Amended Drugs Board Chairman Says "Toxic Capsule" Test Results Not Released as Expected

The company claimed that the selected hollow capsules were from regular companies with complete qualifications and national standards, but no specific names have been disclosed yet. - The reporter Chen Yaqiong revised the pharmaceutical chairman Xiu Yigui and personally disclosed that the results of the reinspection of the Antelope cold capsules will be April 18 It was announced at 8 in the morning, but it was still waiting for the day and it was still not announced. As of press time, it is still a mystery when the re-inspection results are released.

After the revision of the drug scandal was exposed, its official website was hacked by the hackers from the evening of April 15. After a short period of normal recovery, it was hacked again on April 16. At 16:20 pm on April 18th, the reporter saw that the official website of Tonghua Golden Horse [4.82-2.03% Shares Bar] and Qinglandongdan of Qinghai had not yet been repaired, and the official website of the correction drug temporarily returned to normal. "Blessing for common people" is still prominent on the web. The public contact phone has been unsuccessful in dialing.

The spearhead turned to the supplier and was exposed by CCTV's "Weekly Quality Report." It was revised that the chromium content of the antelope cold capsule detected by the pharmaceutical industry was 4.44mg/kg, exceeding the industry standard of 2mg/kg 1 times.

In this regard, the amendment of the pharmaceutical chairman Xiu Yugui said that the exposed product can only be said to mark the "correction", and can not be said to modify the production, because it has not been confirmed by the manufacturer.

In this “toxic capsule” storm, the results of the inspection by the State Food and Drug Administration are of critical importance. According to Xiu Yuegui, the chromium content of the company's self-inspected products is in line with the standards. The Food and Drug Administration has come to sample inspections. Now we wait for the test results and speak with the data.

In fact, Revised Pharmaceuticals issued two statements within one day of April 16. According to the first statement, the company organized a security inspection team for the first time, reviewed relevant product quality, actively cooperated with the relevant national regulatory authorities, and promised that if any quality problems were detected, the company was willing to accept any treatment from the state agency.

However, the amended pharmaceutical industry issued a second statement, deleting the phrase “if any quality problems were detected” and changing it into “a hollow capsule enterprise selected by Lingyang Cold Capsules is a formal enterprise with complete qualifications and national standards. For the re-inspection results, we will retain the power to pursue the relevant suppliers' responsibilities according to law.” Contrasting the two statements before and after, the spearhead was transferred to the hollow capsule supplier.

Regular capsule manufacturers are still "fans"

Yao Longkun, Secretary-General of the China Daily Industrial Association Gelatin Section, told Securities Daily that the key to industrial gelatine imitation of pharmaceutical gelatin capsules lies in the fact that the company did not do a good job and was put into production without testing.

Jilin Huinan Tianyu Pharmaceutical Antiviral Capsules were also identified in the same batch of products with chromium exceeding the standard. The chromium content of the antiviral capsules was 3.54mg/kg. The company contends that in the 2000 edition of the Pharmacopoeia, the test standard did not determine the content of heavy metal chromium, but only specified that the content of heavy metals should not exceed 5 mg/kg. The company's anti-virus capsules (product lot number: 091102) was produced in November 2009 and it implements the 2000 edition of the Pharmacopoeia standard.

In 2007, the Chinese Pharmaceutical Association established the Guild Association Standard for Gelatin Hollow Capsules (YBX-2000-2007), which refers to the standard. The “Food Additive Gelatin” (GB6783-1994) stipulates clearly: “In order to limit the use of gelatin produced from inferior leather to produce capsules, a chromium content index shall be established. The index shall not exceed 2 mg/kg.”

After the “toxic capsule” incident was exposed, Xiu Yugui emphasized that the modified pharmaceutical industry had never purchased capsules from the two companies “Hua Xing” and “Zhuo Kang” mentioned in the CCTV survey. As for where to buy capsules, repairs and your company's statement have not been disclosed.

Jilin Huinan Tianyu Pharmaceutical Co., Ltd. issued a statement on April 17th and revised its pharmaceutical industry in the same way. It stated that “the hollow capsule production enterprise selected by our company's antiviral capsule is a formal capsule manufacturing enterprise with complete formalities and in line with national standards,” and stated that Wait for the results of the inspections of the relevant regulatory authorities. Both companies are located in Jilin Province and they do not know whether they have submitted inspections in the same batch.

It is worth noting that the manufacturers using industrial gelatin capsules exposed by CCTV's "Weekly Quality Report" are all certified by the company.