GNH USA

Europe — EMA

Metronidazol Aurovitas

GNH USA supplies Metronidazol Aurovitas (Metronidazole), an antibiotic for bacterial vaginosis, trichomoniasis and anaerobic infections.

Metronidazole

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What is Metronidazole?

Metronidazole, the active ingredient in Metronidazol Aurovitas, is a nitroimidazole antibiotic presented as an oral dosage form for systemic use. It treats infections caused by anaerobic bacteria and certain protozoa in adult and pediatric patients as prescribed by a healthcare professional.

GNH USA supplies Metronidazol Aurovitas as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Metronidazole used for?

Metronidazol Aurovitas is indicated for infections where anaerobic bacteria or susceptible protozoa are involved.

- Bacterial vaginosis: restores normal vaginal flora by eradicating anaerobic pathogens. - Trichomoniasis: eliminates Trichomonas vaginalis, relieving symptoms and preventing transmission. - Amoebiasis: treats intestinal Entamoeba histolytica infection, reducing dysentery. - Giardiasis: clears Giardia lamblia from the gastrointestinal tract. - Anaerobic bacterial infections (including Clostridioides difficile): controls toxin‑producing anaerobes in the gut and other sites.

What are the side effects of Metronidazole?

Metronidazol Aurovitas may cause a range of adverse reactions.

Common Side Effects: - Nausea: mild to moderate upset stomach. - Metallic taste: transient alteration of taste perception. - Diarrhea: loose stools that may be self‑limiting. - Headache: mild to moderate cranial discomfort.

Serious or Rare Side Effects: - Seizures: convulsive episodes requiring immediate medical attention. - Peripheral neuropathy: tingling or numbness in extremities. - Severe allergic reaction: rash, swelling, or anaphylaxis. - Stevens‑Johnson syndrome: serious skin and mucous membrane disorder. - Pseudomembranous colitis: severe colonic inflammation. - Hepatotoxicity: elevated liver enzymes or liver injury.

What precautions apply to Metronidazole?

Before prescribing Metronidazol Aurovitas, clinicians should consider several safety factors.

- Renal function: assess kidney status, especially in patients with impairment. - Hepatic function: evaluate liver health, as metabolism occurs hepatically. - Alcohol consumption: advise avoidance of alcohol to prevent disulfiram‑like reactions. - Pregnancy status: weigh benefits against potential risks; use only if clearly needed. - Superinfection risk: monitor for overgrowth of non‑susceptible organisms. - Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

What does Metronidazole interact with?

Metronidazol Aurovitas can interact with several medicines, altering efficacy or safety.

Major Interactions (Avoid): - Alcohol: may cause severe flushing, nausea, and tachycardia. - Warfarin: potentiates anticoagulant effect, increasing bleeding risk. - Lithium: can raise lithium levels, leading to toxicity.

Moderate Interactions (Monitor Closely): - Phenytoin: may reduce metronidazole concentrations, decreasing effectiveness. - Cimetidine: can increase metronidazole plasma levels, heightening adverse effects.

Frequently asked questions

What infections is Metronidazol Aurovitas used to treat?+
Metronidazol Aurovitas is prescribed for bacterial vaginosis, trichomoniasis, amoebiasis, giardiasis, and a range of anaerobic bacterial infections such as Clostridioides difficile. It targets organisms that thrive in low‑oxygen environments and certain protozoa, helping to eliminate the infection and relieve symptoms.
How does metronidazole work against these infections?+
Metronidazole penetrates anaerobic microorganisms and is reduced by their internal electron transport proteins. This reduction creates nitro radical anions that damage DNA and inhibit nucleic acid synthesis, ultimately killing the bacteria or protozoa that cause the infection.
What is the usual dose of Metronidazol Aurovitas?+
The specific dose and treatment duration of Metronidazol Aurovitas are determined by the prescribing clinician based on the infection type, severity, patient age, weight, and renal or hepatic function. Patients should follow the exact regimen provided by their healthcare professional.
Is Metronidazol Aurovitas safe to use during pregnancy or breastfeeding?+
Safety in pregnancy and lactation has not been definitively established for Metronidazol Aurovitas. Healthcare providers weigh potential benefits against possible risks before prescribing it to pregnant or nursing individuals. Women should discuss their situation with a qualified professional.
How do I order Metronidazol Aurovitas from GNH USA?+
To request Metronidazol Aurovitas, submit an enquiry on the product page at gnh-usa.com indicating the required quantity. GNH USA 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.
How does Metronidazol Aurovitas compare with other treatments for anaerobic infections?+
Metronidazol Aurovitas belongs to the nitroimidazole class, offering broad activity against anaerobic bacteria and certain protozoa. Compared with alternatives such as clindamycin or carbapenems, metronidazole provides a convenient oral option with a well‑characterized safety profile, though drug‑specific resistance patterns and patient factors guide final selection.
What are the recommended storage conditions for Metronidazol Aurovitas?+
Metronidazol Aurovitas should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight, and excessive heat to maintain its stability and potency throughout its shelf life.
How is Metronidazol Aurovitas administered?+
Metronidazol Aurovitas is taken orally, usually with or without food as directed by the prescriber. The tablets should be swallowed whole with a glass of water and not chewed or crushed unless specifically instructed.
What are the most serious risks associated with Metronidazol Aurovitas?+
Serious risks include seizures, peripheral neuropathy, severe allergic reactions (including anaphylaxis), Stevens‑Johnson syndrome, pseudomembranous colitis, and liver toxicity. Patients should seek immediate medical attention if they experience neurological symptoms, rash, or signs of severe infection.
Who should not use Metronidazol Aurovitas?+
Metronidazol Aurovitas is contraindicated in individuals with a known hypersensitivity to metronidazole or other nitroimidazole derivatives. Caution is also advised for patients with severe hepatic impairment, those who consume alcohol heavily, and individuals with a history of severe neurological reactions to the drug.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Metronidazole
Route
Oral Use
Manufacturer
Aurovitas Pharma Polska Sp. Z O.O
Origin
EU

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