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Description
Abrupt cessation without a transition plan leads to rebound weight gain, metabolic disruption, and frustration

The most commonly reported adverse events are gastrointestinal in nature including nausea, vomiting, and decreased appetite which are typically mild-to-moderate and transient, particularly during the initial dose-escalation phase

The molecular synergy occurs at multiple levels

For generic companies, the Actavis framework creates risk in any settlement where the brand makes a substantial payment in cash or in some other form of value, such as an AG license, a service agreement, or a co-promotion arrangement
