Blister packaging for acute pain regimens
Provided are rapidly bioavailable solid oral dosage forms of acute pain medications, and moisture resistant packaging that enables the formulation of such rapidly bioavailable tablet dosage forms. Also provided is packaging that discourages the use of rapidly bioavailable acute pain medications for off-label chronic pain treatment, and that allows such dosage forms to be manufactured and stored for prolonged periods of time.
1. A method of packaging a rapidly bioavailable diclofenac dosage form demonstrated to have a mean time to maximum plasma concentration (t max ) of from about 5 to about 40 minutes to discourage its administration in the treatment of chronic pain comprising:
a) formulating diclofenac or a pharmaceutically acceptable salt thereof in a rapidly bioavailable tablet dosage form comprising an excipient base; and
b) packaging said drug in a blister package divided into from five to fourteen medication segments, wherein:
i) each medication segment corresponds to one day of treatment,
ii) each medication segment is divided into from one to four unit doses corresponding to a daily dosage for said drug, and
iii) said blister package is imprinted with indicia that distinguishes between said medication segments and instructs on the proper treatment with said drug;
wherein said dosage form comprises from alkali metal carbonate or bicarbonate at a weight ratio to said diclofenac of from about 1:5 to about 4:5.
2. The method of claim 1 wherein said blister package prevents said dosage form from absorbing more than 4 wt. % moisture in three months when stored at 40° C. and 75% relative humidity.
3. The method of claim 1 wherein said dosage form comprises about 50 mg. of diclofenac potassium.
4. The method of claim 1 wherein said dosage form has been demonstrated to have a t max of from about 5 to about 30 minutes, and a mean maximum plasma concentration (C max ) of from about 1700 to about 2300 ng/ml.
5. The method of claim 1 wherein said dosage form has been demonstrated to have a t max of from about 5 to about 30 minutes, and a mean maximum plasma concentration (C max ) of from about 1500 to about 2500 ng/ml wherein said t max exhibits an inter-subject variability of less than about 49%.
6. The method of claim 1 wherein said dosage form has been demonstrated to yield one mean maximum plasma concentration (C max ) peak when orally ingested.
7. The method of claim 1 wherein said dosage form comprises from about 7 to about 20 wt. % of a hygroscopic excipient, having a hygroscopicity of greater than about 1 wt. % water absorption within a twenty four hour period in a humidity chamber maintained at 80% RH and 25 degrees Celcius.
8. The method of claim 1 wherein said dosage form comprises at least 20 wt. % of excipients that are freely soluble in water.
9. The method of claim 1 wherein said dosage form comprises at least 20 wt. % of mannitol, lactose, sucrose, or a combination thereof.
10. The method of claim 1 wherein said dosage form comprises a surfactant.
11. The method of claim 1 wherein said dosage form comprises a surfactant having a hydrophilic lipophilic balance greater than 14.
12. The method of claim 1 wherein said dosage form comprises from about 30 to about 80 wt. % of a hygroscopic diluent and a freely soluble diluent at a weight ratio of from about 1:20 to about 5:1.
13. The method of claim 1 wherein said dosage form comprises an excipient base that is characterized by an inverse relationship between disintegration rate and moisture uptake.
14. The method of claim 1 wherein said excipient base comprises greater than about 20 wt. % of a freely and rapidly soluble diluent.
15. The method of claim 1 wherein said blister package is further imprinted with precautionary indicia discouraging the administration of the drug for the treatment of chronic pain.
16. The method of claim 15 wherein said precautionary indicia states that the safety of the drug has only been studied in short term studies or that the safety of the drug during long term administration has not been adequately investigated.
17. A method of treating acute pain in a host in need thereof comprising:
a) providing diclofenac or a pharmaceutically acceptable salt thereof in a dosage form that comprises:
i) an excipient base which has been demonstrated to yield a time to maximum plasma concentration (t max ) of from about 5 to about 40 minutes; and
i) blister packaging divided into from five to fourteen medication segments, wherein each medication segment corresponds to one day of treatment, each medication segment is divided into from one to four unit doses corresponding to a daily dosage for said drug, and said blister packaging is imprinted with indicia that distinguishes between said medication segments and instructs on the proper treatment with said drug; and
b) administering said diclofenac or pharmaceutically acceptable salt thereof to a patient suffering from acute pain
wherein said dosage form comprises alkali metal carbonate or bicarbonate at a weight ratio to said diclofenac from about 1:5 to about 4:5.
18. The method of claim 17 wherein said blister packaging is further imprinted with precautionary indicia discouraging the administration of the drug for the treatment of chronic pain.
19. The method of claim 18 wherein said precautionary indicia states that the safety of the drug has only been studied in short term studies or that the safety of the drug during long term administration has not been adequately investigated.
20. A method of packaging an acute pain medication to discourage its administration in the treatment of chronic pain comprising:
a) formulating said acute pain medication in a rapidly bioavailable dosage form which has been demonstrated to have a mean time to maximum plasma concentration (t max ) of from about 5 to about 40 minutes; and
b) packaging said drug in a blister package divided into from five to fourteen medication segments, wherein:
i) each medication segment corresponds to one day of treatment,
ii) each medication segment is divided into from one to four unit doses corresponding to a daily dosage for said drug , and
iii) said blister package is imprinted with indicia that distinguishes between said medication segments and instructs on the proper treatment with said drug;
wherein diclofenac is the active ingredient of said medication; and
wherein said dosage form comprises alkali metal carbonate or bicarbonate at a weight ratio to said diclofenac from about 1:5 to about 4:5.
21. The method of claim 20 wherein said blister package is further imprinted with precautionary indicia discouraging the administration of the drug for the treatment of chronic pain.
22. The method of claim 21 wherein said precautionary indicia states that the safety of the drug has only been studied in short term studies or that the safety of the drug during long term administration has not been adequately investigated.