<p> </p>
<p>BREASTFEEDING</p>
<p>ARIXTRA 7.5MG INJECTION is generally not recommended for use in breastfeeding women as it may pass through breast milk. Consult your doctor before receiving it.</p>
<p><img src="https://www.netmeds.com/images/content/icons/kidney.jpg" /></p>
<p>KIDNEY</p>
<p>ARIXTRA 7.5MG INJECTION is not recommended for use in patients with very severe kidney disease unless it is necessary. Consult your doctor before receiving it.</p>
<p><img src="https://www.netmeds.com/images/content/icons/liver.jpg" /></p>
<p>LIVER</p>
<p>ARIXTRA 7.5MG INJECTION should be used with caution in patients with severe liver disease. Consult your doctor before receiving it.</p>
<p><img src="https://www.netmeds.com/images/content/icons/allergy.jpg" /></p>
<p>ALLERGY</p>
<p>Do not receive ARIXTRA 7.5MG INJECTION if you are allergic to Fondaparinux or any of the other ingredients of the medicines.</p>
<p><img src="https://www.netmeds.com/images/content/icons/heart_disease.jpg" /></p>
<p>HEART DISEASE</p>
<p>ARIXTRA 7.5MG INJECTION should not be used in patients with bacterial heart infections. Consult your doctor before receiving it.</p>
<h2>OTHERS</h2>
<p>ARIXTRA 7.5MG INJECTION is not recommended for use if you:</p>
<ul>
<li>Are bleeding excessively</li>
</ul>
<p>Before receiving ARIXTRA 7.5MG INJECTION, inform your doctor if you have/had:</p>
<ul>
<li>Risk of uncontrolled bleeding (hemorrhage) including</li>
<li>Stomach ulcer</li>
<li>Bleeding disorders</li>
<li>Recent bleeding into the brain (intracranial bleeding)</li>
<li>Recent surgery on the brain, spine or eye</li>
</ul>
<p><strong>Use in Pediatrics:</strong></p>
<p>ARIXTRA 7.5MG INJECTION is not recommended for use in children and adolescents (under the age of 17 years). Consult with your child’s doctor.</p>
<p><strong>Use in Geriatrics:</strong></p>
<p>ARIXTRA 7.5MG INJECTION should be used with caution in elderly patients (aged 75 years and above). Consult your doctor before receiving it.</p>
<h2>INTERACTIONS</h2>
<p><strong>A. Drug-Drug interactions:</strong></p>
<p>Before receiving ARIXTRA 7.5MG INJECTION, inform your doctor if you are receiving any of the following medicine:</p>
<ul>
<li>Heparin or heparin-like medicines (used to prevent blood clotting)</li>
</ul>
<p><strong>Overdosage:</strong></p>
<p>ARIXTRA 7.5MG INJECTION will be administered only by a doctor or a nurse in a hospital and so it is unlikely to receive an overdose. However, consult your doctor or nurse if there are any unusual symptoms</p>
<h2>SYNOPSIS</h2>
<table border="0" cellpadding="1" cellspacing="1">
<tbody>
<tr>
<td><strong>Drug</strong></td>
<td>: </td>
<td>Fondaparinux</td>
</tr>
<tr>
<td><strong>Pharmacological Category</strong></td>
<td>: </td>
<td>Anti-thrombotic agents</td>
</tr>
<tr>
<td><strong>Therapeutic Indication</strong></td>
<td>: </td>
<td>Blood clots, some types of heart attack and severe angina</td>
</tr>
<tr>
<td><strong>Dosage Forms</strong></td>
<td>: </td>
<td>Injection, Prefilled syringe (PFS)</td>
</tr>
</tbody>
</table>
<h2>MORE INFORMATION</h2>
<ul>
<li>Keep ARIXTRA 7.5MG INJECTION out of reach of children</li>
<li>Store ARIXTRA 7.5MG INJECTION below 25°C</li>
</ul>
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Composition Details
Fondaparinux (7.5mg)
| Manufacturer |
Glaxo SmithKline Pharmaceuticals Ltd |
| Pack Size |
0.6 ml in 1 vial |
| Product Name |
Arixtra 7.5mg Injection |
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