Hepcinat

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BRAND : HEPCINAT PRICE : 275$ STRENGTH :400MG ACTIVE INGERIDENTS: HEPCINAT-SOFOSBUVIR-400MG COMPANY NAME : NATCO TABLETS COUNT : 28 TABLETS read more

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Drug profile

Hepcinat is comes under the pharmacological category of hepatitis C virus NS5B viral RNA polymerase inhibitor

Hepcinat tablets are prescription medicine, single dose therapy not used ordinarily it is used for the patients who are all having a valid prescription and under the guidance of medical practitioner

In most of the patients, Hepcinat is not combined with peg interferon because of adverse effects produced by peg interferon. Even though this concomitant is avoided, the curable standard of Hepcinat tablet is outstanding rate.


Trade name: Hepcinat

Active ingredient: Sofosbuvir

Strength: 400MG

Mfg: Natco pharma

Package: 28 tablets in a container

Category: Anti-hepaciviral activity


Prescribing information of Hepcinat

The prescribing information of Hepcinat tablets for the patients affected with chronic hepatitis C infection;

Hepcinat is majorly indicated for hepatitis C viral infection therapy by combining with other anti-viral medicines

The effective of Hepcinat is established in the genotype I, II III or IV infections, patients who are having HIV-1/HBV co infection.

Hepcinat mainly prescribed for adolescent patients, and for pediatric patients with age of 12 years or weighing at least 35kg in genotype II or III induced hepatitis C infection


Mechanism of Hepcinat

Hepcinat containing sofosbuvir is a pan genotype, HCV NS5B RNA polymerase inhibitor.

This RNA polymerase enzyme is involved in viral production. Hepcinat is a prodrug which converted into active pharmacological metabolite by undergoing intracellular metabolism.

The active metabolite is known as uridine triphosphate. This metabolite is get inserted into viral RNA by HCV viral RNA polymerase and exhibits anti-viral activity by chain termination process


Absorption

After an oral administration, the peak plasma time of Hepcinat is reaches within 0.5 to 2 hours and its circulating metabolite GS-331007 has peak plasma time 2 to 4 hours


Distribution

The human plasma protein bound capacity with Hepcinat is occur nearly at the range of 61 to 65%

The circulating metabolite has minimal protein bounding property.


Metabolism

Hepcinat is highly metabolized in liver, whereas Hepcinat is a substrate of P-gp & BCRP


Excretion


Hepcinat is eliminated through urine by glomerular filteration

The terminal half life period of Hepcinat is 0.51 hours and its metabolite has 27 hours


How to take the Tablet Hepcinat

Generally Hepcinat is administered with or without food.

Hepcinat tablet is taken as a single dose

Do not crush or chew the tablet, swallow the tablet as whole with some water


Dosage regimens

400mg of Hepcinat (sofosbuvir)

The recommended dosage of Hepcinat by combination with other medicines;

Patients with genotype III hepatitis:

Hepcinat combined with ribavirin and peg interferon alfa and it should be taken as a single dose for 12 weeks

Otherwise Hepcinat with ribavirin should be taken as single dose for 24 weeks

Patient acquired with genotype I, IV, V or VI chronic hepatitis C viral infection:

Hepcinat is combined with ribavirin and peg interferon alfa should be taken as a single dose for 12 weeks

Hepcinat and ribavirin should be taken in case of patients are undesirable to take peg interferon alfa for 24 weeks

Patients suffered with genotype II chronic hepatitis C:

Hepcinat should be combined with ribavirin as a single dose for 12 weeks


In liver transplantation:

Hepcinat should be concurrently used with ribavirin as a single dose until liver transmission.


In pediatric:

Hepcinat tablet is recommended for the children at age 12 or weight of at least 35kg;

In without cirrhosis or with child Pugh A or compensated:

The recommended dosage is one tablet of Hepcinat should be combined with weight based ribavirin as a single dose for 12 weeks


In decompensated cirrhosis:

The prescribed dosage of Hepcinat is one tablet should be used with ribavirin for 24 weeks


Ribavirin dosage:

Ribavirin is recommended to take in two divided doses only with food

Initial dose 600mg slowly increased up to 100mg per day in weight less than 75kg

1200mg should be taken per day with the weight at least 75kg


In pediatric ribavirin dosage;

<47kg: 15mg/kg/day

47 to 49kg: 600mg/day

50 to 65kg: 800mg/day

66 to 80kg: 1000mg/day

>80kg: 1200mg/day

No dosage adjustment is followed in the therapy using Hepcinat in case of renal and hepatic impairment.


Hepcinat caused side effects

General side effects of Hepcinat;

Nausea

Bradycardia

Diarrhea

Fever, chills

Neutropenia

Anemia

Loss of appetite

Rash

Myalgia

HBV reactivation

Pruritus

Depression

Asthenia

Irritability

Influenza like syndrome

Pancytopenia

Fatigue

Headache

Insomnia


Drug interactions

Hepcinat with anticonvulsants like phenytoin, Phenobarbital or carbamazepine causes decreasing the effect of Hepcinat 

Hepcinat with analeptic drug like modafinil causes decreasing the effect of concentration of Hepcinat.

While combining with Hepcinat with amiodarone, no effect of concentration occurs but symptomatic bradycardia occurs

Hepcinat with anti-mycobacterials causes depletion in effect of concentration of Hepcinat 

Hepcinat co administration with P-gp or BCRP inhibitors, causes increasing the plasma concentration of Hepcinat 

Hepcinat is a substrate of P-gp & BCRP transporters. While using Hepcinat with P-gp or BCRP strong inducers like rifampin or st Johns wort may causes decreasing the plasma concentration of sofosbuvir. Thus the results depletion of therapeutic effect of Hepcinat

Hepcinat with vitamin K antagonist, fluctuate the effect of vitamin K antagonist


Food drug interaction

Diet should be followed under the guidance of physician

Drug with herbal interaction occurs like; Hepcinat with st Johns wort may cause depletion of therapeutic effect of Hepcinat

No food drug interaction occurs while taking Hepcinat , but caution should be taken during therapy

Possible contraindications

Hepcinat tablet combined with ribavirin or peg interferon alfa, contraindicated to pregnancy condition

Hypersensitive reaction produce because of patients contraindicated to the component present in Hepcinat tablet

Safety measures

Use with caution in decompensated condition; ribavirin should be combined with Hepcinat . Ribavirin causes fetal abnormalities and death. In pregnancy condition ribavirin not recommended

In HIV-1/HBV co infected patients, HBV reactivation occurs during or after the treatment, to avoid this problem patient must examine to calculate the level of HBV surface antigen & HBV core antibody before starting the treatment

While concomitant amiodarone with Hepcinat , patient must counsel about the exposure of this combination, on the other hand some alternative medicines should be prescribed to reduce the risk of symptomatic bradycardia

Hepcinat combined with P-gp or BCRP strong inducers leading to loss of therapeutic effect. Avoid this combination.


Pregnancy and lactation

Hepcinat comes under pregnancy category B1

Whereas Hepcinat combined with ribavirin in chronic condition, ribavirin has pregnancy category X; which means causes fetal damage even to death

Ribavirin should not be recommended in pregnancy

Breast feeding should not be recommended


Storage and handling

The storage condition of Hepcinat tablets;

Hepcinat tablet container stored at room temperature below 30oC

Container should be kept in dry and cool place, free from moisture, heat & light

Keep out of reach from children

The shelf life of the tablet is around 5 years


Missed dose

Hepcinat is a prescription medicine, if patient fail to take the dose of Hepcinat must consult with physician and take the dose within the time

Otherwise the missed dose should be skipped and follow the regular dosing schedule

Medicine schedule: prescription medicine


Over dosage

The maximum dose of sofosbuvir is 1200mg, there is no distinct antidote is required for over dose of Hepcinat .

If overdose occurs in the patients two possible way to overcome from this difficulty;

Patients first confirmed from the toxicity and Patients should be periodically monitored for their symptoms & clinical status. To maintain safety measures properly

Hemodialysis is another method which is involved in over dosage condition; predominantly eliminate the sofosbuvir circulating metabolite contents from the body with separating at the range of 54%

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