Product image of Holdofeb (Paracetamol) supplied by GNH India

Holdofeb

Active Ingredient:
Paracetamol
Origin:
EU

Holdofeb (Paracetamol)

Holdofeb is an over‑the‑counter oral medication whose active ingredient is paracetamol (acetaminophen). The product is marketed in the European Union and is supplied in tablet or liquid form, with the specific strength not disclosed on the label. As a member of the analgesic and antipyretic class, Holdofeb is intended for temporary relief of fever and mild to moderate pain for short‑term use in adults and children over a certain age.

Manufacturer / TM Owner

Holon S.A.

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Indications & Clinical Uses

Holdofeb is indicated for the temporary relief of common conditions that cause fever or pain. It may be used as part of a broader symptomatic treatment plan when non‑opioid analgesia is appropriate.

  • Fever associated with infections, inflammatory conditions, or post‑vaccination reactions.
  • Mild to moderate headache, including tension‑type and migraine onset.
  • Dental pain, such as after tooth extraction or orthodontic adjustments.
  • Musculoskeletal discomfort, including minor sprains, strains, or backache.
  • Menstrual cramps and other mild visceral pain.
  • Fever in children (≥2 years) when temperature exceeds 38°C (100.4°F).
  • Pain from minor burns or superficial skin injuries.

How It Works

  • Paracetamol, the active ingredient in Holdofeb, reduces pain and fever by inhibiting the activity of cyclooxygenase enzymes in the central nervous system, particularly COX‑2, which leads to decreased synthesis of prostaglandins that sensitize pain pathways and regulate body temperature. The drug’s action is primarily central, with minimal peripheral anti‑inflammatory effects, allowing it to lower temperature set‑points in the hypothalamus and raise the pain threshold.

Side Effects

Like all medicines, Holdofeb may cause unwanted effects, most of which are mild and transient.

Common

  • Nausea or mild stomach upset.
  • Headache.
  • Dizziness.
  • Skin rash or mild itching.
  • Transient fatigue or feeling of weakness.
  • Mild abdominal discomfort.
  • Mild increase in blood pressure (rare).

Serious

  • Severe allergic reaction with swelling of the face, lips, or throat.
  • Liver injury manifested by jaundice, dark urine, or abdominal pain.
  • Blood disorders such as thrombocytopenia or neutropenia.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis (very rare).
  • Acute renal failure in patients with pre‑existing kidney disease.
  • Hypersensitivity reactions such as urticaria.

Precautions & Warnings

When using Holdofeb, certain precautions should be observed to minimize risk and ensure safe use.

  • Do not exceed the recommended daily amount; chronic overuse can harm the liver.
  • Avoid use in individuals with known severe liver disease or active hepatitis.
  • Use caution in patients with renal impairment; dose adjustment may be needed.
  • Limit alcohol consumption while taking Holdofeb, as combined use increases liver toxicity.
  • Consult a healthcare professional before use during pregnancy or breastfeeding, as safety data are limited.
  • Keep out of reach of children; accidental ingestion can cause serious toxicity.
  • Do not combine with other paracetamol‑containing products to avoid accidental overdose.

Avoid Interactions

Holdofeb can interact with other medicines, potentially altering its effectiveness or increasing the risk of adverse effects.

Avoid

  • Concomitant use with other paracetamol‑containing products, which can lead to overdose and liver injury.
  • Co‑administration with strong enzyme‑inducing anticonvulsants (e.g., carbamazepine, phenytoin) that may reduce paracetamol levels.
  • Use with high‑dose aspirin or other NSAIDs in patients at risk for gastrointestinal bleeding.

Use with caution

  • Combination with warfarin or other anticoagulants, as paracetamol may enhance anticoagulant effect.
  • Concurrent use with alcohol, especially in chronic drinkers, due to increased hepatotoxic risk.
  • Administration alongside certain antiviral or antiretroviral agents (e.g., ritonavir) that can affect metabolism.

Frequently Asked Questions

Holdofeb is an over‑the‑counter oral medication marketed in the European Union. Its sole active ingredient is paracetamol, also known as acetaminophen.

Holdofeb lowers fever by inhibiting central cyclooxygenase enzymes, which reduces prostaglandin synthesis in the hypothalamus and resets the body’s temperature set‑point.

Holdofeb is indicated for mild to moderate pain such as headache, dental pain, musculoskeletal aches, menstrual cramps, and other common short‑term pain conditions.

Holdofeb may be used in children aged two years and older when the appropriate dose for weight or age is followed, but it should not be given to infants without medical advice.

Safety data for Holdofeb during pregnancy and lactation are limited. Women who are pregnant or breastfeeding should consult a healthcare professional before using the product.

Common adverse effects include nausea, mild stomach upset, headache, dizziness, skin rash or itching, transient fatigue, mild abdominal discomfort, and rarely a slight increase in blood pressure.

Serious reactions include severe allergic responses (swelling of face, lips, throat), signs of liver injury (jaundice, dark urine, abdominal pain), blood disorders, Stevens‑Johnson syndrome, acute renal failure, or urticaria.

Store Holdofeb at room temperature, away from excess heat, moisture, and direct sunlight. Keep the container tightly closed and out of reach of children.

Holdofeb can be combined with ibuprofen in many cases, but it is advisable to consult a healthcare professional to ensure appropriate dosing and to avoid potential gastrointestinal irritation.

Avoid exceeding the recommended daily dose, using other paracetamol‑containing products, and consuming excessive alcohol while taking Holdofeb.

Holdofeb may enhance the effect of anticoagulants such as warfarin, potentially increasing bleeding risk. Monitoring of coagulation parameters is recommended when both are used together.

Fever reduction usually begins within 30 to 60 minutes after oral administration of Holdofeb, with the greatest effect observed around 2 to 3 hours.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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