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PRE-EXISTING CONDITION IMPROVED side effect

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Aleve Side Effects Report #5658396-9
Consumer or non-health professional from UNITED STATES reported ALEVE problem on Feb 06, 2007. Female patient, weighting 200.6 lb, was diagnosed with arthralgia and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: pre-existing condition improved, . ALEVE dosage: UNIT DOSE: 220 MG. During the same period patient was treated with VITAMIN E, ASCORBIC ACID, VITAMIN B. Patient recovered.

Chantix Side Effects Report #5575169-6
CHANTIX problem was reported by a Health Professional from UNITED KINGDOM on Dec 18, 2007. Male patient, 58 years of age, was diagnosed with depression and was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: pre-existing condition improved, . CHANTIX dosage: unknown. During the same period patient was treated with DULOXETINE. Patient recovered.

Avelox Side Effects Report #5774957-0
Physician from UNITED STATES reported AVELOX problem on Apr 11, 2008. Male patient, 60 years of age, was diagnosed with infection and was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: pre-existing condition improved, . AVELOX dosage: unknown. Patient recovered.

Orencia Side Effects Report #5277053-4
ORENCIA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 28, 2007. Female patient, 50 years of age, weighting 200.6 lb, was diagnosed with rheumatoid arthritis and was treated with ORENCIA. After drug was administered, patient experienced the following problems/side effects: pre-existing condition improved, . ORENCIA dosage: unknown. During the same period patient was treated with TOPROL, HYDROCODONE, METHOTREXATE, LEUCOVORIN CALCIUM, LASIX, POTASSIUM ACETATE. Patient recovered.


Methotrexate Side Effects Report #5685103-6
Consumer or non-health professional from reported METHOTREXATE problem on Mar 24, 2008. Male patient, 67 years of age, was diagnosed with rheumatoid arthritis, tonsil cancer and was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: pre-existing condition improved, tonsil cancer, vertigo, . METHOTREXATE dosage: unknown. During the same period patient was treated with SULFASALAZINE, FOLIC ACID, GOLDECTIONS, CARBOPLATIN, FLUOROURACIL, FOLINIC ACID. Patient recovered.

Byetta Side Effects Report #5240749-4
BYETTA problem was reported by a Physician from UNITED STATES on Sept 29, 2006. Female patient was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: dysgeusia, pre-existing condition improved, weight decreased, . BYETTA dosage: unknown. Patient recovered.

Byetta Side Effects Report #5246263-4
Consumer or non-health professional from UNITED STATES reported BYETTA problem on July 23, 2006. Female patient, 50 years of age, weighting 261.0 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: injection site nodule, pre-existing condition improved, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with LORTAB. Patient recovered.

Lamictal Side Effects Report #5252651-2
LAMICTAL problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 02, 2006. Female patient, 55 years of age, was diagnosed with depression and was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: hypotrichosis, pre-existing condition improved, . LAMICTAL dosage: unknown. During the same period patient was treated with PROTONIX, KLONOPIN, WELLBUTRIN. Patient recovered.

Capecitabine Side Effects Report #5670975-1
Physician from NETHERLANDS reported CAPECITABINE problem on Mar 06, 2008. Male patient, 74 years of age, was treated with CAPECITABINE. After drug was administered, patient experienced the following problems/side effects: diarrhoea, nausea, pre-existing condition improved, . CAPECITABINE dosage: unknown. During the same period patient was treated with BEVACIZUMAB, OXALIPLATIN, CETUXIMAB, PANTOZOL, PRIMPERAN, LOPERAMIDE, DEXAMETHASONE. Patient was hospitalized. Patient died on 12/01/2006.


Forteo Side Effects Report #5485637-3
FORTEO problem was reported by a Consumer or non-health professional from BRAZIL on Oct 05, 2007. Female patient, weighting 143.3 lb, was diagnosed with osteoporosis, arrhythmia, hypertension, arthritis, vitamin supplementation, swelling, bone disorder and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: insomnia, medical device change, pre-existing condition improved, . FORTEO dosage: unknown. During the same period patient was treated with CARDIZEM, ANCORON, ARADOIS, ARAVA, VITERGAN MASTER, LACTULONA, CALCIUM CARBONATE W. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5486384-4
Consumer or non-health professional from BRAZIL reported FORTEO problem on Oct 05, 2007. Female patient, weighting 143.3 lb, was diagnosed with osteoporosis, arrhythmia, hypertension, arthritis, vitamin supplementation, swelling, bone disorder and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: insomnia, medical device change, pre-existing condition improved, . FORTEO dosage: unknown. During the same period patient was treated with CARDIZEM, ANCORON, ARADOIS, ARAVA, VITERGAN MASTER, LACTULONA, CALCIUM CARBONATE W. Patient was hospitalized. Patient recovered.

Mirena Side Effects Report #5735740-5
MIRENA problem was reported by a Consumer or non-health professional from BRAZIL on May 06, 2008. Female patient, 29 years of age, weighting 105.8 lb, was diagnosed with intra-uterine contraceptive device and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: amenorrhoea, ovarian cyst, pre-existing condition improved, procedural pain, uterine leiomyoma, . MIRENA dosage: unknown. During the same period patient was treated with ESTREVA GEL. Patient was hospitalized. Patient recovered.

Yasmin Side Effects Report #5737100-X
Consumer or non-health professional from BRAZIL reported YASMIN problem on May 05, 2008. Female patient, 19 years of age, weighting 125.7 lb, was diagnosed with oral contraception, rhinitis, pelvic pain and was treated with YASMIN. After drug was administered, patient experienced the following problems/side effects: alopecia, menorrhagia, pre-existing condition improved, uterine leiomyoma, . YASMIN dosage: unknown. During the same period patient was treated with BUSONID, BUSCOPAN. Patient was hospitalized. Patient recovered.

Byetta Side Effects Report #5232942-1
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 21, 2006. Female patient, 51 years of age, weighting 252.0 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: decreased appetite, injection site urticaria, pre-existing condition improved, weight decreased, . BYETTA dosage: unknown. Patient recovered.


Byetta Side Effects Report #5249257-8
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Aug 19, 2006. Female patient, 55 years of age, weighting 210.0 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 glucose increased, decreased appetite, pre-existing condition improved, . BYETTA dosage: unknown. During the same period patient was treated with GLIPIZIDE, VERAPAMIL, NORVASC, DIOVAN. Patient recovered.

Byetta Side Effects Report #5254672-2
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 05, 2006. Female patient, 38 years of age, weighting 185.0 lb, was diagnosed with diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: energy increased, injection site urticaria, pre-existing condition improved, therapeutic response unexpected, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with FORTAMET, VITAMIN B, CLARITIN, SEASONALE. Patient recovered.