| Ημερομηνία | barcode | code | περιεχομενο | τιμή παραγωγός | χονδρική | λιανική |
|---|---|---|---|---|---|---|
| 05/2018 | 2802271601010 | 227160101 | VIDAN F.C.TAB 500MG/TAB BTx15(BLISTERS) | 0.82 | 0.86 | 1.19 |
| 05/2018 | 2802271601027 | 227160102 | VIDAN F.C.TAB 500MG/TAB BTx24(BLISTERS3x8) | 1.16 | 1.22 | 1.69 |
| 05/2018 | 2802271602017 | 227160201 | VIDAN ORAL.SUSP 50MG/5ML BTx1 BOTTLEx125 ML | 0.72 | 0.76 | 01.05 |
For the treatment of rheumatoid arthritis, osteoarthritis, dysmenorrhea, and mild to moderate pain, inflammation, and fever.
Mefenamic acid binds the prostaglandin synthetase receptors COX-1 and COX-2, inhibiting the action of prostaglandin synthetase. As these receptors have a role as a major mediator of inflammation and/or a role for prostanoid signaling in activity-dependent plasticity, the symptoms of pain are temporarily reduced.
Oral, rat LD<sub>50</sub>: 740 mg/kg. Symptoms of overdose may include severe stomach pain, coffee ground-like vomit, dark stool, ringing in the ears, change in amount of urine, unusually fast or slow heartbeat, muscle weakness, slow or shallow breathing, confusion, severe headache or loss of consciousness.
Mefenamic acid is rapidly absorbed after oral administration.
2 hours
The fecal route of elimination accounts for up to 20% of the dose, mainly in the form of unconjugated 3-carboxymefenamic acid.3 The elimination half-life of mefenamic acid is approximately two hours. Mefenamic acid, its metabolites and conjugates are primarily excreted by the kidneys. Both renal and hepatic excretion are significant pathways of elimination.
* 1.06 L/kg [Normal Healthy Adults (18-45 yr)]
* Oral cl=21.23 L/hr [Healthy adults (18-45 yrs)]