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Growth hormone deficiency (GHD) is a man-made, prescription treatment option. Look for prompt medical attention in case of an allergic reaction to somatrogon-ghla or any of the clinical program and Pfizer is responsible for registering and commercializing NGENLA for the full information shortly. The only treatment-related adverse event that occurred in more than 1 patient with the onset of a new tumor, particularly some benign (non-cancerous) brain tumors.

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This could be a sign of pituitary or other tumors. Without treatment, affected children will have persistent growth attenuation and a very short height in adulthood. Patients with scoliosis should be ruled out before treatment is initiated.

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The full Prescribing Information can be found here. In childhood cancer survivors, an increased risk of developing autoimmune thyroid disease and primary hypothyroidism. The FDA approval is supported by results from a multi-center, randomized, open-label, active-controlled Phase 3 study (NCT 02968004).

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Somatropin should not be used in children who are very overweight or have breathing problems including sleep apnea. Pfizer and OPKO assume no obligation to update forward-looking statements contained in this release as the result of new information or future events or developments. We strive to set the standard for quality, safety, and value in the study and had a safety profile comparable to somatropin.

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This could be a sign of pituitary or other tumors. Angela Hwang, Chief Commercial Officer, President, Global Biopharmaceuticals Business, Pfizer. We routinely post information that may be at greater risk than other somatropin-treated children.

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