Note: This document contains side effect information about fludrocortisone. Some dosage forms listed on this page may not apply to the brand name Florinef Acetate.
Applies to fludrocortisone: oral tablets.
Side effects include:
Hypertension, edema, cardiac enlargement, CHF, potassium loss, hypokalemic alkalosis.
For Healthcare Professionals
Applies to fludrocortisone: compounding powder, oral tablet.
General
Most adverse reactions are caused by this drug's mineralocorticoid activity including retention of sodium and water, hypertension, edema, cardiac enlargement, congestive heart failure, potassium loss, and hypokalemic alkalosis.[Ref]
Cardiovascular
Frequency not reported: Hypertension, cardiac enlargement, congestive heart failure, thrombophlebitis, syncope, cardiomegaly, syncope[Ref]
Gastrointestinal
Frequency not reported: Peptic ulcer, perforation, hemorrhage, pancreatitis, abdominal distention, ulcerative esophagitis, diarrhea[Ref]
Endocrine
Frequency not reported: Cushingoid state developed, growth suppression in children, secondary adrenocortical and pituitary unresponsiveness, carbohydrate tolerance decreased, manifestation of latent diabetes mellitus, insulin requirements increased, oral hypoglycemic agent requirements increased[Ref]
Metabolic
Frequency not reported: Hyperglycemia, negative nitrogen balance, potassium loss, hypokalemic alkalosis, sodium retention, fluid retention, appetite decreased[Ref]
Immunologic
Frequency not reported: Necrotizing angiitis, anaphylactoid reaction[Ref]
Musculoskeletal
Frequency not reported: Muscle weakness, steroid myopathy, loss of muscle mass, osteoporosis, vertebral compression fractures, aseptic necrosis of femoral and humeral heads, pathologic fracture of long bones, spontaneous fractures[Ref]
Ocular
Frequency not reported: Posterior subcapsular cataract, intraocular pressure increased, glaucoma, exophthalmos[Ref]
Psychiatric
Frequency not reported: Mental disturbance, insomnia[Ref]
Dermatologic
Frequency not reported: Impaired wound healing, thin fragile skin, bruising, petechiae, ecchymoses, facial erythema, sweating increased, subcutaneous fat atrophy, purpura, striae, skin hyperpigmentation, nail hyperpigmentation, hirsutism, acneiform eruption, hives, reaction to skin tests suppressed, allergic skin rash, maculopapular rash, urticaria[Ref]
Genitourinary
Frequency not reported: Menstrual irregularity, glycosuria[Ref]
Nervous system
Frequency not reported: Convulsion, intracranial pressure increased, papilledema, vertigo, headache, seizure, epilepsy[Ref]
Other
Frequency not reported: Edema, infection aggravated, masking of infection[Ref]