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Droxidopa

NORTHERA

What it isNorepinephrine prodrug; neurogenic orthostatic hypotension.

Why this oneUnlike midodrine, it crosses the blood-brain barrier and replaces norepinephrine rather than directly constricting vessels.

What limits itSupine hypertension — the last dose must be at least three hours before lying down. Benefit may wane over months.

FDA-approved for

FDA label

BOXED WARNING Supine hypertension — monitor supine blood pressure before and during treatment; elevate head of bed; reduce or discontinue if uncontrolled.
FDA dosingPopulationStartTargetMax
Neurogenic orthostatic hypotensionAdults100 mg TIDTitrate to symptomatic response600 mg TID (1,800 mg/day)

Titration Titrate in 100 mg TID increments every 24 to 48 hours

Renal GFR <30 mL/min: dosing recommendations cannot be provided

Hepatic Undefined

Instructions

Cautions

Adverse reactions

Pregnancy No human data; animal studies showed reduced live fetuses/embryofetal deaths.

Lactation Breastfeeding not recommended.

⚠ BOXED WARNING

Cost, est. cash$10–$300/month

Generic entry2021

Classes and tags

Clinical profile

Therapeutic safety burden1 / 4
Overdose danger1 / 4
Weight-gain liability0 / 4
Sedation liability0 / 4
QT / Torsades0 / 4
Direct muscarinic antagonism0 / 4
Embryofetal risk1 / 4

Legacy pregnancy categoryUnknown / historical label unavailable

Defining liabilityGenerally tolerated at therapeutic doses; clinically important risks are agent-specific and increase with interactions or organ impairment.

Active metabolites

Mechanism of action: Droxidopa ballicule

Droxidopa ballicule: receptor binding, kinetics and half-life diagram

Open Droxidopa in the interactive console ↗

Memory aids: mascots and interaction avatars

Droxidopa NORTHERA mascot mnemonic cartoon
“Northern Drox”
drox = dog/fox hybrid
general color scheme of the norepinephrine ballicule → metabolized to NE

Open Droxidopa in the interactive console ↗