Vivelle and pain Patient Reports March 20, 2010

Vivelle Side Effects Report #4757524-7
Vivelle side effect was reported by a Consumer or non-health professional from UNITED STATES on Aug 23, 2005. Female patient, 59 years of age, was diagnosed with osteoporosis  and was treated with Vivelle. After drug was administered, patient experienced the following side effects: abdominal pain , bilirubinuria, gallbladder disorder, hepatobiliary disease, liver function test abnormal. Vivelle dosage: 0.025 MG/DAY, BIW. Patient recovered.

Vivelle Side Effects Report #5758896-7
Vivelle side effect was reported by a Consumer or non-health professional from UNITED STATES on June 02, 2008. Female patient, 66 years of age, was diagnosed with menopause , pain  and was treated with Vivelle. After drug was administered, patient experienced the following side effects: arthritis , back pain , depression , hot flush, hyperaesthesia, insomnia, swelling. Vivelle dosage: 0.0375 MG DAILY, 2 X WEEK. During the same period patient was treated with ADVIL. Patient recovered.

Vivelle Side Effects Report #5836480-4
Vivelle side effect was reported by a Consumer or non-health professional from UNITED STATES on Aug 05, 2008. Female patient, 66 years of age, was diagnosed with menopause , pain  and was treated with Vivelle. After drug was administered, patient experienced the following side effects: arthritis , back pain , depression , hot flush, hyperaesthesia, insomnia, oedema peripheral. Vivelle dosage: 0.0375 MG DAILY, 2 X WEEK. During the same period patient was treated with ADVIL. Patient recovered.

Vivelle Side Effects Report #5870655-3
Vivelle side effect was reported by a Consumer or non-health professional from UNITED STATES on Aug 26, 2008. Female patient, 66 years of age, was diagnosed with menopause , pain  and was treated with Vivelle. After drug was administered, patient experienced the following side effects: arthritis , back pain , depression , hot flush, hyperaesthesia, insomnia, swelling. Vivelle dosage: 0.0375 MG DAILY, 2 X WEEK. During the same period patient was treated with ADVIL LIQUI. Patient recovered.


Vivelle Side Effects Report #5185318-X
Vivelle side effect was reported by a Consumer or non-health professional from UNITED STATES on Dec 11, 2006. Female patient, 47 years of age, was treated with Vivelle. After drug was administered, patient experienced the following side effects: application site erythema, application site pruritus, application site reaction, haematoma, lower respiratory tract infection, pain , wound drainage. Vivelle dosage: 0.1 MG/DAY, TWICE WEEKLY. Patient recovered.

Vivelle Side Effects Report #4906194-3
Vivelle side effect was reported by a Consumer or non-health professional from UNITED STATES on Jan 30, 2006. Female patient, 36 years of age, weighting 141.0 lb, was treated with Vivelle. After drug was administered, patient experienced the following side effects: hepatic adenoma, pain . Vivelle dosage: 0.1 MG/DAY, TWICE WEEKLY. Patient recovered.

Vivelle Side Effects Report #4937482-2
Vivelle side effect was reported by a Consumer or non-health professional from UNITED STATES on Jan 30, 2006. Female patient, 36 years of age, weighting 141.0 lb, was treated with Vivelle. After drug was administered, patient experienced the following side effects: hepatic adenoma, migraine , nausea , pain . Vivelle dosage: 0.1 MG/DAY, TWICE WEEKLY. Patient recovered.

Vivelle Side Effects Report #5752564-3
Vivelle side effect was reported by a Consumer or non-health professional from UNITED STATES on May 27, 2008. Female patient was treated with Vivelle. After drug was administered, patient experienced the following side effects: depression , limb injury, pain , tendonitis. Vivelle dosage: 0.05 MG, QD. Patient recovered.

Vivelle Side Effects Report #6047133-4
Vivelle side effect was reported by a Consumer or non-health professional from UNITED STATES on Jan 13, 2009. Female patient was treated with Vivelle. After drug was administered, patient experienced the following side effects: application site rash, discomfort, pain , post procedural complication, pruritus, skin irritation, thermal burn. Vivelle dosage: 0.1 MG, UNK. Patient was hospitalized. Patient recovered.