Europe — EMA
Ogivri (Trastuzumab)
Trastuzumab, the active ingredient in Ogivri, is a monoclonal antibody presented as a 440 mg/10 ml solution for intravenous use. It treats HER2‑positive breast cancer in adult patients.
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What is Trastuzumab?
Trastuzumab, the active ingredient in Ogivri, is a monoclonal antibody presented as a 440 mg/10 ml solution for intravenous use. It treats HER2‑positive breast cancer in adult patients.
GNH USA supplies Ogivri as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres, hospitals and pharmacies worldwide.
What is Trastuzumab used for?
Ogivri is a HER2‑targeted therapy used in the management of cancers that overexpress the HER2 protein. - Early‑stage HER2‑positive breast cancer: improves disease‑free survival when given as part of adjuvant therapy. - Metastatic HER2‑positive breast cancer: prolongs overall survival in combination with chemotherapy. - HER2‑positive gastric or gastro‑oesophageal junction adenocarcinoma: used with chemotherapy in the first‑line setting.
What are the side effects of Trastuzumab?
Adverse reactions to Ogivri may range from mild to severe and are monitored throughout treatment.
Common Side Effects: - Fever, chills and rigour - Nausea or vomiting - Fatigue - Diarrhoea - Headache - Infusion‑related erythema
Serious or Rare Side Effects: - Cardiac dysfunction or decreased left‑ventricular ejection fraction - Severe infusion‑related reactions, including anaphylaxis - Pulmonary toxicity (interstitial pneumonitis) - Thromboembolic events - Hepatitis B reactivation - Severe skin reactions such as Stevens‑Johnson syndrome
What precautions apply to Trastuzumab?
When administering Ogivri, clinicians should observe several safety measures. - Cardiac monitoring: regular echocardiograms or MUGEE studies - Pregnancy : test t t t t ullet ewline - ewline - ullet \
What does Trastuzumab interact with?
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