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Nat-Valganciclovir: Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx) Current status: Cancelled Pre Market
Strength:
450 mg

Patient Medication Information: uses, side effects, how to take - Nat-Valganciclovir

ABOUT THIS MEDICATION

What the medication is used for:

  • NAT-VALGANCICLOVIR is a prescription medication that belongs to the family of drugs known as “antivirals”.
  • NAT-VALGANCICLOVIR is used to treat cytomegalovirus (CMV) retinitis in adults who have acquired immunodeficiency syndrome (AIDS).
  • NAT-VALGANCICLOVIR is also used to prevent cytomegalovirus (CMV) disease in adults who have received a solid organ transplant and are at risk of developing CMV disease.

What it does:

  • NAT-VALGANCICLOVIR works by slowing the growth of CMV virus, the virus that causes CMV retinitis as well as infection at other sites in the body. For most people with CMV retinitis, NAT-VALGANCICLOVIR prevents CMV from progressing (spreading) into healthy cells as quickly as it would without treatment, thereby protecting eyesight from damage due to CMV disease.
  • NAT-VALGANCICLOVIR does not

    • cure CMV retinitis, and some people may experience progression of retinitis during or following treatment with NAT-VALGANCICLOVIR. Therefore, you must follow your doctor’s advice and have your eyes checked regularly.
    • For most patients who have received a solid organ transplant, NAT-VALGANCICLOVIR prevents the occurrence of CMV disease up to 6 months after the transplant.
    • NAT-VALGANCICLOVIR is a prodrug of ganciclovir. This means it is changed to ganciclovir once it is absorbed into the body. Ganciclovir is the active part of the drug that actually slows the growth of CMV virus.

When it should not be used:

Do not take NAT-VALGANCICLOVIR if you have ever had a serious reaction to valganciclovir, ganciclovir (as valganciclovir hydrochloride tablets or ganciclovir capsules or ganciclovir sodium for injection).

Do not take if you have had sensitivity reactions with acyclovir or its pro-drug valacyclovir as a similar reaction can occur with NAT-VALGANCICLOVIR.

Do not take NAT-VALGANCICLOVIR if you have any reaction to any of the non-medicinal ingredients (see “What the non-medicial ingredients are”).

What the medicinal ingredient is:

valganciclovir hydrochloride

What the non-medicinal ingredients are:

NAT-VALGANCICLOVIR tablets contain the following non-medicinal ingredients: crospovidone, microcrystalline cellulose PH101 and PH102, povidone K-29/32, and stearic acid 50. The film-coat applied to the tablets contains hypromellose 2910, polyethylene glycol, titanium dioxide, and FD&C red #40/allura red AC aluminum lake.

What dosage forms it comes in:

NAT-VALGANCICLOVIR is available as a pink 450 mg valganciclovir film-coated tablet (as valganciclovir hydrochloride).

WARNINGS AND PRECAUTIONS

Serious Warnings and Precautions

  • Serious blood problems can occur such as low

numbers of white blood cells, red blood cells or

platelets. (See Side Effects and What to Do About Them)

  • Tumours have been found in laboratory animals

receiving this drug, although at this time there is no similar information from human studies. The drug also has damaging effects on the reproductive system. When used in men, it may decrease the number of sperm in the semen and this may be complete and irreversible. In women, not only may there be suppression of fertility, but pregnancy during treatment is likely to lead to the birth of a malformed child.

BEFORE you use NAT-VALGANCICLOVIR talk to your doctor or pharmacist if:

  • you have ever had a bad reaction to NAT-VALGANCICLOVIR (valganciclovir hydrochloride) or any of the inactive ingredients shown above.
  • you have ever had a bad reaction to ganciclovir, acyclovir or valacyclovir.
  • you are allergic to other medicines, food and dyes.
  • you are taking ANY other medicines (prescription or nonprescription) including herbal or natural products.
  • you have any other illnesses/diseases, including a history of liver or kidney disease.
  • you are receiving hemodialysis as dosage adjustment is required.
  • you have blood problems or have abnormal results on your blood tests.
  • you are breast-feeding or planning to breast feed. You should not take NAT-VALGANCICLOVIR while

    • breastfeeding. Women who are HIV positive should not breast feed because HIV infection can be passed to the baby via the breast milk.

Pregnancy:

Tell your doctor if you are pregnant or planning to become pregnant.

NAT-VALGANCICLOVIR may cause birth defects in humans and should not be used during pregnancy.

If you are a woman of child-bearing potential then you should:

  • avoid pregnancy
  • use effective contraception during treatment and for 30 days after stopping treatment
  • effective contraception includes:
  • a barrier method (e.g. condom) and
  • an additional method (e.g. birth control pills, intrauterine device)

If you are a male taking NAT-VALGANCICLOVIR, whose partner is female, then you should:

  • use a barrier method (e.g. condom) during treatment and for 90 days female partner is not at risk of pregnancy.

This information will help your doctor and you decide whether you should use NAT-VALGANCICLOVIR and what extra care may need to be taken while you are on the medication. You should always consult your doctor or pharmacist before using other medications while on NAT-VALGANCICLOVIR.

INTERACTIONS WITH THIS MEDICATION

Tell your doctor or pharmacist about all medications that you are taking, including those you buy over the counter and herbal or natural products. NAT-VALGANCICLOVIR may change the effect of other medications.

Tell your doctor if you are taking any of the following drugs:

  • that reduce your immunity such as cyclosporine, tacrolimus, mycophenolate mofetil
  • that act against tumours such as vincristine, vinblastine, doxorubicin, hydroxyurea
  • that fight infections such as trimethoprim/sulphonamides, dapsone, amphotericin B, flucytosine, pentamidine
  • pegylated interferons with ribavirin

The following drugs may need to have their dose changed when taken with NAT-VALGANCICLOVIR:

  • Videx® (didanosine, ddI)
  • Retrovir® (zidovudine, ZDV, AZT)
  • Benuryl™ (probenecid)

Imipenem-cilastin -Talk to your doctor if you are taking imipenem-cilastin. Convulsions have occurred in patients taking imipenem-cilastin and ganciclovir. You may discuss different options with your doctor.

PROPER USE OF THIS MEDICATION

Dosing Considerations:

  • Your doctor has prescribed NAT-VALGANCICLOVIR after carefully studying your case. Other people may not benefit from taking this medicine, even though their problems may seem similar to yours. Do not give your NAT-VALGANCICLOVIR to anyone else.

    • To make sure that your therapy is as effective as possible, take your NAT-VALGANCICLOVIR exactly as your doctor prescribes it. Do not skip any doses, or take more than the recommended dose.
    • Take NAT-VALGANCICLOVIR with food.

    • Do not break or crush NAT-VALGANCICLOVIR tablets. Avoid contact with broken NAT-VALGANCICLOVIR tablets on your skin, mucous membranes or eyes. If contact occurs, wash your skin well with soap and water or rinse your eyes well with sterile or plain water if sterile water is not available.

Usual Dose:

Treatment of CMV Retinitis in Patients with AIDS

  • The usual dosage for adults to get active CMV retinitis under control (induction therapy) is two 450 mg tablets twice a day for 21 days.
  • The usual dosage for adults to help keep CMV retinitis under control (maintenance therapy) is two 450 mg tablets once a day.

Prevention of CMV Disease Solid Organ Transplantation

  • The usual dosage to prevent CMV in adults who received a solid organ transplant is two 450 mg tablets once a day starting within 10 days of transplant and continuing until 100 days after the transplant.

Overdose:

In case of drug overdose or suspected drug overdose, particularly accidental oral ingestion, contact a healthcare practitioner (e.g. doctor), hospital emergency department, or regional poison control
centre, even if there are no symptoms.

Missed Dose:

  • If you forget to take a dose of NAT-VALGANCICLOVIR take it as soon as possible, then just carry on with the regular times you take your medication. If you remember your missed dose close to the time for your next dose, do not take the missed dose. Two doses of NAT-VALGANCICLOVIR should not be taken at the same time.
  • Do not let your NAT-VALGANCICLOVIR run out. The amount of virus in your blood may increase if your medicine is stopped, even for a short time.
  • It may be a good idea to ask your doctor or pharmacist ahead of time what to do about missed doses.

SIDE EFFECTS AND WHAT TO DO ABOUT THEM

Unwanted effects are possible with all medicines. Tell your doctor or pharmacist as soon as possible if you do not feel well while you are taking NAT-VALGANCICLOVIR.

Blood problems. NAT-VALGANCICLOVIR can cause serious blood cell problems. These include reduced numbers of certain white blood cells (granulocytopenia, neutropenia, or leukopenia), reduced numbers of red blood cells (anemia), and reduced numbers of platelets (thrombocytopenia). NAT-VALGANCICLOVIR may also cause blood creatinine elevation, increased potassium in the blood, and abnormal liver function. Your doctor should recommend that you have blood tests done on a regular basis.

Kidney problems. NAT-VALGANCICLOVIR can cause an increase in serum creatinine (an indicator of kidney function). An increase in serum creatinine may indicate abnormal kidney function. Your doctor may have blood tests done on a regular basis to monitor your serum creatinine.

Common side effects. NAT-VALGANCICLOVIR can cause other side effects. In studies, the most common side effects with the use of valganciclovir hydrochloride (although not necessarily related to valganciclovir hydrochloride) were diarrhea, nausea, vomiting, fever, headache, trembling, graft rejection, swelling of the legs, constipation, back pain, insomnia (sleeplessness), high blood pressure.

Other side effects. Convulsions, sedation, dizziness, ataxia (unsteadiness) and/or confusion have also been reported with the use of valganciclovir hydrochloride. If they occur, these side effects may affect a person’s ability to drive a car or operate machinery.

Although there is no supporting information from clinical trials in humans, animal studies indicate that valganciclovir hydrochloride may cause cancer and infertility in humans.

SERIOUS SIDE EFFECTS, HOW OFTEN THEY HAPPEN AND WHAT TO DO ABOUT THEM
Symptom / effectTalk with your doctor or pharmacistCall your doctor or pharmacist
Only if severeIn all cases
Common

Blood Problems -Reduced number of white blood cells

Symptoms of infection of the gums, throat, upper airways and skin include: chills, fever (over 100◦F or 38◦C), sore mouth, cough, redness, pain or swelling of any area of your body, or pain or burning when you pass your urine.

-Reduced number of red blood cells

Symptoms: tiredness and weakness.

-Reduced number of platelets

Symptoms: increased bruising and bleeding.

✓
Uncommon

Kidney Problems

-Increase in serum creatinine

Symptoms: decreased urine output, lower back pain or side pain, or swelling of feet or lower legs.

✓

This is not a complete list of side effects. For any unexpected effects while taking NAT-VALGANCICLOVIR, contact your doctor or pharmacist.

HOW TO STORE IT

  • Keep out of the reach of children.
  • Store NAT-VALGANCICLOVIR tablets in a clean dry area at room temperature (15-30°C).
  • Keep container tightly closed.
  • Do not use medication after the expiry date on the package.

REPORTING SUSPECTED SIDE EFFECTS

You can report any suspected adverse reactions associated with the use of health products to the Canada Vigilance Program by one of the following 3 ways:

  • Report online at https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada.html
  • Call toll-free at 1-866-234-2345
  • Complete a Canada Vigilance Reporting Form and:
  • Fax toll-free to 1-866-678-6789, or
  • Mail to: Canada Vigilance Program

    Health Canada

    Postal Locator 1908C

    Ottawa, ON K1A 0K9

Postage paid labels, Canada Vigilance Reporting Form and the adverse reaction reporting guidelines are available on the MedEffect™ Canada Web site at https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada.html.

NOTE: Should you require information related to the management of side effects, contact your health professional. The Canada Vigilance Program does not provide medical advice.

MORE INFORMATION

For more information, please contact your doctor, pharmacist or other healthcare professional.

This leaflet plus the full product monograph, prepared for health professionals, can be obtained by contacting Natco Pharma (Canada) Inc. by:

Phone: 1-800-296-9329

Last prepared: June 30, 2017

About this document

Source: Health Canada – Drug Product Database (DPD) and product monographs · DIN (Drug Identification Number): 02465744

Revision date stated in the text: June 30, 2017

Found a mistake? Write to us via the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Nat-Valganciclovir

Rx or OTC
Prescription (Rx)?
DIN 02465744
Schedule(s) PRESCRIPTION
Active ingredient(s) Valganciclovir (valganciclovir hydrochloride) 450 MG
Dosage form(s) Tablet
Route(s) of administration Oral
Drug class (WHO ATC)
  1. J Antiinfectives for systemic use
    1. J05 Antivirals for systemic use
      1. J05A Direct acting antivirals
        1. J05AB Nucleosides and nucleotides excl. reverse transcriptase inhibitors
          1. J05AB14 Valganciclovir
Company NATCO PHARMA (CANADA) INC
Current status Cancelled Pre Market
Current status date May 14, 2021

Source: Health Canada – Drug Product Database (DPD) and product monographs, data as of November 1, 2026. Data from the Health Canada Drug Product Database, as published there. Not a substitute for the advice of a doctor or pharmacist.