Dosing & Uses
AdultPediatric
Dosage Forms & Strengths
hydrocortisone/acetic acid/propylene glycol diacetate
otic solution
- 1%/ 2%/ 3%
Otitis Externa
Instill 3-5 gtt into affected ear 4-6 times/day
Dosage Forms & Strengths
hydrocortisone/acetic acid otic/propylene glycol diacetate
otic solution
- 1%/ 2%// 3%
Otitis Externa
<3 years
- Safety and efficacy not established
>3 years
- Instill 3-5 gtt into affected ear 4-6 times/day
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Interactions
Interaction Checker
and hydrocortisone/acetic acid otic
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No Interactions Found
Interactions Found
Contraindicated
Serious - Use Alternative
Significant - Monitor Closely
Minor
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Warnings
Contraindications
Hypersensitivity to drugs or components of the formulation; herpes simplex, varicella, vaccinia, perforated lymphatic membrane
Cautions
Use with extreme caution in patients < 3 years old; safety and efficacy not established
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Pregnancy & Lactation
Pregnancy category: C
Lactation: Low amounts excreted into breast milk; use with caution
Pregnancy Categories
A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.
B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk. C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done. D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk. X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist. NA: Information not available.Previous
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Pharmacology
Mechanism of Action
Hydrocortisone elicits anti-inflammatory & antipruritic effects
Acetic acid is used as an antibacterial/antifungal agent
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Images
| BRAND | FORM. | UNIT PRICE | PILL IMAGE |
|---|---|---|---|
| hydrocortisone-acetic acid otic (ear) - | 1-2 % drops |  | |
| hydrocortisone-acetic acid otic (ear) - | 1-2 % drops |  |
Copyright © 2010 First DataBank, Inc.
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Medscape prescription drug monographs are based on FDA-approved labeling information, unless otherwise noted, combined with additional data derived from primary medical literature.
