Quick Answer: What Is General Medication?

What is a medication error?

A medication error is defined as “any preventable event that may cause or lead to inappropriate medication use or patient harm while the medication is in the control of the healthcare professional, patient, or consumer,” according to the National Coordinating Council for Medication Error Reporting and Prevention..

What is a Class 1 drug?

Schedule I drugs, substances, or chemicals are defined as drugs with no currently accepted medical use and a high potential for abuse. Some examples of Schedule I drugs are: heroin, lysergic acid diethylamide (LSD), marijuana (cannabis), 3,4-methylenedioxymethamphetamine (ecstasy), methaqualone, and peyote. Schedule II.

What does pom stand for?

Another explanation – now generally considered to be a false etymology – was that “Pom” or “Pommy” were derived from an acronym such as POM (“Prisoner of Millbank”), POME (“Prisoner of Mother England”) or POHMS (“Prisoner of Her Majesty’s Service”).

What is the definition of a medication?

A medication is a substance that is taken into or placed on the body that does one of the following things: Most medications are used to cure a disease or condition. For example, antibiotics are given to cure an infection. Medications are also given to treat a medical condition.

What does GSL mean in medication?

general sale listPharmacy medicine ( P ) to the general sale list ( GSL ) Under the provisions of The Human Medicines Regulations 2012, regulation 62(5), GSL is appropriate for medicines which can, with reasonable safety, be sold or supplied otherwise than by or under the supervision of a pharmacist.

What two names are medicines known by?

Many medicines have at least 2 different names:the brand name – created by the pharmaceutical company that made the medicine.the generic name – the name of the active ingredient in the medicine.

What does surgery mean?

“Surgery” means a procedure performed for the purpose of structurally altering the human body by incision or destruction of tissues and is part of the practice of medicine for the diagnostic or therapeutic treatment of conditions or disease processes by any instruments causing localized alteration or transportation of …

What is a MHRA Licence?

To make, assemble or import human medicines, you need a manufacturer licence, issued by the Medicines and Healthcare Products Regulatory Agency (MHRA). To qualify for a manufacturer licence you need to show MHRA that you comply with EU good manufacturing practice ( GMP ) and pass regular GMP inspections of your site.

What are the 3 categories of medicines?

There are, therefore, three classes of products under the Medicines Act 1968, namely: (1) General Sale List medicines (GSL). (2) Pharmacy medicines (P). (3) Prescription Only Medicines (POM). The legal requirements that apply to the sale, supply, dispensing and labelling of each class are dealt with separately below.

Is paracetamol generic name?

For example, paracetamol is a generic name. There are several companies that make this with brand names such as Panadol®, Calpol®, etc.

What is the difference between GSL and P medicines?

P: pharmacy-only medicines, obtained without a prescription (colloquially, ‘over the counter’) from, or under the supervision of, a qualified pharmacist. GSL: general sales list medicines, obtained without a prescription from, for example, a pharmacy or a supermarket.

What medication can a pharmacist prescribe?

Pharmacists can prescribe drugs for minor health problemsMild acne.Atopic dermatitis (eczema) requiring use of low-to-moderate potency corticosteroids.Diaper rash in newborns.

What are the 7 classifications of drugs?

DREs classify drugs in one of seven categories: central nervous system (CNS) depressants, CNS stimulants, hallucinogens, dissociative anesthetics, narcotic analgesics, inhalants, and cannabis.

What is an MHRA inspection?

The Medicines and Healthcare Products Regulatory Agency (MHRA) are required under European law to inspect Clinical Trials of Investigational Medicinal Products (CTIMPs) conducted by both commercial and non-commercial organisations. (See MHRA page on Risk Based Inspections). …

What does MHRA stand for?

Medicines and Healthcare products Regulatory Agencythe Medicines and Healthcare products Regulatory Agency ( MHRA ), the UK’s regulator of medicines, medical devices and blood components for transfusion, responsible for ensuring their safety, quality and effectiveness.

How do you use medicine in a sentence?

Use “medication” in a sentence | “medication” sentence examples The medication should ease the suffering. I’m not taking any medication. … He is currently on/taking medication for his heart. She stopped the medication because of side effects. He was epileptic and refused to take medication for his condition.More items…•

Why do doctors prescribe brand name drugs?

Typically lower in cost and as effective as their branded counterparts, they help control pharmacy spending and increase access to important therapies for patients who could be deterred by the high cost of some branded drugs.

What is difference between medicine and medication?

Medicating is the treatment of a condition using drugs or potions in any form as opposed to surgery. A medication is any drug or potion in any form that is used to fight a disease or heal a condition. Medicine and medication, when discussing the use of drugs and potions, mean the same thing.

What are the 4 categories of medicine?

The 4 Categories of MedicationGeneral Sales List (GSL) GSLs are a type of medicine that have few legal restrictions. … Pharmacy Medicines. Pharmacy Medicines are only available to purchase behind the counter at a pharmacy. … Prescription Only Medicines. … Controlled Drugs.

Why do meds have 2 names?

Every drug has an approved generic or medical name, decided on by an expert committee. Many drugs are also known by a brand or trade name chosen by the pharmaceutical company making and selling that drug as a medicine. So, for example, the drug infliximab (generic name) is also known as Remicade (brand name).

What powers do the MHRA have?

MHRA is the designated competent authority that administers and enforces the law on medical devices in the UK. It has a range of investigatory and enforcement powers to ensure their safety and quality.