Skip to main content

Painkillers: brand names for paracetamol (= acetaminophen) in foreign countries

Do you ever need a medication when in a foreign country, but in this country the medication you need is not available under a certain name? It's useful to know the active compound of the medication! In this case, I will present to you a list of brand names which contain paracetamol (= acetaminophen) throughout the world.

When you are in the local pharmacy, ask about the active compound ("paracetamol" or "acetaminophen") and they will know immediately what you mean! If you talk about a brand from your own country it can take a while until the pharmacist knows what you mean.

Useful: in almost all countries, generic brands are available, usually under the name of the active compound, so just ask for "paracetamol" or "acetaminophen" if you would like the cheapest product.

Paracetamol = Acetaminophen

EUROPE

Austria: Ben-u-ron, Mexalen
Belgium: Algostase, Dafalgan
Croatia: Daleron, Lekadol, Plicet
Czech Republic/Czechia: Paralen
Denmark: Pamol, Panodil, Pinex
Germany: Ben-u-ron, Enelfa, RubieMol (suppository)
Finland: Pamol, Panadol
France: Claradol, Dafalgan, Doliprane
Greece: Apotel, Depon, Panadol
Great-Britain (UK): Alvedon, Panadol,
Italy: Acetamol, Efferalgan, Sanipirina, Tachipirina
The Netherlands: Panadol
Norway: Pamol, Panodil, Paracet, Pinex
Poland: Codipar, Efferalgan, Panadol
Portugal: Ben-u-ron, Dafalgan, Panadol, Panasorbe, Supofen
Serbia: Febricet
Spain: Antidol, Apiretal, Efferalgan, Febrectal, Gelocatil, Termalgin
Sweden: Alvedon, Panodil
Switzerland/Suisse: Acetalgin, Becatemol, Ben-u-ron, Dafalgan, Panadol
Turkey: Minoset, Panadol, Parasedol, Parol, Setamol, Tamol, Termacet, Tylol

OTHER

Brasil: Dorico
Canada: Tylenol
Egypt: Abimol, Paramol, Pyral
Japan: Calonal
United States of America (USA): Acephen, Cetylev, Tylenol
South-Africa: Empaped






Comments

Popular posts from this blog

Erythropoietin: definition, structure, synthesis in vivo

Definition: EPO: = erythropoietin   A glycoprotein hormon-like structure, a sialoglycoprotein, which is an important factor in the survival, growth and proliferation of erythroid precursor cells (EPC) and it improves the de novo creation, differentation and growth of red blood cells (RBC). Thus, EPO controls the erythropoiesis = production of RBC. EPC: these are cells that are located in the bone marrow, will eventually form the RBC. RBC: cells responsible for the transport and distribution of oxygen throughout the body. Structure: Built out of 165 aminoacids (AA). They are all connected and form 1 polypeptide chain.  Although, within the chain, there are 2 disulfide bonds.  Respectively on positions: Cys7-161 and Cys29-33  Cys = cystein and the numbers indicate the positions these AA are located. Cystein structure. Available  sulfide  group for bonding There are also 4 positions where there is a possibility for glycosylation  Namel...

Alkylhalides: Substitution reactions 6 (Sn1)

Alkylhalides: Substitution Nucleophile substitution reaction ( Sn1 reaction ) Sn1 side reactions I will now discuss some side reactions that can occur when a Sn1 reaction takes place. Carbocation shift Illustrated in the scheme below: Benzyl- and allylhalides  Benzyl- and allylhalides can undergo Sn1 AND Sn2 reactions. How to distinct them? Sn1 conditions: protic solvent and by adding a weak attacking nucleophile. Note: Benzyl- and allylhalides easily undergo Sn1 reactions, because their carbocations are very stable. Sn2 conditions: aprotic solvent and by adding a strong attacking nucleophile. Note: tertiary benzylhalides and tertiary allylhalides will NOT undergo a Sn2 reaction because of the steric effects (see chapter Sn2 reaction blogposts). Sn2 reaction examples Sn1 reaction examples Sn1 and Sn2 reactions in biology, nature and medicines S-Adenosyl methionine This is a biological methylating agens, also known as SAM . It is a frequen...

Alkanes and radicals 1: Introduction

Alkanes and radicals Introduction Let's start with one of the most complex compounds consisting of alkanes and cycloalkanes (naftenes) that can be separated by distillation: Petroleum . Some tips when writing reactions with radicals, have a look on these reactions below, when an heterolytic bond gets cleaved, the arrowhead gets two barbs. When there is a homolytic bond that gets cleaved the arrowhead that shows the direction of the radical, gets one barb, have a look: Alkanes are little reactive, they will not react fast and heavily, because they only contain strong  sigma  σ bindings (single bonds). They also only have non-partial charged atoms. Although, alkanes DO react with Cl2 and Br2. The reactions are listed below, have a look, first the actual reaction, then shown in detail with different steps :