XEFO

This brand name is authorized in Austria, Brazil, Estonia, Israel, Lithuania, Poland, Romania, South Africa, Turkey.

Active ingredients

The drug XEFO contains one active pharmaceutical ingredient (API):

1	Lornoxicam UNII ER09126G7A - LORNOXICAM
	Lornoxicam is a non-steroidal anti-inflammatory drug with analgesic properties and belongs to the class of oxicams. Lornoxicams mode of action is mainly related to the inhibition of the prostaglandin synthesis (inhibition of the cyclooxygenase enzyme) leading to desensitisation of peripheral nociceptors and consequently inhibition of inflammation. A central effect on nociception, which seems to be independent of anti-inflammatory effects has also been suggested.
	Read more about Lornoxicam

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
XEFO Film-coated tablets	MPI, EU: SmPC	Health Products Regulatory Authority (IE)
XEFO Powder and solvent for solution for injection	MPI, EU: SmPC

Medicine classification

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

ATC Group		Classification
M01AC05	Lornoxicam	M Musculo-skeletal system → M01 Antiinflammatory and antirheumatic products → M01A Antiinflammatory and antirheumatic products, non-steroids → M01AC Oxicams
Discover more medicines within M01AC05

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
BR	Câmara de Regulação do Mercado de Medicamentos	504114105116315, 504114106112313
EE	Ravimiamet	1024209, 1024210, 1103522, 1134638, 1134649, 1147339, 1519860, 1519882, 1519893, 1519905, 1519938, 1519949, 1519950, 1519961, 1519972, 1519983, 1519994, 1520187, 1520198, 1520200, 1520222, 1520255, 1520277, 1521672, 1521683, 1541809, 1764356, 1764367, 1764378, 1764389, 1764390, 1764413, 1770522, 1805712, 1805723, 1805734, 1805745, 1805756, 1805767, 1805778, 1830608, 1830664, 1834332, 1847572, 1847583, 1847594, 1847606
IL	מִשְׂרַד הַבְּרִיאוּת	4680
LT	Valstybinė vaistų kontrolės tarnyba	1003271, 1003272, 1004262, 1004274, 1012602, 1012603, 1012604, 1014586, 1026461, 1026462, 1026463, 1026465, 1026466, 1026467, 1026469, 1026470, 1026471, 1026472, 1026473, 1026474, 1026475, 1074199, 1079566, 1080043, 1081746, 1082311, 1084871, 1085245, 1085349, 1085351, 1085496, 1085690, 1087697, 1087807, 1087808, 1088322, 1088444, 1088445, 1088538, 1088697, 1088698, 1091410, 1091411, 1093177, 1093178, 1093179, 1093180
PL	Rejestru Produktów Leczniczych	100209978, 100373040, 100383038, 100405886, 100417180, 100426279, 100427824
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W62178001, W62178002, W62178003, W62178004, W62178005, W62178006, W62178007
TR	İlaç ve Tıbbi Cihaz Kurumu	8682758090032, 8699456090103
ZA	Health Products Regulatory Authority	33/3.1/0247, 33/3.1/0248, 33/3.1/0249, 44/3.1/0331