Medicine expiry date,energy bills compared,boosting energy levels during pregnancy chart - You Shoud Know

admin 11.12.2014

Hi, I'd like a pic of a prescription pill bottle with a magnifier on the expiry date and that date being some date in 2003.
I intimate them for the same and send them snaps of those medicine and they ready to dispatch right medicine again so i do nothing and waiting for the consignment, when it was received i check there is wrong medicine is dispatch to me it was FORMINAL 500 SR and 4 numbers of Stips was badly handled and packed so medicines are come out from its packing so i call them again and they ask me to send back medicine to them and i denied. Q.2 What is the difference in the control between Western medicine and Chinese medicine in Hong Kong? Q.3 How can I know more about the legal requirements of handling pharmaceutical products in Hong Kong?
Sale of unregistered pharmaceutical products is an offence under the Pharmacy and Poisons Ordinance. A.5Registered pharmaceutical products are subject to various kinds of control over their sale to protect the health of the public. Some Part 1 poisons are further classified into First Schedule and the Third Schedule with additional restrictions on their sale at the retailers. The sales requirement of various categories of pharmaceutical products is summarized in the Appendix I. A.6According to the Pharmacy and Poisons Ordinance, all Part 1 poisons and Part 2 poisons must be labelled with the word “Poison ??” or other applicable words specified in the above Ordinance. The word “Poison ??” serves as a warning to consumers as using incorrect dosage or improper use of these medicines may cause serious health damage.
A.8A pharmaceutical product that is registered in Hong Kong does not necessarily mean that it is locally available.
To find out whether a product is available in Hong Kong, you can seek advice from a local pharmacy (ASP) or medicine store (LSP) or you can contact the registration certificate holder. Q.9 As registered pharmaceutical products are regulated by the relevant authority, does it mean that they will not cause harm to consumers? A.9A pharmaceutical product or medicine must meet the criteria of safety, quality and efficacy for approval of registration. Furthermore, medicines may cause adverse effects and response that vary amongst individuals. A.10Healthcare professionals will balance the risks and benefits of a particular treatment for their patients according to their conditions. A.11According to the information from World Health Organization, over 50% of the medicines purchased via the Internet from sites that conceal their physical address have been found to be counterfeit.
You are, therefore, advised not to purchase pharmaceutical product from sources that are doubtful, including from Internet sites with unknown origin or seller with unknown address, as the product’s safety, quality and efficacy cannot be guaranteed. You are advised to seek advice from healthcare professionals before using any medicine instead of choosing one by yourself, especially if you have persistent symptoms of unknown cause. A.13In Hong Kong, pharmaceutical products must be registered before sale and it is unlawful to sell unregistered pharmaceutical products.
In addition, even if the product is registered, their sale may be subject to different levels of control (please refer to A.5) and you may contravene the relevant legislation in dealing with or trading pharmaceutical products without the appropriate licences or authorisation. Q.14 I am taking some medicines which are prescribed by my doctor in my hometown and I have to stay in Hong Kong for a period of time.
Q.15 Can I buy some pharmaceutical products overseas for my own use and bring them back to Hong Kong? A.15Importation of pharmaceutical products and medicine are controlled under the Import and Export Ordinance (Cap. Q.16 Why can’t I sell these pharmaceutical products that I bought abroad in Hong Kong, even over the Internet?
A.16It is a legal requirement that pharmaceutical product must be registered before sale in Hong Kong.
A.18Listed Seller of Poisons (LSP), or referred to as “medicine stores” are different from pharmacies (ASP) in that there are no pharmacists on duty in the former.
Q.20When I buy medicines from a medicine store, what information should I pay attention to? A.20Medicine stores (LSP) are authorized to sell medicines that are non-poisons or Part 2 poisons, such as cold and flu medications.
The dosage instructions and cautionary statement (if any) should be labelled in both English and Chinese.

A.21Products with very similar names or appearance may contain different ingredients while products with the same ingredients may have different product names or appearance.
On the other hand, medicines with fewer serious side effects or those used for treating or alleviating minor illness can be sold without prescription in pharmacies (ASP) or medicine stores (LSP). A.23A prescription should be given by a registered medical practitioner, registered dentist or registered veterinary surgeon. A.25It is a legal requirement for pharmacies (ASP) to retain prescriptions dispensed and keep the records for 2 years. At the time of dispensing a prescription which can be dispensed more than once, the name and address of the pharmacy (ASP) and the date on which the prescription is dispensed should be noted on the prescription by the person dispensing the prescription. A.27As the responses to a medicine may vary amongst individuals, you should tell the doctor or pharmacist who give you the medicine about your symptoms after taking medicine.
You should tell your doctor or pharmacist any of your known drug allergies as there may be cross-sensitivity among drugs in the same class. A.28Decision on the treatment regime for a patient needs professional evaluation of patient’s symptoms, signs, medical history, and their response to medications. If you have query concerning your treatment or medical condition, you should discuss with healthcare professionals such as your family doctor or pharmacist.
Q.29If I want to raise a complaint about a product marketed with a Hong Kong registration number, what should I do? However, if the product’s registration number is indicated as HKP-XXXXX, HKNT-XXXXX or HKC-XXXXX, it is a proprietary Chinese medicine. Parents and caregivers should follow the instructions for use for all medicines given to children.
Children should be supervised when taking any dose form of medicine; particular attention should be paid for taking soft gel capsules due to the risk of choking. Proper storage of medicines is not only to maintain the potency of medicine, but also to protect children from accidental ingestion. A.9Any labeling should not contravene the provisions of the Undesirable Medical Advertisements Ordinance (Cap. 138A), "pharmaceutical products" must be registered before they can be sold, offered for sale, distributed or possessed for the purposes of sales, distribution or other use in Hong Kong.
The maximum penalty is a fine at level 6 of Criminal Procedure Ordinance Cap 221 ($100,000) and two years' imprisonment.
In Hong Kong, the Poisons List under the Tenth Schedule of Pharmacy and Poisons Regulation (Cap.
For example, pharmaceutical products that do not contain any poisons or contain Part 2 poisons are referred as Over-The-Counter medicines (OTC). The sale of pharmaceutical products containing Part 1 First Schedule poisons further requires keeping sales records which include the date of the sale, the name, number of identity card, address and signature of the purchaser, the name and quantity of the medicine as well as the purpose for which it is required. These medicines should only be obtained from licensed retailers and be used upon the professional advice of healthcare professionals.
It is important that these medicines should be taken upon the advice or instruction of healthcare professionals to ensure the safe use of these medicines. The decision on whether to market a pharmaceutical product in Hong Kong is made by its registration certificate holder. You should seek healthcare professionals’ advice on whether a medicine is appropriate for your health condition or management of your disease. If a medicine is used in accordance with the advice from your doctor or pharmacist, the health benefits you gain from the treatment should outweigh the risks of adverse events. In addition, improper storage of a pharmaceutical product during transit might adversely affect the quality of the product. They can give you the most appropriate treatment option after considering your conditions as well as the risks and benefits of the medicine.
Any illegal sale of unregistered pharmaceutical products will contravene the Pharmacy and Poisons Ordinance (Cap.138) and the maximum penalty is a fine at level 6 of Criminal Procedure Ordinance Cap 221 ($100,000) and imprisonment for 2 years upon conviction.
You should also discuss with a local healthcare professional, such as a doctor or pharmacist to check whether you can obtain the same medicines in Hong Kong or to advise to switch to another substitute if they are not available.
60), thus must be covered by a licence issued by Department of Health under delegated authority of the Director-General of Trade and Industry Department.

Only an Authorized Seller of Poisons (ASP), often referred to as a “pharmacy”, can sell prescription medicines under the authority of a prescription with the supervision of a pharmacist. They cannot sell pharmaceutical products containing Part 1 poisons, including prescription medicines, and are prohibited from using or displaying the “Rx” logo. Therefore, self-medications may lead to overdose or increase the risks of side effects, posing significant risk to your health. Examples include medicines used for the treatment of high blood pressure, diabetes, bacterial infections and medicines that help you to sleep.
Examples include drugs used for relieving common cold, treating fever and some painkillers. In the prescription provided by a dentist, it should be written “For dental treatment only” and in the prescription given by a veterinary surgeon, it should be written “For animal treatment only”. The pharmacist in the shop has to maintain prescription records which should be readily available for inspection.
The prescription will be retained by the pharmacy which carried out the last and final dispensing of the prescription. In more severe cases, one may experience reactions like shortness of breath and in such case, you should seek medical treatment immediately. The Drug Office is a drug regulatory agency and is not able to advise individual patients on their treatment.
The former can be sold in any retail shops while the latter can be sold in Authorized Sellers of Poisons (ASP, usually known as pharmacies or dispensaries) and Listed Sellers of Poisons (LSP, usually known as medicine stores). The sale of pharmaceutical products containing prescription only medicines (Part 1 Third Schedule poisons) must be authorized by a prescription from a registered medical practitioner, a registered dentist or a registered veterinary surgeon.
Prior to a product’s registration, information is only available from pre-market studies of the product and reference from reputable literatures.
Some risks of a medicine will not be revealed until after the drug has been used in larger populations and in different types of patients. At these premises, a pharmacist will be on duty at specified hours and it is allowed to use or display the “Rx” logo. However, they are authorized to sell medicines that are non-poisons or Part 2 poisons, such as cold and flu medications. You should always seek advice from a qualified healthcare professional before taking any medicines.
These prescription-only medicines must be dispensed and sold on doctor’s prescription in registered pharmacies (ASP) under the direct supervision of registered pharmacists. Some poisons are further categorized under different Parts of the Poisons List and other different Schedules under the Pharmacy and Poisons Regulations (Cap.
Pharmaceutical products containing Part 1 poisons can only be sold in pharmacies (ASP) in the presence and under the supervision of registered pharmacist.
In addition, some adverse effects of a medicine will only be noted after the product is marketed and used in the general population. You are therefore encouraged to report to a healthcare professional any adverse effects you experience after taking a medicine. The sale, manufacturing, dispensing or compounding of Chinese herbal medicines or proprietary Chinese medicines as defined in section 2 of the Chinese Medicine Ordinance (Cap 549) or other materials of herbal, animal or mineral origin customarily used by the Chinese for medicinal purpose is exempted from regulation under the Pharmacy and Poisons Ordinance (Cap.
Therefore, assessment of a product prior to its registration can only be based on information available at that time.
Healthcare professionals will then report any adverse drug reactions that deemed medically significant to our office.
If you have any further questions on giving medicine to children, consult your doctor or your pharmacist.

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