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ACYCLOVIR 1 GM FTV INJECTION

 

 
 

 

GENERIC NAMES

MANUFACTURERS 

MEDICAL GROUP

MEDICAL ARTICLES

 

DRUGS IN :

 

 

FDA DRUGS

UNITED STATES

CANADA

UNITED KINGDOM

AUSTRALIA

GERMANY

FRANCE

MIDDLE EAST

KUWAIT

LEBANON

EGYPT

SYRIA

BAHRAIN

IRAN

JORDAN

SAUDI ARABIA

UNITED ARAB EMIRATES

 

 

 
 

SIZE:

1 GM FTV

 

GENERIC NAME:

ACYCLOVIR

 

MANUFACTURER:

ABBOTT LABORATORIES

 

UNIT:

 

ADMINISTRATION ROUTE:

 

FDA PREGNANCY GROUP:

C; B

 

INDICATIONS:

Herpes genitalis

Herpes labialis

Herpes simplex encephalitis

Herpes zoster

Infection, herpes simplex

Infection, varicella- zoster

Varicella

 

SIDE EFFECTS:

elevated liver function tests

fever

hallucinations

leukopenia

lymphadenopathy

peripheral edema

seizures

skin reactions, such as erythema multiforme, pruritus, rash, Stevens-Johnson syndrome, toxic epidermal necrolysis, or urticaria

visual abnormalities

Gastrointestinal disturbances

lightheadedness

Malaise

Gastrointestinal disturbances

headache

lightheadedness

Agitation

alopecia

dizziness

myalgia

paresthesia

somnolence

Phlebitis or inflammation at the injection site

Acute renal failure

Encephalopathic changes

hematologic abnormalities, such as anemia

leukocytosis, neutropenia or neutrophilia

thrombocytopenia or thrombocytosis

hematuria

urticaria

Disseminated intravascular coagulation (DIC)

hemolysis

hypotension

psychological disturbances, such as delirium

mental obtundation

psychosis

Anaphylaxis

confusion

 

ABSOLUTE CONTRAINDICATIONS :

 

RELATIVE CONTRAINDICATIONS :

>> Dehydration

>> Renal function impairment, pre-existing

Hypersensitivity to acyclovir, ganciclovir, or valacyclovir

Neurological abnormalities

Prior neurologic reactions to cytotoxic medications

 

ADULT DOSE:

Genital herpes infections, severe, initial episode-Intravenous infusion, 5 mg (base) per kg of body weight every eight hours for five days. Administer at a constant rate over at least a one-hour period. Herpes simplex (HSV-1 and HSV-2) infections, mucocutaneous, in immunocompromised patients-Intravenous infusion, 5 mg (base) per kg of body weight every eight hours for seven days. Administer at a constant rate over at least a one-hour period. Herpes simplex encephalitis -Intravenous infusion, 10 mg (base) per kg of body weight every eight hours for ten days. Administer at a constant rate over at least a one-hour period. Herpes zoster, caused by varicella zoster virus, in immunocompromised patients-Intravenous infusion, 10 mg (base) per kg of body weight every eight hours for seven days. Administer at a constant rate over at least a one-hour period. Note: Adults with acute or chronic renal impairment require a reduction in dose and/or dosing interval as follows : Creatinine clearance (mL/min)/(mL/sec) Dose (base) Dosing interval (hr) > 50/0.83 100% 8 25-50/0.42-0.83 100% 12 10-25/0.17-0.42 100% 24 0-10/0-0.17 50% 24 Hemodialysis patients require administration of an additional dose following each hemodialysis session . No additional dosing is required for peritoneal dialysis patients .

 

MAXIMUM ADULT DOSE:

30 mg (base) per kg of body weight, or 1.5 grams per square meter of body surface area, daily.

 

PEDIATRIC DOSE:

Genital herpes infections, severe, initial episode-Infants and children up to 12 years of age: Intravenous infusion, 250 mg (base) per square meter of body surface area every eight hours for five days. Administer at a constant rate over at least a one-hour period. Children 12 years of age and over: See Usual adult and adolescent dose . Herpes simplex (HSV-1 and HSV-2) infections, mucocutaneous, in immunocompromised patients-Infants and children up to 12 years of age: Intravenous infusion, 10 mg (base) per kg of body weight every eight hours for seven days. Administer at a constant rate over at least a one-hour period. Children 12 years of age and over: See Usual adult and adolescent dose . Herpes simplex infections, neonatal -Infants from birth to 3 months of age: Intravenous infusion, 10 mg (base) per kg of body weight every eight hours for ten days. Administer at a constant rate over at least a one-hour period. Note: Intravenous doses of 15 or 20 mg (base) per kg of body weight every eight hours, administered at a constant rate over at least a one-hour period, have been used; however, the safety and efficacy of these doses have not been established. Herpes simplex encephalitis -Infants 3 months and older and children up to 12 years of age: Intravenous infusion, 20 mg (base) per kg of body weight every eight hours for ten days. Administer at a constant rate over at least a one-hour period. Children 12 years of age and older: See Usual adult and adolescent dose . Herpes zoster, caused by varicella zoster virus, in immunocompromised patients-Children up to 12 years of age: Intravenous infusion, 20 mg (base) per kg of body weight every eight hours for seven days. Administer at a constant rate over at least a one-hour period. Children 12 years of age and older: See Usual adult and adolescent dose . Note: Patients with acute or chronic renal impairment require a reduction in dose and/or dosing interval as follows : Creatinine clearance (mL/min)/(mL/sec) Dose (base) Dosing interval (hr) > 50/0.83 100% 8 25-50/0.42-0.83 100% 12 10-25/0.17-0.42 100% 24 0-10/0-0.17 50% 24 Hemodialysis patients require administration of an additional dose following each hemodialysis session . No additional dosing is required for peritoneal dialysis patients . 

 

MAXIMUM PEDIATRIC DOSE:

 

ELDERLY DOSE:

 

 

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