Actoplus and dyspnoea Patient Reports February 12, 2012

Actoplus Side Effects Report #6125244-2
Actoplus side effect was reported by a Health Professional from UNITED STATES on Mar 19, 2009. Female patient, weighting 205.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with Actoplus. After drug was administered, patient experienced the following side effects: brain natriuretic peptide increased, cardiac failure congestive, dyspnoea, fibrin d dimer increased, oedema peripheral. Actoplus dosage: unknown. During the same period patient was treated with BYSTOLIC. Patient was hospitalized. Patient recovered.

Actoplus Side Effects Report #5054466-7
Actoplus side effect was reported by a Health Professional from UNITED STATES on July 05, 2006. Female patient, 61 years of age, weighting 235.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actoplus. After drug was administered, patient experienced the following side effects: dyspnoea, movement disorder , muscular weakness, myalgia, tenderness. Actoplus dosage: 15/500 MG, TWICE DAILY, PER ORAL. During the same period patient was treated with TRICOR, AVANDAMET. Patient recovered.

Actoplus Side Effects Report #5079781-2
Actoplus side effect was reported by a Health Professional from UNITED STATES on Aug 01, 2006. Female patient, 61 years of age, weighting 235.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actoplus. After drug was administered, patient experienced the following side effects: dyspnoea, mobility decreased, muscular weakness, myalgia. Actoplus dosage: 15/500 MG, TWICE DAILY, PER ORAL. During the same period patient was treated with ACE INHIBITOR, TRICOR, AVANDAMET. Patient recovered.

Actoplus Side Effects Report #5118484-2
Actoplus side effect was reported by a Health Professional from UNITED STATES on Sept 18, 2006. Female patient, 61 years of age, weighting 235.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actoplus. After drug was administered, patient experienced the following side effects: asthenia, dyspnoea, hyperaesthesia, movement disorder , muscular weakness, myalgia. Actoplus dosage: 15/500 MG, TWICE DAILY, PER ORAL. During the same period patient was treated with ACE INHIBITOR, TRICOR, AVANDAMET. Patient recovered.


Actoplus Side Effects Report #5118494-5
Actoplus side effect was reported by a Physician from UNITED STATES on Sept 18, 2006. Female patient was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actoplus. After drug was administered, patient experienced the following side effects: dyspnoea, rash , throat tightness, urticaria, wheezing. Actoplus dosage: unknown. During the same period patient was treated with METFORMIN. Patient recovered.

Actoplus Side Effects Report #5389191-6
Actoplus side effect was reported by a Consumer or non-health professional from UNITED STATES on July 02, 2007. Male patient, 64 years of age, weighting 250.0 lb, was diagnosed with diabetes mellitus and was treated with Actoplus. After drug was administered, patient experienced the following side effects: anaemia, cardiac failure, cardiomegaly, dyspnoea, influenza, pulmonary oedema. Actoplus dosage: 15/500 MG, DAILY, PER ORAL. Patient was hospitalized. Patient recovered.

Actoplus Side Effects Report #5419570-X
Actoplus side effect was reported by a Consumer or non-health professional from UNITED STATES on Aug 15, 2007. Male patient, 42 years of age, weighting 192.0 lb, was diagnosed with blood glucose increased and was treated with Actoplus. After drug was administered, patient experienced the following side effects: abdominal distension, asthenia, dyspnoea, fluid retention. Actoplus dosage: unknown. Patient recovered.

Actoplus Side Effects Report #5008127-0
Actoplus side effect was reported by a Physician from UNITED STATES on Dec 08, 2005. Female patient was treated with Actoplus. After drug was administered, patient experienced the following side effects: cardiac failure congestive, dyspnoea, oedema, weight increased. Actoplus dosage: 15/850 MG, PER ORAL. During the same period patient was treated with LIPITOR. Patient recovered.