AGP Limited Secures 1st Position at BCSR Awards 2023

AGP collaborates with Childlife Foundation on Children’s Day 2023

AGP Launched Peridots – A Thanda Solution to Acidity, Gas and Indigestion

AGP secures 2nd Position at BCR Awards 2022

AGP wins Top Exporter Award at 6th PPMA Summit

AGP sponsors KDSP Carnival 2023

AGP bags big win at GDEIB Awards 2023

AGP continues partnership with IBA

AGP continues collaboration with TCF

AGP joins hands with SKMF

AGP continues partnership with ACF

AGP conducts Allergy Awareness Session At Pak Turk Maarif

Gong-Ringing Ceremony of AGP at PSX

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Poze G

Generic:

Glimepiride, Pioglitazone HCI

 

Therapeutic Class:

Glitazone & S-Urea Combs

 

Composition:

Poze G Tab 30 mg/ 2 mg: 
Each tablet contains 30 mg pioglitazone hydrochloride with 2 mg
glimepiride.

Poze G Tab 30 mg/ 4 mg: 
Each tablet contains 30 mg pioglitazone hydrochloride with 4 mg
glimepiride.

 

Description:

Poze G tablets contain two oral antihyperglycemic agents used in the management of type 2 diabetes: pioglitazone hydrochloride and glimepiride. Pioglitazone hydrochloride acts primarily by decreasing insulin resistance. It improves sensitivity to insulin in muscle and adipose tissue and inhibits hepatic gluconeogenesis. It reduces circulating insulin levels and improves glycemic control. Glimepiride is an oral
glucose-lowering drug of the sulphonylurea class, which acts by increasing
the release of insulin from the pancreatic beta cells.

 

Indications:

Poze G is indicated as an
adjunct to diet and exercise as a once-daily combination therapy to improve
glycemic control in patients with type 2 diabetes who are already treated
with a combination of pioglitazone and a sulfonylurea or whose diabetes is
not adequately controlled with a sulfonylurea alone, or for those patients
who have initially responded to pioglitazone alone and require additional
glycemic control.

 

Dosage:

Poze G tablets are available as a 30 mg pioglitazone plus 2 mg glimepiride or a 30 mg pioglitazone plus 4 mg glimepiride formulation for oral administration. The maximum recommended daily dose for pioglitazone is 45 mg and the maximum recommended daily dose for glimepiride is 8 mg. Poze G should therefore not be given more than once daily at any of the tablet strengths.   

 

General:

The use of antihyperglycemic therapy in the management of type 2 diabetes should be individualized on the basis of effectiveness and tolerability.

Dosage Recommendations:

Selecting the starting dose of Poze G should be based on the patient’s current regimen of pioglitazone and/or sulfonylurea. It is recommended that a single dose of Poze G be administered once daily with the first main meal.

Starting dose for patients currently on glimepiride monotherapy:

Based on the usual starting dose of pioglitazone (15 mg or 30 mg daily), Poze G may be initiated at 30 mg/2 mg or 30 mg/4 mg tablet strengths once daily, and adjusted after assessing adequacy of therapeutic response.

Starting dose for patients currently on pioglitazone monotherapy:

Based on the usual starting doses of glimepiride (1 mg or 2 mg once daily), and pioglitazone 15 mg or 30 mg, Poze G may be initiated at 30 mg/2 mg once daily, and adjusted after assessing adequacy of therapeutic response.

Starting dose for patients switching from combination therapy of pioglitazone plus glimepiride as separate tablets:

Poze G may be initiated with 30 mg/2 mg or 30 mg/4 mg tablet strengths based on the dose of pioglitazone and glimepiride already being taken. Patients who are not controlled with 15 mg of pioglitazone in combination with glimepiride should be carefully monitored when switched to Poze G.

Maximum Recommended Dose:

Poze G tablets are available as a 30 mg pioglitazone plus 2 mg glimepiride or a 30 mg pioglitazone plus 4 mg glimepiride formulation for oral administration. The maximum recommended daily dose for pioglitazone is 45 mg and the maximum recommended daily dose for glimepiride is 8 mg. Poze G should therefore not be given more than once daily at any of the tablet strengths. 

 

 

Presentations:

  • Poze G 30 mg/ 2 mg is available in 14’s
  • Poze G 30 mg/ 4 mg is available in 14’s

 

Posterisan

Generic:

Bacterial Culture Suspension

 

Therapeutic Class:

Topical Antihaemorrhoidal

 

Composition:

Bacterial cultural suspension

 

Description:

1 gm of Posterisan forte
ointment contains in 166.7 mg aqueous suspension 330 million dead E.coli
(corpuscular components and metabolites) and 3.3 mg liquefied phenol
(corresponding to 3.0 mg pure phenol) in an inert ointment base (water/oil
emulsion)

 

Indications:

For the treatment of
haemorrhoids, eczema and itching in the region of the anus (anal eczema and
pruritus anal), anal fissures and cracks (rhagades).

 

Dosage:

Ointment is applied several
times daily in a thin layer on the parts of skin or of the mucosa that must
be treated

 

Presentations:

10 gm ointment

 

Posterisan Forte

Generic:

Bacterial Culture Suspension,
Hydrocortisone

 

Therapeutic Class:

 

Topical Antihaemorrhoidal

 
 

Composition:

 

Bacterial cultural suspension
and hydrocortisone

 
 

Description:

 

1 gm of Posterisan forte
ointment in 166.7 mg aqueous suspension contains 500 million dead E.coli
(corpuscular components and metabolites), 3.3 mg liquefied phenol
(corresponding to 3.0 mg pure phenol) and 2.5 mg hydrocortisone in an inert
ointment base (water/oil emulsion)

 
 

Indications:

 

Persistent haemorrhoids
complaints, acute or ulcerous eczemas, itching and painful cracks and chaps
(rhagades and fissures) in the anal region

 
 

Dosage:

 

Ointment is applied several
times daily in a thin layer on the parts of skin or of the mucosa that must
be treated

 
 

Presentations:

 

10 gm ointment

 

 

 

Phyllocontin

Generic:

Aminophylline Hydrate

Therapeutic Class:

Xanthines – Systemic

Composition:

Each Phyllocontin continus
tablet contains aminophylline hydrate 225 mg.

Description:

Phyllocontin continus tablet
contains aminophylline that is the salt of theophylline most commonly used
for therapeutic purposes. It acts as a bronchodilator (dilates the bronchi
i.e. air passage). It improves breathing by opening air passages in the
lungs.

Indications:

  • Treatment and prophylaxis of bronchospasm associated with asthma. emphysema & chronic bronchitis
  • Prevention of
    exercise-induced bronchoconstriction

Dosage:

1-2 tablets 12 hourly ensure 24
hours protection

Presentations:

225 mg tabs 50’s

Osnate-D Tablets

Generic:

Ossein Mineral Complex

 

Therapeutic Class:

 

Calcium

 
 

Composition:

 
Each Osnate-D tablet contains:

  • Vitamin D……………………… 400 IU
  • Ossein Mineral Complex …….. 830 mg
  • Corresponding to:
  • Calcium …………………….. 177.6 mg*
  • Phosphorus ………………… 82.2 mg*
  • Residual Mineral Salts …… 24.9 mg
  • Collagen ……………………. 224  mg
  • Other proteins …………….. 66.4 mg
  • Trace elements ……………. Fl, Mg, Fe, Zn, Cu, Ni.

* Corresponding to approximately 440 mg Hydroxyapatite.

 
 

Description:

 
Osnate-D contains the organic matrix (Ossein) and the mineral components (Hydroxyapatite) of bone tissue in physiological proportions along with Vitamin D.  
 

Indications:

 
Osnate-D is indicated in the following conditions:

  • Increased mineral requirements during pregnancy, lactation and growth
  • Osteoporosis
  • Osteomalacia
  • Hypocalcemia
  • Bone pain
  • Increased bone fragility
  • Prophylaxis against dental caries
  • As adjuvant in fractures with delayed callus formation 
 
 

Dosage:

 
Usual dosage: 1-2 tabs daily before meals with some liquid.

Special dosage instruction:  In Osteoporosis: As advised by the physician.

 
 

Presentations:

 
Osnate-D Tabs are available in pack of 30’s.  
 

 

Osnate-D suspension

Generic:

Ossein Mineral Complex, Vitamin D

 

Therapeutic Class:

 

Calcium

 
 

Composition:

 
Each 5 ml of Osnate-D suspension contains:

  • Vitamin
    D ………………………………………… 400 IU
  • Ossein Mineral Complex (AGP Specs)… 400 mg

 

Corresponding to:

  • Calcium ……………………….. 85.59 mg*
  • Phosphorus ………………….. 39.61mg*
  • Residual Mineral Salts …… 12.00 mg
  • Collagen ……………………… 107.95 mg
  • Other proteins ………………. 32.00 mg
  • Trace elements ……………… (Fl, Mg, Fe, Zn, Cu & Ni)

* Corresponding to approx. 212 mg Hydroxyapatite.

 
 

Description:

 

Osnate-D suspension contains the organic matrix (Ossein) and the mineral components (Hydroxyapatite) of bone tissue in physiological proportions along with Vitamin D.

 
 

Indications:

 
Osnate-D suspension is indicated for the prevention or treatment of the following conditions:

  • Poor bone & teeth development
  • Rickets
  • Osteoporosis
  • Osteomalacia
  • Bone pain
  • Increased bone fragility
  • Hypocalcemia
  • Increased mineral requirements during pregnancy, lactation & growth
  • Prophylaxis against dental caries
  • As adjuvant in fractures with delayed callus formation
 
 

Dosage:

 
Children: 1 to 2 teaspoonfuls daily before meals or as directed by the physician.

Adult: 2 to 4 teaspoonfuls daily before meals or as directed by the physician.

Special dosage instruction:  In Osteoporosis: As advised by the physician.

 
 

Presentations:

 

Osnate-D suspension is available in 120 ml bottle.

 
 

Osnate Tablet

Generic:

Ossein Mineral Complex

 

Therapeutic Class:

 

Calcium

 
 

Composition:

 
Each Osnate tab contains:

  • OSSEIN MINERAL COMPLEX————830.0 mg

Corresponding to:

  • Trace Elements————————– FI, Mg, Fe, Zn, Cu,Ni

Corresponding to approx. 440 mg Hydroxyapatite

  • Calcium———————————–177.6 mg
  • Phosphorus——————————-82.2 mg
  • Residual Mineral Salts——————-24.9 mg
  • Collagen———————————-224.0 mg
  • Other proteins—————————66.4 mg

 

 

Description:

 
Osnate is a calcium preparation (Ossein-hydroxyapatite compound) of unique composition. It contains the  organic matrix and the mineral components of bone tissue in physiological proportions.  
 

Indications:

 
Increased calcium requirement like in

  • Pregnancy
  • Lactation
  • Osteoporosis
 
 

Dosage:

 
Osteoporosis: 2-4 tabs twice daily.

Pregnancy & lactation: 1-2 tabs daily.

 
 

Presentations:

 
800 mg tabs 30’s  
 

Osnate suspension

Generic:

Ossein Mineral Complex

 

Therapeutic Class:

Calcium

 

Composition:

Each 5 ml contains:

Ossein Mineral Complex (AGP Specs) …. 400 mg

Corresponding to :

  •    Calcium ………………………………………….. 85.59 mg*
  •    Phosphorus ……………………………………… 39.61mg*
  •    Residual Mineral Salts ………………………… 12.00 mg
  •    Collagen …………………………………………. 107.95 mg
  •    Other proteins ………………………………….. 32.00 mg
  • Trace elements …………………………………. (Fl, Mg, Fe, Zn, Cu & Ni)

* Corresponding to approx. 212 mg Hydroxyapatite.

 

Description:

Osnate suspension contains the organic matrix and the minerals components of bone tissue in physiological proportions.

 

Indications:

Calcium and phosphorus deficiencies, growth and Osteoporosis. As adjuvant in fractures with delayed callus formation.

 

Dosage:

Children: 1 to 2 teaspoonfuls daily before meals or as directed by the physician.

 

Presentations:

60 ml susp

Novafol

Generic:

L-Methylfolate

 

Therapeutic Class:

 
Oth Anti-Anaem – Folic Acid  
 

Composition:

 

Each Novafol tablet contains
L-Methylfolate 400 mcg.

 
 

Description:

 

Novafol (L-methylfolate) which
is structurally analogous to the reduced and active form of folic acid
5-methyltetrahydrofolate (L-Methylfolate), is absorbed directly in the
active form that can immediately diffuses into the blood and is available
for its immediate biological action.

 
 

Indications:

 
Novafol tablets are for the
specific dietary management of impaired metabolic processes in those women
with distinct nutritional requirement for any of the following conditions.

  • High risk recurrent pregnancy loss
  • Impaired folic acid absorption and impaired metabolism
  • Hyperhomocysteinemia during pregnancy
 
 

Dosage:

 
Usual dosage of Novafol Tab is 1
or 2 tablets daily.
For folic acid deficiency:

The typical dose is 250-1000 mcg (micrograms) per day.

For preventing neural tube defects: 
At least 400 mcg of folic acid per day from supplements or fortified food should be taken by women capable of becoming pregnant and continued through the first month of pregnancy. Women with a history of previous pregnancy complicated by such neural tube defects usually take 4 mg per day beginning one month before and continuing for three months after conception

For treating high levels of homocysteine in the blood:

  • 0.5-5 mg (milligrams)/day has been used, although 0.8-1 mg/day is appears to be more effective.
  • In people with end-stage renal disease, high homocysteine levels may be more difficult to treat, and doses of 0.8
  • 15 mg/day have been used. Other dosage plans such as 2.5-5 mg 3 times weekly have also been used. Doses higher than 15 mg daily do not seem to be more effective.
 
 

Presentations:

 
  • 400 mcg Tab 30’s
 

 

Nebcin

Generic:

Tobramycin Sulphate

 

Therapeutic Class:

Aminoglycosides
 

Composition:

Nebcin 10 mg:
Each ampoule contains 10 mg of tobramycin sulphate in 1 ml solution.

Nebcin 20 mg:
Each ampoule contains 20 mg of tobramycin sulphate in 1 ml solution.

Nebcin 80 mg:
Each ampoule contains 80 mg of tobramycin sulphate in 2 ml solution.

 

Description:

Tobramycin sulfate, a
water-soluble antibiotic of the aminoglycoside group, is derived from the
actinomycete Streptomyces tenebrarius. Nebcin injection is a clear and
colorless sterile aqueous solution for parenteral administration

 

Indications:

  • Septicemia
  • Lower respiratory tract infections
  • Serious central-nervous-system infections
  • Intra-abdominal infections
  • Skin, bone, and skin structure infections
  • Complicated and recurrent urinary tract infections
 

Dosage:

Neonates:
0-7 days: 2 mg/kg every 12 hours,
More than 7 days: 2 mg/kg every 8 hours

Children:

6-7.5 mg/kg/day in 3-4 divided doses

Adult:

3-5 mg/kg/day in 3-4 divided doses

 

Presentations:

  • 10 mg/1 ml inj,
  • 20 mg/1 ml inj,
  • 80 mg/2 ml inj,