ASPIRIN 500 MG 20 TABLETS Specifications & 2026 Price
| Retail Price in Turkey | 117,40 TL |
|---|---|
| Drug Status | Active |
| Origin | Manufacture |
| Active Ingredient | Asetilsalisilik Asit |
| Manufacturer | Bayer Türk Kimya San. Ltd. Şti. |
| Prescription Type | White Prescription |
|---|---|
| Packaging | 20 |
| Form | TABLET |
| Route of Admin. | Oral |
| Barcode | 8699546010011 |
Summary
Active ingredient: 500 mg acetylsalicylic acid in each tablet
Excipients: Corn starch, cellulose.
Before you start using this medicine, read this INSTRUCTIONS FOR USE carefully, because it contains important information for you.
What is it used for?
Detailed information for this product is available in the patient information leaflet.
How to use?
Instructions for proper use and dosage/frequency of administration
Unless your doctor gives a separate recommendation, the maximum daily dose should not exceed 8 tablets (4 g), 1-2 tablets at a time at intervals of 4-8 hours for adolescents aged 16 years and over and adults.
Do not use ASPIRIN for more than 4 days or in high doses without consulting your doctor.
If you take the medicine by mistake, consult your doctor.
After meals, it is swallowed with some liquid without chewing. Do not use the medicine on an empty stomach.
Side Effects
Like all medicines, side effects may occur in people who are sensitive to the ingredients contained in ASPIRIN.
If any of the following occur, stop using ASPIRIN and IMMEDIATELY inform your doctor or go to the emergency department of your nearest hospital.
These are all very serious side effects. If you have one of these, it means you have a serious allergy to ASPIRIN. You may need emergency medical attention or hospitalization.
If you experience any side effects not mentioned in this instruction manual, inform your doctor or pharmacist.
If you experience any side effects, whether listed in the Instructions for Use or not, talk to your doctor, pharmacist or nurse. Also, report the side effects you encounter to the Turkish Pharmacovigilance Center (TÜFAM) by clicking on the “Drug Side Effect Reporting” icon on the website www.titck.gov.tr or by calling the side effect reporting line at 0 800 314 00 08. By reporting any side effects that occur, you will contribute to obtaining more information about the safety of the medicine you are using.
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