→Appendix 1: hydralazine
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▶Common or very common Angina pectoris. diarrhoea.
dizziness. flushing. gastrointestinal disorders. headache.
hypotension. joint disorders. lupus-like syndrome (after
long-term therapy with over 100 mg daily (or less in
women and in slow acetylator individuals)). myalgia.
nasal congestion. nausea. palpitations. tachycardia.
vomiting
▶Rare or very rare Acute kidney injury. agranulocytosis.
anaemia. anxiety. appetite decreased. conjunctivitis.
depression. dyspnoea. eosinophilia. eye disorders. fever.
glomerulonephritis. haematuria. haemolytic anaemia.
hallucination. heart failure. hepatic disorders.
leucocytosis. leucopenia. lymphadenopathy. malaise.
nerve disorders. neutropenia. oedema. pancytopenia.
paradoxical pressor response. paraesthesia. pleuritic pain
. proteinuria. skin reactions. splenomegaly.
thrombocytopenia. urinary retention. vasculitis. weight
decreased
SIDE-EFFECTS, FURTHER INFORMATION The incidence of
side-effects is lower if the dose is kept below 100mg daily,
but systemic lupus erythematosus should be suspected if
there is unexplained weight loss, arthritis, or any other
unexplained ill health.
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Neonatal thrombocytopenia reported, but
risk should be balanced against risk of uncontrolled
maternal hypertension. Manufacturer advises avoid before
third trimester.
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Present in milk but not known to be
harmful.
Monitoring Monitor infant in breast-feeding.
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Manufacturer advises caution (risk
of accumulation).
Dose adjustments Manufacturer advises adjust dose or
dosing interval according to clinical response.
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Dose adjustments Reduce dose if eGFR less than
30 mL/minute/1.73 m2.
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Manufacturer advises test
for antinuclear factor and for proteinuria every 6 months
and check acetylator status before increasing dose above
100 mg daily, but evidence of clinical value unsatisfactory.
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