COMBINATION PRODUCT USING 3,4-METHYLENEDIOXYMETHAMPHETAMINE AND CARVEDILOL FOR THE TREATMENT OF PSYCHIATRIC DISORDERS

1 . A composition for treating an individual while reducing acute adverse effects of an empathogen/entactogen, comprising effective amounts of an empathogen/entactogen and an adverse effect-reducing agent.

2 . The composition of claim 1 , wherein said empathogen/entactogen is a serotonin/oxytocin releaser chosen from the group consisting of MDMA, MDMA-analogs, MDMA-prodrugs, MDA, MDEA, MDAI, mephedrone, methylone, 3-MMC, 4-FA, PMA, PMMA, 2,5-dimethoxy-4-iodoamphetamine (DOI), 2,5-dimethoxy-4-bromoamphetamie (DOB), salts thereof, analogs thereof, and homologues thereof.

3 . The composition of claim 1 , wherein said empathogen/entactogen is present in an amount that results in cardiovascular stimulant and/or thermogenic effects.

4 . The composition of claim 3 , wherein said empathogen/entactogen is present in an amount of 50-300 mg and is chosen from the group consisting of MDMA, MDA, MDAI, mephedrone, methylone, or 3-MMC.

5 . The composition of claim 1 , wherein said adverse effect-reducing agent is an adrenergic α and β-receptor antagonist.

6 . The composition of claim 5 , wherein said adverse effect-reducing agent is chosen from the group consisting of carvedilol, labetalol, salts thereof, analogs thereof, and homologs thereof.

7 . The composition of claim 6 , wherein said carvedilol is present in an amount of 5-150 mg.

8 . The composition of claim 1 , wherein said empathogen/entactogen and adverse effect-reducing agent are in dosage units chosen from the group consisting of separate dosage units, in the same dosage unit with the same release profiles, and in the same dosage unit with different release profiles.

9 . The composition of claim 1 , wherein said adverse effect-reducing agent is an α-blocker.

10 . A method of treating an individual with an empathogen/entactogen and reducing its acute adverse effects, including the steps of:

administering an empathogen/entactogen to the individual;

administering an adverse effect-reducing agent to the individual; and

reducing the acute adverse effects of the empathogen/entactogen.

11 . The method of claim 10 , wherein the adverse effect-reducing agent is administered at the same time or up to 24 hours after administering the empathogen/entactogen.

12 . The method of claim 10 , wherein the acute adverse effects are chosen from the group consisting of cardiostimulant effects and thermogenic effects.

13 . The method of claim 10 , wherein the empathogen/entactogen is a serotonin/oxytocin releaser chosen from the group consisting of MDMA, MDMA-analogs, MDMA-prodrugs, MDA, MDEA, MDAI, mephedrone, methylone, 3-MMC, 4-FA, PMA, PMMA, 2,5-dimethoxy-4-iodoamphetamine (DOI), 2,5-dimethoxy-4-bromoamphetamie (DOB), salts thereof, analogs thereof, and homologues thereof.

14 . The method of claim 10 , wherein the adverse effect-reducing agent is an adrenergic α and β-receptor antagonist.

15 . The method of claim 10 , wherein the adverse effect-reducing agent is chosen from the group consisting of carvedilol, labetalol, salts thereof, analogs thereof, and homologs thereof.

16 . The method of claim 10 , wherein the individual is already treated with a β-blocker and the adverse effect-reducing agent is an α-blocker.

17 . A method of stopping acute cardiostimulant and hyperthermic actions of an empathogen/entactogen in an individual, including the steps of:

administering an adverse effect-reducing agent to the individual after the individual has taken the empathogen/entactogen; and

stopping the acute adverse effects of the empathogen/entactogen.

18 . The method of claim 17 , wherein the individual is experiencing adverse effects due to an overdose of the empathogen/entactogen.

19 . The method of claim 17 , wherein the empathogen/entactogen is a serotonin/oxytocin releaser chosen from the group consisting of MDMA, MDMA-analogs, MDMA-prodrugs, MDA, MDEA, MDAI, mephedrone, methylone, 3-MMC, 4-FA, PMA, PMMA, 2,5-dimethoxy-4-iodoamphetamine (DOI), 2,5-dimethoxy-4-bromoamphetamie (DOB), salts thereof, analogs thereof, and homologues thereof.

20 . The method of claim 17 , wherein the adverse effect-reducing agent is an adrenergic α and β-receptor antagonist.

21 . The method of claim 17 , wherein the adverse effect-reducing agent is chosen from the group consisting of carvedilol, labetalol, salts thereof, analogs thereof, and homologs thereof.

22 . A method of treating an individual at risk of cardiovascular events and/or hyperthermia with an empathogen/entactogen, including the steps of:

administering an empathogen/entactogen to the individual who is at risk of cardiovascular events and/or hyperthermia;

administering an adverse effect-reducing agent to the individual; and

providing psychotropic effects of empathogen/entactogen to the individual while reducing risk of cardiovascular events and/or hyperthermia.

23 . The method of claim 22 , wherein the empathogen/entactogen is a serotonin/oxytocin releaser chosen from the group consisting of MDMA, MDMA-analogs, MDMA-prodrugs, MDA, MDEA, MDAI, mephedrone, methylone, 3-MMC, 4-FA, PMA, PMMA, 2,5-dimethoxy-4-iodoamphetamine (DOI), 2,5-dimethoxy-4-bromoamphetamie (DOB), salts thereof, analogs thereof, and homologues thereof.

24 . The method of claim 22 , wherein the adverse effect-reducing agent is an adrenergic α and β-receptor antagonist.

25 . The method of claim 22 , wherein the adverse effect-reducing agent is chosen from the group consisting of carvedilol, labetalol, salts thereof, analogs thereof, and homologs thereof.

26 . The method of claim 22 , wherein the individual is already treated with a β-blocker and the adverse effect-reducing agent is an α-blocker.