Index
ToggleWhat is prodoline?
Prodolina® is the trademark of a synthetic medicine that uses sodium metamizole as an active ingredient , a chemical compound belonging to the line of analgesic, antipyretic and spasmolytic medicines, with an effect on painful processes of various etymologies .
To highlight: This pharmaceutical product is made in Mexico by the company named SANOFI-WINTHROP, SA DE CV . (1)
What is prodoline used for?
- Thanks to the mechanism of action of metamizole, prodoline® acts by neuronal impregnation in peripheral receptors and in the central nervous system , exerting a local analgesic, antipyretic, anti-inflammatory and spasmolytic effect on some conditions that cause pain for various reasons. (two)
- It is used to treat:
- Pain of mild to moderate intensity, whether acute or chronic.
- Fever of different etiology .
- Some cases of visceral pain.
Dosage and routes of administration of prodoline
The presentation of prodolina® is in the form of a box with 10 tablets containing metamizol sodium 500 mg. The administration is orally and the informative dosage can be as follows:
- Adults: From one tablet to two, 3 to 4 times a day as directed by the treating physician.
Prodoline Side Effects
Treatment with prodolina® can cause some of the following adverse reactions in certain types of patients :
- Possible allergic manifestations due to patient contact with any of the components of the formula.
- Skin rash, itching, hives and itching.
- Chest tightness, asthma and facial swelling.
- Tachycardia, fever and inflammation.
- Risk of decreased white blood cells , thrombocytopenia, leukopenia.
- Bullous type reactions in skin and mucous membranes (Steven Johnson Syndrome, Lyell Syndrome ).
- Proteinuria, oliguria, interstitial nephritis and gastric irritation.
Important: There is a possibility that the patient during treatment with prodolina®, may manifest any of these symptoms or another that is not on the list. If this occurs please discontinue use and consult your doctor .
Contraindications and warnings of prodoline
The use of prodolina® is contraindicated in any of the following cases:
- Patient hypersensitivity to any of the components of the formula.
- Patients with glucose 6-phosphate dehydrogenase deficiency.
- People with liver failure and hepatic porphyria.
- Patients with acute myocardial infarction, shock, polytrauma.
- During the pregnancy period.
- During breastfeeding .
You should know: Before starting treatment with this drug, the patient must provide their doctor with all the information about their health history .
Avoid it if you have:
- History of hypersensitivity to pyrazolones.
- Arterial hypotension below 100 mm Hg.
- Agranulocytosis, nephritis, hepatitis and blood dyscrasias.
Warnings:
- Pharmaceutical products such as prodolina® must be administered with a prescription or prescription.
- Do not alter the indicated dose.
- Follow your doctor’s instructions throughout the course of treatment with this drug.
- Do not mix this product with beverages containing alcohol.
- Do not consume this medicine without medical authorization, if you are being medicated for other pathologies.
- Keep this product out of the reach of children.

University Professional in the area of Human Resources, Postgraduate in Occupational Health and Hygiene of the Work Environment, 14 years of experience in the area of health. Interested in topics of Psychology, Occupational Health, and General Medicine.