Classes
DEA Class; Rx
Common Brand Names; Zovirax, Avaclyr, Zovirax topical, Sitavig
- Antivirals, Other;
- Antivirals, HSV;
- Antivirals, VZV
Description
Synthetic antiviral with activity against herpes simplex virus type 1 and 2 and varicella-zoster virus
Used to treat herpes labialis, herpes genitalis, herpes simplex encephalitis, herpes simplex keratitis, neonatal herpes infection, chickenpox (varicella), shingles (zoster)
Potent activity against herpes simplex viruses type 1 and 2 and much less activity against varicella-zoster virus
Indications
Indicated for the treatment of neonatal herpes simplex virus infection.
Contraindications
Hypersensitivity
Adverse Effects
Oral
- Malaise (≤12%)
Parenteral
- Inflammation or phlebitis at injection site (9%)
- Nausea (7%)
- Vomiting (7%)
- Rash or hives (2%)
- Elevated transaminase levels (1-2%)
Eye pain (stinging)
Punctuate keratitis
Follicular conjunctivitis
Burning/stinging (30%)
Pruritus (4%)
Dry lips (<1%)
Rash (0.3%)
Warnings
Avoid rapid infusion because of risk of renal damage
Renal failure, resulting in death, has occurred
Use with caution in immunocompromised patients (potential risk of thrombotic thrombocytopenic purpura [TTP]/hemolytic uremic syndrome [HUS])
Use with caution in patients with renal impairment
Treatment should begin within 24 hours of appearance of rash
Use with caution in patients receiving nephrotoxic drugs
Maintain adequate hydration during PO or IV therapy
Thrombocytopenic purpura/hemolytic uremic syndrome reported
Pregnancy and Lactation
Drug is minimally absorbed systemically following topical route of administration, and maternal use is not expected to result in fetal exposure to drug
Drug is minimally absorbed systemically following topical route of administration, and breastfeeding is not expected to result in exposure of child to drug
Maximum Dosage
30 mg/kg/day IV per FDA-approved product labeling; however, up to 45 mg/kg/day IV is used off-label; 4,000 mg/day PO; 50 mg/dose buccal.
30 mg/kg/day IV per FDA-approved product labeling; however, up to 45 mg/kg/day IV is used off-label; 4,000 mg/day PO; 50 mg/dose buccal.
30 mg/kg/day IV per FDA-approved product labeling; however, up to 45 mg/kg/day IV is used off-label. 80 mg/kg/day PO (Max: 3,200 mg/day) per FDA-approved product labeling; however, 4,000 mg/day has been used off-label; safety and efficacy of buccal tablet not established.
12 years: 30 mg/kg/day IV per FDA-approved product labeling; however, up to 45 mg/kg/day IV is used off-label; 80 mg/kg/day PO (Max: 3,200 mg/day) per FDA-approved product labeling; however, 4,000 mg/day has been used off-label; safety and efficacy of buccal tablet not established.
2 to 11 years: 60 mg/kg/day IV; 80 mg/kg/day PO (Max: 3,200 mg/day); safety and efficacy of buccal tablet not established.
1 year: 60 mg/kg/day IV; safety and efficacy of oral acyclovir have not been established; however, 80 mg/kg/day PO has been used off-label.
60 mg/kg/day IV; safety and efficacy of oral acyclovir have not been established; however, 80 mg/kg/day PO has been used off-label.
60 mg/kg/day IV; safety and efficacy of oral acyclovir have not been established; however, 900 mg/m2/day PO has been used off-label for suppressive therapy of neonatal herpes.
How supplied
Acyclovir sodium
injectable solution
- 50mg/mL
injection, lyophilized powder for reconstitution
- 500mg/vial
- 1000mg/vial
oral suspension
- 200mg/5mL
tablet
- 400mg
- 800mg
capsule
- 200mg
ophthalmic ointment
- 3% (3.5g tube)
topical cream
- 5%
topical ointment
- 5%
mucoadhesive buccal tablet
- 50mg (Sitavig)