TOLFIKIND-MR BOLUS
Out of Stock
Tolfikind MR Bolus by Veticura Mankind, the premium clinical veterinary division of Mankind Pharma Limited, is a revolutionary, first-of-its-kind oral bolus formulation that brings together three pharmacologically complementary active ingredients, namely Tolfenamic Acid, Paracetamol, and Chlorzoxazone, in a single, convenient bolus for large animal use. This triple-action combination addresses one of the most complex and clinically challenging pain scenarios in livestock medicine: the simultaneous presentation of acute inflammation, systemic fever, and painful skeletal muscle spasm that accompanies conditions such as acute mastitis, bovine respiratory disease, metritis, foot rot, musculoskeletal injury, and the postoperative and peri-parturient period. Single-active NSAID boluses traditionally manage only the inflammatory and pyrexic components of pain, leaving muscle tension and spasm, which significantly compound animal distress and impede recovery, unaddressed. Tolfikind MR Bolus closes this therapeutic gap definitively, delivering complete multi-modal pain relief from a single oral dose under veterinary prescription. It is classified as a Schedule H prescription veterinary pharmaceutical and must be administered under the supervision of a registered veterinary practitioner. Animeal is proud to offer Tolfikind MR Bolus as part of its curated range of advanced prescription veterinary medicines for the health, productivity, and welfare of your livestock
Ingredients:
Tolfenamic Acid (Fenemate Class NSAID): Tolfenamic acid is a potent, veterinary-approved non-steroidal anti-inflammatory drug of the fenemate class, closely structurally related to flunixin meglumine and widely used across the European Union and India for pain, fever, and inflammation management in cattle, pigs, dogs, and cats. Its primary mechanism of action operates through balanced, non-selective inhibition of both the COX-1 and COX-2 cyclooxygenase enzyme isoforms. These enzymes are responsible for converting arachidonic acid into the pro-inflammatory prostaglandin cascade, specifically PGE2, PGI2, and thromboxane A2, which are the key molecular mediators that sensitise peripheral nociceptors to pain stimuli, sustain vasodilation and oedema at the site of tissue injury, and activate the hypothalamic thermostat to maintain elevated body temperature during fever. By competitively inhibiting both COX isoforms, tolfenamic acid rapidly reduces prostaglandin synthesis at the tissue level, alleviating the cardinal signs of inflammation including heat, redness, swelling, and pain, while simultaneously normalising body temperature through the hypothalamic pathway. Tolfenamic acid is especially well-established in the treatment of respiratory disease in cattle, acute mastitis as adjunct therapy alongside antibiotics, and musculoskeletal disorders, and its pharmacological profile as a balanced COX inhibitor offers both anti-inflammatory potency and a well-characterised safety margin when used at recommended doses.
Paracetamol (Acetaminophen, Phenylacetic Acid Class): Paracetamol complements the anti-inflammatory action of tolfenamic acid by providing a distinct and additive analgesic and antipyretic mechanism that operates primarily through central nervous system pathways. Unlike NSAIDs, paracetamol's analgesic effect involves the inhibition of prostaglandin synthesis specifically within the central nervous system, modulation of the endocannabinoid system through the AM404 metabolite, and enhancement of descending serotonergic pain-inhibitory pathways in the spinal cord. At the thermoregulatory level, paracetamol reduces hypothalamic prostaglandin signalling, reinforcing the antipyretic action already initiated by tolfenamic acid and providing faster and more complete normalisation of elevated core body temperature. The pharmacokinetic profile of paracetamol, with its rapid gastrointestinal absorption and relatively short half-life, complements the sustained anti-inflammatory action of tolfenamic acid, providing immediate analgesic relief in the early post-dosing period while the NSAID component establishes its full therapeutic tissue concentration. This dual-mechanism analgesic synergy delivers a more comprehensive pain relief experience than either compound alone.
Chlorzoxazone (Benzoxazolone Derivative, Centrally Acting Muscle Relaxant): Chlorzoxazone is a centrally acting benzoxazolone-class muscle relaxant that represents the defining innovation in the Tolfikind MR formulation, distinguishing it from all single-NSAID or NSAID-paracetamol combination boluses available in the Indian market. Its mechanism of action involves modulation of GABA-A and GABA-B receptors in the spinal cord and supraspinal regions, inhibiting multisynaptic reflexes that drive sustained skeletal muscle hypertonicity and painful spasm following musculoskeletal injury, inflammation, or neurological sensitisation. By depressing the exaggerated reflex arcs that sustain muscle tension around inflamed or injured tissue, chlorzoxazone reduces the secondary mechanical pain and movement restriction that accompanies primary inflammatory pain, allowing the animal to ambulate, feed, and rest more normally during the recovery period. This muscle relaxant action is particularly therapeutically valuable in conditions such as foot rot with associated limb musculature guarding, respiratory disease with intercostal and diaphragmatic splinting, and post-calving or post-surgical musculoskeletal strain, where reflex muscle spasm significantly amplifies clinical pain scores and delays return to productive function. Chlorzoxazone is notably well-established in its long-standing use as a combination partner to paracetamol, with this pairing providing synergistic pain relief with improved tolerability in clinical settings.
