Drug intelligence / Profile preview

hydromorphone + ropivacaine

Development stage
Unknown
Modality
Small Molecules
Administration
Epidural, Intrathecal, Caudal, Peripheral Nerve Block
01

Overview

Hydromorphone + ropivacaine is a combination of two pharmaceutical agents used primarily for regional anesthesia and postoperative pain management. Hydromorphone is a potent semisynthetic opioid analgesic that acts as an agonist at the mu-opioid receptor, providing strong analgesia. Ropivacaine is an amide-type local anesthetic that blocks sodium channels in nerve cells, inhibiting nerve impulse conduction and thus producing local or regional anesthesia. The combination is administered via epidural, spinal, caudal, or peripheral nerve block routes to enhance postoperative pain control while potentially reducing the required dose of each agent and minimizing side effects compared to higher doses of single agents alone. This combination has been studied in various surgical settings including cesarean section, breast surgery (e.g., modified radical mastectomy), hemorrhoidectomy, and pediatric surgeries[1][2][3][4][5]. Clinical studies indicate improved analgesic efficacy with this combination versus either drug alone or other opioid/local anesthetic combinations.

Other names
Hydromorphone combined with ropivacaine
02

Targets

SCN9A (Sodium channel protein type 9 subunit alpha)MOR (Mu opioid receptor)SCN8A (NaV1.6)

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