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Sitavig Side Effects

Generic name: acyclovir

Medically reviewed by Drugs.com. Last updated on Sep 28, 2024.

Note: This document provides detailed information about Sitavig Side Effects associated with acyclovir. Some dosage forms listed on this page may not apply specifically to the brand name Sitavig.

Applies to acyclovir: capsule, powder for solution, solution, suspension, tablet.

Other dosage forms:

Serious side effects of Sitavig

Along with its needed effects, acyclovir (the active ingredient contained in Sitavig) may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.

Check with your doctor immediately if any of the following side effects occur while taking acyclovir:

More common side effects

- For acyclovir injection only
  • pain, swelling, or redness at place of injection

Less common side effects

  • abdominal or stomach pain
  • decreased frequency of urination or amount of urine
  • increased thirst
  • loss of appetite
  • nausea or vomiting
  • unusual tiredness or weakness

Rare side effects

  • black, tarry stools
  • blood in urine or stools
  • chills, fever, or sore throat
  • confusion
  • convulsions (seizures)
  • hallucinations (seeing, hearing, or feeling things that are not there)
  • hives
  • pinpoint red spots on skin
  • trembling
  • unusual bleeding or bruising

Frequency not determined

Other side effects of Sitavig

Some side effects of acyclovir may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.

Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:

More common side effects

- Especially seen with high doses
  • general feeling of discomfort or illness

Less common side effects

- Especially seen with long-term use or high doses
  • diarrhea
  • headache

Frequency not determined

For healthcare professionals

Applies to acyclovir: buccal tablet, compounding powder, intravenous powder for injection, intravenous solution, oral capsule, oral suspension, oral tablet.

General adverse events

The more commonly reported adverse reactions include malaise, nausea, vomiting, diarrhea, and headache.[Ref]

Gastrointestinal

Nausea and vomiting are more frequent in elderly subjects.[Ref]

Renal

Renal pain may be associated with renal failure and crystalluria. Renal impairment is generally reversible but may progress to acute renal failure.[Ref]

Local

Severe local inflammatory reactions, including tissue necrosis, have occurred following infusion into extravascular tissues. Application site pain and application site irritation have occurred with the buccal tablets.[Ref]

Nervous system

Dizziness, somnolence, and coma more frequent in elderly subjects.[Ref]

Dermatologic

Cardiovascular

Hematologic

Hepatic

Hypersensitivity

Ocular

Musculoskeletal

Other

Genitourinary

Metabolic

Psychiatric

Hallucinations, psychosis, confusion, aggressive behavior, agitation may be more marked in older adults and those with renal impairment.[Ref]

Respiratory

References

1. Cerner Multum, Inc. "UK Summary of Product Characteristics."

2. Cerner Multum, Inc. "Australian Product Information."

3. (2017) "Product Information. Sitavig (acyclovir)." Innocutis Holdings LLC

4. (2017) "Product Information. Acyclovir (acyclovir)." West-Ward Pharmaceuticals Corporation (previously Roxane Laboratories Inc)

5. (2017) "Product Information. Zovirax (acyclovir)." Mylan Pharmaceuticals Inc

Frequently asked questions

Further information

Sitavig side effects can vary depending on the individual. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Note: Medication side effects may be underreported. If you are experiencing side effects that are not listed, submit a report to the FDA by following this guide.