Sri Lanka News, Apetamin-P

Insect in bottle:

Temporary ban on Apetamin-P syrup sale

Dharma SRI ABEYRATNE

The Cosmetic Devices and Drug Regulatory Authority of Sri Lanka has imposed a temporary ban on the sale of Apetamin-P Syrup in the country following an incident where an insect was found in an Apetamin-P syrup bottle sold by a private pharmacy in Maho.

The bottle of syrup which contained the insect has been forwarded to the Food and Drug Inspector in Kurunegala District by the customer who bought the drug from the pharmacy.

The Food and Drug Inspector has sent the bottle to the Cosmetic Devices and Drug Regulatory Authority for further investigations. Apetamin-P syrup is used for allergies and to get an appetite.

This consignment of the drug has been imported from a company in India.

According to Cosmetic Devices and Drug Regulatory Authority Director Dr Hemantha Beneragama, the selling of Apetamin-P by private pharmacies has been temporary banned due to this incident.

The Cosmetic Devices and Drug Regulatory Authority has already issued a circular banning the selling of Apetamin-P since such contaminations indicate a huge failure in production process. Therefore, a complete laboratory test is being carried out by the Cosmetic Devices and Drug Regulatory Authority, Dr Beneragama said.

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Product Description

APETAMIN VITAMIN SYRUP

Apetamin contains a unique combination of Cyproheptadine, Lysine and Vitamins. Cyproheptadine and lysine being essential in limiting amino acid helps to promote appetite. Beside helping in the synthesis of collagen tissue, lysine also helps to improve immunity during infancy, childhood & adolescence. The water soluble vitamins in Apetamin being coenzymes helps to absorb the amino acid lysine through the intestinal villi faster. Hence, Also assist in better utilization of Lysine. They also improve immunity and help to correct marginal vitamin deficiency.

Each 5ml contains: Cyproheptadine Hydrochloride (anhydrous) BP 2g. L-Lysine Hydrochloride USP 150mg. Thiamine Hydrochloride BP 2mg. Pyridoxine Hydrochloride BP 1mg. Nicotinamide BP 15mg. Dexpanthenol BP 4.5mg.

Loss of appetite and poor eating habits, Anorexia after a brief illness. Patients experiencing loss of appetite during convalescence following surgery or after any major illness.

SAFETY: It is generally safe to use both in children and adults. However, precaution should be taken while using other CNS depressants and sedatives. Warnings: Beware that Apetamin may cause drowsiness in the first few days. Then your body will adjust. DOSAGE: Children: (2-6 years): 5 ml, 2 to 3 times daily before food. (7-14 years): 10ml, 2 to 3 times daily before food. Adults: 10ml, 3 times daily before food.

Benefits: Apetamin will increase you appetite quickly.

You will definitely receive lots of compliments.

DISCLAIMER: BEFORE STARTING ANY NEW MEDICATION OR SUPPLEMENT CONSULT WITH YOUR PHYSICIAN DO NOT TAKE THIS PRODUCT IF YOU ARE PREGNANT BREASTFEEDING, OR ALLERGIC TO ANTIHISTAMINES

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The new extended-release tablets was a new formulation of this well-known medicinal product Panodil. The new paracetamol tablet contains 665 mg, compared to 500 mg in ordinary tablets. A dosage of two 665 mg tablets three times daily of the new product has been found to be therapeutically equivalent to two 500 mg tablets four times daily. Due to the risk of overdose, the new product is prescription-only, like Panodil Retard and Panodil 1 g.

Panodil new extended-release tablets was marketed on Monday, 1 April.

The advantage of the new extended-release tablets is that the number of daily doses for chronic pain can be reduced from four to three daily. Compared to Panodil Retard, the new product involves a reduction in the number of tablets per dose from four to two, but patients must take it more often: three times daily instead of two.

The disadvantage is that one month?s therapy costs three times as much as ordinary paracetamol tablets or Panodil 1 g. On the other hand, the new Panodil costs a little less than Panodil Retard.

Extended-release tablets (also Panodil Retard) should not be crushed as ordinary tablets can be, since this causes them to lose their time-release capability. Caregivers should be made aware of this fact if the new tablets are prescribed.

The shelf life of extended-release tablets is substantially shorter than that of ordinary tablets (two years in plastic bottles and three years in blister packs), which is yet another reason why the new product should only be used to treat chronic pain.

All in all, Panodil 1 g seems to be the best choice for chronic pain treatment at this time, when both cost and compliance are taken into consideration. On the other hand, there is no generic product which can be substituted for it and thus no competition in the longer term.

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DRUG DESCRIPTION

Glucocorticoids are adrenocortical steroids, both naturally occurring and synthetic, which are readily absorbed from the gastrointestinal tract. Prednisolone (prednisolone (prednisolone (prednisolone tablets) tablets) tablets) is a white crystalline powder, very slightly soluble in water. It is designated chemically as pregna-1,4-diene-3,20-dione,11,17,21-trihydroxy-,(11β)-. The structural formula is represented below:

Prednisolone Tablets USP 5 mg contain the following inactive ingredients: anhydrous lactose, colloidal silicon dioxide, crospovidone, D&C Yellow No.10, docusate sodium, FD&C Yellow No. 6, magnesium stearate and sodium benzoate.

Last reviewed on RxList: 6/20/2008 This monograph has been modified to include the generic and brand name in many instances.

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DRUG DESCRIPTION

Glucocorticoids are adrenocortical steroids, both naturally occurring and synthetic, which are readily absorbed from the gastrointestinal tract. Prednisolone (prednisolone (prednisolone (prednisolone tablets) tablets) tablets) is a white crystalline powder, very slightly soluble in water. It is designated chemically as pregna-1,4-diene-3,20-dione,11,17,21-trihydroxy-,(11β)-. The structural formula is represented below:

Prednisolone Tablets USP 5 mg contain the following inactive ingredients: anhydrous lactose, colloidal silicon dioxide, crospovidone, D&C Yellow No.10, docusate sodium, FD&C Yellow No. 6, magnesium stearate and sodium benzoate.

Last reviewed on RxList: 6/20/2008 This monograph has been modified to include the generic and brand name in many instances.

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Further recall of paracetamol tablets

The Irish Medicines Board (IMB) has issued an urgent notice for patients who have been dispensed any batch of the paracetamol product, Paratabs 500mg Tablets.

This announcement is an extension of a recall announced last month, in which one batch of the tablets was recalled due to fears of contamination. Since then, 'contamination of several additional batches' has been identified. The cause of this contamination is being investigated, but it is likely to be a mould.

Paratabs 500mg Tablets could not have been purchased over the counter in grocery stores or in pharmacies. They would only have been dispensed by your pharmacist on foot of a prescription from your doctor.

Blister pack of Paratabs or other paracetamol products are not affected.

Details of the product distributed in Ireland are as follows:

-Product name: Paratabs 500mg Tablets.

-Active substance: Paracetamol.

-PA number: PA281/74/1.

-Batch number: 6022.

-Expiry date: 02/2008.

-Marketing authorisation holder: Pinewood Laboratories Ltd (trading as Pinewood Healthcare).

The IMB is calling on all patients who have been dispensed Paratabs 500mg Tablets since August 29 to immediately check the label of their drugs to see if they are part of the affected batch.

If they are, or if you are unsure about the drugs you have been dispensed, do not take any more of the tablets. Return them immediately to the pharmacist, who will be able to dispense alternative paracetamol tablets.

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I'm hoping someone can help me with a question on a pharmacy medication.

I am taking Voltaren Tablets for inflammation (Diclofenac), I have seen on another thread that the Voltaren gel is available in France. Do they sell the tablets as well?

I don't want to leave with an enormous supply from home & I was wondering if these are available OTC in France. Last time I was in Paris I was taking Nurofen Plus (Ibuprofen & Codeine), these were not available only Ibuprofen on it's own.

My Dr has now put me on Voltaren tablets & they seem to be much better for the inflammation. They are OTC here, but if I need a script, I could have one written by my Dr here, before I leave.

Thank you for any help!

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#1,149 of 1,811 hotels in Paris

Hong D June 21, 2016

1. Re: Voltaren Tablets

May 15, 2012, 8:44 AM

Always, always travel with a copy of your prescription. It will make your life far easier should something happen to the ones you packed. (someone here dropped a pill bottle down the loo. so it doesn't have to be loss or theft!)

Bring the tablets you need for your comfort and well-being. Don't count on buying something you *need*.

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Thanks for all the replies, and thank you Pvoyageuse. That's what I wanted to know. Voltaren are OTC here, so I'll bring extra.

It is only a pain reliever, not a life saving medication. I would be fine on Ibuprofen, if I had to. I just wanted to know if it was OTC in France.

This is why I like to have a hotel with a bath (thank goodness they are common in France) - a nice soak after a long day sightseeing usually does wonders as well!

Thank you again, every time I get on this forum, I thank goodness I'm not travelling 30 years ago, before the internet. LOL !

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