4.4.0.0 Ap­proved Weight-‍Loss Med­i­ca­tions

The U.S. Food and Drug Ad­min­is­tra­tion (FDA) has ap­proved med­i­ca­tions for both short-‍term and long-‍term weight man­age­ment as ad­juncts to diet, ex­er­cise, and be­hav­ioral ther­a­py. Near­ly all FDA- ap­proved med­i­ca­tions for weight loss have been shown to im­prove glycemic con­trol in pa­tients with type 2 di­a­betes and delay pro­gres­sion to type 2 di­a­betes in pa­tients at risk (41). Phen­ter­mine is in­di­cat­ed as short-‍term (≤12 weeks) treat­ment (42). Five weight-‍loss med­i­ca­tions (or com­bi­na­tion med­i­ca­tions) are FDA-‍ap­proved for long-‍term use (more than a few weeks) by pa­tients with BMI ≥27 kg/m2 with one or more obe­si­ty-‍as­so­ci­at­ed co­mor­bid con­di­tions (e.g., type 2 di­a­betes, hy­per­ten­sion, and dys­lipi­demia) who are mo­ti­vat­ed to lose weight (41). Med­i­ca­tions ap­proved by the FDA for the treat­ment of obe­si­ty and their ad­van­tages and disad­van­tages are sum­ma­rized in Table 8.2. The ra­tio­nale for weight-‍loss med­i­ca­tions is to help pa­tients to more con­sis­tently ad­here to low-‍calo­rie diets and to rein­force lifestyle changes. Providers should be knowl­edge­able about the prod­uct label and should bal­ance the po­ten­tial benefits of suc­cess­ful weight loss against the po­ten­tial risks of the med­i­ca­tion for each pa­tient. These med­i­ca­tions are contrain­di­cat­ed in women who are preg­nant or ac­tive­ly try­ing to con­ceive. Women of reprod­uctive po­ten­tial must be coun­seled re­gard­ing the use of re­li­able meth­ods of con­tra­cep­tion.

Table 8.2—Med­i­ca­tions ap­proved by the FDA for the treat­ment of obe­si­ty

All medications are contraindicated in women who are or may become pregnant. Women of reproductive potential must be counseled regarding the use of reliable methods of contraception. Select safety and side effect information is provided; for a comprehensive discussion of safety considerations, please refer to the prescribing information for each agent. b.i.d., twice daily; ER, extended release; MEN 2, multiple endocrine neoplasia syndrome type 2; MTC, medullary thyroid carcinoma; OTC, over the counter; PBO, placebo; q.d., daily; Rx, prescription; t.i.d, three times daily; XR, extended release.
*Use lowest effective dose; maximum appropriate dose is 37.5 mg.
Duration of treatment was 28 weeks in a general obese adult population.
Enrolled participants had normal (79%) or impaired (21%) glucose tolerance.
§Maximum dose, depending on response, is 15 mg/92 mg q.d.
||Approximately 68% of enrolled participants had type 2 diabetes or impaired glucose tolerance.