SOLPADEINE

This brand name is authorized in Cyprus, Estonia, Ireland, Lithuania, Malta, Poland, Romania, United Kingdom

Active ingredients

The drug SOLPADEINE contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII 362O9ITL9D - ACETAMINOPHEN
 

Paracetamol is a medication used to treat pain and fever. It does appear to selectively inhibit COX activities in the brain, which may contribute to its ability to treat fever and pain.

 
Read more about Paracetamol
2
UNII GSL05Y1MN6 - CODEINE PHOSPHATE
 

Codeine is a centrally acting weak analgesic. Codeine exerts its effect through μ opioid receptors, although codeine has low affinity for these receptors, and its analgesic effect is due to its conversion to morphine. Codeine, particularly in combination with other analgesics such as paracetamol, has been shown to be effective in acute nociceptive pain. The anti-tussive activity of codeine is probably due to its depressant effect on the medullary cough centre in the brain.

 
Read more about Codeine
3
UNII 3G6A5W338E - CAFFEINE
 

Caffeine is structurally related to the methylxanthines theophylline and theobromine. Caffeine’s main action is as a CNS stimulant.

 
Read more about Caffeine

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
N02BE51 Paracetamol, combinations excl. psycholeptics N Nervous system → N02 Analgesics → N02B Other analgesics and antipyretics → N02BE Anilides
Discover more medicines within N02BE51

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
EE Ravimiamet 1028001, 1076655, 1149443, 1149454, 1149465, 1149476, 1149487
GB Medicines & Healthcare Products Regulatory Agency 107262, 107264, 180758, 19642, 19643, 49242, 49249
IE Health Products Regulatory Authority 46790, 47029
LT Valstybinė vaistų kontrolės tarnyba 1008790, 1027079
MT Medicines Authority MA1005/00101, MA1005/00401
PL Rejestru Produktów Leczniczych 100061814, 100204774, 100237489, 100381810
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W68638001, W68638002, W68638003, W68638004, W68638005, W68639001, W68639002, W68639009, W68639010, W68639011, W68639012, W68640001, W68640002, W68640003, W68640004, W68640005, W68640006, W68640007

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