Lofexidine may potentiate CNS depressant effects of alcohol.
Source: NLP:lofexidine
Brand names: Lofexidine
Route: Oral
Contraindications
4 CONTRAINDICATIONS None. None (4)
Pregnancy & Breastfeeding
8.1 Pregnancy Risk Summary The safety of lofexidine tablets in pregnant women has not been established. In animal reproduction studies, oral administration of lofexidine during organogenesis to pregnant rats and rabbits caused a reduction in fetal weights, increases in fetal resorptions, and litter loss at exposures below that in humans. When oral lofexidine was administered from the beginning of organogenesis through lactation, increased stillbirths and litter loss were noted along with decreased viability and lactation indices. The offspring exhibited delays in sexual maturation, auditory startle, and surface righting. These effects occurred at exposures below that in humans [see Animal Data] . The background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies carry some risk of birth defect, loss, or other adverse outcomes. The background risk of major birth defects in the U.S. general population is 2% to 4% and of miscarriage is 15% to 20% of clinically recognized pregnancies. Data Animal Data Increased incidence of resorptions, decreased number of implantations, and a concomitant reduction in the number of fetuses were observed when pregnant rabbits were orally administered lofexidine hydrochloride during organogenesis (from gestation day [GD] 7 to 19) at a daily dose of 5.0 mg/kg/day (approximately 0.08 times the maximum recommended human dose [MRHD] of 2.88 mg lofexidine base on an AUC basis). Maternal toxicity evidenced by increased mortality was noted at the highest tested dose of 15 mg/kg/day (approximately 0.4 times the MRHD on an AUC basis). Decreased implantations per dam and decreased mean fetal weights were noted in a study in which pregnant rats were treated with oral lofexidine hydrochloride during organogenesis (from GD 7 to 16) at a daily dose of 3.0 mg/kg/day (approximately 0.9 times the MRHD on an AUC basis). This dose was associated with maternal toxicity (decreased body weight gain and mortality
6 interactions on record
Lofexidine may potentiate CNS depressant effects of alcohol.
Source: NLP:lofexidine
Lofexidine may potentiate CNS depressant effects of barbiturates.
Source: NLP:lofexidine
Both methadone and lofexidine prolong QT interval. ECG monitoring is recommended when used concomitantly.
Source: NLP:lofexidine
Coadministration may reduce efficacy of oral naltrexone if taken within 2 hours of lofexidine due to altered pharmacokinetics.
Source: NLP:lofexidine
Lofexidine potentiates CNS depressant effects of benzodiazepines.
Source: NLP:lofexidine
CYP2D6 inhibitor that increases lofexidine plasma levels by 28%. Monitor for orthostatic hypotension and bradycardia.
Source: NLP:lofexidine