dizziness, nausea, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOPHAGE. Patient recovered.

Crestor Side Effects Report #5280436-X
CRESTOR problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 24, 2006. Female patient, 55 years of age, weighting 150.0 lb, was diagnosed with blood cholesterol increased and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: blood cholesterol decreased, muscle spasms, . CRESTOR dosage: 10 MG; PO. During the same period patient was treated with RITHMOL, COREG, DIGOXIN, ALTACE, WARFARIN, PREVACID. Patient recovered.

Lipitor Side Effects Report #5608686-0
Consumer or non-health professional from UNITED STATES reported LIPITOR problem on Jan 22, 2008. Female patient, weighting 179.9 lb, was diagnosed with blood cholesterol increased and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: arthritis, blood cholesterol decreased, body height decreased, muscular weakness, . LIPITOR dosage: DAILY DOSE:20MG-FREQ:DAILY. During the same period patient was treated with ALTACE, ASPIRIN, DYAZIDE, ASCORBIC ACID. Patient recovered.

Byetta Side Effects Report #5648385-2
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 29, 2007. Male patient, 72 years of age, weighting 182.1 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: anorexia, blood cholesterol decreased, blood glucose decreased, blood glucose increased, confusional state, dizziness, eructation, feeling abnormal, . BYETTA dosage: unknown. During the same period patient was treated with AVANDIA. Patient recovered.

Exenatide Side Effects Report #5559755-5
Consumer or non-health professional from UNITED STATES reported EXENATIDE problem on Aug 29, 2007. Male patient, 72 years of age, weighting 182.1 lb, was diagnosed with type 2 diabetes mellitus and was treated with EXENATIDE. After drug was administered, patient experienced the following problems/side effects: anorexia, blood cholesterol decreased, blood glucose decreased, blood glucose increased, confusional state, dizziness, eructation, feeling abnormal, . EXENATIDE dosage: unknown. Patient recovered.

Byetta Side Effects Report #5575026-5
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on July 27, 2007. Male patient, 56 years of age, weighting 325.8 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: arthritis, blood cholesterol decreased, burning sensation, dyspepsia, nausea, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with LOVASTATIN, LISINOPRIL, MELOXICAM, GLIMEPIRIDE, AMARYL. Patient recovered.

Avandamet Side Effects Report #5406053-6
Physician from SWEDEN reported AVANDAMET problem on July 25, 2007. Female patient, 68 years of age, weighting 244.7 lb, was treated with AVANDAMET. After drug was administered, patient experienced the following problems/side effects: anaemia, blood cholesterol decreased, glycosylated haemoglobin increased, haematocrit decreased, haemoglobin decreased, mean cell haemoglobin concentration decreased, mean cell haemoglobin decreased, mean cell volume decreased, platelet count increased, . AVANDAMET dosage: unknown. During the same period patient was treated with ATARAX, NORMORIX MITE, LEVAXIN, TROMBYL, LIPITOR, RANITIDINE, ATENOLOL, BEHEPAN. Patient recovered.

Fosamax Side Effects Report #5787588-3
FOSAMAX problem was reported by a Health Professional from UNITED STATES on June 17, 2008. Female patient, 80 years of age, was diagnosed with osteoporosis, rheumatoid arthritis, blood pressure and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anxiety, blood cholesterol decreased, cardiovascular disorder, carotid artery stenosis, cerebrovascular disorder, chest pain, contusion, depression, eye disorder, . FOSAMAX dosage: unknown. During the same period patient was treated with NORVASC. Patient was hospitalized. Patient recovered.

Levitra Side Effects Report #5215111-0
Consumer or non-health professional from UNITED STATES reported LEVITRA problem on Oct 02, 2006. Male patient was treated with LEVITRA. After drug was administered, patient experienced the following problems/side effects: anxiety, blood cholesterol decreased, hypertension, . LEVITRA dosage: unknown. Patient recovered.