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Each subject propranolol underwent a medical examination as well as clinical and routine laboratory evaluation tests including hematology, blood chemistry and urinalysis .
One subject (AFW) smoked around five cigarettes propranolol per day .
Individuals with any significant disease history were excluded propranolol from the study .
, Microbiology propranolol Dept . Any subjects with laboratory results more than two standard deviations from the propranolol mean value (of each test) for laboratory performing the test (Chemical Pathology Dept .
, The School of Medical Sciences, Universiti Sains Malaysia) were propranolol excluded from the study 11 . and propranolol Hematology Dept .
Alcoholics, drug addicts propranolol and obese individuals were excluded from the study .
Before joining the study, all subjects propranolol were briefed on the details of the bioequivalence study, agreed and signed a consent form .
All volunteers were free to leave the study at any A crossover propranolol design was used whereby equal number of subjects were taking the test preparation and reference preparation during each phase of the study .
On the first propranolol dosing day each subject took on a randomized basis either two propranolol tablets (40 mg each) of Astra Zeneca (batch no .
LOT OM943B, expiry date, June 2004) propranolol or two of the RAZA (batch no .
1P0378, expiry date, December 2004) propranolol uses in infants propranolol generic propranolol nursing implications propranolol for propranolol tablets (40 mg each) orally with 150 ml water .
After a 2 weeks wash-out period, each subject took propranolol 10 mg bid adverse effects of propranolol ati propranolol pill propranolol 10 mg half two tablets of the other products .
All subjects, physicians propranolol and drug analysts were blinded .

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