TABLE 1.
Characteristics of Medications Tried for OH
| Medication | Mechanism of Action | Dose Range | Contraindications | Side Effects |
| Atomoxetine | A selective norepinephrine reuptake inhibitor, increasing norepinephrine available in the synapse | 18 mg used in trials (OD) Not licensed for OH in United Kingdom |
Phaeochromocytoma; severe cardiovascular disease; and severe cerebrovascular disease | Anxiety: appetite decreased; asthenia; chills (in adults); constipation; depression; dizziness; drowsiness; gastrointestinal discomfort; headaches; hyperhidrosis; menstrual cycle irregularities; altered mood); nausea); prostatitis; sexual dysfunction; thirst; vomiting; and weight loss |
| Caffeine | Wide ranging and poorly understood mechanism—thought to stimulate catecholamine release causing vasoconstriction (when used irregularly) | 100 mg used (OD) | No absolute CI, caution advised with history of severe anxiety; cardiovascular disease or symptomatic arrhythmias; peptic ulcer disease or gastroesophageal reflux disease | Restlessness and shakiness, insomnia, headaches, dizziness, tachycardia, dehydration, and anxiety |
| Droxidopa (L-DOPS) | A norepinephrine precursor, which is metabolised in the brain, allowing the norepinephrine to act on α-adrenergic receptors causing vasoconstriction and on beta-adrenergic receptors to stimulate heart contraction and dilate arteries | 100–600 mg (TDS) Not available in United Kingdom |
Neuroleptic malignant syndrome, supine hypertension, coronary artery disease, arrhythmia, chronic heart failure | Nausea, headache, increased blood pressure, hallucination, and anorexia |
| Ergometrine | An ergot alkaloid, which causes arterial vasoconstriction by stimulation of α-adrenergic and serotonin receptors as well as inhibiting the release of endothelial-derived relaxation factor | 1 mg used in trials (OD) Licensed for 250–500 μg in postpartum haemorrhage |
Eclampsia; first stage of labor; induction of labor; s stage of labor; sepsis; severe cardiac disease; severe hypertension; vascular disease | Abdominal pain; arrhythmias; chest pain; coronary vasospasm; dizziness; dyspnoea; headache; hypertension; myocardial infarction; nausea; palpitations; pulmonary edema; rash; tinnitus; vasoconstriction; and vomiting |
| Midodrine | A prodrug that is converted into desglymidodrine, which works on α1-adrenergic receptors to increase vascular tone | 2.5–10 mg TDS | Aortic aneurysm; blood vessel spasm; bradycardia; cardiac conduction disturbances; cerebrovascular occlusion; congestive heart failure; hypertension; hyperthyroidism; myocardial infarction; narrow-angle glaucoma; proliferative diabetic retinopathy; serious prostate disorder; urinary retention | Chills; flushing; gastrointestinal discomfort; headache; nausea; paraesthesia; piloerection; scalp pruritus; supine hypertension (dose-dependent); and urinary disorders |
| Pyridostigmine | An anticholinesterase that reduces the breakdown of acetylcholine in the synaptic cleft | 60 mg used in trials (30 mg BD/60 mg OD) 30–120 mg licensed for multiple sclerosis |
Intestinal obstruction; urinary obstruction | Abdominal cramps; diarrhoea; excessive tearing; hypersalivation; nausea; and vomiting |
| Yohimbine | Presynaptic α2-adrenergic receptor antagonist, which may lead to increased norepinephrine release | 2–5.4 mg (TDS) used in clinical trials | Pregnancy, hypersensitivity, children, and panic disorder | Anxiety; irritability; headache; sweating; nausea; tachycardia; priapism; worsening of panic attacks; vomiting; dizziness; nervousness; restlessness; reduced urination; hypertension; tremors; and skin flushing |