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Bupivacaine Hydrochloride + Dextrose is a hyperbaric ("heavy") local anesthetic solution indicated for producing subarachnoid block (spinal anesthesia) in adults undergoing surgical procedures.
Bupivacaine Hydrochloride + Dextrose is a hyperbaric ("heavy") local anesthetic solution indicated for producing subarachnoid block (spinal anesthesia) in adults undergoing surgical procedures. The dextrose component increases the specific gravity of the solution above that of cerebrospinal fluid, allowing the anesthesia provider to control the spread of the block within the subarachnoid space by positioning the patient.
Bupivacaine Hydrochloride + Dextrose is intended for use only by, or under the direct supervision of, clinicians experienced in the techniques of spinal anesthesia, with resuscitation equipment and drugs immediately available.
Bupivacaine Hydrochloride + Dextrose is for subarachnoid (spinal/intrathecal) injection ONLY, to be administered by or under the direct supervision of clinicians experienced in spinal anesthesia, in a setting equipped with full resuscitation and continuous cardiovascular/respiratory monitoring. Dose depends on the procedure, desired block height, and patient factors, and must be individualized by the treating anesthesiologist.
| Indication/Procedure | Typical Adult Dose |
|---|---|
| Vaginal delivery | Approximately 6 mg (starting dose), titrated as needed |
| Lower extremity and perineal procedures | Approximately 7.5 mg |
| Lower abdominal procedures | Approximately 12 mg |
| Cesarean section | Approximately 7.5 mg to 10.5 mg |
The syringe must always be aspirated before and during injection to check for blood or cerebrospinal fluid. Vital signs (blood pressure, heart rate, oxygen saturation, respiratory rate) must be monitored continuously during and after administration of Bupivacaine Hydrochloride + Dextrose because of the risk of high spinal block, severe hypotension, and cardiorespiratory compromise. Dose reduction and careful titration are recommended in elderly, pregnant, and debilitated patients. Do not use if the solution is discolored, cloudy, or contains particulate matter; discard any unused portion as this is a single-dose, preservative-free product.
Adverse effects of Bupivacaine Hydrochloride + Dextrose are largely related to the physiological effects of spinal anesthesia (sympathetic blockade) and, rarely, to systemic absorption or inadvertent intravascular exposure.
Bupivacaine Hydrochloride + Dextrose is contraindicated in patients with:
Disclaimer
The information provided is accurate to the best of our knowledge, but it does not replace professional medical advice. We cannot guarantee its completeness or accuracy, and the absence of specific information about a drug should not be taken as an endorsement. We are not responsible for any consequences arising from this information, so please consult a healthcare professional for any concerns or questions.