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Drug Database

N01AH06 remifentanil

Approved by UK Medicines & Healthcare Products Regulatory Agency & the European Medicines Agency.

Learning Zones

8 year old child with redness and peeling of the skin on the body.
Overview
Atopic Dermatitis in Paediatric Patients
1 mins
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Learning Zone
Type 2 Inflammation in COPD
1 mins
Advances in Lymphoma
Learning Zone
Advances in Lymphoma
1 mins
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Learning Zone
Advances in HS
30 mins
UCARE Landing page
Learning Zone
All Things Angioedema and Urticaria: Podcasts
30 mins
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Learning Zone
Ulcerative colitis Learning Zone
90 mins
Plaque psoriasis
Learning Zone
Psoriasis Academy
910 mins
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Learning Zone
Alopecia areata Learning Zone
60 mins
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Learning Zone
mCRPC in focus
1 mins
Pediatric Eosinophilic Esophagitis teaser image
Learning Zone
Type 2 Inflammation in Gastroenterology
160 mins
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Learning Zone
Pompe Disease: Key findings from WMS 2022
150 mins
Doctor holding patients hand in consultation
Learning Zone
Supportive care in oncology Learning Zone
150 mins
Doctor separates blood and plasma
Learning Zone
Albumin in fluid management
115 mins
Image of AI generated blood clot formation that would require pharmacological treatments available for various vascular conditions, such as anticoagulants, anti platelet agents, and vasodilators
Learning Zone
Antiplatelet therapy in ACS: Choices and Controversies
270 mins
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Learning Zone
Chronic Kidney Disease Learning Zone
340 mins
Woman with gut pain
Learning Zone
Inflammatory Bowel Disease Learning Zone
100 mins
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Learning Zone
CDK4/6 inhibitors in breast cancer
199 mins
Fibrinogen Deficiency
Learning Zone
Fibrinogen Deficiency in Bleeding Learning Zone
160 mins
Oral Anti Coagulation Reversal
Learning Zone
Oral Anticoagulation Reversal Learning Zone
355 mins

 

 

Disclaimer

The drug SPC information (indications, contra-indications, interactions, etc), has been developed in collaboration with eMC (www.medicines.org.uk/emc/). Medthority offers the whole library of SPC documents from eMC.

Medthority will not be held liable for explicit or implicit errors, or missing data.

Reporting of suspected adverse reactions 

Drug Licencing

Drugs appearing in this section are approved by UK Medicines & Healthcare Products Regulatory Agency (MHRA), & the European Medicines Agency (EMA).