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Tamsulosin
HCl
API |
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Haorui supplies high quality Tamsulosin HCl API produced by our
GMP facility that has been successfully inspected by the
FDA.
We offer
competitive prices and support our products with reliable technical and
regulatory services. Tamsulosin HCl API is available from R&D to
commercial quantities. Please contact us for more details. |
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The following
information is provided for general information purposes
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What is Tamsulosin?
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Tamsulosin is used to treat
the symptoms of benign prostatic hyperplasia (BPH).
Tamsulosin hydrochloride is an antagonist
of alpha1A adrenoceptors in the prostate.
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Tamsulosin
HCl is (-)-(R)-5-[2-[[2-(0-ethoxyphenoxy) ethyl]
amino] propyl]-2-methoxybenzenesulfonamide,
monohydrochloride. Tamsulosin HCl occurs as white
crystals that melt with decomposition at approximately 230°C. It is sparingly soluble in water and in
methanol, slightly soluble in glacial acetic acid and in ethanol, and practically insoluble
in ether. The empirical formula of tamsulosin HCl is C20H28N2O5S HCl. The molecular weight of
tamsulosin HCl is 444.98. Its structural formula is:
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The history of Tamsulosin
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Tamsulosin was approved by the FDA in 1997.
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What is Tamsulosin used for?
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Tamsulosin is a drug for
the treatment of men who are having difficulty
urinating because of benign prostatic hyperplasia (BPH). In men, the tube which
carries urine from the bladder to the penis (called
the urethra) travels through the prostate gland. As
men get older, the prostate gland enlarges, and the
muscle cells within the prostate gland and the neck
of the bladder (which control the flow of urine)
tighten. The combination of enlargement and
tightening of muscles compresses the urethra and
obstructs the flow of urine. This results in
difficulty urinating and retention of urine within
the bladder. The tightening or contraction of the
muscle cells is controlled by nerves.
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One
type of nerve, the alpha adrenergic nerves, cause
the muscle cells to tighten by releasing a chemical
related to epinephrine (adrenalin). Tamsulosin
blocks the effects of this chemical on the muscle
cells and causes the muscles to relax. This results
in a decrease in obstruction to the flow of urine.
There are other drugs which block alpha adrenergic
nerves throughout the body and which are used in
treating diseases of the heart, blood vessels, and
prostate for example, prazosin (Minipress), terazosin (Hytrin), doxazosin (Cardura), and alfuzosin (Uroxatral).
Tamsulosin is more active against the alpha
adrenergic nerves of the prostate and bladder neck
than these other drugs and has a lesser effect on
alpha adrenergic nerves elsewhere in the body.
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For this reason, tamsulosin causes fewer side effects,
especially low blood pressure, than other alpha adrenergic blocking
drugs. Moreover, tamsulosin therapy can be started
at the optimum dose whereas other alpha adrenergic
blocking drugs need to be started at low doses with
the doses slowly increased over time in order to
minimize the side effects.
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Tamsulosin
mode of action
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Each
capsule
for oral administration
contains tamsulosin HCl 0.4 mg, and the following
inactive ingredients: methacrylic acid
copolymer, microcrystalline cellulose, triacetin, polysorbate 80, sodium lauryl
sulfate, calcium stearate, talc, FD&C blue No. 2, titanium
dioxide, ferric
oxide, gelatin, and trace amounts of shellac, industrial methylated spirit 74 OP,
n-butyl, alcohol, isopropyl alcohol, propylene
glycol, dimethylpolysiloxane, and black iron oxide E172.
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Tamsulosin
side effects
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Although
side effects from tamsulosin are not common, they
can occur. Tell your doctor if any of these symptoms
are severe or do not go away:
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dizziness
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sleepiness
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runny
nose
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 | sexual dysfunction (difficulty ejaculating)
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Disclaimer:
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Information on
this page is provided for general information
purposes. You should not make a clinical treatment
decision based on information contained in this page
without consulting other references including the
package insert of the drug, textbooks and where
relevant, expert opinion. We cannot be held
responsible for any errors you make in administering
drugs mentioned on this page, nor for use of any
erroneous information contained on this page.
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