|
|
 |
| |
| |
Page updated on 01st
September 2008
|
New Introductions
- Cipla
|
| |
Ocugard: For Your Eyes Only |
As long as we are alive, eating and breathing in
a polluted world, our bodies will have to contend
with free radicals and we will need antioxidants
to help reduce the impact and minimize the damage
they cause. Normally, the body can handle free radicals,
but if antioxidants are unavailable, or if the free-radical
production becomes excessive, damage can occur.
Of particular importance is that free radical damage
accumulates with age.
As we get older our eyes have a harder time fighting
off free radicals that cause oxidative stress damage.
Aging process brings about anatomical changes in
the eye, which results in physiological changes
simultaneously.
Ocugard is a comprehensive blend
of essential carotenoids, free radicascavengers,
multivitamins and other vital ingredients designed
for protection of eyes against age related macular
degeneration (AMD), cataract, glaucoma and diabetic
retinopathy. Ocugard thus plays an important role
in preventing the damage to the human eye due to
destructive action of free radicals as it contains
antioxidants.
Ocugard plays an important role
in preventing the damage to the human eye due to
destructive action of free radicals as it vital
ocular antioxidants like rutin , alpha-lipoic
acid , ginkgo biloba extracts , bilberry extracts
, lutein , zeaxanthin , zinc ,selenium , vitamin
C , vitamin E and beta-carotene .
Indications
- Ocugard can be given as an adjunct in patients
with age related macular degeneration.
- Patients sufferings / at high risk from cataract.
- Patients suffering / at high risk from glaucoma.
- Postoperative patients of cataract or glaucoma.
- Diabetic patients as a prophylaxis against cataract.
- Patients with idiopathic raised intraocular pressure,
and in patients with diabetic retinopathy.
What is the recommended dosage of Ocugard?
The recommended dosage of Ocugard
is two tablets at a time daily or as recommended
by the doctor.
Warnings
Current and Former Smokers: Consult
your eye care professional about the risks associated
with smoking and using beta-carotene.
|
| |
IF1
Eye drops: For Itch Free Eyes with Enhanced Patient
Compliance |
Ocular allergy occurs in approximately 15%-20%
of the general population. Seasonal allergic conjunctivitis
(SAC) is the most common form of this disease. Transient
ocular itching and hyperemia, the primary signs
and symptoms of SAC, are manifested typically during
the spring, summer.
IF1 contains olopatadine
0.2%, which is a long-acting multiple-action
topical agent with mast cell stabilizing and antihistaminic
properties.
Olopatadine is the first dual-action agent approved
by the US FDA combining antihistaminic properties
with mast-cell stabilizing activity, thus creating
an eye-drop with strong immediate efficacy as well
as long-lasting therapy.
Olopatadine is a relatively selective histamine
H1 antagonist and
an inhibitor of the release of histamine from the
mast cells. Decreased chemotaxis and inhibition
of eosinophil activation has also been demonstrated.
Olopatadine decreases adhesion molecule expression
results in decreased leukocyte infiltration and
prevention of other events which lead to inflammatory
process associated with allergy
Olopatadine is devoid of effects on alpha-adrenergic,
dopaminergic, and muscarinic type 1 and 2 receptors.
Indications
Olopatadine hydrochloride 0.2% ophthalmic
solution is indicated for the treatment of ocular
itching associated with allergic conjunctivitis.
Dosage and Administration
The recommended dose of olopatadine 0.2%
is one drop in each affected eye once a day
IF1 Highlights
(1)Potent anti-histaminic ability and
mast cell stabilizing activity
- Olopatadine 0.2% has also demonstrated its ability
to act as a potent antihistamine, on a level superior
to other selective H1
antihistamines
- Olopatadine is the first topical ophthalmic anti-allergy
agent that has clinically shown mast-cell stabilization
in human eyes.
(2)
Fast Acting
Reduces itching symptoms within 3
minutes of administration to the eyes
(3)
Long lasting relief
Dual mechanism of action gives an
immediate and a long lasting relief for upto 24
hrs
(4)
Comparison with other dual acting agents
- Olopatadine has been shown to inhibit 96% of histamine
release from human conjunctival mast cells
in vitro , even at 10 times the clinically
maximally effective dose.
- On the other hand, results for other dual acting
agents revealed a biphasic response, whereby low
concentrations suppressed histamine release, but
as the concentration was increased, histamine release
was actually stimulated.
(5) Soothes the eyes
- Olopatadine 0.2% formulation contains povidone,
which makes it soothing and well tolerated on the
ocular surface.
- Olopatadine 0.2% can be used in allergic conjunctivitis
patients with mild to moderate dry eye also.
(6)
Convenient dosing
- Simple once a day dosing – helps in increasing
patient compliance
- Safe and well tolerated, improves quality
of life of patients with allergic conjunctivitis.
|
| |
EPINA
Ophthalmic Solution: Redness to Relief |
Epinastine 0.05%
Ocular allergy occurs in approximately
15%-20% of the general population. Seasonal allergic
conjunctivitis (SAC) is the most common form of
this disease. Transient ocular itching and hyperemia,
the primary signs and symptoms of SAC, are manifested
typically during the spring, summer.
Epinastine ophthalmic solution 0.05% is a clear,
colorless, sterile isotonic solution containing
epinastine HCl, an antihistamine and an inhibitor
of histamine release from the mast cell for
topical administration to the eyes.
Epinastine is a topically active, direct H
1 -receptor antagonist and an inhibitor of
the release of histamine from the mast cell.
Epinastine is selective for the histamine
H 1 -receptor and
has affinity for the histamine H 2
-receptor. Epinastine also possesses affinity for
the a 1 -, a 2
-, and 5-HT 2 -receptors.
Epinastine does not penetrate the blood/brain barrier
and, therefore, is not expected to induce side effects
of the central nervous system.
Indications
Epina eye drops are indicated for
the prevention of itching associated with allergic
conjunctivitis
Dosage and Method
of Administration
The recommended dosage is one drop in each
eye twice a day.
Treatment should be continued throughout the period
of exposure (i.e., until the pollen season is over
or until exposure to the offending allergen is terminated),
even when symptoms are absent.
EPINA Highlights
Mechanism of Action
Multi-action control of signs
and symptoms
Affinity for both H1
and H2 receptors
,thus providing relief from
Ocular itch
Vasodilatation , eye lid swelling
, redness , facial edema
Mast cell stabilizing action
100-200 times higher affinity for
H1 receptors as compared to histamine
Non-sedating antihistaminic action
Onset and Duration of Action
Fast acting: Onset of action
within 3 mins .
Long Lasting sustained relief for more
than 12 hours
Soothing For Ocular Surface
Soothing effect: Comfortable
on the ocular surface
Does not exacerbate ocular surface
drying.
Compliance, Comfort and Tolerability
Simple BID dosing :May increase
compliance
Safe and effective for up to 8 weeks,
without evidence of tachyphylaxis
|
| |
Fiteye:
All That Eyes Need |
As long as we are alive, eating and breathing in
a polluted world, our bodies will have to contend
with free radicals and we will need antioxidants
to help reduce the impact and minimize the damage
they cause. Normally, the body can handle free radicals,
but if antioxidants are unavailable, or if the free-radical
production becomes excessive, damage can occur.
Of particular importance is that free radical damage
accumulates with age.
As we get older our eyes have a harder time fighting
off free radicals that cause oxidative stress damage.
Aging process brings about anatomical changes in
the eye, which results in physiological changes
simultaneously.
Fiteye contains Vitamin C, Vitamin
E, Vitamin A, Vitamin B 2 , Zinc, Copper, Selenium
, Manganese , L-Glutathione , Lutein , Zeaxanthin
and Rutin .
Fiteye plays an important
role in preventing the damage to the human eye due
to destructive action of free radicals as it contains
antioxidants
Who should take Fiteye?
Fiteye is formulated to provide nutritional and
antioxidant support for the eye and is recommended
for patients who are not taking a multi-vitamin
supplement. Fiteye is recommended for all people
over 50 years of age as a valuable part of daily
eye health care regimen.
Fiteye is particularly beneficial to those exposed
to environmental pollution or stress, which increases
the risk of damage by free radicals, those who suffer
from diabetes, cardiovascular disorders, cataracts,
age related macular degeneration etc.
Dosage
The recommended dosage of Fiteye is one
tablet one or two times daily , or as recommended
by the physician
Warnings
Current and Former Smokers: Consult
your eye care professional about the risks associated
with smoking and using Beta-Carotene.
|
| |
Flomex
Eye Ointment - Offers Desired Benefit Without Risk |
Fluometholone 0.1%
Steroidal eye ointments are preferred in
certain conditions like blepharitis, keratitis,
scleritis, episcleritis, post external and internal
ocular surgeries, post refractive surgeries and
ocular injuries.
Clinical Efficacy
- Post (ALT) fluorometholone decreases ocular
inflammation and discomfort during the early post-operative
period.
- Post PRK fluorometholone reduces postoperative
inflammatory response, and decreases the stromal
reparative response.
Flomex Eye ointment enables
- Maximum contact time of the fluorometholone
- Increases the bioavailability of the same,
- Maintains consistent dosage of the drug.
Safety Profile
- Lower propensity to raise IOP
- Safe for Glaucoma Patients
- Safe for long term use
- Safe for steroid responders
- Safe for elderly people
- Safe for children over 2 years of age
Indications
Fluorometholone ophthalmic ointment is indicated
for the treatment of steroid-responsive inflammation
of the palpebral and bulbar conjunctiva, cornea
and anterior segment of the globe.
Dosage
A small amount (approximately 1 / 2 inch ribbon)
of ointment should be applied to the conjunctival
sac one to three times daily. During the initial
24 to 48 hours, the frequency of dosing may be increased
to one application every four hours.
The dosing of fluorometholone ophthalmic ointment
may be reduced, but care should be taken not to
discontinue therapy prematurely. In chronic conditions,
withdrawal of treatment should be carried out by
gradually decreasing the frequency of applications.
|
| |
Moxicip
Eye Ointment - Genetically Smart Fluoroquinolone |
Moxifloxacin 0.5% Eye Ointment
Moxifloxacin available in India for the
first time as an eye ointment, with the advantage
of being preservative free.
Moxifloxacin is a 8-methoxy fluoroquinolone anti
infective. Moxicip eye ointment is a semisolid preparation
in which the active drug moxifloxacin is dissolved
in required quantity.
Antimicrobial Spectrum
- Moxifloxacin is a broad spectrum antibiotic
- Moxifloxacin possesses enhanced activity against
gram-positive organisms while maintaining its
efficacy against the gram-negative organisms.
- Strengthened potential against gram-positive
cocci like Staphylococcus aureus , Streptococcus
pneumoniae.
- Hinders resistance.
- 8 to 16 times more potent against gram-positive
organisms than previous generation quinolones
. Demonstrates susceptibility
for isolates that are second and third generation
fluoroquinolone resistant.
Clinical Efficacy
Moxifloxacin cures more than 80% of neonates
with bacterial conjunctivitis Moxicip Eye ointment
enables:
- Maximum contact time of the moxifloxacin
- Increases the bioavailability of the same,
- Maintains consistent dosage of the drug.
Indications
- Moxifloxacin eye ointment is
indicated for treatment of external bacterial
infections of the eyes like conjunctivitis, meibomianitis,
chalazion, stye, blepheritis.
- It is an ideal agent for empiric treatment of
superficial ocular infections and ocular infections
requiring prolonged contact time of the drug.
- Treatment of conjunctivitis in neonates and
pediatrics.
- Treatment of bacterial keratitis.
- Efficacious for postoperative ocular pad dressings
and night time use.
Dosage
Apply half-inch ribbon three times a day
on the first two days. For the next five days apply
half-inch ribbon two times a day.
Highlights
- World's first preservative free moxifloxacin
eye ointment
- Preservative free
- Can be used in pediatrics
|
| |
Adlube
- Overnight Shielding For Dry Eyes |
Adlube is an ocular lubricant
containing white petrolatum (57.5%) and mineral
oil (42.5%).
Highlights
It is the FIRST STERILE PRESERVATIVE FREE
ocular lubricating ointment available in India.
It is one of the BEST ocular
lubricant combinations. It has no preservative and
hence, gentle enough to be used as often as needed
without damaging the eye vision. It is safe and
effective for dry eye. It is thicker and greasier
and hence, stays in eye for a much longer time than
eye drops. It provides long lasting relief for dry
eye. It prevents abrasion at night and reduces need
for artificial tears and warm compressors. It has
provided a new therapeutic approach to provide steady
levels of medication to ocular surface. It also
prevents brittleness and / or breaking of eyelashes.
Indications
For the temporary relief of burning, irritation
and discomfort due to dryness of the eye or due
to exposure to wind or sun. Also may be used as
a protectant against further irritation.
Dosage and Method of Administration
For topical ocular administration.
Wash your hands before use. Pull down the lower lid
of the affected eye and apply a small amount (one
fourth inch) of ointment to the inside of the eyelid.
(Ideal for use at bedtime). There is no variation
in dosage for age. To avoid contamination, do not
touch tip of the container to any surface. Replace
cap after using. |
| |
Brimocom
Eye Drops - Added Reduction with Neuroprotection |
Brimocom (Brimonidine-timolol)
consists of two active substances: brimonidine tartrate
and timolol maleate. These two components decrease
elevated intraocular pressure (IOP) by complementary
mechanisms of action and the combined effect results
in additional IOP reduction compared to either compound
administered alone. Brimocom has
a rapid onset of action.
Highlights
- Brimocom contains 2 well trusted established
medications in glaucoma therapy i.e Timolol,
which is well-established gold standard beta-blocker
in glaucoma treatment and brimonidine is well
tolerated by patients and has favorable ocular
and systemic safety profile
- Brimocom has dual mechanism
of action i.e it increases outflow as well as
decreases production of aqueous humor.
- Brimonidine-timolol fixed combination produces
a statistically significant greater lowering of
IOP as compared to either Timolol or Brimonidine
monotherapy.
- Brimonidine-timolol fixed combination reduced
IOP by up to 33% (7.6 mm Hg) from an untreated
baseline of 23.3mmHg.
- Brimocom contains Brimonidine, which confers
the added advantage of Neuroprotection
- Brimocom is dosed twice daily
, which offers BD convenience,
Indications
Brimonidine-timolol fixed combination is indicated
for reduction of intraocular pressure (IOP) in patients
with chronic open-angle glaucoma or ocular hypertension
who are insufficiently responsive to topical beta-blockers
Dosage and Method of Administration
The recommended dose in adults is one drop of Brimocom
in the affected eye(s) twice daily, approximately
12 hours apart. If more than one topical ophthalmic
product is to be used, the different products should
be instilled at least 5 minutes apart. |
| |
IF2
Eye Drops - The New Age Anti-Allergic |
Olopatadine hydrochloride 0.1%
w/v eye drops
IF2 eye drops for Itch Free Eyes: Twice
daily convenience with a dual mechanism of action
Olopatadine is the first dual-action agent
with antihistaminic properties with mast-cell stabilizing
activity to be approved by the FDA in 1996 for all
the signs and symptoms of allergic conjunctivitis.
Olopatadine Demonstrates Mast cell stabilizing
activity
It is the first topical ophthalmic anti-allergy
agent that has clinically shown mast-cell stabilization
in human eyes.
Inhibits 96% of histamine release from conjunctival
mast cells in vitro
Olopatadine decreases adhesion molecule expression
results in decreased leukocyte infiltration and
prevention of other events which lead to inflammatory
process associated with allergy
Olopatadine: Antihistaminic agent
Olopatadine is a potent antihistamine with
high affinity for H1 receptors and some affinity
for H2 receptors
Effectively block the action of histamine on various
sites namely
(1)Nerve endings thus relieves the eyes from ocular
itch
(2)Blood vessel walls thus reducing chemosis
(3) Eyelids thereby decreasing lid edema
Indications
Olopatadine hydrochloride ophthalmic solution is
indicated for the treatment of the signs and symptoms
of allergic conjunctivitis.
Dosage and Administration
The recommended dose of olopatadine is one drop in
each affected eye two times per day at an interval
of 6 to 8 hours.
Highlights
Potent mast cell stabilizing ability: Olopatadine
is the first topical ophthalmic anti-allergy agent
that has clinically shown mast-cell stabilization
in human eyes.
Fast Acting: Olopatadine reduces
itching within 3 minutes of administration to the
eyes
Long lasting relief: Dual mechanism
of action of olopatadine gives an immediate and
a long lasting relief for upto 8 hrs
Superior Efficacy: Olopatadine
is 43% more effective than Ketotifen, 37% more effective
than Azelastine and 30% more effective than Epinastine
at 5 minutes post challenge for relief of ocular
itching.
Soothes the eyes: Olopatadine is
more comfortable on the ocular surface as compared
to levocabastine and ketotifen.
Convenient dosing: Olopatadine
has a simple twice a day dosing – helps in
increasing patient compliance
|
| |
Gatiquin-P
Power to Outperform |
Corticosteroids are the most effective
of clinically available agents for the non-specific
treatment of corneal inflammation.
Corticosteroids suppress the inflammatory
response to a variety of agents but they probably
delay or slow healing. Since corticosteroids may
inhibit the body's defense mechanism against infection,
a concomitant antimicrobial drug may be used when
this inhibition is considered to be clinically significant.
Gatiquin-P is a fixed
combination of the most potent steroid Prednisolone
and Gatifloxacin the first US FDA approved 4 th
generation ophthalmic fluoroquinolone.
Prednisolone is a potent
steroid , while the antibiotic gatifloxacin
in the combination is included to provide action
against the susceptible organisms.
Gatifloxacin is highly effective
against most of the pathogenic bacteria causing
ocular infections such as
Aerobes, Gram-positive:
Cornyebacterium propinquum,Staphylococcus
aureus, Staphylococcus epidermidis, Streptococcus
mitis, Streptococcus pneumoniae
Aerobes, Gram-negative
: Haemophilus influenzae
It is also known to be effective
against nontuberculous Mycobacteria, which are largely
responsible for post LASIK keratitis
It appears that when a bactericidal
antibiotic and a corticosteroid are instilled concurrently
a favorable balance is struck.
Thus, a combination of prednisolone,
a potent corticosteroid and gatifloxacin, a broad
spectrum antibiotic in a topical formulation will
together effectively resolve inflammation and infection
in severe eye conditions.
The combination can be administered
to treat post-operative inflammation. This combination
will enhance the patient compliance and provide
easy dosage administration. Thus there exists a
potential role for the combination in coexisting
infection and inflammation.
Gatiquin-P
is indicated for steroid-responsive inflammatory
ocular conditions for which a corticosteroid is
indicated and where bacterial infection or a risk
of bacterial ocular infection exists. The use of
a combination drug with an anti-infective component
is indicated where the risk of infection is high
or where there is an expectation that potentially
dangerous numbers of bacteria will be present in
the eye.
The combination can also be used
for post-operative inflammation and any other ocular
inflammation associated with infection.
Dosage and Administration
One or two drops instilled into
the conjunctival sac(s), every 4 to 6 hours. During
the initial 24 to 48 hours, the dosage may be increased
to 1 or 2 drops every two hours.
Frequency must be decreased gradually
or warranted by improvement in clinical signs. Care
should be taken not to discontinue the therapy prematurely
|
| |
Latim
- One drop. Drops IOP better. |
(Latanoprost 0.005% +
Timolol maleate 0.5%)
Latim (LTFC)
is a combination of Timolol maleate 0.5% a (ß
blocker) and Latanoprost 0.005% (a prostaglandin
analogue). The two components work together to result
into an additive IOP lowering effect than the two
components administered individually.
The rationale for the fixed dose
combination of Latanoprost, an outflow facilitator
and Timolol, an aqueous suppressor is based on the
complementary mechanism of action and efficacy of
the two components. Thus combining the benchmark
topical ß blocker (Timolol) and the prostaglandin
analogue Latanoprost confers a superior efficacy
on LTFC
Amongst a number of combination
therapies, which have been studied, Latanoprost-timolol
fixed combination (LTFC) is observed to lower the
IOP by 49% post single dose
Latim not only
brings about a powerful reduction in IOP, but with
a easy once daily dosing regimen, it also increases
patient compliance, convenience and therapeutic
efficacy.
Latim offers
- Improved diurnal IOP control
- 13-36 % additional IOP reductions
with LTFC as compared to those on monotherapy.
- Efficacy maintained over a period
of 12 months.
Latim
is indicated for the reduction of intraocular pressure
(IOP) in patients with open angle glaucoma and ocular
hypertension who are not controlled on, or are intolerant
to, monotherapy with compounds other than latanoprost
and timolol.
The recommended dosage is one
drop in the affected eye(s) once daily.
|
| |
Propcaine
– Promises Quality, Promises Success |
Proparacaine hydrochloride 0.5%
Eye drops
Proparacaine 0.5%
- The only topical anaesthetic approved for ocular
administration by U.S. FDA
Propcaine
contains proparacaine, which is an ester type of
specific surface acting local anaesthetic available
in a 0.5% w/v.
After topical application to the
eye, proparacaine penetrates to sensory nerve endings
in the corneal tissue. It blocks both the initiation
and conduction of nerve impulses thereby causing
anaesthesia.
Proparacaine eye drops provides
complete analgesia during surgery, wears off rapidly
following surgery and does not interfere with the
patient's ability to blink, see or move the eye.
Propcaine: Highlights
- Rapid onset of action
- Relatively short duration
- No Mydriasis
- No IOP change
- Minimal pain on instillation
- No cross allergy with tetracaine
- Repeated applications can be
used during intraocular surgery/operations
- Fewer allergic reactions as compared
to other topical ocular anaesthetics
Indications
Proparacaine ophthalmic solution
is indicated for the following procedures:
- Corneal anaesthesia of short
duration e.g. Tonometry, Gonioscopy,
- Removal of corneal foreign bodies
and for short corneal and conjunctival procedures.
Dosage and Administration
For removal of foreign bodies
and sutures and for tonometry:
• 1-2 drops (in single instillations) in each eye
before operating.
For short corneal and conjunctival
procedures:
• 1 drop in each eye every 5-10 minutes for 5-7
doses.
|
| |
|
|