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Pirfenex 200mg 15 Tablets

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marketed by CIPLA LTD (RESPI_ORAL)

15TAB

Prescription Required


343.68

M.R.P.:  381.87

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Product description

Pirfenex tablet is a prescription medicine that belongs to a group of compounds called respiratory agents. It is used in the treatment of idiopathic pulmonary fibrosis. It reduces scarring and swelling in the lungs and helps to breathe better. Idiopathic pulmonary fibrosis is a lung disease caused by lung tissue becoming thick and stiff and eventually forming scar tissue within the lungs. The

Cholestasis, hepatic disease, hepatitis, hepatotoxicity, jaundice. Dialysis, renal disease, renal failure, renal impairment. Tobacco smoking. Sunlight (uv) exposure..

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FAQ

1. Is a pirfenex tablet a steroid?
Ans: No, a pirfenex tablet is not a steroid. It belongs to the pyridines group of medicines. It is used to treat idiopathic pulmonary fibrosis (ipf) in adults. In ipf, the tissues of the lungs get scarred and swell with time, which creates problems in breathing. This medicine helps reduce these effects to make you breathe better.
2. How do I know that the pirfenex tablet is right for me?
Ans: Only you and your doctor can decide if the pirfenex tablet is right for you. The doctor will only prescribe this tablet after assessing your condition. Based on your response to treatment and tolerability, you should continue the medicine.
3. If my disease is stable, can I stop the pirfenex tablet?
Ans: Idiopathic pulmonary fibrosis is a progressive disease though its progression is unpredictable. Do not stop the medication without consulting the doctor. Continue taking pirfenex tablets to slow down the progression of the disease.
4. What should I avoid while taking a pirfenex tablet?
Ans: You should restrict sun exposure while taking a pirfenex tablet. Wear sunblock daily and cover your arms, legs, and head to reduce exposure to sunlight. Along with that, avoid smoking as it decreases the effect of this tablet.
5. What is the survival rate of pulmonary fibrosis?
Ans: The median survival of patients with pulmonary fibrosis is 2-3 years, yet some people live much longer. The factors which can be held responsible for shortened survival are older age, smoking history, and lower body mass index.