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DRUG FOR THE WEEK
NESINA
NESINA
•Therapeutic class:-Dipeptidyl peptidase 4-inhibitor
•Generic name:-Alogliptin benzoate
•Trade name:-Nesina
•FDA Approved date :- 26 January 2013
•Company name:- Takeda
•Cost:- 25 mg (Rs.209.40) ,12.5 mg(Rs.112.20), 6.25mg
(Rs.60.40)
•
•Indications:- Type 2 diabetes mellitus
•Dosage:-
• Adults:- Usual- 25mg- qd
• Renal Impairment: Moderate : 12.5mg qd
•. End-Stage Renal Disease/severe: 6.25mg qd.
•Pregnancy:-
•Category B
•Mechanism of action:-
It increases the activation of incretin hormones, thereby
increasing their bloodstream concentrations and reducing fasting
postprandial glucose concentrations .
•Pharmacokinetics:-
Absorption:- Absolute bioavailability (100%)
Distribution:- 20% plasma protein binding
Metabolism:- hepatic metabolism occurs
Elimination:- Feces (13%), Urine (76%), T1/2=21 hrs
•Adverse drug reactions:-
• Hypoglycemia
• Nasopharyngitis
•Throbbing headache
•Drug interactions:-
• Bexarotene
• Gatifloxacin
•Warning and Precautions:-
•Not for use in type 1 diabetes, diabetes ketoacidosis
•D/c if pancreatitis is suspected
•Use with caution in patients with abnormal LFTs
Patient counselling:-
•Avoid alcohol consumption
•If a dose is missed not to take a double dose
•Inform signs / symptoms of pancreatitis
•Instruct to inform physician if unusual symptom
develops or if a symptom persists/worsens.
Nesina

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Nesina

  • 1. DRUG FOR THE WEEK NESINA
  • 2. NESINA •Therapeutic class:-Dipeptidyl peptidase 4-inhibitor •Generic name:-Alogliptin benzoate •Trade name:-Nesina •FDA Approved date :- 26 January 2013
  • 3. •Company name:- Takeda •Cost:- 25 mg (Rs.209.40) ,12.5 mg(Rs.112.20), 6.25mg (Rs.60.40) • •Indications:- Type 2 diabetes mellitus •Dosage:- • Adults:- Usual- 25mg- qd • Renal Impairment: Moderate : 12.5mg qd •. End-Stage Renal Disease/severe: 6.25mg qd. •Pregnancy:- •Category B
  • 4. •Mechanism of action:- It increases the activation of incretin hormones, thereby increasing their bloodstream concentrations and reducing fasting postprandial glucose concentrations . •Pharmacokinetics:- Absorption:- Absolute bioavailability (100%) Distribution:- 20% plasma protein binding Metabolism:- hepatic metabolism occurs Elimination:- Feces (13%), Urine (76%), T1/2=21 hrs
  • 5. •Adverse drug reactions:- • Hypoglycemia • Nasopharyngitis •Throbbing headache •Drug interactions:- • Bexarotene • Gatifloxacin
  • 6. •Warning and Precautions:- •Not for use in type 1 diabetes, diabetes ketoacidosis •D/c if pancreatitis is suspected •Use with caution in patients with abnormal LFTs Patient counselling:- •Avoid alcohol consumption •If a dose is missed not to take a double dose •Inform signs / symptoms of pancreatitis •Instruct to inform physician if unusual symptom develops or if a symptom persists/worsens.