Oral tolfenamic acid for acute migraine
Clinical bottom line:
Oral tolfenamic acid has been tested in only a single small trial in acute migraine, involving about 80 patients. It is unsafe to draw any conclusions.
This information comes from an as-yet unpublished systematic review. The only outcome reported here is that of headache response at two hours, though other outcomes may be available in the full paper.
- Date review completed: September 2000
- Number of trials included: One randomised controlled trial
- Control group: Active and placebo
- Main outcomes: Headache intensity and duration
Inclusion criteria were: treatment of acute migraine; randomised allocation to treatment groups; double-blind design; adult population and headache outcomes.
Search
Comprehensive searches of the following databases were made: MEDLINE (1966 - July 2000), EMBASE (1980 - June 2000), Cochrane Library (Issue 3, 2000) and the Oxford Pain Relief Database (1950 - 1994). A series of free text searches were undertaken, using generic and trade names. There was no restriction to language. Retrieved reports were searched for additional trials. Neither individual authors nor pharmaceutical companies were contacted for unpublished data.
Findings
Tables with all included trials and excluded trials are available.
For oral tolfenamic acid rapid release (200 mg plus a further 200 mg at 60 minutes if headache not improved), 33/43 patients had a headache response at two hours compared with 12/41 with placebo.
Adverse effects
Adverse effects are not reported in any way that makes obvious sense.