Ozagrel Sodium
Ozagrel is an antiplatelet agent working as a thromboxane A2 synthesis inhibitor.
Primary Characteristics
It is of Synthetic origin.
It is classified in Antiplatelet Agent pharmacological group.
Molecular Weight: 500 · Solubility in Water: freely · Non-proprietary name: Lacosamide.

Pharmacokinetics
None recorded.
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Indications
Ozagrel Sodium is primarily indicated in conditions like Cerebral infarction.
Contraindications
None recorded.
Dosage
Ozagrel Sodium's dosage details are as follows:
| Dose | Single Dose | Frequency | Route | Instructions |
|---|---|---|---|---|
| Adult Dosage | ||||
| 120 mg | 120 mg | Every 2h | IV | solute in 500ml normal saline or 5% glucose solution, intravenous infusion, treatment duration is 2 weeks. |
| Paediatric Dosage (20kg) | ||||
| No data. | ||||
| Neonatal Dosage (3kg) | ||||
| No data. | ||||
Drug Interactions
Always consult your physician for the change of dose regimen or an alternative drug of choice that may strictly be required.
Side Effects
Ozagrel Sodium in overdosage may give rise to further complications which include hemorrhagic cerebral infraction, extradural hemorrhage, encephalic hemorrhage, gastrointestinal hemmorahe, subcutaneous hemorrhag.
Ozagrel Sodium is known to cause more or less tolerable side effects which are usually transient. These include Abdominal distension, Anorexia , Diarrhea, Fever, Headache, Hypotension, Nausea and vomiting, Skin rashes, Supraventricular arrythemia, Urticaria.
Warnings / Precautions
Interference in Pathology
Ozagrel Sodium may interfere in the diagnosis of BUN increased, GOT increased, GPT incresed.
Available Brands
None recorded.
Storage Conditions
Drug Classification
- 1.10.2 — Anticoagulants/Platelet deaggregators