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FDA-approved clinical protocols specify 1.75 mg subcutaneous injection administered 45 minutes before anticipated sexual activity, with no more than one dose per 24 hours and a maximum of eight doses per month

10.1042/bj3400001 171 JohnstonD

Individuals, health practitioners and businesses must ensure they are meeting all their obligations under Commonwealth and State legislation, in addition to relevant regulatory requirements and professional practice standards, including AHPRA and the Pharmacy Board of Australia

Because the compound is unproven in people and material sold as a research chemical is not manufactured to pharmaceutical standards, the full profile of potential effects is uncharacterised

Smaller gauge and shorter needles provide almost painless injections

302 , F730F741 (2012)