Description:
Coryton (Losartan potassium), the
first of a new class of agents for
the treatment of hypertension, is
an angiotensin II receptor (type AT)
antagonist. Coryton (Losartan potassium)
and its principal active metabolite
block the vasoconstrictor and aldosterone
secreting effects of angiotensin II
by selectively blocking the binding
of angiotensin II to the AT, receptor
found in many tissues (e.g. vascular
smooth muscle, adrenal gland).Coryton
(Losartan potassium) is a reversible,
competitive inhibitor of the AT, receptor.
Presentation:
Coryton Tablet : Pack of 2x 10’s
tablets.
Composition:
Each film coated tablet contains :
Losartan (as Potassium) ....... 50mg.
Indications:
Coryton is indicated for the treatment
of hypertension.
Dosage
and Administration:
The usual starting and maintenance
dose is 50mg once daily for most patients.
The maximal antihypertensive effect
is attained 3-6 weeks after initiation
of therapy. Some patients may receive
an additional benefit by increasing
the dose to 100 mg once daily. Coryton
may be administered with other antihypertensive
agents. Coryton may be administered
with or without food .
Side
Effects:
Hypersensitivity: Anaphylactic
reactions, angioedema including swelling
of the larynx and glottis causing
airway obstruction and/or swelling
of the face, lips, pharynx and/or
tongue has been reported rarely in
patients treated with losartan.
Gastrointestinal: Hepatitis
(reported rarely), liver function
abnormalities.
Hematologic: Anemia.
Musculoskeletal: Myalgia.
Nervous System psychiatric:
Migraine.
Respiratory: Cough.
Skin: Urticaria, pruritus.
Contraindications:
Coryton is contraindicated in patients
who are hypersensitive to any component
of this product.
Cautions:
Hypotension and Electrolyte /
Fluid Imbalance
In patients who are intravascularly
volume-depleted (e.g. those treated
with high-dose diuretics), symptomatic
hypotension may occur. These conditions
should be corrected prior to administration
of Coryton or a lower starting dose
should be used.
Liver
Function Impairment
Based on pharmacokinetic data which
demonstrate significantly increased
plasma cocentrations of losartan in
cirrhotic patients, a lower dose should
be considered for patients with a
history of hepatic impairment.
Renal
Function Impairment
As a consequence of inhibiting the
renin angiotensin system, changes
in renal function including renal
failure have been reported in susceptible
individuals.
Other
drugs that affect the renin angiotensin
system may increase blood urea and
serum creatinine in patients with
bilateral renal artery stenosis or
stenosis of the artery to a solitary
kidney. Similar effects have been
reported with Coryton, these changes
in renal function may be reversible
upon discontinuation of therapy.
Use in Pregnancy and Lactation:
When used in pregnancy during the
second and third trimesters, drugs
that act directly on the renin angiotensin
system can cause injury and even death
in the developing foetus. When pregnancy
is detected Coryton should be discontinued
as soon as possible.
It
is not known whether losartan is excreted
in human milk but because of the potential
for adverse effects on the nursing
infant, a decision should be made
whether to discontinue nursing or
discontinue the drug, taking into
account the importance of the drug
to the mother.
Drug
Interactions:
In clinical pharmacokinetic trials,
no drug interactions of clinical significance
have been identified with hydrochlorothiazide,
digoxin, warfarin, cimetidine, phenobarbital,
ketoconazole, and erythromycin.
Concomitant
use of potassium-sparing diuretics.
(e.g. spironolactone, triamterene,
amiloride) potassium supplements,
or salt substitutes containing potassium
may lead to increase in serum potassium.
The
antihypertensive effect of losartan
may be attenuated by the non-steroidal
anti-inflammatory drug indomethacin.
Over
Dosage:
The
most likely manifestation of overdosage
would be hypotension and tachycardia,bradycardia
could occur from parasympathetic (vagal)
stimulation. If symptomatic hypotension
does occur, then institute supportive
therapy.
Storage:
Store below 30 C.
Protect from moisture.
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