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Patients cannot substitute one for the other without proper medical supervision and dosing adjustments
and evaluation of baseline glucose control, especially with prediabetes or diabetes
The FDA Adverse Event Reporting System (FAERS) has received reports of pancreatitis in patients taking tirzepatide, but these reports do not prove causation, as patients with type 2 diabetes and obesity have inherently elevated baseline risk for pancreatitis independent of medication use
We meet the standards of Polish law and commonly used global pharmaceutical industry standards
The FDA issued a warning letter in 2023 regarding companies marketing BPC-157 with therapeutic claims, reinforcing that this peptide lacks the evidence base required for approved drug status [2]
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