Product image of Juluca (Dolutegravir Sodium, Rilpivirine Hydrochloride) supplied by GNH India

Juluca

Active Ingredient:
Dolutegravir Sodium, Rilpivirine Hydrochloride
Origin:
EU

Juluca (Dolutegravir Sodium, Rilpivirine Hydrochloride)

Dolutegravir sodium and rilpivirine hydrochloride, the active ingredients in Juluca, are an integrase strand transfer inhibitor and a non‑nucleoside reverse transcriptase inhibitor presented as an oral tablet for systemic use. It treats HIV‑1 infection in treatment‑experienced adults.

GNH India supplies Juluca as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Viiv Healthcare B.V.

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Indications & Clinical Uses

  • Juluca is an antiretroviral medication that targets HIV‑1 replication in adults who have previously received therapy.
  • HIV‑1 infection in treatment‑experienced adults: provides virologic suppression when combined with a suitable background regimen.

How It Works

  • Dolutegravir sodium binds to the HIV‑1 integrase enzyme, preventing the insertion of viral DNA into the host genome, while rilpivirine hydrochloride attaches to the reverse transcriptase enzyme at a non‑nucleoside site, blocking the conversion of viral RNA to DNA. Together they halt viral replication and reduce plasma HIV RNA levels.

Side Effects

Juluca may cause a range of adverse reactions, most of which are mild to moderate.

Common Side Effects

  • Nausea: mild stomach upset reported by some patients.
  • Headache: transient headache episodes.
  • Fatigue: feeling of tiredness or reduced energy.
  • Diarrhea: loose stools, usually self‑limiting.
  • Insomnia: difficulty falling or staying asleep.
  • Rash: mild skin irritation or erythema.

Serious or Rare Side Effects

  • Hepatotoxicity: signs of liver injury such as jaundice.
  • Severe hypersensitivity: swelling, breathing difficulty, or anaphylaxis.
  • QT prolongation: cardiac rhythm changes detectable on ECG.
  • Depression or mood changes: new or worsening psychiatric symptoms.
  • Elevated serum creatinine: indicating possible renal impact.
  • Pancreatitis: abdominal pain with elevated enzymes.

Precautions & Warnings

  • Before initiating Juluca, consider the following safety measures.
  • Baseline liver function: assess hepatic enzymes to detect pre‑existing liver disease.
  • Drug resistance testing: ensure no prior resistance to integrase inhibitors or NNRTIs.
  • Concomitant medications: review for potential interactions that affect drug levels.
  • Pregnancy and breastfeeding: discuss risks with a healthcare professional.
  • Adherence counseling: emphasize the importance of consistent daily dosing.
  • Store at ambient temperature: keep tablets in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Juluca can interact with several drug classes; monitoring is essential.

Major Interactions (Avoid)

  • Antacids containing aluminum or magnesium: reduce rilpivirine absorption.
  • Rifampin or other strong enzyme inducers: markedly lower dolutegravir levels.
  • Proton pump inhibitors: may decrease rilpivirine exposure.

Moderate Interactions (Monitor Closely)

  • Certain anticonvulsants (e.g., carbamazepine): modestly reduce dolutegravir concentrations.
  • St. John’s wort: may lower rilpivirine levels.
  • Hormonal contraceptives: potential reduction in efficacy, consider alternative methods.

Frequently Asked Questions

Juluca is prescribed for adults with HIV‑1 infection who have previously received antiretroviral therapy and need a regimen that combines an integrase inhibitor with a non‑nucleoside reverse transcriptase inhibitor to maintain viral suppression.

Dolutegravir sodium inhibits the HIV‑1 integrase enzyme, preventing the viral DNA from integrating into the host cell’s genome, which blocks a critical step in the viral replication cycle.

The prescribed dose of Juluca is determined by the treating physician based on the patient’s clinical status, prior treatment history, and any relevant laboratory results.

Safety in pregnancy and lactation has not been fully established; clinicians should weigh potential benefits against risks and discuss options with the patient before prescribing.

Submit an enquiry on the Juluca product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Juluca uniquely combines an integrase strand transfer inhibitor (dolutegravir) with a non‑nucleoside reverse transcriptase inhibitor (rilpivirine) in a single tablet, offering a convenient two‑drug option for patients who are virologically suppressed on prior therapy, whereas many alternatives require three or more agents.

Store Juluca tablets at ambient temperature, below 25 °C, in the original blister pack, protected from moisture and direct sunlight to maintain potency.

Juluca is taken orally, usually once daily with a meal, to improve absorption of the rilpivirine component; patients should follow the dosing schedule prescribed by their healthcare provider.

Serious risks include liver toxicity, severe hypersensitivity reactions, QT‑interval prolongation, and rare psychiatric effects; patients should be monitored for these events and seek immediate medical attention if they occur.

Juluca is contraindicated in patients with known hypersensitivity to dolutegravir, rilpivirine, or any excipients, and should be avoided in individuals with significant resistance to either drug class or those taking contraindicated interacting medications.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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