Northera Blue Flamingo
Medication icon

NORTHERA offers customized dosing and a streamlined prescription process1,2

Northera Blue Flamingo
Medication icon

NORTHERA offers customized dosing and a streamlined prescription process1,2

Customize dosing and titration for each patient based on symptomatic response and tolerability to optimize treatment1,2

Northera titration over time illustration
Northera titration over time illustration
  • NORTHERA® (droxidopa) is available in 100 mg, 200 mg, and 300 mg strength capsules1
  • NORTHERA can be titrated to symptomatic response in increments of 100 mg three times a day every 24 to 48 hours, allowing for personalized dosing1
  • Monitor supine blood pressure prior to and during treatment and more frequently when increasing doses1
Morning icon Midday icon Late afternoon icon
Morning icon Midday icon Late afternoon icon
  • Patients should be advised to elevate the head of the bed when resting or sleeping1
  • If supine hypertension is not well managed, NORTHERA may increase the risk of cardiovascular events, particularly stroke1
  • Reduce or discontinue NORTHERA if supine hypertension persists1
NORTHERA capsules should be taken whole, the same way each time, either with food or without food1

For oral administration. Not actual sizes.

  • If a dose is missed, the next dose should be taken at the regularly scheduled time. The patient should not double the next dose1
  • Use of or change in dose of dopa-decarboxylase inhibitors may require dose adjustments for NORTHERA1
  • Administering NORTHERA in combination with other agents that increase blood pressure (e.g., norepinephrine, ephedrine, midodrine, and triptans) would be expected to increase the risk for supine hypertension1
  • Clinical experience with NORTHERA in patients with severe renal function impairment (GFR <30 mL/min) is limited; therefore, dosing recommendations cannot be provided for these patients1

Total daily dosing

~70% of patients received a maintenance dose of at least 1200 mg (400 mg three times a day)2

Total Daily Dosing Experience Graph
Total Daily Dosing Experience Graph
  • About 40% of patients received the maximum dose of 1800 mg (600 mg three times a day)2
  • Dose escalation was stopped if2:
    • Sustained supine SBP rose to ≥180 mm Hg or DBP to ≥110 mm Hg
    • The patient became asymptomatic, reached the maximum dose, or was unable to tolerate side effects believed to be related to the study drug
  • Fewer than 10% of patients remained at the starting dose of 300 mg (100 mg three times a day)2

NORTHERA Treatment Form

The NORTHERA Treatment Form allows for customized dosing and a streamlined prescription process1,2

Fill out the NORTHERA Treatment Form completely, either online or via downloadable PDF, and fax it in to the Northera Support Center to start the prescription process. Once the Northera Support Center receives the completed form, a representative will:
Contact your patient, provide information on starting NORTHERA, and be available to answer frequently asked questions.
Contact your patient’s insurance provider to confirm coverage and determine eligibility for patient support.
Coordinate with the specialty pharmacy to arrange for fulfillment and delivery of your patient's NORTHERA prescription.
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We want to help you stay connected. Sign up for email updates with information about nOH and NORTHERA as they become available.

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The Northera Support Center offers resources for coverage and support to eligible patients.

References:

1. NORTHERA [package insert]. Deerfield, IL: Lundbeck. 2. Data on file. Deerfield, IL: Lundbeck.

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NORTHERA CONNECT:

Please see Important Safety Information, including Boxed Warning for supine hypertension.

For more information, see the full Prescribing Information.

Indications and Usage

NORTHERA (droxidopa) is indicated for the treatment of orthostatic dizziness, lightheadedness, or the “feeling that you are about to black out” in adult patients with symptomatic neurogenic orthostatic hypotension (nOH) caused by primary autonomic failure (Parkinson’s disease [PD], multiple system atrophy, and pure autonomic failure), dopamine beta-hydroxylase deficiency, and non-diabetic autonomic neuropathy. Effectiveness beyond 2 weeks of treatment has not been established. The continued effectiveness of NORTHERA should be assessed periodically.

Important Safety Information

WARNING: SUPINE HYPERTENSION

Monitor supine blood pressure prior to and during treatment and more frequently when increasing doses. Elevating the head of the bed lessens the risk of supine hypertension, and blood pressure should be measured in this position. If supine hypertension cannot be managed by elevation of the head of the bed, reduce or discontinue NORTHERA.

CONTRAINDICATIONS

  • NORTHERA is contraindicated in patients who have a history of hypersensitivity to the drug or its ingredients.

WARNINGS AND PRECAUTIONS

  • Supine Hypertension: NORTHERA therapy may cause or exacerbate supine hypertension in patients with nOH, which may increase the risk of cardiovascular events if not well managed, particularly stroke.
  • Hyperpyrexia and Confusion: Cases of a symptom complex resembling neuroleptic malignant syndrome (NMS) have been reported with NORTHERA use during post-marketing surveillance. Observe patients carefully when the dosage of NORTHERA is changed or when concomitant levodopa is reduced abruptly or discontinued, especially if the patient is receiving neuroleptics. NMS is an uncommon but life-threatening syndrome characterized by fever or hyperthermia, muscle rigidity, involuntary movements, altered consciousness, and mental status changes. The early diagnosis of this condition is important for the appropriate management of these patients.
  • Ischemic Heart Disease, Arrhythmias, and Congestive Heart Failure: NORTHERA therapy may exacerbate existing ischemic heart disease, arrhythmias, and congestive heart failure. Careful consideration should be given to this potential risk prior to initiating therapy.
  • Allergic Reactions: Hypersensitivity reactions, including anaphylaxis, angioedema, bronchospasm, urticaria, and rash have been reported in post-marketing experience, with some resulting in emergency treatment. If a hypersensitivity reaction occurs, discontinue the drug and initiate appropriate therapy.
  • This product contains FD&C Yellow No. 5 (tartrazine), which may also cause allergic-type reactions (including bronchial asthma) in certain susceptible persons. Although the overall incidence of FD&C Yellow No. 5 (tartrazine) sensitivity in the general population is low, it is frequently seen in patients who also have aspirin hypersensitivity.

ADVERSE REACTIONS

  • The most common adverse reactions (>5% and ≥3% difference compared to placebo) were headache, dizziness, nausea, and hypertension.

DRUG INTERACTIONS

  • Administering NORTHERA in combination with other agents that increase blood pressure (e.g., norepinephrine, ephedrine, midodrine, and triptans) would be expected to increase the risk for supine hypertension.
  • Dopa-decarboxylase inhibitors may require dose adjustments for NORTHERA.
  • The concomitant use of selective MAO-B inhibitors, such as rasagiline or selegiline, was permitted in the NORTHERA clinical trials. However, based on mechanism of action, the use of non-selective MAO inhibitors and linezolid should be avoided as there is a potential for increased blood pressure when taken with NORTHERA.

USE IN SPECIFIC POPULATIONS

  • There are no available data on use of NORTHERA in pregnant women and risk of major birth defects or miscarriage. Because of the potential for serious adverse reactions, including reduced weight gain in breastfed infants, advise a woman not to breastfeed during treatment with NORTHERA.
  • The safety and effectiveness of NORTHERA in pediatric patients have not been established. No overall differences in safety or effectiveness were observed between patients aged 75 years and older and younger patients in clinical trials, but greater sensitivity of some older individuals cannot be ruled out.
  • Clinical experience with NORTHERA in patients with severe renal function impairment (GFR <30 mL/min) is limited; therefore, dosing recommendations cannot be provided for these patients.

For more information, please see the full Prescribing Information, including Boxed Warning for supine hypertension.