Drug Interactions between fospropofol and st. john's wort
This report displays the potential drug interactions for the following 2 drugs:
- fospropofol
- st. john's wort
Interactions between your drugs
St. John's wort fospropofol
Applies to: st. john's wort and fospropofol
GENERALLY AVOID: An isolated case report suggests that St. John's wort may prolong the sedative effects of some drugs used in general anesthesia. The case patient was a 21-year-old woman who received general anesthesia with fentanyl 1 mcg/kg and propofol 3 mg/kg IV, and sevoflurane in oxygen and nitrous oxide via a facemask. Total anesthesia time was approximately 10 minutes. Thirty minutes after anesthesia, the patient could not be aroused, even when subjected to painful stimulation. She was not easily rousable until 90 minutes postanesthesia. A subsequent interview revealed nothing unusual except for use of St. John's wort for the past three months. At the time of the procedure, the patient was taking St. John's wort 1000 mg (500 mg tablets standardized to 0.3% hypericin) three times a day. The authors suggested that St. John's wort may have caused profound sedation by interacting with anesthetic agents centrally, at neurotransmitter (GABA) receptor sites, and at hepatocellular enzyme sites.
MANAGEMENT: Based on the suspected interaction, it may be appropriate to advise patients to discontinue use of St. John's wort 5 days before surgery.
References (1)
- Crowe S, McKeating K (2002) "Delayed Emergence and St. John's Wort." Anesthesiology, 96, p. 1025-7
Drug and food interactions
St. John's wort food
Applies to: st. john's wort
GENERALLY AVOID: An isolated case report suggests that foods containing large amounts of tyramine may precipitate a hypertensive crisis in patients treated with St. John's wort. The mechanism of interaction is unknown, as St. John's wort is not thought to possess monoamine oxidase (MAO) inhibiting activity at concentrations achieved in vivo. The case patient was a 41-year-old man who had been taking St. John's wort for seven days prior to presentation at the emergency room with confusion and disorientation. The patient recalled last eating aged cheese and having a glass of red wine approximately 10 hours prior to admission. No other cause of delirium or hypertension could be identified. In addition, alcohol may potentiate some of the pharmacologic effects of St. John's wort. Use in combination may result in additive central nervous system depression and/or impairment of judgment, thinking, and psychomotor skills.
MANAGEMENT: Until further information is available, patients treated with St. John's wort should consider avoiding consumption of protein foods in which aging or breakdown of protein is used to increase flavor. These foods include cheese (particularly strong, aged or processed cheeses), sour cream, wine (particularly red wine), champagne, beer, pickled herring, anchovies, caviar, shrimp paste, liver (particularly chicken liver), dry sausage, figs, raisins, bananas, avocados, chocolate, soy sauce, bean curd, yogurt, papaya products, meat tenderizers, fava beans, protein extracts, and dietary supplements. Caffeine may also precipitate hypertensive crisis so its intake should be minimized as well. Patients should also be advised to avoid or limit consumption of alcohol.
References (1)
- Patel S, Robinson R, Burk M (2002) "Hypertensive crisis associated with St. John's Wort." Am J Med, 112, p. 507-8
Therapeutic duplication warnings
No warnings were found for your selected drugs.
Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.
See also
Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan. | |
No interaction information available. |
Further information
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