Registered Zambia · ZAMRA

M+PAC

Mycoplasma hyopneumonia 1 ml

ZAMRA-VM-26-34 Emulsion for injection 1 ml

What it does

Hyopneumonia is a vaccine for the prevention of swine enzootic pneumonia.

Commonly used for: swine enzootic pneumonia (Mycoplasma hyopneumoniae infection)

Read more in plain English ↓

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

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Registration & product details

Registration no.
ZAMRA-VM-26-34
Registration date
2026-03-06
Expiry date
2031-03-05
Status
Registered/Compliant
Active ingredient
Mycoplasma hyopneumonia 1 ml
Strength
1 ml
Pack size
-
Therapeutic class
-
Manufacturer / MAH
Intervet
Country of origin
Germany
Manufacturer location
Feldstraße 1A, 85716 Unterschleißheim, Germany

Source: Zambia Medicines Regulatory Authority · fetched 2026-03-12 00:08:02 · updated 2026-10-29 03:40:27

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

About hyopneumonia

Hyopneumonia is a vaccine for the prevention of swine enzootic pneumonia.

What it treats

  • swine enzootic pneumonia (Mycoplasma hyopneumoniae infection)

How it works

It works by helping the body's immune system to fight against the bacteria that cause swine enzootic pneumonia.

Who it's for

Pigs

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

About mycoplasma

Mycoplasma is a type of bacteria that can cause various infections, particularly in the respiratory system.

What it treats

  • respiratory infections
  • urethritis (inflammation of the urethra)
  • pneumonia

How it works

Mycoplasma bacteria can disrupt normal cell function and lead to illness.

Who it's for

This condition can affect anyone, but it is more common in young adults and those with weakened immune systems.

Cautions

  • • May require specific tests for accurate diagnosis.
  • • Treatment may vary based on the type of infection.

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

Clinical monograph: hyopneumonia

Hyoscyamine is an anticholinergic medication used to treat various conditions such as peptic ulcer disease, gastrointestinal disorders, and symptomatic relief of smooth muscle spasm in conditions like asthma, bronchitis, and pertussis. It is also used to treat conditions associated with excessive salivation and bronchial secretions.

Indications

  • Community-acquired pneumonia
  • Hospital-acquired pneumonia
  • Ventilator-associated pneumonia

Dosage

Children: Refer to the BNF for Children for specific pediatric dosing instructions, as the recommended dose may vary depending on the age and weight of the child.

Adults: The recommended adult dose of hyoscyamine is typically 0.125-0.25 mg orally, 3-4 times a day. However, this dose may vary depending on the specific indication and patient response.

Mechanism of action

Hydrophneumonia acts as a broad-spectrum antibiotic, inhibiting bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs) located inside the bacterial cell wall. This leads to the disruption of the bacterial cell wall and ultimately, cell death.

Pharmacodynamics

Hyoscyamine's anticholinergic effects include reduced salivation, bronchial secretions, and gastrointestinal motility. It also causes dilation of pupils, increased heart rate, and decreased sweating.

Pharmacokinetics

Hyoscyamine is rapidly absorbed after oral administration, with peak plasma concentrations occurring within 1-2 hours. It is extensively metabolized by the liver, primarily through the cytochrome P450 system, and has a half-life of approximately 3-4 hours.

Contra-indications

  • Hypersensitivity to the active substance or any of the excipients
  • Severe renal impairment

Adverse effects

  • Headache
  • Nausea
  • Diarrhoea
  • Vomiting
  • Rash
  • Hypersensitivity reactions

Interactions

  • May increase the risk of bleeding when co-administered with warfarin or other anticoagulants
  • May increase the risk of nephrotoxicity when co-administered with other nephrotoxic agents

Precautions

  • Monitor liver function tests
  • Monitor renal function tests
  • Monitor for signs of hypersensitivity reactions

Pregnancy

Use only if the potential benefits outweigh the risks.

Breast-feeding

Unknown

Storage

Store in a cool, dry place. Protect from light.

Formulations

  • Tablets
  • Injectable solution
  • Powder for reconstitution

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: mycoplasma

Mycoplasma refers to a genus of bacteria that are notable for their lack of a cell wall, making them inherently resistant to antibiotics that target cell wall synthesis. They are some of the smallest self-replicating organisms and can cause a variety of diseases in humans, including respiratory infections and atypical pneumonia. Mycoplasma pneumoniae is the most clinically significant species and is known to cause infections primarily in children and young adults.

Indications

  • Mycoplasma pneumonia
  • Atypical pneumonia
  • Respiratory tract infections
  • Sinusitis
  • Bronchitis
  • Chronic cough

Dosage

Children: Refer to specific antibiotic guidelines as the dosage depends on the antibiotic chosen for treatment

Adults: Refer to specific antibiotic guidelines as the dosage depends on the antibiotic chosen for treatment.

Mechanism of action

Mycoplasma species, particularly Mycoplasma pneumoniae, adhere to the respiratory epithelial cells and disrupt normal cellular processes. They utilize surface proteins and lipids to anchor themselves to host cells, leading to cell damage through inflammatory responses. They do not produce toxins but can induce host immune responses that contribute to the pathogenicity of the infection.

Pharmacodynamics

Mycoplasma are unique bacteria that lack a cell wall, which makes them resistant to many common antibiotics, such as penicillins and cephalosporins. The treatment of infections caused by Mycoplasma typically involves the use of antibiotics that target protein synthesis, such as macrolides (e.g., azithromycin) or tetracyclines (e.g., doxycycline). These antibiotics inhibit bacterial growth by disrupting essential processes within the bacteria, leading to cell death or stasis.

Pharmacokinetics

The pharmacokinetics of antibiotics used to treat Mycoplasma infections can vary. For example, macrolides are well-absorbed orally and have good tissue penetration, allowing them to reach the site of infection effectively. They are metabolized in the liver and excreted primarily through bile. Tetracyclines also have good oral bioavailability and are distributed widely in body tissues, but should be avoided in children under 8 years due to potential effects on bone and tooth development. The half-lives of these antibiotics can range from several hours to a day, depending on the specific drug and patient factors.

Pregnancy

Mycoplasma infections should be treated with caution during pregnancy. The use of antibiotics may be necessary, but the choice of medication should consider safety profiles and potential risks to the fetus.

Breast-feeding

Caution is advised when treating Mycoplasma infections in breastfeeding individuals. Certain antibiotics may be excreted in breast milk, so a risk-benefit assessment is essential.

Storage

Store in a cool, dry place away from direct sunlight. Specific conditions may vary depending on the antibiotic used for treatment.

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

This drug in other countries

The same active ingredient registered across other registries we cover - including different brands.