Consumer vs. Physicians Attitudes Toward Health Products Advertising

* Within this Register, each drug, form and strength must have a separate bound book or section within a bound book with the product name and strength written at the top of each page.

A prescription can be identified as legally authorised written instruction by a prescribing officer to a pharmacist to dispense medication.

There are several types of medication, each has a purpose and function needed for their administration via the different routes.

There are proponents of DTC prescription drug ads. They argue that “the ads inform patients about diseases and possible treatments, encourage people to seek medical advice, help remove stigma associated with medical conditions, and provide needed sales revenue to fund costly research and development (R&D) of new drugs (Drug Ads ProCon.org).” On the flip side opponents argue “that DTC drug ads misinform patients, promote drugs before long-term safety-profiles can be known, medicalize and stigmatize normal conditions and bodily functions like wrinkles and low testosterone, waste valuable medical appointment time, and have led to our society’s overuse of prescription drugs (Drug Ads ProCon.org).”

* All medication should be recorded and signed for by the receiving pharmacist and a proper record maintained in-house.

There are several legislations in place with protocols for the administration of medication which I have listed below. The main policy re admin of drugs and storing of drugs and medicines is the Control Of Substances Hazardous to Health or COSHH but along with this there are other policies in place as per the list below.

So to conclude, although both positives and negatives are associated with DTC prescription drug ads, the negatives outweigh the positives because of the detrimental effects they can have on the consumer. The ads misinform patients, stigmatize normal conditions, have led to the overuse of prescription drugs, and promote drugs before long-term safety information can be known. DTC prescription drug ads are endangering the viewers in our society. In the long run, banning DTC prescription drug ads, or at the very least increasing regulation, would be best for the

In regards to the price of prescription drugs, supporters note that the advertising promotes competition among the drug companies, thus driving the drug prices down. Assuming that this is true, which is disputable in itself, “some opponents also suggest that DTCPA increases health care costs because visits to the physician prompted by a drug ad can be a waste of time and money”.(nih.gov) So if the prices are driven down then that would be of benefit to some and if they are, in fact, increased that would be of impact to all consumers. This ethical analysis does not require an answer as to which point of view is true.

12. The FDA would not let unsafe replications of drugs onto the market, prescription or over the counter medications

Advertisements have one primary purpose that is to persuade. Prescription medications Ads tell the consumers to get treatment and also imply that they have the need for it to solve their problems. Since prescription Ads have been introduced, the pharmaceutical

Some people believe pharmacy should be allowed to advertise prescription medical, they think that it give consumers valuable information, others disagrees, and believe that pharmacy shouldn’t be allowed to advertise prescription medical on TV because it compromise kinds of carry giving to patients. The pharmacy companies should not be allowed advertise prescription drugs on TV because prescription drugs should only be allowed to doctors and physicians, it’s up to their doctors to decide if the patients will be benefit from the drugs without pressure form the patients, they know everything and particular drugs consumers need, while a person who learned about the

After the Pharmacy technicians checks the solution for exactness, and may convey it to the patient. The expert then duplicates the data about the endorsed pharmaceutical onto the patient's profile. Specialists likewise may amass a 24-hour supply of medication for each patient. They bundle and mark every measurement independently. The bundles are then set in the drug cupboards of patients until the administering pharmacist checks them for precision, and at exactly that point is the prescription given to the patients.

A pharmacopoeias book is a lawfully assortment prepared by a national or regional authority of standards and with quality specifications for medicines utilized in that specific country. A high quality specification consists of a group of acceptable tests that may make sure the identity, purity and efficacy of the product. Ensure the strength or amount of the active pharmaceutical ingredient and performance

Safe and effective medicine is an essential element to healthcare. Counterfeit drugs, which may not be safe or efficacious, have become a growing problem around the globe and are compromising treatment of disease and patient health. A counterfeit drug is essentially fake medicine. The World Health Organization (WHO) defines a counterfeit drug to be a product which has been deliberately or fraudulently mislabeled in regards to its identity and source. A counterfeit drug may have the wrong ingredients, no active ingredients, insufficient active ingredients or have fake packaging (WHO, 2005).

Counterfeit medicines are “deliberately and fraudently mislabelled with respect to identity and / or source. Counterfeiting may include products with the correct ingredients or with the wrong ingredients , without active ingredeients, with insufficient active ingredient or with fake packaging”(Wondemagegnehu, 1999).