Generic Flomax .04mg 20 Caps, Tamsulosin Hydrochloride, Tamsulosina
Tamsulosin binds selectively and competitively to postsynaptic á1-adrenoceptors, in particular to subtypes
alpha1A and alpha1D. It brings about relaxation of prostatic and urethral smooth
FLOMAX 0.4 increases the maximum urinary flow rate. It relieves obstruction by relaxing smooth muscle in prostate and
It also improves the irritative symptoms in which bladder instability plays an important role.
These effects on storage and voiding symptoms are maintained during long-term therapy. The need for surgical treatment is
Alpha1-blockers can reduce blood pressure by lowering peripheral resistance. No reduction in blood pressure of any clinical
significance was observed during studies with FLOMAX 0.4.
Uniformity of absorption can be promoted by the patient always taking FLOMAX 0.4 after the same meal.
Tamsulosin shows linear kinetics.
After a single dose of FLOMAX 0.4 in the fed state, plasma levels of tamsulosin peak at around 6 hours and in the steady state, which is reached by day 5 of multiple dosing, Cmax in patients is about two-thirds higher than that reached after a single dose. Although this was seen in elderly patients, the same finding would also be expected in young
There is a considerable inter-patient variation in plasma levels both after single and multiple dosing.
In humans tamsulosin is about 99% bound to plasma proteins and the volume of distribution
is small (about 0.2L/kg).
Tamsulosin has a low first pass effect, being metabolized slowly. Most tamsulosin is present in plasma in the form of unchanged medicine. It is metabolized in the liver.
Tamsulosin and its metabolites are mainly excreted in the urine with about 9% of a dose being
present in the form of unchanged medicine.
After a single dose of FLOMAX 0.4 in the fed state, and in the steady state in patients, elimination half-lives of about 10 and 13
hours respectively have been measured.
The presence of renal impairment does not warrant lowering the dose.
Treatment of functional symptoms of benign prostatic hyperplasia (BPH).
One capsule daily, to be taken after breakfast, or the first meal of the day.
The capsule should be swallowed whole and should not be crushed or chewed as this will interfere with the modified release of the active ingredient.
Hypersensitivity to tamsulosin hydrochloride or any other component of the product.
A history of orthostatic hypotension.
Severe hepatic insufficiency.
As with other alpha1-blockers, reduction in blood pressure can occur in individual cases during treatment with FLOMAX 0.4, as a result of which, very rarely, syncope can occur. At the first signs of orthostatic hypotension (dizziness, weakness), the patient should sit or lie down until the symptoms have disappeared.
Before therapy with FLOMAX 0.4 is initiated, the patient should be examined in order to exclude the presence of other conditions which can cause the same symptoms as benign prostatic hyperplasia. Digital rectal examination and, when necessary, determination of prostate specific antigen (PSA) should be performed before treatment and at regular intervals
The treatment of severely renally impaired patients (creatinine clearance of < 10ml/min) should be approached with caution as
these patients have not been studied.
Effects On Ability To Drive And Use Machines
No data is available on whether FLOMAX 0.4 adversely
The following adverse reactions have been reported during the use of FLOMAX 0.4: dizziness, abnormal ejaculation and, less
frequently (1-2%), headache, asthenia, postural hypotension and palpitations.
No interactions have been seen when FLOMAX 0.4 was given concomitantly with either atenolol, enalapril, or nifedipine. Concomitant cimetidine brings about a rise in plasma levels of tamsulosin, and furosemide a fall, but as levels remain within the normal range posology need not be changed.
In vitro, neither diazepam nor propranolol, trichlormethiazide, chlormadinon, amitriptyline, diclofenac, glibenclamide,
simvastatin nor warfarin change the free fraction of tamsulosin in human plasma. Neither does tamsulosin change the free fractions of diazepam, propranolol, trichlormethiazide and chlormadinon.
No interactions at the level of hepatic metabolism have been seen during in vitro studies with liver microsomal fractions
(representative of the cytochrome P450-linked drug metabolizing enzyme system), involving amitriptyline, salbutamol, glibenclamide and finasteride. Diclofenac and warfarin, however, may increase the elimination rate of tamsulosin.
Concurrent administration of other á1-adrenoceptor antagonists could lead to hypotensive effects.
No cases of acute overdosage have been reported. However, acute hypotension could theoretically occur after overdosage
in which case cardiovascular support should be given. Blood pressure can be restored and heart rate brought back to normal by lying the patient down. If this does not help then volume expanders and, when necessary, vasopressors could be employed. Renal function should be monitored and general supportive measures applied. Dialysis is unlikely to be of help as tamsulosin is very highly bound to plasma proteins.
Measures, such as emesis, can be taken to impede absorption. When large quantities are involved, gastric lavage can be applied and activated charcoal and an osmotic laxative, such as sodium sulphate, can be administered.
Special Precautions For Storage
Store below 30°C.
FLOMAX 0.4mg modified release capsules can be used up to four years after manufacture. The
expiry date is printed on the package.
Please consult your medical doctor for more information and usage.