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Achilles Side Effects Report #5705192-X
Physician from UNITED STATES reported ACHILLES TENDON problem on Mar 14, 2008. Female patient, 42 years of age, was diagnosed with soft tissue disorder, surgery and was treated with ACHILLES TENDON. After drug was administered, patient experienced the following problems/side effects: incision site pain, osteoarthritis, post procedural swelling, synovial cyst, . ACHILLES TENDON dosage: unknown. During the same period patient was treated with ACHILLES TENDON, STAPLE. Patient recovered.

Dianeal Side Effects Report #5555189-8
DIANEAL problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 03, 2007. Male patient, 36 years of age, weighting 174.2 lb, was diagnosed with peritoneal dialysis, anaemia, insomnia, hyperphosphataemia and was treated with DIANEAL. After drug was administered, patient experienced the following problems/side effects: incision site pain, peritonitis, pneumonia, ventricular fibrillation, . DIANEAL dosage: unknown. During the same period patient was treated with RENAGEL, EPOGEN, AMIODARONE, METOPROLOL, RESTORIL, CYTAMEN. Patient was hospitalized. Patient died on 09/17/2007.

Dianeal Side Effects Report #5495446-7
Consumer or non-health professional from UNITED STATES reported DIANEAL problem on Oct 17, 2007. Male patient, 36 years of age, was diagnosed with peritoneal dialysis and was treated with DIANEAL. After drug was administered, patient experienced the following problems/side effects: incision site pain, peritonitis, pneumonia, ventricular fibrillation, . DIANEAL dosage: unknown. Patient was hospitalized. Patient died on 09/17/2007.

Rebif Side Effects Report #5705049-4
REBIF problem was reported by a Physician from UNITED STATES on Mar 27, 2008. Female patient, 34 years of age, weighting 127.0 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: incision site pain, injection site reaction, ovarian cyst, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.


Betaseron Side Effects Report #5652416-3
Consumer or non-health professional from UNITED STATES reported BETASERON problem on Feb 21, 2008. Female patient, 57 years of age, weighting 220.5 lb, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: appendicitis, incision site pain, scar, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.

Achilles Side Effects Report #5695383-9
ACHILLES TENDON MUSCULOSKELETAL SOFT problem was reported by a Physician from UNITED STATES on Mar 14, 2008. Female patient, 42 years of age, was diagnosed with soft tissue injury and was treated with ACHILLES TENDON MUSCULOSKELETAL SOFT. After drug was administered, patient experienced the following problems/side effects: graft complication, incision site pain, oedema peripheral, synovial cyst, . ACHILLES TENDON MUSCULOSKELETAL SOFT dosage: unknown. During the same period patient was treated with STAPLE. Patient recovered.

Temozolomide Side Effects Report #5607397-5
Consumer or non-health professional from UNITED STATES reported TEMOZOLOMIDE problem on Jan 28, 2008. Male patient, weighting 202.8 lb, was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: incision site complication, incision site pain, wound infection, . TEMOZOLOMIDE dosage: 1950 MG. Patient was hospitalized. Patient recovered.

Byetta Side Effects Report #5650270-7
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 17, 2007. Male patient, 58 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 glucose increased, incision site pain, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOPHAGE. Patient recovered.

Achilles Side Effects Report #5763741-X
Physician from UNITED STATES reported ACHILLES TENDON problem on June 10, 2008. Female patient, 42 years of age, was diagnosed with soft tissue disorder and was treated with ACHILLES TENDON. After drug was administered, patient experienced the following problems/side effects: incision site complication, incision site pain, osteoarthritis, swelling, synovial cyst, . ACHILLES TENDON dosage: unknown. During the same period patient was treated with STAPLE. Patient recovered.


Motrin Side Effects Report #5327092-X
MOTRIN problem was reported by a Consumer or non-health professional from UNITED STATES on May 02, 2007. Female patient, weighting 170.0 lb, was diagnosed with procedural pain and was treated with MOTRIN. After drug was administered, patient experienced the following problems/side effects: chest discomfort, incision site pain, . MOTRIN dosage: unknown. During the same period patient was treated with CHANTIX, ACETAMINOPHEN AND HYDROCODONE BITARTRATE. Patient recovered.

Musculoskeletal Side Effects Report #5341314-0
Health Professional from UNITED STATES reported MUSCULOSKELETAL SOFT problem on May 18, 2007. Female patient was diagnosed with soft tissue disorder and was treated with MUSCULOSKELETAL SOFT. After drug was administered, patient experienced the following problems/side effects: incision site oedema, incision site pain, pyrexia, . MUSCULOSKELETAL SOFT dosage: unknown. Patient was hospitalized. Patient recovered.

Byetta Side Effects Report #5644427-9
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 17, 2008. Female patient was diagnosed with type 2 diabetes mellitus, blood cholesterol increased, gastrooesophageal reflux disease and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: abdominoplasty, hypoaesthesia, incision site pain, incorrect dose administered, nausea, . BYETTA dosage: unknown. During the same period patient was treated with VYTORIN, NEXIUM, ACTOS, METFORMIN. Patient was hospitalized. Patient recovered.

Betaseron Side Effects Report #5557877-6
Consumer or non-health professional from UNITED STATES reported BETASERON problem on Nov 25, 2007. Female patient, 57 years of age, was diagnosed with multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: appendicitis, incision site pain, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.

Byetta Side Effects Report #5421278-1
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 14, 2007. Female patient, 59 years of age, weighting 192.0 lb, was diagnosed with type 2 diabetes mellitus, depression, hypertension, stomach discomfort, fluid retention and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood glucose increased, incision site pain, incisional hernia, irritable bowel syndrome, stress, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOPHAGE, GLIPIZIDE, CYMBALTA, DIOVAN, ACIPHEX, LASIX, POTASSIUM CHLORIDE. Patient was hospitalized. Patient recovered.


Procrit Side Effects Report #5398630-6
Physician from UNITED STATES reported PROCRIT problem on Feb 27, 2007. Male patient, weighting 162.0 lb, was diagnosed with pre-existing disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: gastric mucosal lesion, hypersensitivity, incision site pain, injection site abscess, oedema, pain in extremity, scar, scar pain, skin lesion, . PROCRIT dosage: unknown. During the same period patient was treated with ULTRAM, FLEXERIL, XANAX, INDOMETHACIN. Patient recovered.

Procrit Side Effects Report #5398630-6
PROCRIT problem was reported by a Physician from UNITED STATES on Feb 27, 2007. Male patient, weighting 162.0 lb, was diagnosed with pre-existing disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: gastric mucosal lesion, hypersensitivity, incision site pain, injection site abscess, oedema, pain in extremity, scar, scar pain, skin lesion, . PROCRIT dosage: unknown. During the same period patient was treated with ULTRAM, FLEXERIL, XANAX, INDOMETHACIN. Patient recovered.

Geodon Side Effects Report #5757585-2
Health Professional from UNITED STATES reported GEODON problem on May 22, 2008. Male patient, weighting 300.0 lb, was diagnosed with intermittent explosive disorder and was treated with GEODON. After drug was administered, patient experienced the following problems/side effects: erectile dysfunction, extrapyramidal disorder, incision site pain, oedema, physical assault, post procedural haematoma, priapism, suicide attempt, weight increased, . GEODON dosage: unknown. During the same period patient was treated with XANAX, OXYCODONE, DIAZEPAM, PROLIXIN. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5347120-5
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on May 24, 2007. Male patient, 52 years of age, weighting 160.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: chest wall mass, iatrogenic injury, incision site pain, metastatic neoplasm, neoplasm malignant, procedural complication, salivary gland cancer, viith nerve injury, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Lamotrigine Side Effects Report #5326335-6
Physician from UNITED STATES reported LAMOTRIGINE problem on May 14, 2007. Male patient, 27 years of age, was treated with LAMOTRIGINE. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, appendicitis perforated, incision site pain, . LAMOTRIGINE dosage: 100MG PER DAY. During the same period patient was treated with OLANZAPINE. Patient was hospitalized. Patient recovered.


Forteo Side Effects Report #5331358-7
FORTEO problem was reported by a Consumer or non-health professional from UNITED STATES on May 10, 2007. Female patient, 58 years of age, was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: benign neoplasm, gastrooesophageal reflux disease, incision site pain, injection site bruising, nausea, surgery, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.