
Sarozar2 mg
Beacon Pharmaceuticals PLC
Saroglitazar Magnesium is a dual PPAR-alpha/gamma agonist indicated for the following uses: Established/Approved Use Diabetic dyslipidemia and hypertriglyceridemia in patients with type 2 diabetes…
Saroglitazar Magnesium is a dual PPAR-alpha/gamma agonist indicated for the following uses:
Saroglitazar Magnesium is a relatively newer, regionally-approved agent; it should be used within its approved indications and under physician supervision.
| Indication | Recommended Dose |
|---|---|
| Diabetic dyslipidemia / hypertriglyceridemia with type 2 diabetes (add-on to statin) | 4 mg once daily (as two 2 mg tablets or one 4 mg tablet), taken orally with or without food |
| NAFLD/NASH (in markets where approved) | 4 mg once daily, per treating physician's assessment and local approved labeling |
Tablets should be swallowed whole with water. Dose should not be adjusted or increased without physician advice. Periodic monitoring of lipid profile, blood glucose, and liver function is recommended during treatment. See Precautions and Warnings for renal/hepatic impairment considerations.
The most commonly reported adverse effects of Saroglitazar Magnesium (occurring in more than 2% of patients) include:
Other reported effects include mild elevations in liver enzymes, myalgia, and increases in serum creatinine. Most adverse events have been mild to moderate and generally did not require discontinuation. See Precautions and Warnings for fluid retention/edema and hepatic monitoring guidance.
Saroglitazar Magnesium is contraindicated in patients with known hypersensitivity to Saroglitazar Magnesium or to any excipient in the formulation.
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