Tirzepatide is a dual GIP and GLP-1 receptor agonist. It is a modified 39-amino-acid peptide containing a C20 fatty diacid moiety that promotes albumin binding and prolongs its duration of action.
Tirzepatide selectively activates both glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptors. It enhances both first- and second-phase insulin secretion and reduces glucagon secretion in a glucose-dependent manner.
Through these actions, tirzepatide helps improve blood glucose regulation in adults with type 2 diabetes.
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Wikijet is indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.
In the event of an overdose, treatment should be based on the patient's clinical signs and symptoms. Appropriate supportive care and medical observation may be required.
Because tirzepatide has a long duration of action, symptoms following an overdose may require prolonged monitoring. Its elimination half-life is approximately 5 days.
Seek immediate medical attention if an excessive dose has been administered.
If a dose is missed:
The weekly injection day may be changed if necessary, provided there are at least 72 hours (3 days) between two doses.
Poorly controlled diabetes during pregnancy can pose risks to both the mother and fetus. Wikijet should be used during pregnancy only when the potential benefits are considered to outweigh the potential risks.
Women who are pregnant or planning pregnancy should discuss tirzepatide treatment with their healthcare provider.
The benefits of breastfeeding should be considered alongside the mother's clinical need for tirzepatide and any potential effects on the breastfed infant. Discuss the use of Wikijet with a healthcare professional before starting or continuing treatment while breastfeeding.
Patients should be informed about the potential risk of thyroid C-cell tumors associated with tirzepatide. Seek medical advice if symptoms such as a neck lump, difficulty swallowing, difficulty breathing, or persistent hoarseness develop.
Patients should be monitored for signs and symptoms of pancreatitis, such as persistent or severe abdominal pain that may radiate to the back, with or without vomiting.
If pancreatitis is suspected, Wikijet should be discontinued and appropriate medical evaluation and treatment initiated.
The risk of hypoglycemia may increase when tirzepatide is used together with insulin or insulin secretagogues such as sulfonylureas. The dose of these medicines may need to be reduced under medical supervision.
Serious allergic or hypersensitivity reactions may occur. Discontinue Wikijet and seek immediate medical attention if symptoms such as severe rash, facial or throat swelling, difficulty breathing, or other signs of a serious allergic reaction develop.
Monitor renal function when initiating or increasing the dose in patients with renal impairment who experience severe gastrointestinal reactions such as prolonged vomiting or diarrhea, as dehydration may affect kidney function.
Patients with a history of diabetic retinopathy should be monitored for changes or progression in their eye condition, particularly when blood glucose levels improve rapidly.
If symptoms suggestive of gallbladder disease occur, such as persistent upper abdominal pain, nausea, vomiting, or jaundice, appropriate clinical evaluation and gallbladder investigations may be required.
Concomitant use with insulin or insulin secretagogues such as sulfonylureas may increase the risk of hypoglycemia. Your doctor may reduce the dose of these medicines when Wikijet is initiated.
Tirzepatide delays gastric emptying, which may affect the absorption of certain oral medicines. Patients taking medicines that depend on specific blood concentrations for effectiveness or have a narrow therapeutic index, such as warfarin, may require additional monitoring.
Because tirzepatide can affect gastric emptying, oral hormonal contraceptive effectiveness may potentially be reduced during treatment initiation and dose escalation.
Patients using oral hormonal contraceptives should discuss contraceptive options with their healthcare provider. A non-oral contraceptive method or an additional barrier method may be recommended for 4 weeks after starting tirzepatide and for 4 weeks after each dose increase.
Non-oral hormonal contraceptives are not expected to be affected in the same manner.
⚠️Disclaimer:
At ePharma, we’re committed to providing accurate and accessible health information. However, all content is intended for informational purposes only and should not replace medical advice from a qualified physician. Please consult your healthcare provider for personalized guidance. We aim to support, not substitute, the doctor-patient relationship.