This information is for educational purposes only. It is not intended as medical advice. Always consult a qualified healthcare professional.
CONDRODIN 400MG Hard capsule — Description, Dosage, Side Effects | PillsCard
OTC
CONDRODIN 400MG Hard capsule
400 mg, Kapsułki twarde
INN: Chondroitini natrii sulfas
Data updated: 2026-04-08
Available in:
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Form
Kapsułki twarde
Dosage
400 mg
Route
—
Storage
—
About This Product
User Reviews
Reviews reflect personal experiences and are not medical advice. Always consult your doctor.
Manufacturer
Reig Jofre Sp. z o.o.
ATC Code
M01AX25
Source
URPL
Pharmacotherapeutic group: other non-steroidal anti-inflammatory and antirheumatic agents, ATC code:
M01AX25
The active substance in Condrodin, chondroitin sulfate sodium salt, is a polysaccharide belonging to the glycosaminoglycan group.
Chondroitin sulfate is one of the major components of cartilage, as it forms part of its main protein, proteoglycan, which is the basis for the mechanical and elastic properties of cartilage.
The therapeutic effects of chondroitin sulfate in patients with osteoarthritis are based on an anti-inflammatory effect at the cellular level (in vivo), stimulation of endogenous proteoglycan synthesis (in vitro) and hyaluronic acid synthesis (in vivo), and reduction of the catabolic activity of chondrocytes (in vivo) by inhibiting certain proteolytic enzymes (e.g. collagenase, elastase, proteoglycanase, phospholipase A2, N-acetyl-glucosaminidase) (in vitro, in vivo) as well as formation of other substances damaging cartilage (in vitro).
Clinical studies in patients with osteoarthritis have shown that treatment with chondroitin sulfate eliminates or improves osteoarthritis symptoms of the knees and hips, such as pain and functional limitation. The effect manifests within 6–8 weeks and persists for 2–3 months after completion of treatment. For short-term pain relief, diclofenac has superior efficacy.
⚠️ Warnings
Patients with cardiac disease and/or renal impairment:
Very rarely (<1/10,000), oedema and/or fluid retention may occur. This is due to the osmotic effect of chondroitin sulfate.
Patients with hepatic impairment:
There is no experience with chondroitin sulfate in patients with hepatic impairment. Therefore, particular caution should be exercised when treating these patients.
In clinical studies, no adverse effects of chondroitin sulfate on platelets were observed at recommended doses. In rats, signs of platelet aggregation inhibition were observed at substantially higher doses (50 mg/kg/day, corresponding to a daily dose of 4000 mg in humans). This effect must be taken into account when chondroitin sulfate is used concomitantly with platelet aggregation inhibitors such as acetylsalicylic acid, dipyridamole, clopidogrel, and ticlopidine.
The dosage of concomitantly used analgesics should be regularly reviewed, as the use of chondroitin sulfate may reduce the need for pain-relieving medications.
Onset of action is slow; therefore, the product is not suitable for the treatment of acute pain.