Fenoldopam (Corlopam) - Uses, Dose, Side effects, MOA

Fenoldopam (Corlopam) is a dopamine (D-1 receptor) agonist with minimal adrenergic effects. It is a rapidly acting vasodilator and is used in situations where a rapid decrease in the blood pressure is required such as hypertensive urgency and emergency.

Fenoldopam Uses:

  • Severe hypertension:

    • It is indicated for the short-term treatment of uncontrolled hypertension (up to 48 hours while the patient is in the hospital).
    • It is also used to treat patients with malignant hypertension, in patients with deteriorating end-organ dysfunction secondary to uncontrolled hypertension, and for the reduction of blood pressure in children.

Fenoldopam (Corlopam) Dose in Adults

Fenoldopam (Corlopam) Dose in the treatment of Severe hypertension:

  • It is administered intravenously at a dose of 0.01 - 0.3 mcg/kg/minute initially.
  • The dose may be increased in increments of 0.05 - 0.1 mcg/kg/minute every 15 minutes until the target blood pressure is achieved.
  • The maximum rate of infusion has been reported in clinical studies as 1.6 mcg/kg/minute.
  • The drug is usually administered for a period of 48 hours while the patient is in the hospital.

Note: Patients may continue oral antihypertensive medications while on treatment or after the infusion.

Fenoldopam (Corlopam) Dose in Childrens

Fenoldopam (Corlopam) Dose in the treatment of Severe hypertension:

  • Infants, Children, and Adolescents: IV:

    • Continuous IV infusion:
      • initially, 0.2 mcg/kg/minute as a continuous intravenous infusion.
      • The dose may be increased at a rate of 0.3 to 0.5 mcg/kg/minute every 20 - 30 minutes.
      • The maximum dose is 0.8 mcg/kg/minute.
      • Higher doses may not have additional blood pressure lowering effects and may worsen tachycardia.

Pregnancy Risk Factor B

  • Only use it during pregnancy if clearly indicated.
  • However, it has not yet been investigated in human pregnancies. Animal reproduction studies have not shown any evidence of fetal harm.

Fenoldopam use during breastfeeding:

  • The data on the presence of the drug is not available.
  • The manufacturer suggests that breastfeeding be stopped because of the possibility of serious side effects in infants breastfeeding with the drug.
  • This is in line with the mother's rights and the risks to the infant from drug exposure.

Dose in Kidney Disease:

  • The manufacturer has not recommended any dosage adjustment in the dose.
  • The effects of hemodialysis on the drug have not been evaluated.

Dose in Liver disease:

The manufacturer has not recommended any dosage adjustment in the dose.

Side Effects of Fenoldopam (Corlopam):

  • Cardiovascular:

    • Flushing
    • Hypotension
  • Central nervous system:

    • Headache
  • Gastrointestinal:

    • Nausea

Less Common Side Effects of Fenoldopam (Corlopam):

  • Cardiovascular:

    • Angina Pectoris
    • Bradycardia
    • Cardiac Failure
    • Chest Pain
    • ECG Abnormality (ST-T Abnormalities)
    • Extrasystoles
    • Inversion T Wave On ECG
    • Myocardial Infarction
    • Orthostatic Hypotension
    • Palpitations
    • Tachycardia
  • Central Nervous System:

    • Anxiety
    • Dizziness
    • Insomnia
  • Dermatologic:

    • Diaphoresis
  • Endocrine & Metabolic:

    • Hyperglycemia
    • Hypokalemia
    • Increased Lactate Dehydrogenase
  • Gastrointestinal:

    • Abdominal Distention
    • Abdominal Pain
    • Constipation
    • Diarrhea
    • Vomiting
  • Genitourinary:

    • Oliguria
    • Urinary Tract Infection
  • Hematologic & Oncologic:

    • Hemorrhage
    • Leukocytosis
  • Hepatic:

    • Increased Serum Transaminases
  • Local:

    • Injection Site Reaction
  • Neuromuscular & Skeletal:

    • Back Pain
    • Muscle Cramps (Limbs)
  • Ophthalmic:

    • Increased Intraocular Pressure
  • Renal:

    • Increased Blood Urea Nitrogen
    • Increased Serum Creatinine
  • Respiratory:

    • Dyspnea
    • Nasal Congestion
  • Miscellaneous:

    • Fever

Contraindications to Fenoldopam (Corlopam):

The manufacturer's labeling does not contain any contraindications.

Warnings and precautions

  • Hypokalemia

    • Hypokalemia may occur in patients who receive the infusion within six hours.
    • It is important to monitor potassium levels.
  • Tachycardia

    • Tachycardia is possible, particularly if the rate of infusion exceeds 0.01 mcg/kg/minute for adults and 0.8 mg/kg/minute for children.
    • Reflex tachycardia is less likely when the infusion rate is lower than 0.1 mg/kg/minute, and the drug is titrated slower.
  • Angina

    • Tachycardia may occur due to an increase in myocardial oxygen requirement.
    • Patients with obstructive or persistent coronary artery disease should not use it.
  • Glaucoma:

    • Patients with intraocular hypertension and glaucoma may experience an increase in intraocular pressure that is dose-dependent.
    • The intraocular pressure will return to baseline in two hours if the rate of infusion decreases.

Fenoldopam: Drug Interaction

Note: Drug Interaction Categories:

  • Risk Factor C: Monitor When Using Combination
  • Risk Factor D: Consider Treatment Modification
  • Risk Factor X: Avoid Concomitant Use

Risk Factor C (Monitor therapy)

Alfuzosin May enhance the hypotensive effect of Blood Pressure Lowering Agents.
Amphetamines May diminish the antihypertensive effect of Antihypertensive Agents.
Antipsychotic Agents (Second Generation [Atypical]) Blood Pressure Lowering Agents may enhance the hypotensive effect of Antipsychotic Agents (Second Generation [Atypical]).
Barbiturates May enhance the hypotensive effect of Blood Pressure Lowering Agents.
Benperidol May enhance the hypotensive effect of Blood Pressure Lowering Agents.
Brigatinib May diminish the antihypertensive effect of Antihypertensive Agents. Brigatinib may enhance the bradycardic effect of Antihypertensive Agents.
Brimonidine (Topical) May enhance the hypotensive effect of Blood Pressure Lowering Agents.
Dexmethylphenidate May diminish the therapeutic effect of Antihypertensive Agents.
Diazoxide May enhance the hypotensive effect of Blood Pressure Lowering Agents.
DULoxetine Blood Pressure Lowering Agents may enhance the hypotensive effect of DULoxetine.
Herbs (Hypertensive Properties) May diminish the antihypertensive effect of Antihypertensive Agents.
Herbs (Hypotensive Properties) May enhance the hypotensive effect of Blood Pressure Lowering Agents.
Hypotension-Associated Agents Blood Pressure Lowering Agents may enhance the hypotensive effect of Hypotension-Associated Agents.
Levodopa-Containing Products Blood Pressure Lowering Agents may enhance the hypotensive effect of Levodopa-Containing Products.
Lormetazepam May enhance the hypotensive effect of Blood Pressure Lowering Agents.
Methylphenidate May diminish the antihypertensive effect of Antihypertensive Agents.
Molsidomine May enhance the hypotensive effect of Blood Pressure Lowering Agents.
Naftopidil May enhance the hypotensive effect of Blood Pressure Lowering Agents.
Nicergoline May enhance the hypotensive effect of Blood Pressure Lowering Agents.
Nicorandil May enhance the hypotensive effect of Blood Pressure Lowering Agents.
Nitroprusside Blood Pressure Lowering Agents may enhance the hypotensive effect of Nitroprusside.
Pentoxifylline May enhance the hypotensive effect of Blood Pressure Lowering Agents.
Pholcodine Blood Pressure Lowering Agents may enhance the hypotensive effect of Pholcodine.
Phosphodiesterase 5 Inhibitors May enhance the hypotensive effect of Blood Pressure Lowering Agents.
Prostacyclin Analogues May enhance the hypotensive effect of Blood Pressure Lowering Agents.
Quinagolide May enhance the hypotensive effect of Blood Pressure Lowering Agents.
Yohimbine May diminish the antihypertensive effect of Antihypertensive Agents.

Risk Factor D (Consider therapy modification)

Amifostine Blood Pressure Lowering Agents may enhance the hypotensive effect of Amifostine. Management: When amifostine is used at chemotherapy doses, blood pressure lowering medications should be withheld for 24 hours prior to amifostine administration. If blood pressure lowering therapy cannot be withheld, amifostine should not be administered.
Obinutuzumab May enhance the hypotensive effect of Blood Pressure Lowering Agents. Management: Consider temporarily withholding blood pressure lowering medications beginning 12 hours prior to obinutuzumab infusion and continuing until 1 hour after the end of the infusion.

Risk Factor X (Avoid combination)

Bromperidol May diminish the hypotensive effect of Blood Pressure Lowering Agents. Blood Pressure Lowering Agents may enhance the hypotensive effect of Bromperidol.

Monitoring parameters:

  • Blood pressure,
  • heart rate,
  • ECG
  • serum potassium concentrations

How to administer Fenoldopam (Corlopam)?

It is administered as a continuous intravenous infusion.

Fenoldopam Mechanism of action:

It is a selective postsynaptic dopamine agonist (D-1-receptors). It exerts rapid hypotensive effects by:

  • decreasing peripheral vascular resistance and increased renal blood flow,
  • diuresis, and
  • natriuresis;

It is six times more potent than dopamine in producing renal vascular dilation and has minimal adrenergic effects.

The onset of action when administered intravenously:

  • Children: 5 minutes;
  • Adults: 10 minutes;
  • Note: Most of the effects of the drug can be seen within 15 minutes.

Duration of action: IV:

  • 1 hour

Half-life elimination: IV:

  • Children: 3 to 5 minutes;
  • Adults:  about 5 minutes

Metabolism:

  • It is metabolized in the liver via methylation, glucuronidation, and sulfation;
  • the 8-sulfate metabolite may have some activity;
  • It has an extensive first-pass effect

Excretion:

  • Urine (90%);
  • feces (10%)

International Brand Names of Fenoldopam:

  • Corlopam

Fenoldopam Brand Names in Pakistan:

No Brands Available in Pakistan.

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