Pharmaceutical composition for idiopathic pulmonary fibrosis and application thereof
A pulmonary fibrosis, idiopathic technology, applied in the field of medicine, to achieve the effect of improving the quality of life, slowing down acute exacerbations, and alleviating pulmonary interstitial fibrosis
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Embodiment 1
[0016] Embodiment 1: The patient, male, 54 years old, the main clinical symptoms of the patient were intermittent cough, expectoration, and chest tightness for 3 years, which aggravated for 1 month. The patient was diagnosed with acute exacerbation of idiopathic pulmonary fibrosis (AE-IPF) and was given oral pirfenidone capsules starting from 200 mg each time, 3 times a day, and the dose was increased by 200 mg each week, and then gradually increased by 600 mg each time. 3 times a day, plus dextromethorphan 7.5mg once a day. After 1 month of drug treatment, the patient had no further progression of idiopathic pulmonary fibrosis on chest CT scan. After continuing to take the medicine orally for 3 months, the patient felt that the symptoms such as cough and chest tightness were relieved compared with before, and the chest CT showed that the ground-glass opacities and grid shadows in both lungs were relieved compared with before. The re-examination of the patient's lung function...
Embodiment 2
[0017] Example 2: The patient, male, 82 years old, the main clinical symptoms of the patient were intermittent cough and expectoration for more than 10 years, which aggravated with wheezing for 1 week. The patient was diagnosed with idiopathic pulmonary fibrosis (IPF) on CT scan 10 years ago. The patient did not receive any special treatment. In the past 1 week, the patient felt that his cough had worsened with wheezing. The examination of both lungs showed diffuse interstitial changes, and the interstitial fibrosis in both lungs was worse than before. , consider the patient as AE-IPF. Oral administration of pirfenidone capsules starting from 200mg each time, 3 times a day, increasing the dose by 200mg each time a week, and then gradually increasing 400mg 3 times a day for anti-fibrosis treatment, and at the same time adding dextromethorphan 7.5mg a day 1 time. A one-month re-examination of chest CT showed no significant progression of interstitial fibrosis in both lungs. Th...
Embodiment 3
[0018] Embodiment 3: The patient, male, 70 years old, the main clinical symptom of the patient is intermittent wheezing for 2 years, which aggravates with wheezing for 1 week. The patient's chest CT scan in May 2019 showed increased diffuse ground-glass shadows, mesh shadows, and honeycomb shadows in both lungs, and pulmonary interstitial fibrosis had progressed compared with before. Lung function check showed FEV1% pred 57.8%, FVC% pred 44.6%. The patient took oral pirfenidone capsules starting from 200mg each time, 3 times a day, and increased the dose by 200mg each time a week, and then gradually increased 400mg 3 times a day for anti-fibrosis treatment. At the same time, dextromethorphan 7.5mg was added every day 1 time a day. After 4 months of oral administration, the patient's re-examination of chest CT showed that the interstitial fibrosis of both lungs was less than before, and the ground-glass opacity of both lungs was less than before. The results are as follows: ...
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