Clonidine Interactions

Brand names: Clonidine

Central alpha-2 Adrenergic Agonist · Adrenergic alpha2-Agonists

Route: Oral

FDA Black Box Warning

The 500 mcg/mL strength product should be diluted prior to use in an appropriate solution. NOTE: Clonidine hydrochloride injection (epidural clonidine) is not recommended for obstetrical, post-partum, or peri-operative pain management. The risk of hemodynamic instability, especially hypotension and bradycardia, from epidural clonidine may be unacceptable in these patients. However, in a rare obstetrical, post-partum or peri-operative patient, potential benefits may outweigh the possible risks.

Contraindications

4 CONTRAINDICATIONS History of a hypersensitivity reaction to clonidine. Reactions have included generalized rash, urticaria, angioedema.( 4 ) Clonidine hydrochloride extended-release tablets are contraindicated in patients with a history of a hypersensitivity reaction to clonidine. Reactions have included generalized rash, urticaria, and angioedema [see Adverse Reactions ( 6 )].

Pregnancy & Breastfeeding

8.1 Pregnancy Pregnancy Exposure Registry There is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to ADHD medications, including clonidine hydrochloride extended-release tablets, during pregnancy. Healthcare providers are encouraged to register patients by calling the National Pregnancy Registry for ADHD Medications at 1-866-961-2388 or visiting https://womensmentalhealth.org/adhd-medications/. Risk Summary Prolonged experience with clonidine in pregnant women over several decades, based on published literature, including controlled trials, a retrospective cohort study and case reports, have not identified a drug associated risk of major birth defects, miscarriage, and adverse maternal or fetal outcomes. In animal embryofetal studies, increased resorptions were seen in rats and mice administered oral clonidine hydrochloride from implantation through organogenesis at 10 and 5 times, respectively, the maximum recommended human dose (MRHD) given to adolescents on a mg/m 2 basis. No developmental effects were seen in rabbits administered oral clonidine hydrochloride during organogenesis at doses up to 3 times the MRHD (see Data) . The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriages in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively. Data Animal Data Oral administration of clonidine hydrochloride to pregnant rabbits during the period of embryo/fetal organogenesis at doses of up to 80 mcg/kg/day (approximately 3 times the oral maximum recommended daily dose [MRHD] of 0.4 mg/day given to adolescents on a mg/m 2 basis) produced no developmental effects. In pregnant rats, however, doses as low as 15 mcg/kg/day (1/3 the MRHD given to adolescents on a mg/m 2 basis) were assoc

52 interactions on record

Metoprolol may exacerbate rebound hypertension following clonidine withdrawal. Withdraw metoprolol several days before gradual clonidine withdrawal.

Source: NLP:metoprolol tartrate

Negative chronotrope. Potentiates electrophysiologic and hemodynamic effects resulting in bradycardia, sinus arrest, and AV block.

Source: NLP:amiodarone hydrochloride

Beta-blockers may exacerbate rebound hypertension following clonidine withdrawal; careful withdrawal timing required.

Source: NLP:atenolol

Beta-blockers may exacerbate rebound hypertension following clonidine withdrawal; beta-blocker should be withdrawn several days before gradual clonidine cessation.

Source: NLP:atenolol and chlorthalidone

Bisoprolol fumarate should be discontinued several days before clonidine withdrawal to avoid excessive sympathetic rebound.

Source: NLP:bisoprolol fumarate

May cause hypotension and bradycardia; beta-blocker should be discontinued first when terminating concomitant therapy.

Source: NLP:carvedilol

Concomitant use may cause hypotension and bradycardia; beta-blocker should be discontinued first when stopping both drugs.

Source: NLP:carvedilol phosphate

Sinus bradycardia resulting in hospitalization and pacemaker insertion has been reported with clonidine and diltiazem concomitantly.

Source: NLP:clonidine

Sinus bradycardia resulting in hospitalization and pacemaker insertion reported with concurrent use. Heart rate monitoring required.

Source: NLP:diltiazem hydrochloride

Beta blockers increase risk of clonidine-withdrawal rebound hypertension. If antihypertensive therapy must be interrupted, discontinue beta blocker first and gradually.

Source: NLP:esmolol hydrochloride

Increases bradycardia risk; beta-blockers may exacerbate rebound hypertension following clonidine withdrawal. Withdraw metoprolol several days before gradual clonidine withdrawal.

Source: NLP:metoprolol

Beta-blocker may exacerbate rebound hypertension following clonidine withdrawal. Withdraw metoprolol several days before gradual clonidine withdrawal, or delay metoprolol introduction for several days after stopping clonidine.

Source: NLP:metoprolol succinate

Beta-blocker may exacerbate rebound hypertension following clonidine withdrawal. Withdraw metoprolol several days before gradual clonidine withdrawal.

Source: NLP:metoprolol succinate er tablets

Beta-blocker withdrawal several days before clonidine withdrawal required to avoid exacerbating rebound hypertension; concomitant use also increases risk of bradycardia.

Source: NLP:metoprolol tartrate and hydrochlorothiazide

Discontinue nebivolol several days before gradual tapering of clonidine to avoid excessive reduction of sympathetic activity.

Source: NLP:nebivolol

May produce excessive reduction of sympathetic activity. Nebivolol must be discontinued several days before gradual tapering of clonidine.

Source: NLP:nebivolol hydrochloride

α-2 adrenergic agonist that increases the pressor effect of phenylephrine hydrochloride.

Source: NLP:phenylephrine hci

Beta-blockers may antagonize clonidine's antihypertensive effects and rebound hypertension may result if clonidine is withdrawn abruptly. Withdraw beta-blocker several days before clonidine withdrawal.

Source: NLP:propranolol hydrochloride

Concomitant use increases risk of bradycardia and rebound hypertension upon discontinuation. Withdraw sotalol several days before gradual clonidine withdrawal.

Source: NLP:sotalol hydrochloride

Sinus bradycardia resulting in hospitalization and pacemaker insertion has been reported with clonidine and verapamil concomitantly.

Source: NLP:clonidine

Sinus bradycardia resulting in hospitalization and pacemaker insertion reported. Monitor heart rate during concurrent use.

Source: NLP:verapamil hydrochloride

Clonidine may potentiate the CNS-depressive effects of alcohol.

Source: NLP:clonidine

Caution advised with simultaneous use of clonidine and other similar pharmacologic agents.

Source: NLP:apraclonidine

Clonidine may potentiate the CNS-depressive effects of barbiturates.

Source: NLP:clonidine

Monitor heart rate in patients receiving clonidine concomitantly with calcium channel blockers, which affect sinus node function or AV nodal conduction.

Source: NLP:clonidine

Monitor heart rate in patients receiving clonidine concomitantly with digitalis, which affects sinus node function or AV nodal conduction.

Source: NLP:clonidine

May lead to either potentiation or weakening of glimepiride's glucose-lowering effect. May also reduce signs of hypoglycemia.

Source: NLP:glimepiride

May lead to either potentiation or weakening of glucose-lowering effect; may mask hypoglycemia signs.

Source: NLP:glipizide

May increase or decrease the blood glucose lowering effect and blunt signs/symptoms of hypoglycemia. Increased glucose monitoring required.

Source: NLP:insulin aspart

May increase or decrease blood glucose lowering effect and blunt signs/symptoms of hypoglycemia. Increased glucose monitoring required.

Source: NLP:insulin aspart-szjj

May increase or decrease blood glucose lowering effect and blunt hypoglycemia signs/symptoms. Dosage adjustment and increased glucose monitoring may be required.

Source: NLP:insulin degludec

May increase or decrease blood glucose lowering effect and blunt signs/symptoms of hypoglycemia. Dosage adjustment and increased glucose monitoring required.

Source: NLP:insulin glargine

May increase or decrease blood glucose lowering effect and may blunt signs/symptoms of hypoglycemia. Dose adjustment and increased glucose monitoring required.

Source: NLP:insulin glulisine

May increase or decrease blood glucose effect and blunt hypoglycemia signs; increased glucose monitoring required.

Source: NLP:insulin human

May increase or decrease blood glucose lowering effect and may blunt signs/symptoms of hypoglycemia; increased glucose monitoring required.

Source: NLP:insulin lispro

May increase or decrease blood glucose lowering effect and blunt signs/symptoms of hypoglycemia. Dose adjustment and increased glucose monitoring required.

Source: NLP:insulin lispro-aabc

May transiently elevate growth hormone concentrations and impact accuracy of MACRILEN diagnostic test. Avoid concomitant use.

Source: NLP:macimorelin acetate

May blunt signs and symptoms of hypoglycemia. Increased frequency of glucose monitoring may be required.

Source: NLP:nateglinide

Concomitant use can potentiate electrophysiologic and hemodynamic effects, resulting in bradycardia, sinus arrest, and AV block.

Source: NLP:nexterone (amiodarone hci)

Oral beta-blockers may exacerbate rebound hypertension following clonidine withdrawal, though no reports with ophthalmic timolol.

Source: NLP:timolol hemihydrate

Oral beta-adrenergic blocking agents may exacerbate rebound hypertension following clonidine withdrawal, though no reports exist for ophthalmic timolol maleate.

Source: NLP:timolol maleate

Amitriptyline in combination with clonidine enhances the manifestation of corneal lesions in animal studies.

Source: NLP:clonidine