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What You Should Know About Northera (Droxidopa)

Droxidopa (Northera)

Droxidopa is a generic form of the brand-name drug called Northera. This prescription medication was first approved by the FDA in 2014 for treating the symptoms of neurogenic orthostatic hypotension (NOH), which involves fainting, dizziness, or lightheadedness when standing after sitting or lying down. Droxidopa is a type of prodrug (a drug that is converted into an active form once it reaches its target area) and belongs to the class of alpha and beta-adrenergic agonists. 

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This medication is indicated to regulate standing blood pressure by temporarily increasing the level of norepinephrine in your body. Norepinephrine, also known as noradrenaline, is a type of neurotransmitter (brain chemical) that is needed to regulate blood pressure. 

Droxidopa is available in oral capsule form and can only be obtained via a doctor’s prescription. 

What Is Droxidopa Used To Treat?

Droxidopa is used to treat symptomatic neurogenic orthostatic hypotension a chronic and potentially debilitating condition characterized by a sustained drop of blood pressure upon standing due to low production or release of norepinephrine. This condition may arise as a result of autonomic failure and mainly occurs in patients suffering from certain neurologic disorders such as pure autonomic failure (PAF), multiple system atrophy (MSA), and Parkinson’s disease (PD).

These neurologic disorders mainly affect the patient’s autonomic nervous system (typically involved in regulating various involuntary functions such as heart rate, breathing, and blood pressure), which leads to inadequate release of norepinephrine. The dysregulation in norepinephrine release results in low blood pressure in neurogenic OH patients whenever they stand. 

Due to a drop in blood pressure, neurogenic OH patients experience severe dizziness, lightheadedness, syncope, blurred vision, faintness (feeling of passing out), and loss of consciousness. 

Between 80,000 150,000 people are thought to suffer from the symptoms of neurogenic OH in the United States. 

How Does Droxidopa Work?

Droxidopa works to improve the symptoms of NOH by increasing the norepinephrine level in the body. Norepinephrine, upon release, normalizes the blood pressure by constricting (narrowing) the peripheral blood vessels. 

Mechanism of Action

Once inside the body, droxidopa prodrug is converted into norepinephrine by an enzyme called dopa-decarboxylase. Norepinephrine then exhibits its pharmacological action throughout the body and increases blood flow to the brain, which prevents the symptoms of NOH.

Dosage Form and Strengths

Droxidopa is available in capsule form with strengths of 100 mg, 200 mg, and 300 mg. 

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Droxidopa Dosage

Dosing Information

The recommended initial (starting) dose is 100 mg 3 times a day during waking hours (in the morning, at midday, and in the late afternoon at least 3 hours before bedtime). The dose of droxidopa is titrated (adjusted) according to symptomatic response (where the patient’s symptoms respond to the drug). 

Depending on the symptomatic response, the droxidopa dose can be increased by increments of 100 mg 3 times a day, up to a maximum dose of 600 mg three times a day. The maximum recommended total daily dose of droxidopa is 1,800 mg. Dose titration and adjustment must be done by the treating doctor.

The dose of droxidopa could vary from patient to patient and is done in a very stringent fashion to improve neurogenic OH symptoms and avoid an excessive increase in blood pressure. 

What To Do if You Miss a Dose 

Take your dose consistently as prescribed by your doctor. In case of a missed dose, avoid taking a double dose of droxidopa to compensate for the missed dose.

If you accidentally took your dose less than 3 hours before bedtime, consult your healthcare provider immediately to reduce the risk of supine hypertension

How Is Droxidopa Used?

Droxidopa capsules are taken orally (by mouth). Since the elimination half-life of this medication is 2 to 3 hours, it is prescribed to be taken three times a day to maintain a consistent effect.

Droxidopa capsules should be taken consistently with or consistently without food upon waking up in the morning, at midday, and in the late afternoon at least 3 hours prior to bedtime. The capsules should be swallowed whole without opening, crushing, chewing, or breaking them.

Possible Side Effects of Droxidopa

Nurse checking blood pressure of droxidopa patient

Some common side effects reported by patients taking droxidopa include but are not limited to:

  • Nausea
  • Dizziness
  • Headache
  • Hypertension (increased blood pressure)

These symptoms are temporary and can be managed easily. However, if the symptoms persist and do not go away within two weeks during therapy, you should report to your healthcare provider immediately. 

Moreover, some side effects can be severe and require immediate medical attention, such as:

Supine Hypertension

Droxidopa can cause or worsen supine hypertension in NOH patients. Supine hypertension is a condition in which a patient’s blood pressure rises when they lie flat on their back. Supine hypertension increases the risk of stroke if not appropriately managed.  

Doctors recommend that patients should check their blood pressure before going to bed, and while resting or sleeping, they should elevate the head of the bed to avoid the risk of supine hypertension. Blood pressure should also be monitored whenever changing the dose. 

Arrhythmias, Congestive Heart Failure, and Ischemic Heart Disease

Droxidopa therapy may exacerbate existing arrhythmias, congestive heart failure, and ischemic heart disease. It is recommended to discuss your health status with your doctor before initiating droxidopa. 

Severe Allergic Reaction

Droxidopa contains tartrazine (a lemon yellow azo dye used in food coloring and medication), which may cause a severe allergic reaction (including bronchial asthma) in some patients with NOH. 

Hyperpyrexia and Confusion

Hyperpyrexia (a condition where the body temperature goes above 106.7 degrees Fahrenheit) and confusion symptoms are also reported in patients receiving droxidopa therapy during post-marketing surveillance. 

Therefore, it is recommended to carefully observe the patients when the dosage is changed. 

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Droxidopa Interaction With Other Drugs

There is a high possibility that other drugs may interact with droxidopa and increase the risk of supine hypertension in patients with NOH. Some of the medications that need to be avoided or adjusted include:

Before taking droxidopa, consult your healthcare provider if you take the medications mentioned above. You should always inform your doctor and pharmacist about all the medications you’re currently taking before starting any new medications.


It is recommended to consult your doctor before taking droxidopa. You should not take droxidopa in the following cases:

  • You have a history of asthma, irregular heartbeat, heart failure, and kidney disease.  
  • You are pregnant or planning to become pregnant.
  • You are breastfeeding a child or plan to breastfeed.
  • You are less than 18 years old.

US Boxed 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 droxidopa.


  1. Kaufmann, H., Norcliffe-Kaufmann, L., & Palma, J. A. (2015). Droxidopa in neurogenic orthostatic hypotension. Expert review of cardiovascular therapy13(8), 875-891.
  2. Kaufmann, H., Freeman, R., Biaggioni, I., Low, P., Pedder, S., Hewitt, L. A., … & Mathias, C. J. (2014). Droxidopa for neurogenic orthostatic hypotension: a randomized, placebo-controlled, phase 3 trial. Neurology83(4), 328-335.
  3. US. Food and Drug Administration. Droxidopa prescribing information
This information is not a substitute for medical advice or treatment. Talk to your doctor or healthcare provider about your medical condition prior to starting any new treatment. AmeriPharma™ Specialty Care assumes no liability whatsoever for the information provided or for any diagnosis or treatment made as a result, nor is it responsible for the reliability of the content. AmeriPharma™ Specialty Care does not operate all the websites/organizations listed here, nor is it responsible for the availability or reliability of their content. These listings do not imply or constitute an endorsement, sponsorship, or recommendation by AmeriPharma™ Specialty Care. This webpage may contain references to brand-name prescription drugs that are trademarks or registered trademarks of pharmaceutical manufacturers not affiliated with AmeriPharma™ Specialty Care.

Rafik Boctor, RPh was born and raised in Cairo, Egypt. He received his degree from the Faculty of Pharmacy, Helwan University in 2011. The most rewarding part of his job is making positive changes in patients' health and well-being on a daily basis. His areas of expertise include immunoglobulins, chemotherapy and biologics. In his free time, he enjoys playing guitar, singing, and Latin dancing.

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