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Accutane Side Effects Report #5661558-8
Physician from UNITED STATES reported ACCUTANE problem on Mar 04, 2008. Female patient, weighting 145.1 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: adenoma benign, colitis, colitis ulcerative, crohn's disease, depression, dry skin, gastrointestinal disorder, inflammatory bowel disease, irritable bowel syndrome, . ACCUTANE dosage: REPORTED AS 40MG OD. During the same period patient was treated with ORTHO TRI, CLINDAMYCIN LOTION, SULFAMETHOXAZOLE AND TRIMETHOPRIM, SULFAMETHOXAZOLE AND TRIMETHOPRIM, SULFAMETHOXAZOLE AND TRIMETHOPRIM, CLEOCIN T, CLEOCIN T. Patient recovered.

Accutane Side Effects Report #5662624-3
ACCUTANE problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 06, 2008. Female patient, 43 years of age, weighting 128.1 lb, was diagnosed with anxiety and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: adenoma benign, blood cholesterol increased, diverticulitis, elbow operation, gallbladder polyp, haemangioma of liver, haemorrhage, haemorrhoids, hydronephrosis, . ACCUTANE dosage: unknown. During the same period patient was treated with AMNESTEEM, XANAX. Patient was hospitalized. Patient recovered.

Parlodel Side Effects Report #5630350-2
Consumer or non-health professional from BRAZIL reported PARLODEL problem on Feb 11, 2008. Female patient, 49 years of age, weighting 147.7 lb, was diagnosed with hyperprolactinaemia, menopause and was treated with PARLODEL. After drug was administered, patient experienced the following problems/side effects: adenoma benign, . PARLODEL dosage: 0.125 MG/DAY. During the same period patient was treated with ESTRADIOL, DUFASTON. Patient recovered.

Accutane Side Effects Report #5636654-1
ACCUTANE problem was reported by a Physician from UNITED STATES on Feb 13, 2008. Female patient, weighting 145.1 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: adenoma benign, colitis, colitis ulcerative, crohn's disease, depression, dry skin, gastrointestinal disorder, inflammatory bowel disease, irritable bowel syndrome, . ACCUTANE dosage: REPORTED AS 40MG OD. During the same period patient was treated with ORTHO TRI, CLINDAMYCIN LOTION, SULFAMETHOXAZOLE AND TRIMETHOPRIM, SULFAMETHOXAZOLE AND TRIMETHOPRIM, SULFAMETHOXAZOLE AND TRIMETHOPRIM, CLEOCIN T, CLEOCIN T. Patient recovered.


Accutane Side Effects Report #5645028-9
Physician from UNITED STATES reported ACCUTANE problem on Feb 21, 2008. Female patient, weighting 145.1 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: adenoma benign, colitis, colitis ulcerative, crohn's disease, depression, dry skin, gastrointestinal disorder, inflammatory bowel disease, irritable bowel syndrome, . ACCUTANE dosage: REPORTED AS 40MG OD. During the same period patient was treated with ORTHO TRI, CLINDAMYCIN LOTION, SULFAMETHOXAZOLE AND TRIMETHOPRIM, SULFAMETHOXAZOLE AND TRIMETHOPRIM, SULFAMETHOXAZOLE AND TRIMETHOPRIM, CLEOCIN T, CLEOCIN T. Patient recovered.

Humira Side Effects Report #5597729-9
HUMIRA problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Jan 11, 2008. Female patient, weighting 125.7 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: adenoma benign, adhesion, intestinal obstruction, . HUMIRA dosage: unknown. During the same period patient was treated with LEFLUNOMIDE, CALCIUM GLUCONATE, ERGOCALCIFEROL, FERROUS SULPHATE, MELOXICAM. Patient was hospitalized. Patient recovered.

Accutane Side Effects Report #5604485-4
Consumer or non-health professional from UNITED STATES reported ACCUTANE problem on Jan 15, 2008. Female patient, weighting 145.1 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: adenoma benign, colitis ulcerative, crohn's disease, depression, dry skin, gastrointestinal disorder, inflammatory bowel disease, irritable bowel syndrome, mouth cyst, . ACCUTANE dosage: REPORTED AS 40MG OD. During the same period patient was treated with ORTHO TRI. Patient recovered.

Accutane Side Effects Report #5562955-1
ACCUTANE problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 06, 2007. Female patient, 43 years of age, weighting 128.1 lb, was diagnosed with anxiety and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: adenoma benign, blood cholesterol increased, diverticulitis, elbow operation, haemorrhage, haemorrhoids, hypersensitivity, hysterectomy, intervertebral disc protrusion, . ACCUTANE dosage: unknown. During the same period patient was treated with AMNESTEEM, XANAX. Patient was hospitalized. Patient recovered.

Aredia Side Effects Report #5564303-X
Physician from UNITED STATES reported AREDIA problem on Dec 14, 2007. Male patient, 75 years of age, weighting 190.0 lb, was diagnosed with myalgia and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: adenoma benign, anal polyp, apical granuloma, arthralgia, asthenia, bone disorder, bone lesion, bone pain, bronchitis chronic, . AREDIA dosage: unknown. During the same period patient was treated with ZOMETA, ANTINEOPLASTIC AGENTS, PREDNISONE, DURAGESIC, VICODIN. Patient was hospitalized. Patient died.


Accutane Side Effects Report #5574436-X
ACCUTANE problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 21, 2007. Female patient, 43 years of age, weighting 128.1 lb, was diagnosed with anxiety and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: adenoma benign, blood cholesterol increased, diverticulitis, elbow operation, haemorrhage, haemorrhoids, hydronephrosis, hypersensitivity, hysterectomy, . ACCUTANE dosage: unknown. During the same period patient was treated with AMNESTEEM, XANAX. Patient was hospitalized. Patient recovered.

Aredia Side Effects Report #5513761-5
Physician from UNITED STATES reported AREDIA problem on Nov 05, 2007. Male patient, 75 years of age, weighting 190.0 lb, was diagnosed with myalgia and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: adenoma benign, anal polyp, apical granuloma, arthralgia, asthenia, bone disorder, bone lesion, bone pain, bronchitis chronic, . AREDIA dosage: unknown. During the same period patient was treated with ZOMETA, ANTINEOPLASTIC AGENTS, PREDNISONE, DURAGESIC, VICODIN. Patient was hospitalized. Patient recovered.

Byetta Side Effects Report #5582055-4
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 16, 2007. Female patient, 61 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: adenoma benign, blood glucose increased, intestinal polyp, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with NOVOLIN. Patient recovered.

Parlodel Side Effects Report #5482090-0
Consumer or non-health professional from BRAZIL reported PARLODEL problem on Oct 03, 2007. Female patient, 25 years of age, weighting 114.6 lb, was diagnosed with blood prolactin increased and was treated with PARLODEL. After drug was administered, patient experienced the following problems/side effects: adenoma benign, dizziness, malaise, nausea, surgery, . PARLODEL dosage: 2.5 MG, QID. During the same period patient was treated with RIFOCINA. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5490840-2
FOSAMAX problem was reported by a Physician from UNITED STATES on Oct 15, 2007. Female patient, 58 years of age, weighting 134.5 lb, was diagnosed with osteopenia, osteoporosis, sleep disorder and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adenoma benign, anxiety, arthralgia, blood alkaline phosphatase increased, chest pain, gamma-glutamyltransferase increased, insomnia, jaw cyst, laryngitis, . FOSAMAX dosage: unknown. During the same period patient was treated with CLONAZEPAM, NEXIUM, TRAZODONE HYDROCHLORIDE, TAMOXIFEN CITRATE. Patient recovered.


Dostinex Side Effects Report #5491092-X
Physician from BRAZIL reported DOSTINEX problem on Oct 08, 2007. Male patient, weighting 187.4 lb, was diagnosed with prolactinoma, blood cholesterol increased, benign prostatic hyperplasia, osteopenia and was treated with DOSTINEX. After drug was administered, patient experienced the following problems/side effects: adenoma benign, visual disturbance, . DOSTINEX dosage: unknown. During the same period patient was treated with VYTORIN, DOXAZOSIN MESYLATE, CALTRATE, FOSAMAX. Patient recovered.

Pegasys Side Effects Report #5405231-X
PEGASYS problem was reported by a Consumer or non-health professional from IRELAND on July 24, 2007. Male patient, 46 years of age, weighting 179.9 lb, was diagnosed with hepatitis c and was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: adenoma benign, dysphonia, pharyngolaryngeal pain, . PEGASYS dosage: unknown. During the same period patient was treated with COPEGUS. Patient recovered.

Fosamax Side Effects Report #5385969-3
Physician from UNITED STATES reported FOSAMAX problem on July 02, 2007. Female patient, 58 years of age, weighting 134.5 lb, was diagnosed with osteopenia, osteoporosis, sleep disorder and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adenoma benign, anxiety, arthralgia, blood alkaline phosphatase increased, chest pain, gamma-glutamyltransferase increased, insomnia, jaw cyst, laryngitis, . FOSAMAX dosage: unknown. During the same period patient was treated with CLONAZEPAM, NEXIUM, TRAZODONE HYDROCHLORIDE, TAMOXIFEN CITRATE. Patient recovered.

Pegasys Side Effects Report #5390197-1
PEGASYS problem was reported by a Consumer or non-health professional from UNITED STATES on July 12, 2007. Male patient, 54 years of age, was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: adenoma benign, . PEGASYS dosage: unknown. During the same period patient was treated with RIBAVIRIN. Patient recovered.

Fosamax Side Effects Report #5385969-3
Physician from UNITED STATES reported FOSAMAX problem on July 02, 2007. Female patient, 58 years of age, weighting 134.5 lb, was diagnosed with osteopenia, osteoporosis, sleep disorder and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adenoma benign, anxiety, arthralgia, blood alkaline phosphatase increased, chest pain, gamma-glutamyltransferase increased, insomnia, jaw cyst, laryngitis, . FOSAMAX dosage: unknown. During the same period patient was treated with CLONAZEPAM, NEXIUM, TRAZODONE HYDROCHLORIDE, TAMOXIFEN CITRATE. Patient recovered.


Pegasys Side Effects Report #5390197-1
PEGASYS problem was reported by a Consumer or non-health professional from UNITED STATES on July 12, 2007. Male patient, 54 years of age, was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: adenoma benign, . PEGASYS dosage: unknown. During the same period patient was treated with RIBAVIRIN. Patient recovered.

Kadian Side Effects Report #5766722-5
Health Professional from UNITED STATES reported KADIAN problem on May 29, 2008. Male patient, 43 years of age, weighting 177.5 lb, was diagnosed with pain and was treated with KADIAN. After drug was administered, patient experienced the following problems/side effects: adenoma benign, bronchopneumonia, cardiomegaly, cardiovascular disorder, cholesterosis, completed suicide, coronary artery stenosis, depressed level of consciousness, . KADIAN dosage: 30 MG PO Q12 HOURS PRN. During the same period patient was treated with ALPRAZOLAM, HYDROCODONE, CYCLOBENZAPRINE, HYDROMORPHONE, DARVON. Patient died on 02/02/2008.

Modafinil Side Effects Report #5776633-7
MODAFINIL problem was reported by a Health Professional from JAPAN on June 03, 2008. Male patient, 63 years of age, was diagnosed with sleep apnoea syndrome and was treated with MODAFINIL. After drug was administered, patient experienced the following problems/side effects: adenoma benign, atrophy, biliary dilatation, blood alkaline phosphatase increased, dilatation intrahepatic duct acquired, gamma-glutamyltransferase increased, gastric disorder, pancreatic carcinoma, pancreatic duct dilatation, . MODAFINIL dosage: 200 MG QD ORAL. During the same period patient was treated with DEXART, LIDOCAINE. Patient was hospitalized. Patient recovered.

Accutane Side Effects Report #5730125-X
Physician from UNITED STATES reported ACCUTANE problem on Apr 29, 2008. Female patient, weighting 145.1 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: adenoma benign, adnexa uteri mass, back pain, colitis, colitis ulcerative, crohn's disease, depression, dry skin, gastrointestinal disorder, . ACCUTANE dosage: REPORTED AS 40MG OD. During the same period patient was treated with ORTHO TRI, ORTHO TRI, CLINDAMYCIN LOTION, SULFAMETHOXAZOLE AND TRIMETHOPRIM, SULFAMETHOXAZOLE AND TRIMETHOPRIM, SULFAMETHOXAZOLE AND TRIMETHOPRIM, SULFAMETHOXAZOLE AND TRIMETHOPRIM. Patient recovered.

Accutane Side Effects Report #5715871-6
ACCUTANE problem was reported by a Physician from UNITED STATES on Apr 16, 2008. Female patient, weighting 145.1 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: adenoma benign, colitis, colitis ulcerative, crohn's disease, depression, dry skin, gastrointestinal disorder, inflammatory bowel disease, irritable bowel syndrome, . ACCUTANE dosage: REPORTED AS 40MG OD. During the same period patient was treated with ORTHO TRI, ORTHO TRI, CLINDAMYCIN LOTION, SULFAMETHOXAZOLE AND TRIMETHOPRIM, SULFAMETHOXAZOLE AND TRIMETHOPRIM, SULFAMETHOXAZOLE AND TRIMETHOPRIM, SULFAMETHOXAZOLE AND TRIMETHOPRIM. Patient recovered.

Nolvadex Side Effects Report #5354126-9
Physician from AUSTRIA reported NOLVADEX problem on June 04, 2007. Female patient, weighting 196.2 lb, was diagnosed with breast cancer and was treated with NOLVADEX. After drug was administered, patient experienced the following problems/side effects: adenoma benign, endometrial hyperplasia, . NOLVADEX dosage: unknown. Patient was hospitalized. Patient recovered.

Zelnorm Side Effects Report #5364687-1
ZELNORM problem was reported by a Consumer or non-health professional from UNITED STATES on June 13, 2007. Male patient, 55 years of age, was diagnosed with constipation, diabetes mellitus and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: adenoma benign, colon polypectomy, colonic polyp, coronary angioplasty, diverticulum intestinal, haemorrhoids, myocardial infarction, . ZELNORM dosage: 6 MG, BID. During the same period patient was treated with GLYBURIDE AND METFORMIN, PRANDIN, AVANDIA, LOPRESSOR, LISINOPRIL, ZOCOR, NEXIUM, SINGULAIR. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5327113-4
Physician from UNITED STATES reported REMICADE problem on May 08, 2007. Female patient, weighting 155.0 lb, was diagnosed with crohn's disease and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: adenoma benign, leiomyoma, . REMICADE dosage: unknown. Patient was hospitalized. Patient recovered.

Zelnorm Side Effects Report #5330713-9
ZELNORM problem was reported by a Consumer or non-health professional from UNITED STATES on May 10, 2007. Female patient, 40 years of age, weighting 149.0 lb, was diagnosed with irritable bowel syndrome and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: adenoma benign, chest pain, cholecystectomy, dyspepsia, dyspnoea, flatulence, . ZELNORM dosage: 6 MG, BID. Patient was hospitalized. Patient recovered.

Champix Side Effects Report #5290920-0
Health Professional from UNITED KINGDOM reported CHAMPIX problem on Mar 28, 2007. Female patient, 48 years of age, weighting 154.3 lb, was diagnosed with ex-smoker and was treated with CHAMPIX. After drug was administered, patient experienced the following problems/side effects: adenoma benign, gastrointestinal obstruction, pneumococcal bacteraemia, . CHAMPIX dosage: unknown. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5291750-6
ZYPREXA problem was reported by a Physician from UNITED STATES on Mar 29, 2007. Female patient, 18 years of age, was diagnosed with schizophrenia, paranoid type and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: adenoma benign, blood prolactin increased, . ZYPREXA dosage: 20 MG, UNK. During the same period patient was treated with CYMBALTA, LAMICTAL, GEODON. Patient recovered.

Valsartan Side Effects Report #5311239-5
Consumer or non-health professional from TAIWAN, PROVINCE OF CHINA reported VALSARTAN AND HYDROCHLOROTHIAZIDE problem on Apr 17, 2007. Male patient, 49 years of age, weighting 176.4 lb, was diagnosed with hypertension and was treated with VALSARTAN AND HYDROCHLOROTHIAZIDE. After drug was administered, patient experienced the following problems/side effects: adenoma benign, ileus, . VALSARTAN AND HYDROCHLOROTHIAZIDE dosage: unknown. Patient was hospitalized. Patient recovered.

Nolvadex Side Effects Report #5258691-1
NOLVADEX problem was reported by a Physician from AUSTRIA on Feb 28, 2007. Female patient, weighting 196.2 lb, was diagnosed with breast cancer and was treated with NOLVADEX. After drug was administered, patient experienced the following problems/side effects: adenoma benign, endometrial hyperplasia, . NOLVADEX dosage: unknown. Patient was hospitalized. Patient recovered.

Estraderm Side Effects Report #5259212-X
Consumer or non-health professional from UNITED STATES reported ESTRADERM problem on Feb 26, 2007. Female patient, 56 years of age, weighting 118.0 lb, was diagnosed with osteoporosis prophylaxis, hot flush and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: adenoma benign, anal haemorrhage, basal cell carcinoma, benign tumour excision, breast cancer, breast cyst, breast tenderness, bursa disorder, chronic obstructive pulmonary disease, . ESTRADERM dosage: 0.05 MG, UNK. During the same period patient was treated with PREMARIN, AMITRIPTYLINE, ZYRTEC, CLIMARA. Patient was hospitalized. Patient recovered.

Diovan Side Effects Report #5262898-7
DIOVAN AMLO problem was reported by a Consumer or non-health professional from BRAZIL on Feb 27, 2007. Female patient, 42 years of age, weighting 180.8 lb, was diagnosed with hypertension and was treated with DIOVAN AMLO. After drug was administered, patient experienced the following problems/side effects: adenoma benign, arrhythmia, blood pressure fluctuation, cardiovascular disorder, fatigue, feeling hot, formication, hypertension, . DIOVAN AMLO dosage: VALS 160 / AMLO 5 MG/DAY. During the same period patient was treated with ATENSINA, PURAN T. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5674760-6
Physician from UNITED STATES reported FOSAMAX problem on Mar 10, 2008. Female patient, 74 years of age, weighting 130.1 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, adenoma benign, anaemia, anxiety, asthma, atrioventricular block first degree, back pain, breathing-related sleep disorder, bronchitis, . FOSAMAX dosage: unknown. During the same period patient was treated with PREMPRO, NEXIUM. Patient was hospitalized and became disabled. Patient recovered.

Fosamax Side Effects Report #5640945-8
FOSAMAX problem was reported by a Physician from UNITED STATES on Feb 18, 2008. Female patient, 74 years of age, weighting 130.1 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, adenoma benign, anaemia, anxiety, asthma, atrioventricular block first degree, back pain, breathing-related sleep disorder, bronchitis, . FOSAMAX dosage: unknown. During the same period patient was treated with PREMPRO, NEXIUM. Patient was hospitalized and became disabled. Patient recovered.

Estraderm Side Effects Report #5585741-5
Consumer or non-health professional from UNITED STATES reported ESTRADERM problem on Jan 07, 2008. Female patient, 72 years of age, weighting 205.0 lb, was diagnosed with menopause and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: acute myocardial infarction, adenoma benign, anxiety, arachnoid cyst, breast calcifications, breast cancer, breast mass, cerebral ischaemia, cerebrovascular accident, . ESTRADERM dosage: 0.5 MG, UNK. During the same period patient was treated with CELEXA, PREMARIN, PROVERA, CYCRIN, ZESTRIL, METOPROLOL TARTRATE, LORTAB. Patient was hospitalized. Patient recovered.

Clofarabine Side Effects Report #5614673-9
CLOFARABINE problem was reported by a Physician from UNITED STATES on Jan 23, 2008. Male patient, 67 years of age, weighting 189.6 lb, was diagnosed with myeloid leukaemia and was treated with CLOFARABINE. After drug was administered, patient experienced the following problems/side effects: acute myeloid leukaemia, adenoma benign, aggression, aspiration, atelectasis, biopsy bone marrow abnormal, cerebral calcification, deep vein thrombosis, depressed level of consciousness, . CLOFARABINE dosage: 30 MG/M2, INTRAVENOUS. During the same period patient was treated with ACETAMINOPHEN, LOVENOX, TOBRAMYCIN, VANCOMYCIN, DOUBUTAMINE, ALBUMIN, NOREPINEPHRINE BITARTRATE, MEROPENEM. Patient was hospitalized. Patient recovered.

Lexotan Side Effects Report #5375831-4
Consumer or non-health professional from BRAZIL reported LEXOTAN problem on June 20, 2007. Female patient, 45 years of age, weighting 136.7 lb, was diagnosed with insomnia, pain, constipation, blood prolactin abnormal and was treated with LEXOTAN. After drug was administered, patient experienced the following problems/side effects: abdominal pain, adenoma benign, carpal tunnel syndrome, dizziness, dyspnoea, dyspnoea exertional, erythema, . LEXOTAN dosage: 3 MG/DAY. During the same period patient was treated with BEXTRA, ZELMAC, DOSTINEX, NIFUROXAZIDE. Patient recovered.

Estraderm Side Effects Report #5388980-1
ESTRADERM problem was reported by a Consumer or non-health professional from UNITED STATES on July 06, 2007. Female patient, 72 years of age, weighting 205.0 lb, was diagnosed with menopause and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: acute myocardial infarction, adenoma benign, anxiety, arachnoid cyst, breast cancer, breast mass, breast microcalcification, cerebral ischaemia, cerebrovascular accident, . ESTRADERM dosage: 0.5 MG, UNK. During the same period patient was treated with CELEXA, PREMARIN, PROVERA, CYCRIN, ZESTRIL, METOPROLOL SUCCINATE, LORTAB. Patient was hospitalized. Patient recovered.

Lexotan Side Effects Report #5375831-4
Consumer or non-health professional from BRAZIL reported LEXOTAN problem on June 20, 2007. Female patient, 45 years of age, weighting 136.7 lb, was diagnosed with insomnia, pain, constipation, blood prolactin abnormal and was treated with LEXOTAN. After drug was administered, patient experienced the following problems/side effects: abdominal pain, adenoma benign, carpal tunnel syndrome, dizziness, dyspnoea, dyspnoea exertional, erythema, . LEXOTAN dosage: 3 MG/DAY. During the same period patient was treated with BEXTRA, ZELMAC, DOSTINEX, NIFUROXAZIDE. Patient recovered.

Estraderm Side Effects Report #5388980-1
ESTRADERM problem was reported by a Consumer or non-health professional from UNITED STATES on July 06, 2007. Female patient, 72 years of age, weighting 205.0 lb, was diagnosed with menopause and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: acute myocardial infarction, adenoma benign, anxiety, arachnoid cyst, breast cancer, breast mass, breast microcalcification, cerebral ischaemia, cerebrovascular accident, . ESTRADERM dosage: 0.5 MG, UNK. During the same period patient was treated with CELEXA, PREMARIN, PROVERA, CYCRIN, ZESTRIL, METOPROLOL SUCCINATE, LORTAB. Patient was hospitalized. Patient recovered.

Estraderm Side Effects Report #5742973-0
Consumer or non-health professional from UNITED STATES reported ESTRADERM problem on May 14, 2008. Female patient, 72 years of age, weighting 205.0 lb, was diagnosed with menopause and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: acute myocardial infarction, adenoma benign, arachnoid cyst, arterial stenosis, arteriosclerosis, breast cancer, breast mass, cerebral ischaemia, cerebrovascular accident, . ESTRADERM dosage: 0.5 MG, UNK. During the same period patient was treated with CELEXA, PREMARIN, PROVERA, CYCRIN, ZESTRIL, METOPROLOL TARTRATE, LORTAB. Patient was hospitalized. Patient recovered.

Tysabri Side Effects Report #5710583-7
TYSABRI problem was reported by a Health Professional from UNITED STATES on Mar 31, 2008. Female patient, 60 years of age, weighting 154.8 lb, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: abdominal pain, adenoma benign, back pain, blood glucose increased, blood potassium increased, burning sensation, emphysema, myelomalacia, neck pain, . TYSABRI dosage: 300 MG QM IV. During the same period patient was treated with PROVIGIL, SINGULAIR, PRILOSEC, LYRICA, THEOPHYLLINE, LIDOCAINE. Patient was hospitalized. Patient recovered.

Viagra Side Effects Report #5351051-4
Consumer or non-health professional from UNITED STATES reported VIAGRA problem on May 29, 2007. Male patient, weighting 160.1 lb, was diagnosed with erectile dysfunction, hypertension and was treated with VIAGRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, adenoma benign, arthritis, cerumen impaction, dizziness, dyspnoea, erectile dysfunction, . VIAGRA dosage: unknown. During the same period patient was treated with ACCUPRIL, CIALIS, TRIAMTERENE AND HYDROCHLOROTHIAZIDE, LUMIGAN, ACETYLSALICYLIC ACID SRT, VITAMIN CAP, FISH OIL. Patient recovered.

Champix Side Effects Report #5332621-6
CHAMPIX problem was reported by a Health Professional from UNITED KINGDOM on May 11, 2007. Female patient, 48 years of age, weighting 154.3 lb, was diagnosed with ex-smoker and was treated with CHAMPIX. After drug was administered, patient experienced the following problems/side effects: abdominal pain lower, adenoma benign, gastrointestinal obstruction, pneumococcal bacteraemia, pyrexia, . CHAMPIX dosage: unknown. Patient was hospitalized. Patient recovered.

Aredia Side Effects Report #5268034-5
Physician from UNITED STATES reported AREDIA problem on Mar 05, 2007. Male patient, 71 years of age, weighting 173.0 lb, was diagnosed with myalgia and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: abscess, adenoma benign, anal polyp, apical granuloma, arthralgia, asthenia, bone disorder, bone lesion, bone pain, . AREDIA dosage: unknown. During the same period patient was treated with ZOMETA, PREDNISONE, DURAGESIC, VICODIN, DARVON. Patient was hospitalized. Patient recovered.

Accutane Side Effects Report #5754294-0
ACCUTANE problem was reported by a Consumer or non-health professional from UNITED STATES on May 19, 2008. Female patient, weighting 143.1 lb, was diagnosed with oral contraception, musculoskeletal pain and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: abdominal distension, abortion spontaneous, adenoma benign, anaemia, anhedonia, anxiety, arthritis, back pain, bilirubin urine, . ACCUTANE dosage: unknown. During the same period patient was treated with BIRTH CONTROL S, ORTHO TRI, ORTHO TRI, PHENERGAN, TYLENOL, ZANTAC, IBUROFEN. Patient was hospitalized and became disabled. Patient recovered.