General Information
NOTE: This monograph discusses the use of acetic acid; hydrocortisone combination product for treatment of selected otic infections. Clinicians may wish to consult the individual drug monographs for more information about each specific agent.
Corticosteroid hypersensitivity
Acetic acid; hydrocortisone is contraindicated in patients with a known or suspected hypersensitivity to any of the product ingredients, such as hydrocortisone sensitivity (corticosteroid hypersensitivity). VoSoL HC also contains propylene glycol and benzethonium chloride. Discontinue use immediately if irritation or a rash develops.
Herpes infection, varicella
Acetic acid; hydrocortisone otic is listed by the manufacturer as being contraindicated in patients with herpes infection (e.g., herpes simplex or vaccinia) and varicella. It is recommended that acetic acid; hydrocortisone should not be used for longer than 10 days to avoid development of secondary infections. If the initial infection is not improved after 7—10 days of therapy, cultures are recommended to guide further treatment.
Tympanic membrane perforation
All otic medications are generally contraindicated in patients with tympanic membrane perforation (e.g., ruptured eardrum). Otic preparations, such as acetic acid; hydrocortisone, should be used sparingly to prevent accumulation of excess debris (i.e., cerumen) in the ear.
Ocular exposure, ophthalmic administration, parenteral administration
Avoid ocular exposure of acetic acid; hydrocortisone otic preparations. Acetic acid; hydrocortisone is not for ophthalmic administration or parenteral administration.
Children, infants, neonates
The safety and effectiveness of acetic acid; hydrocortisone in children below the age of 3, including infants and neonates, have not been established.
Pregnancy
Acetic acid; hydrocortisone otic solution is classified in FDA pregnancy risk category C and should be used with caution during pregnancy. Significant systemic absorption of the otic product components is not expected in normal prescription use of limited duration (i.e., 7—10 days). However, no adequate and well controlled studies have been conducted in pregnant women.
Breast-feeding
The manufacturer does not make any recommendations for the use of acetic acid; hydrocortisone otic solution during breast-feeding. Drugs, such as acetic acid, administered via the otic route generally exert a local effect and may result in minimal systemic absorption; clinically significant breast milk concentrations are not expected. Hydrocortisone is excreted into breast milk after systemic administration. Trace amounts of endogenous hydrocortisone (cortisol) are excreted in breast milk; however, no reports of exogenous hydrocortisone excretion into breast milk exist. The American Academy of Pediatrics (AAP) states that another steroid, prednisone, is usually compatible with breast-feeding. Another report states that systemic steroids used in asthma patients are compatible with breast-feeding. Consider the benefits of breast-feeding, the risk of potential infant drug exposure, and the risk of an untreated or inadequately treated condition. If a breast-feeding infant experiences an adverse effect related to a maternally administered drug, healthcare providers are encouraged to report the adverse effect to the FDA.