Inhouse product
Indications
Genazopt Ophthalmic
Suspension is indicated in the treatment of elevated intraocular pressure in
patients with ocular hypertension or open-angle glaucoma.
* রেজিস্টার্ড চিকিৎসকের পরামর্শ মোতাবেক ঔষধ সেবন করুন'
Pharmacology
Carbonic anhydrase
(CA) is an enzyme found in many tissues of the body including the eye. It
catalyzes the reversible reaction involving the hydration of carbondioxide and
the dehydration of carbonic acid. Inhibition of carbonic anhydrase in the
ciliary processes of the eye decreases aqueous humor secretion, presumably by
slowing the formation of bicarbonate ions with subsequent reduction in sodium
and fluid transport. The result is a reduction in intraocular pressure (IOP).
Dosage & Administration
Shake well before use.
Insert 1 drop in the affected eye(s) three times daily. It may be used
concomitantly with other topical ophthalmic products to lower intraocular
pressure. If more than one topical ophthalmic drug is being used, the drugs
should be administered at least ten minutes apart.
Pediatric Use: One drop in the affected eye(s) 2 times
daily in pediatric patient (4 weeks to 5 years age)
Geriatric Use: No overall differences in safety or
effectiveness have been observed between elderly and younger patients.
* রেজিস্টার্ড চিকিৎসকের পরামর্শ মোতাবেক ঔষধ সেবন করুন'
Interaction
In patients treated
with oral carbonic anhydrase inhibitors, rare instances to drug interactions
have occurred with high-dose salicylate therapy. Therefore, the potential for
such drug interactions should be considered in patients receiving Genazopt.
Contraindications
It is contraindicated
in patients who are hypersensitive to any component of this product.
Side Effects
The most frequently
reported adverse events associated with Genazopt were blurred vision and
bitter, sour or unusual taste. These events occurred in approximately 5-10% of
patients. Blepharitis, dermatitis, dry eye, foreign body sensation, headache,
hyperemia, ocular discharge, ocular discomfort, ocular keratitis, ocular pain,
ocular pruritus reactions were reported at an incidence below 1%: allergic
reactions, alopecia, chest pain, conjunctivitis, dizziness, dry mouth, dyspnea,
dyspepsia, eye fatigue, hypertonia, keratoconjunctivitis, lid margin crusting
or sticky sensation, nausea, pharyngitis, tearing and urticaria.
Pregnancy & Lactation
Pregnancy Category C.
There are no adequate and well-controlled studies in pregnant women. It should
be used during pregnancy only if the potential benefit justifies the potential
risk to the fetus. It should be used only if the potential benefit justifies the
potential risk to the baby.
Precautions & Warnings
Genazopt is a
sulfonamide and although administered topically it is absorbed systemically.
Therefore, the same types of adverse reactions that are attributable to
sulfonamides may occur with topical administration of Genazopt. Fatalities have
occurred, although rarely, due to severe reactions to sulfonamides including
Stevens-Johnson syndrome, toxic epidermal necrolysis, fulminant hepatic
necrosis, agranulocytosis, aplastic anemia, and other blood dyscrasias.
Sensitization may occur when a sulfonamide is re-administered irrespective of
the route of administration. If signs of serious reactions or hypersensitivity
occur, discontinue the use of Genazopt. Because Genazopt and its metabolite are
excreted predominantly by the kidney, Genazopt is not recommended in renal
impairment patients. Genazopt- has not been studied in patients with hepatic
impairment and should be used with caution in such patients.
Overdose Effects
Although no human data
are available, electrolyte imbalance, development of an acidosis state, and
possible nervous system effects may occur following oral administration of an
overdose. Serum electrolyte levels (particularly potassium) and blood pH levels
should be monitored.
Therapeutic Class
Drugs for miotics and
glaucoma
Storage Conditions
Store at room
temperature & protect from light. Do not touch dropper tip to any surface.
It is desirable that the contents should not be used more than four weeks after
first opening of the bottle. Protect from freezing.
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