not so much licensing- but rather government scheduling, which dictates how (eg supermarket, vending machine, door to door, or pharmacy) and what quantities are legal to sell in an unscheduled manner.IntoxInc wrote:sometimes the reason why some medicines from same category are 'OTC drug' and others are 'Prescription drug' are purely based on licensing. (even though they both may have exactly the same potential adverse effects)
:arrow: question : how would i know?
:arrow: answer : part of the job...
Sohaib Khawaja
CDM - Asia Hub
Global Development Operations
Bristol-Myers Squibb Company
[ www.bms.com ]
i understand what you mean, but your example of 'so many mg of drug A per tablet' is too general in this case... Drug A and Drug B may not have the same 'mg' in a typical dose. So you can't classify them based on that. However, I don't know the regulations in Australia, so can't comment on that.Anonymous wrote:For eg, up to 20 tablets of drug A is legal to sell in supermarket, with so many mg of the drug per tablet, but go one tablet up or a mg higher & it falls into the pharmacy medicine category (S2) in the case of australia, or S3 which is "pharmacist only" whereby pharmacist needs to be a part of the transaction to ensure there's a therapeutic need, safety etc,.
Occasionally scheduling does change with more information as in the case of Nurofen. Previously it was in the S3 category which required pharmacists to be a part of sale process,.. Later, there was a study done which proved that nurofen in children gave no more adverse reactions than liquid paracetamol, which opened the door to all the childrens iburprofen products on the market and the downscheduling. Now, it's available in supermarkets in aust - although with controversy, as the medicine does interfere with some medications and can be potentially harmful, like lithium for example.
it's got nothing to do with comparing how many mg between two drugs. In australia, the SUSDP (Standard of Uniform Scheduling of Drugs and Poisons) dictates what quantities of each drug, and how many tablets per packet are allowed, and it doesn't bundle Drug A into same category necessarily as Drug B based on amount of mg. I think I might have confused you there.IntoxInc wrote:i understand what you mean, but your example of 'so many mg of drug A per tablet' is too general in this case... Drug A and Drug B may not have the same 'mg' in a typical dose. So you can't classify them based on that. However, I don't know the regulations in Australia, so can't comment on that.Anonymous wrote:For eg, up to 20 tablets of drug A is legal to sell in supermarket, with so many mg of the drug per tablet, but go one tablet up or a mg higher & it falls into the pharmacy medicine category (S2) in the case of australia, or S3 which is "pharmacist only" whereby pharmacist needs to be a part of the transaction to ensure there's a therapeutic need, safety etc,.
Occasionally scheduling does change with more information as in the case of Nurofen. Previously it was in the S3 category which required pharmacists to be a part of sale process,.. Later, there was a study done which proved that nurofen in children gave no more adverse reactions than liquid paracetamol, which opened the door to all the childrens iburprofen products on the market and the downscheduling. Now, it's available in supermarkets in aust - although with controversy, as the medicine does interfere with some medications and can be potentially harmful, like lithium for example.
I recently read that ibuprofen is connected with heart attacks. Does anyone have anymore information on this?Strong Eagle wrote:I don't get it... and maybe someone can explain it.
I can buy aspirin off the shelf.
I can buy paracetamol, a tylenol type drug, off the shelf.
But, if I want to buy ibuprofen (aka Advil), I have to get it from the pharmacist. There is only one brand, Nuprofen, and it is quite expensive.
What's with dat???
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