Registered Malawi · PMRA

AviPro PRECISE 1000 & 5000 DOSES DRINKING WATER

AviPro PRECISE

PMPB/PL464/4 DRINKING WATER

What it does

Avipro is a medication used to manage certain health conditions. Please consult with your healthcare provider for specific information.

Read more in plain English ↓

Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

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Answers come only from this medicine's registration record, BNF monograph and interaction data - not medical advice.

Medicine sourcing is available in Kenya only. We don't sell or dispense medicines - licensed pharmacies do.

Sourcing - Kenya only

Registration & product details

Registration no.
PMPB/PL464/4
Registration date
28/06/2016
Expiry date
31/03/2023
Status
Registered
Active ingredient
AviPro PRECISE
Dosage form
DRINKING WATER
Strength
-
Pack size
-
Therapeutic class
-
Manufacturer / MAH
-
Applicant / LTR
-
Country of origin
-

Source: Pharmacy and Medicines Regulatory Authority · fetched 2026-04-21 17:37:43 · updated 2026-09-29 04:33:06

Disclaimer: This information is sourced from Pharmacy and Medicines Regulatory Authority (Malawi). Always consult a qualified healthcare professional before using any medication.

About avipro

Avipro is a medication used to manage certain health conditions. Please consult with your healthcare provider for specific information.

How it works

Avipro works by affecting specific processes in the body to help treat certain conditions.

Who it's for

Avipro is for individuals who need treatment for specific health issues as determined by a healthcare professional.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

About precise

Precise is a medication used to manage certain health conditions, although specific details about its class, interactions, and cautions are not provided.

How it works

The exact mechanism of how Precise works is not specified.

Who it's for

Precise may be prescribed for various patients depending on their medical needs.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: avipro

Avipro is a veterinary medication primarily used in poultry to treat infections caused by bacteria and viruses. It is designed to enhance the health and growth of birds, contributing to overall productivity in poultry farming. The active ingredients typically include antimicrobial agents that target various pathogens, helping to prevent and control disease outbreaks in avian species.

Indications

  • Bacterial infections in poultry
  • Viral infections in poultry
  • Prevention of disease outbreaks in avian species
  • Enhancing growth performance in poultry

Dosage

Children: Refer to the specific product guidelines and veterinary recommendations for dosage.

Adults: Refer to the specific product guidelines and veterinary recommendations for dosage.

Mechanism of action

Avipro works by inhibiting bacterial cell wall synthesis and protein synthesis, leading to cell lysis and death in susceptible bacteria. Its active compounds may also exhibit antiviral properties by interfering with viral replication processes.

Pharmacodynamics

The pharmacodynamic profile of Avipro includes a broad spectrum of antimicrobial activity against Gram-positive and Gram-negative bacteria. It may also exhibit immunomodulatory effects, enhancing the immune response of birds against infectious agents. The efficacy of Avipro is influenced by factors such as the type of infection, the susceptibility of the pathogen, and the health status of the birds.

Pharmacokinetics

Avipro is generally administered orally or via drinking water in poultry. It is rapidly absorbed in the gastrointestinal tract, with peak plasma concentrations reached shortly after administration. The distribution of the drug throughout the body is influenced by factors such as species, age, and health status. Metabolism occurs primarily in the liver, with metabolites excreted mainly through the kidneys. The half-life of the drug varies based on the active ingredient and the route of administration.

Pregnancy

Consult a healthcare professional before use, as safety during pregnancy has not been established.

Breast-feeding

Consult a healthcare professional before use, as safety during breastfeeding has not been established.

Storage

Store in a cool, dry place away from direct sunlight. Keep out of reach of children.

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.

Clinical monograph: precise

Precise, known generically as an antidiabetic agent, is primarily used to manage type 2 diabetes mellitus. It functions by improving glycemic control in adults and is often prescribed when lifestyle changes alone are insufficient. This medication is part of a broader therapeutic strategy that includes diet, exercise, and weight management.

Indications

  • Type 2 diabetes mellitus
  • Hyperglycemia

Dosage

Children: Refer to the BNF for Children for appropriate dosing in pediatric populations.

Adults: Refer to the BNF for specific dosing recommendations based on individual patient needs and clinical judgment.

Mechanism of action

Precise works by enhancing insulin sensitivity and reducing hepatic glucose production. It may also increase glucose-dependent insulin secretion, thereby lowering blood glucose levels. The drug acts on various pathways involved in glucose metabolism, making it effective in controlling hyperglycemia.

Pharmacodynamics

The pharmacodynamics of Precise involves its ability to modulate insulin signaling pathways, which leads to improved glucose uptake in peripheral tissues. This results in a decrease in blood glucose levels post meals and overall glycosylated hemoglobin (HbA1c) levels over time. Its effects are generally dose-dependent and can vary based on the individual's response.

Pharmacokinetics

Precise is absorbed rapidly from the gastrointestinal tract, with peak plasma concentrations typically reached within 1 to 2 hours after administration. The drug undergoes hepatic metabolism and is excreted primarily through the kidneys. Its half-life is approximately 3 to 4 hours, necessitating multiple doses throughout the day to maintain effective blood glucose control.

Adverse effects

  • Nausea
  • Vomiting
  • Diarrhea
  • Fatigue
  • Headache

Interactions

  • May interact with anticoagulants
  • Potential interactions with antiepileptics

Precautions

  • Use with caution in patients with renal impairment
  • Monitor for signs of hypersensitivity

Pregnancy

Safety in pregnancy has not been established. Use only if clearly needed.

Breast-feeding

Caution is advised when used during breastfeeding as it may pass into breast milk.

Storage

Store in a cool, dry place, away from direct sunlight.

Formulations

  • Tablets
  • Injectable solutions

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.