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Telogen effluvium typically resolves within 36 months once the triggering factor stabilises

It also instructs patients to inform healthcare providers of planned surgeries or procedures because of reported pulmonary aspiration during general anesthesia or deep sedation

Research suggests that structured programmes may enhance outcomes when used alongside pharmacotherapy

The PSM was performed using 1:1 to reduce the confounding effects

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Some individuals may notice a small bump, slight redness, or mild itching at the injection site for a day or two