MedPath
EMA Approval

Dynastat

M01AH04

parecoxib

Basic Information

M01AH04

parecoxib

Therapeutic indication

For the short-term treatment of postoperative pain in adults.

Overview Summary

Dynastat is a painkilling medicine for use in adults for the short-term relief of pain after an operation.

It contains the active substance parecoxib.

Authorisations (1)

EMEA/H/C/000381

Pfizer Europe MA EEIG,Boulevard de la Plaine 17,1050 Bruxelles,Belgium

Authorised

March 22, 2002

Active Substances (2)

parecoxib sodium

parecoxib sodium

Documents (13)

Dynastat-H-C-381-II-0032 : EPAR - Scientific Discussion - Variation

May 7, 2009

CHANGES_SINCE_INITIAL_AUTHORISATION

Dynastat : EPAR - All Authorised presentations

November 14, 2005

AUTHORISED_PRESENTATIONS

Dynastat : EPAR - Procedural steps taken and scientific information after authorisation

March 5, 2025

CHANGES_SINCE_INITIAL_AUTHORISATION

Dynastat-H-C-381-A18-20 : EPAR - Scientific Conclusion

November 14, 2005

CHANGES_SINCE_INITIAL_AUTHORISATION

Dynastat : EPAR - Scientific Discussion

November 14, 2005

INITIAL_MARKETING_AUTHORISATION_DOCUMENTS

Dynastat : EPAR - Product Information

January 7, 2010

DRUG_PRODUCT_INFORMATION

Dynastat : EPAR - Steps taken after authorisation when a cutoff date has been used

November 14, 2005

CHANGES_SINCE_INITIAL_AUTHORISATION

Dynastat : EPAR - Procedural steps taken before authorisation

November 14, 2005

INITIAL_MARKETING_AUTHORISATION_DOCUMENTS

Dynastat : EPAR - Medicine overview

April 14, 2009

OVERVIEW_DOCUMENT

Dynastat-H-C-PSUSA-00002314-202303 : EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation

February 19, 2024

CHANGES_SINCE_INITIAL_AUTHORISATION

Dynastat : EPAR - Scientific Discussion

November 14, 2005

CHANGES_SINCE_INITIAL_AUTHORISATION

Dynastat : EPAR - Procedural steps taken and scientific information after authorisation (archive)

January 7, 2010

CHANGES_SINCE_INITIAL_AUTHORISATION

Dynastat : EPAR - Procedural steps taken before authorisation

November 14, 2005

CHANGES_SINCE_INITIAL_AUTHORISATION

Overview Q&A (7)

Question

Other information about Dynastat

Answer

Dynastat received a marketing authorisation valid throughout the EU on 22 March 2002.

Question

How is Dynastat used?

Answer

Dynastat is available as an injection and it can only be obtained with a prescription.

Dynastat can be given into a vein or a muscle. The first dose of 40 mg is followed by further doses of 20 or 40 mg every 6 to 12 hours, up to a maximum total dose of 80 mg a day.

For more information about using Dynastat, see the package leaflet or contact your doctor or pharmacist.

Question

How does Dynastat work?

Answer

The active substance in Dynastat, parecoxib, is converted to valdecoxib in the body. Valdecoxib is a non?steroidal anti?inflammatory drug (NSAID) that belongs to the group of medicines called cyclo?oxygenase?2 (COX?2) inhibitors. It blocks the COX?2 enzyme, resulting in reduced production of prostaglandins, substances that are involved in inflammation. By reducing prostaglandins, Dynastat helps to reduce the symptoms of inflammation, including pain.

Question

What benefits of Dynastat have been shown in studies?

Answer

Dynastat was studied in over 2,500 adults who had surgical procedures including dental, orthopaedic (bone) and gynaecological surgery (surgery on the female reproductive system). Dynastat was compared with placebo (a dummy treatment) as well as with other painkillers such as ibuprofen, ketorolac, morphine, tramadol and valdecoxib. Dynastat was generally more effective than placebo and as effective as other painkillers. Dynastat also reduced the need for morphine.

Question

What are the risks associated with Dynastat?

Answer

The most common side effect with Dynastat (which may affect more than 1 in 10 people) is nausea (feeling sick). The most serious side effects (which may affect fewer than 1 in 100 people) include myocardial infarction (heart attack), severe reduction in blood pressure and allergic reactions.

Dynastat must not be used in patients who have had a serious allergic reaction to a medicine, have allergies to a class of medicines called sulfonamides or have certain illnesses including those affecting the gastrointestinal system, liver and heart. Women must not be given Dynastat during the last 3 months of pregnancy or if they are breast-feeding. It must not be used to relieve pain after certain types of heart surgery.

For the full list of side effects and restrictions of Dynastat, see the package leaflet.

Question

Why is Dynastat authorised in the EU?

Answer

Dynastat was found effective for relieving pain after surgery and its side effects are manageable.

The European Medicines Agency therefore decided that Dynastat’s benefits are greater than its risks and it can be authorised for use in the EU.

Question

What measures are being taken to ensure the safe and effective use of Dynastat?

Answer

Recommendations and precautions to be followed by healthcare professionals and patients for the safe and effective use of Dynastat have been included in the summary of product characteristics and the package leaflet.

As for all medicines, data on the use of Dynastat are continuously monitored. Side effects reported with Dynastat are carefully evaluated and any necessary action taken to protect patients.

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