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Home > Drugs > Miscellaneous antifungals > Ancobon > Ancobon Side Effects
Miscellaneous antifungals

Ancobon Side Effects

Note: This document contains side effect information about flucytosine. Some dosage forms listed on this page may not apply to the brand name Ancobon.

Applies to flucytosine: oral capsule.

Warning

Oral route (Capsule)

Use with extreme caution in patients with impaired renal function. Close monitoring of hematologic, renal, and hepatic status of all patients is essential.

Serious side effects of Ancobon

Along with its needed effects, flucytosine (the active ingredient contained in Ancobon) 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 flucytosine:

Incidence not known

  • Agitation
  • black, bloody, tarry stools
  • blistering, peeling, or loosening of the skin
  • bloody or cloudy urine
  • burning, crawling, itching, numbness, prickling, "pins and needles", or tingling feelings
  • burning upper abdominal or stomach pain
  • change in consciousness
  • chest pain or tightness
  • chills
  • confusion
  • cough or hoarseness
  • dark urine
  • decreased urine output
  • depression
  • diarrhea
  • dizziness
  • dry mouth
  • feeling of constant movement of self or surroundings
  • fever
  • headache
  • hearing loss
  • hives, itching, skin rash
  • increased sensitivity of the skin to sunlight
  • irregular heartbeat
  • irritability
  • joint or muscle pain
  • light-colored stools
  • loss of appetite
  • loss of consciousness
  • lower back or side pain
  • mood changes
  • muscle cramps or twitching
  • nausea
  • no blood pressure or pulse
  • no breathing
  • numbness or tingling in the hands, feet, or lips
  • painful or difficult urination
  • pain in the lower back or side
  • pale skin
  • rapid weight gain
  • rectal bleeding
  • red irritated eyes
  • red skin lesions, often with a purple center
  • redness of the skin
  • seeing, hearing, or feeling things that are not there
  • seizures
  • sensation of spinning
  • severe sunburn
  • shakiness and unsteady walk
  • sore throat
  • sores, ulcers, or white spots on the lips or in the mouth
  • stopping of the heart
  • swelling of the face, ankles, or hands
  • swollen glands
  • thirst
  • trouble breathing
  • unpleasant breath odor
  • unsteadiness, trembling, or other problems with muscle control or coordination
  • unusual bleeding or bruising
  • unusual drowsiness, dullness, tiredness, weakness or feeling of sluggishness
  • vomiting
  • vomiting of blood or material that looks like coffee grounds
  • weakness in the arms, hands, legs, or feet
  • weight loss
  • yellow eyes or skin

For Healthcare Professionals

Applies to flucytosine: oral capsule.

Cardiovascular

Frequency not reported: Cardiac arrest, myocardial toxicity, ventricular dysfunction, cardiac toxicity with ST elevation[Ref]

Dermatologic

Frequency not reported: Rash, pruritus, urticaria, photosensitivity, Lyell's syndrome[Ref]

Gastrointestinal

Frequency not reported: Nausea, vomiting/emesis, abdominal pain, diarrhea, dry mouth, duodenal ulcer, gastrointestinal hemorrhage/bleeding, enterocolitis, ulcerative colitis[Ref]

Genitourinary

Frequency not reported: Crystalluria[Ref]

Hematologic

Frequency not reported: Anemia, agranulocytosis, aplastic anemia, eosinophilia, leukopenia, pancytopenia, thrombocytopenia, bone marrow aplasia (fatal cases), bone marrow toxicity[Ref]

Hepatic

Frequency not reported: Jaundice, hepatic dysfunction, elevated bilirubin, increased hepatic enzymes, acute hepatic injury, hepatic necrosis, hepatitis, alterations in liver function tests[Ref]

Acute hepatic injury including hepatic necrosis with possible fatal outcome in debilitated patients has been reported.

Alterations in liver function tests were generally dose related and reversible.[Ref]

Hypersensitivity

Frequency not reported: Allergic reactions, anaphylaxis[Ref]

Metabolic

Frequency not reported: Anorexia, hypoglycemia, hypokalemia

Nervous system

Frequency not reported: Ataxia, hearing loss, headache, paresthesia, parkinsonism, peripheral neuropathy, vertigo, sedation, convulsions[Ref]

Other

Frequency not reported: Pyrexia, fatigue, weakness[Ref]

Psychiatric

Frequency not reported: Confusion, hallucinations, psychosis[Ref]

Renal

Frequency not reported: Azotemia, elevated creatinine, elevated BUN, renal failure[Ref]

Respiratory

Frequency not reported: Dyspnea, chest pain, respiratory arrest[Ref]

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