DIDREX (benzphetamine) Tablets should not be used in combination with other anorectic agents,
including prescribed drugs, over-the-counter preparations and herbal products.
In a case-control epidemiological study, the use of anorectic agents was associated
with an increased risk of developing pulmonary hypertension, a rare, but often
fatal disorder. The use of anorectic agents for longer than three months was
associated with a 23-fold increase in the risk of developing pulmonary hypertension.
Increased risk of pulmonary hypertension with repeated courses of therapy cannot
be excluded. It should be noted that benzphetamine was not specifically studied
in this case-control study.
The onset or aggravation of exertional dyspnea, or unexplained symptoms of
angina pectoris, syncope, or lower extremity edema suggest the possibility of
occurrence of pulmonary hypertension. Under these circumstances, DIDREX (benzphetamine) Tablets
should be immediately discontinued, and the patient should be evaluated for
the possible presence of pulmonary hypertension.
Valvular heart disease associated with the use of some anorectic agents
such as fenfluramine and dexfenfluramine has been reported. Possible contributing
factors include use for extended periods of time, higher than recommended dose,
and/or use in combination with other anorectic drugs. However, no cases of this
valvulopathy have been reported when benzphetamine has been used alone.
The potential risk of possible serious adverse effects such as valvular heart
disease and pulmonary hypertension should be assessed carefully against the
potential benefit of weight loss. Baseline cardiac evaluation should be considered
to detect pre-existing valvular heart diseases or pulmonary hypertension prior
to initiation of benzphetamine treatment. DIDREX (benzphetamine) Tablets are not recommended
in patients with known heart murmur or valvular heart disease. Echocardiogram
during and after treatment could be useful for detecting any valvular disorders
which may occur. To limit unwarranted exposure and risks, treatment with DIDREX (benzphetamine)
Tablets should be continued only if the patient has satisfactory weight loss
within the first 4 weeks of treatment (i.e., weight loss of at least 4 pounds,
or as determined by the physician and patient).
When tolerance to the anorectic effect develops, the recommended dose should
not be exceeded in an attempt to increase the effect; rather, the drug should
be discontinued.
DIDREX (benzphetamine) Tablets are not recommended for severely hypertensive patients or for
patients with symptomatic cardiovascular disease including arrhythmias.
DIDREX (benzphetamine) Tablets are not recommended for patients who used any anorectic agents
within the prior year.