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Brand Vs Generic – IPA President Speaks to Life Science World

April 2, 2013 in association, DRUGS CONTROL, health ministry, medical news, pharma industry, pharmacist

Abhay Kumar, President-Indian Pharmacist Association

The Health Ministry’s directive asking the doctors to prescribe Generic medicines is a very positive and legitimate directive as a whole. As far as the Pharmacist is considered, he/she would be the most happy to see a prescription with the generic medicine, as he will be not bounded by the “Brands” which some Physician restrict for ‘not to be substitute’. This step of the GOI not only will lead to cheaper medicine to the under-deprived patients but will also encourage several other Pharmaceutical companies to market their product in Generic as well. As we all know that potency and pharmacological value of these generic drugs are as good as the branded one, there should any misconception among the common people about the “Generic medicine”. So, government should also launch some awareness campaign about the efficacy of the generic drugs in addition to issuing such directive to the Physician to prescribe generic medicine.

At the end we at the IPA welcome this step of Govt. of India and would request all those who stands on the other side in this regard to support this for the betterment of the common people of India, who needs this cost effective  ‘Generic Medicine” the most.

http://www.lifescienceworld.in/brand-vs-generics-a-war.html

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Use of Nimesulide Should ordinarily be restricted to 10 Days

April 20, 2012 in health ministry, medical news, Patient counseling, pharma industry, pharmacist

The Drugs Controller General of India has asked the manufacturers to add “box warning” on its label, suggesting that its use to be restricted to 10 days.  If longer clinical use is necessary then liver function test should be assessed periodically.

Manufacturers are directed to incorporate the said box warning in a conspicuous manner on label, carton, package insert and other promotional literature of the drug.

 

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Pharmacy college develops ointment to tackle skin ailments

November 7, 2011 in pharma industry, pharmacist

Not many medicines available have been known to be effective against skin ailments like eczema and athlete’s foot. A city-based pharmacy college, however, has developed anointment that may prove to be a boon for people with these conditions. The formula of the ointment has already been bought by a manufacturer.

Researchers from Sharad Pawar College of Pharmacy have taken a leaf from tribal and ancient knowledge about the sal tree to make this medicine. Not only has the college applied for a patent of the cream, they have already sold the formula to city-based pharma company, Vaidik Remedies.

“The medicinal properties of sal have been well known among the tribal population. It also finds a mention in some ancient scriptures. We only tried to give some scientific base to the ancient knowledge through our research,” said N J Duragkar, one of the researchers and a teacher at the college. He insisted that this step would be in reiterating the effectiveness of ancient medical practices like ayurveda over other forms of medicine. “It has been a big issue with practitioners of modern medicine that systems like ayurveda do not have enough documentation and there is an absence of a scientific explanation about the properties of their medicines. We have made a conscious effort to modernize our ancient medical system and ease out the criticism,” he explained.

Principal of the college, KP Bhusari was also a part of the research team. He said, “We have been able to extract and isolate the compound of the sal tree that helps fight against these skin diseases. We conducted a clinical trial on around 100 people who were grouped according to their ages. The two-year long trials included people from eight years of age to 75 year olds. Besides us, the team from Vaidik Remedies, also conducted an independent trial.” He informed that both the trials showed that the ointment worked effectively against itching and the various bacterial and fungal infections that affect the skin.

Housewives, housemaids and others who are more prone to develop fungal infections constituted the trial group of Vaidik Remedies. “We also found the cream to be effective against cuts and blisters. In fact, I tried it on my family members, too,” revealed Satish Vyavahare, MD of the company. He believes that such tie-ups would be mutually beneficial as both the research as well as pharma industries scene in Vidarbha has a lot of scope to develop.

Source: The Times of India

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Health ministry to withdraw ban on ads on morning after pills

October 18, 2011 in DRUGS CONTROL, pharma industry

The Union health ministry will soon withdraw its ban on advertisements on emergency contraceptive pills like Unwanted-72, Option-72 and I-Pill. The ministry had imposed the ban in January last year after experts raised concern that these advertisements may promote the misuse of the pill by the young generation.

According to sources, the Drugs Technical Advisory Board (DTAB) of the union health ministry in its meeting held on October 10 has decided to allow the advertisements on  emergency contraceptive pills with some riders. As per the new DTAB guidelines, a committee consisting of the principal of a reputed girls college, representatives from civil society groups and the advertising council should screen the ads and the scripts before they are on air.

Ever since the drug companies launched advertisements on emergency contraceptive pills like Unwanted-72, Option-72 and I-Pill, experts and public interest groups in the country have been raising concern that these advertisements may promote the misuse of the pill by the young generation who have started looking at the pills as a regular contraceptive method as the advertisements are said to have failed to drive home the message clearly that these pills are emergency contraceptives.

Apart from the civil society organisations, gynaecologists in the country have also been expressing concern on the misuse of the pill by the young generation. It triggered a debate in sexually conservative India with critics arguing that the easy availability of such pills would encourage promiscuity among the millions of young people. There was also criticism that the easy availability of these drugs will also promote unsafe sex among younger generation and may result in promotion of diseases like HIV/AIDS in the country.

When the public criticism reached its crescendo after the companies started airing competitive ads on these pills, the Drugs Controller General of India (DCGI) banned the advertisements on these emergency pills and left the matter to the DTAB, which is the highest authority of health experts on technical matters under the union health ministry.

Now that the DTAB has taken a final decision in favour of the pharma companies, they can start advertisements on these pills.

Source: Pharmabiz

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Madras HC quashes ban on PPA, verdict on nimesulide yet to come

September 14, 2011 in pharma industry

Phenylpropanolamine (PPA), one of the six drugs banned by the Union health ministry early this year for its adverse effects, can now be manufactured and marketed by the pharma companies in the country as the Madras High Court has quashed the ban on PPA.

Delivering its final judgment on September 9 on a writ petition filed by drug major Cipla Ltd, the Madras High Court has quashed the Union health ministry’s notification dated February 10, 2011, insofar as Phenylpropanolamine is concerned.  In the notification, the ministry had banned six of the most controversial drugs— nimesulide (below 12 years age), cisapride, PPA, human placenta extracts, sibutramine & its formulations and R-sibutramine & its formulations.

Cipla had filed a writ petition in the Madras High Court on March 23 this year, praying to allow the company to manufacture and market PPA. But, the court merged the Cipla case with that of a similar case filed by manufacturers association Confederation of Indian Pharmaceutical Industries (CIPI) and after hearing the parties, the court in its interim order stayed the entire notification of the ministry (GSR 82 E) dated February 10, 2011.

In yet another case filed by Unichem Laboratories for marketing nimesulide (below 12 years age), the court is yet to deliver the final judgment.

In the gazette notification dated February 10, the ministry had banned these controversial drugs for their adverse effects on human health. The ministry’s decision was based on the recommendations of the Drugs Technical Advisory Board (DTAB) and its recommendations are normally followed by the ministry. Earlier, the DCGI had brought these controversial drugs under the radar of the DTAB in the wake of serious concern raised by the medical experts in the country over their side-effects.

Source: Pharmabiz

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India patent case threatens cheap drug supply: MSF

September 5, 2011 in pharma industry

Supply of cheap, copycat drugs for the developing world could be badly threatened if Swiss firm Novartis wins a challenge to India’s patent law, medical charity MSF said on Monday.

The warning came as the Supreme Court was due to hear more arguments Tuesday in an appeal by Novartis seeking patent protection for a newer version of its leukaemia drug Glivec — a case watched closely by global pharmaceutical firms.

“If the patent law challenge is successful, it would have a devastating impact on access to affordable medicines across the developing world,” Leena Menghaney, India representative of Medecins Sans Frontieres (MSF), told a news conference.

Novartis is contesting the Indian patent office’s rejection of a patent application for the updated version of Glivec that is better absorbed by the body. MSF calls the improvement a “minor modification”.

The drugmaker’s challenge goes to the heart of India’s patent act, which says a patent cannot be granted for an old drug unless changes make it significantly more therapeutically effective.

The Supreme Court case is the final act in a lengthy legal battle between Novartis and patient rights groups in India, where local firms produce generic drugs at a fraction of the cost of brand-name originals.

Indian generic versions of Glivec sell for 8,000 rupees ($174) for a month’s treatment compared with 120,000 rupees for the brand-name version, MSF said.

Pharmaceutical multinationals argue that protecting patents is crucial to stimulating the research and development of new drugs.

India, known as the “pharmacy to the developing world,” has long been a key provider of cheap generic medicines as it did not issue drug patents until 2005, when it was obliged to adhere to WTO intellectual property regulations.

Now, India allows patents for new inventions after 1995 or for an updated drug showing much greater therapeutic efficacy. The base compound for Glivec was discovered in 1993.

But India rejects applications for minor changes to existing drugs, which critics say are aimed at extending the life of original patent monopolies from their original 20 years — a practice known as “evergreening”.

A spokesman for Novartis said on Monday the court’s decision was essential to the “viability of the innovative pharmaceutical business in this country”, adding that Glivec had received patent protection in nearly 40 countries.

The cost difference between generic and brand name drugs is crucial for poor people around the world, MSF said, noting generics from India have pushed down prices for older anti-AIDS drugs by 99 percent.

MSF buys 80 percent of its generic AIDS drugs from India and the humanitarian group said it is currently keeping 170,000 people in 19 countries alive on the treatment.

“We couldn’t afford to treat them all without these generic drugs,” Joanna Keenan, spokesman for Geneva-based MSF, told AFP.

If the court accepts Novartis’s arguments, the ruling could set a precedent allowing firms to acquire patents on modified versions of existing medicines — extending the time of their exclusive right to make drugs, MSF said.

“It would create a scenario in which only the richest survive. The outcome of this case is literally a matter of life and death for people,” Loon Gangte, who heads an Indian group representing people living with HIV/AIDS, told AFP.

Source: The Economic Times

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Medical representative’s strike on Aug 17

August 14, 2011 in pharma industry

Around 1.5 lakh medical representatives of country will observe strike on August 17 to press their 15-point charter of demands.

The call for strike was given by the Federation of Medical and Sales Representatives Association of India in its meeting held in February.

According to Arvind Tiwari, secretary, Kanpur unit of Uttar Pradesh Medical and Sales Representatives Association, another around 1 lakh sales promotion employees working in small and medium pharmaceutical companies and other industries would support the strikers. Tiwari said that the sales promotion employees engaged in the marketing of drugs were deprived of leave facilities and job records as per provisions of sales Promotion Employees (condition of services) Act-1976.

Source: The Times of India

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AICDF calls for pharmacy bandh in Delhi & Haryana against govt’s decision to include Schedule HX in D&C Rules

July 20, 2011 in DRUGS CONTROL, pharma industry, pharmacist

The All India Chemists and Distributors Federation (AICDF) has called for pharmacy bandh on August 1 in Delhi and Haryana in protest against the Union government’s decision to include Schedule HX in Drugs & Cosmetics Rules 1945 through an amendment.

Speaking to Pharmabiz over telephone from New Delhi, AICDF president  Kailash Gupta said that chemists from all the states in the country have expressed solidarity with his organization and given support for the bandh. He said the association members will assemble at Jantar Mantar at 9 am on the day and hold a protest march to Parliament. Wholesalers, retailers and pharmacists from hospital pharmacies will join the march by wearing black badges.

According to the organization, the government has decided to amend the D&C Rules to include the new schedule because of pressure from multinational companies. This will lead to acute shortage and non-availability of vital life saving drugs. The situation will also lead to corruption and black marketing.

According to Gupta 70 per cent of the total Indian population resides in rural and remote areas where basic health services are not available. By introducing this controversial schedule HX, the Health ministry is depriving the poor people from accessing life saving drugs.

Ashok Khandelwal, organizing secretary of AICDF said, part A of this schedule HX restricts the availability of 16 various life saving drugs to limited number of hospital pharmacies. It will cause harassment of patients and attendants.

Source: Pharmabiz

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Kerala drug authorities register case against Geltec & Abbott for selling vitamin products without licence

July 14, 2011 in DRUGS CONTROL, pharma industry

The Assistant Drugs Control (ADC) office at Ernakulam in Kerala has registered cases of violation against the healthcare companies, Geltec Private Limited, Bangalore and Abbott Health Care Private Limited, Mumbai for manufacturing and selling the vitamin products, Follihair tablets and Supractive capsules, without drug manufacturing licence.

Revi S Menon, the ADC at Ernakulam said these products were sold along with drugs through medical stores on prescriptions of doctors. The people were purchasing them as drugs. Drug inspectors from his office while inspecting the sales premises of Abbot Healthcare private limited in Kochi have found that the products have been sold without drug manufacturing licences.

He said the products were manufactured by Geltec Private Limited, Bangalore and marketed by Abbott Health Care Private Limited, Mumbai.

According to the ADC, both the products are combinations of vitamins, minerals and amino acids and these types of products come under price control fixed by NPPA. In order to circumvent the provisions of DPCO, Abbott was selling these products as proprietary food. The products are in pharmaceutical dosage forms- tablets and capsule, and are meant for therapeutic purposes, he said.

He said there are so many instances of drug manufacturers circumventing the provisions of the DPCO, and recently the Chemicals and Fertilizers Ministry had directed the National Pharmaceutical Pricing Authority to take up such cases with the Union health ministry to put an end to such illegal trade. He added that so many multi-vitamins are sold as food supplements and these come under DPCO and their prices are fixed by NPPA, but the manufacturers are violating the norms of the DPCO.

The retail price of Follicare tablets (10 tab) was Rs.95 and of Supractive capsules (15 cap), Rs.99. The products were distributed through pharmaceutical wholesalers, and the public got it from retail shops on prescription of doctors.

Since they were being sold without drug manufacturing licences, the inspectors seized the items from the marketing company’s store and produced before the Chief Judicial Magistrate Court at Ernakulam. The companies were given notices to stop the sale of the products in Kerala, he said.

More inspections will be conducted in the coming days in all the retail and wholesale shops to find out whether these products are marketed or not, he added.

Source: Pharmabiz

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Health ministry issues Guidelines on IV Fluid’s storage, distribution and administration

June 30, 2011 in health ministry, pharma industry

Aiming to ensure maximum precaution in the use and handling of IV Fluids to avoid any adverse reactions in the country, the union health ministry has issued Guidelines on IV Fluid’s storage, distribution and administration.

Intravenous Fluids are liable to microbial growth, contamination of particulate matter leading to adverse drug reaction. LVPs are marketed in various primary packaging materials which needs careful handling to prevent  damage from cracks which leads to contamination of fluids meant for IV administration. It is in this context, the ministry has decided to issue the guideline which will ensure maximum precautions during temporary storage, transportation and handling.

The administration of intravenous fluids is one of the most common and universal interventions in medicine. Crystalloid solutions are the most frequently chosen, by far, with normal saline (NS) and lactated Ringer’s (RL) both being frequent choices globally. Of interest, the choice of intravenous fluids has remained one of the most controversial subjects in critical care over the past half a century.

On the issue of distribution of IV solution, the Guidelines define that criteria for selection and agreement should include the transporter and the vehicles which meets the acceptance criteria defined to ensure safety of the product. During transportation transporter should ensure: that ?the product identity is not lost & also ensure that cartons and labelling are in good condition; adequate precaution should be taken against spillage, breakage or theft or other adverse influences; and the Product and its pack are secured and not subjected to unacceptable degree of heat, cold, light, moisture or other adverse influences nor to attack by microorganisms or pests.

To maintain proper practices to ensure quality, efficacy and safety of IV Fluids after receiving the same in the hospital store till the end users points, it is recommended in the Guidelines in the tune of recommendation made by the committee appointed by National Human Rights Commission (NHRC) in the year 1999 that the head of hospital pharmacy with the approval and co-operation of the hospital pharmacy and therapeutics committee must develop a Hospital Formulary.

The Guidelines also give in detail about the good administration practices of IV Fluids.

Infusion therapy has increased in complexity over the years. These guidelines are intended to help individual practitioners ensure that patients receive the most appropriate care for their individual circumstances.