Minipress and condition aggravated Patient Reports February 12, 2012

Minipress Side Effects Report #4871258-X
Minipress side effect was reported by a Consumer or non-health professional from UNITED STATES on Dec 16, 2005. Female patient, 62 years of age, was diagnosed with hypertension, blood cholesterol increased and was treated with Minipress. After drug was administered, patient experienced the following side effects: arthralgia, blood cholesterol increased, body height decreased, cervical dysplasia, condition aggravated, eye haemorrhage, hypertension. Minipress dosage: 2 MG (1 MG, BID INTERVAL: EVERY DAY) , ORAL. During the same period patient was treated with PRAZOSIN GITS, ZETIA, ANTIHYPERTENSIVES, LEVOXYL. Patient recovered.

Minipress Side Effects Report #4911652-1
Minipress side effect was reported by a Consumer or non-health professional from UNITED STATES on Feb 02, 2006. Female patient, 62 years of age, was diagnosed with hypertension, blood cholesterol increased and was treated with Minipress. After drug was administered, patient experienced the following side effects: anxiety , blood cholesterol increased, blood pressure increased, body height decreased, condition aggravated, eye haemorrhage. Minipress dosage: 2 MG (1 MG, BID, INTERVAL: EVERY DAY), ORAL. During the same period patient was treated with PRAZOSIN GITS, ZETIA, ANTIHYPERTENSIVES, LEVOXYL. Patient recovered.

Minipress Side Effects Report #4609436-7
Minipress side effect was reported by a Physician from on Mar 01, 2005. Male patient was diagnosed with hypertension and was treated with Minipress. After drug was administered, patient experienced the following side effects: arrhythmia , atrial fibrillation , bradycardia, condition aggravated, raynaud's phenomenon. Minipress dosage: 2 MG (1 MG, 1 IN 2 D). During the same period patient was treated with NEBIVOLOL. Patient recovered.