Gemcitabin Hexal 200 mg/vial (IV Infusion)
Medicine Details
Category | Details |
---|---|
Generic | Gemcitabine |
Company | Sandoz a novartis division |
Also available as |
Title
Gemcitabin Hexal
Categories
- Cytotoxic Chemotherapy
Indications
- Non-Small Cell Lung Cancer
- Pancreatic Cancer
- Bladder Cancer
- Breast Cancer
- Ovarian Cancer
Pharmacology
- Metabolism by nucleoside kinases
- Inhibition of DNA synthesis
- Induction of apoptosis
Dosage & Administration
- Non-Small Cell Lung Cancer:
- Single-agent Use
- Combination Use
- Pancreatic Cancer:
- Weekly injections followed by a week of rest
- Bladder Cancer:
- Single agent use
- Combination use
- Breast Cancer:
- Combination with Paclitaxel
- Ovarian Cancer:
- Combination with Carboplatin
Interaction
No confirmed interactions reported
Contraindications
- Known hypersensitivity to Gemcitabine or any other components
Side Effects
- Haematological Toxicity
- Hepatic Toxicity
- Gastrointestinal Effects
- Genito-Urinary Toxicity
- Pulmonary Toxicity
- Allergic Toxicity
- Neurotoxicity
- Alopecia
Pregnancy & Lactation
Pregnancy Category D
Precautions & Warnings
- Caution in patients with risk of toxicity
- Hepatic Toxicity
- Embryofetal Toxicity
Use in Special Populations
- Elderly Patients
- Renal and Hepatic Impairment
- Children
Overdose Effects
No known antidote
Storage Conditions
Store at 20°C to 25°C, away from light
Dimensions
Standard vial sizes
Color Options
N/A
Materials
Glass vials, chemical components
Usability Features
- Intravenous infusion
- Use in combination therapy
Technical Specifications
- Metabolism by nucleoside kinases
- Inhibition of DNA synthesis
- Induction of apoptosis
Design Elements
Standard pharmaceutical vial design
Functions
Cytotoxic chemotherapy for various cancers
Absorption Rate
N/A
Half-Life
Affected by age
Dosage Forms
Intravenous infusion
Age Group
- Elderly Patients
- Children
Hazardous Properties
Cytotoxicity
Toxicity Levels
- Mild to moderate myelosuppression
Efficacy
Treatment of various types of cancer
Safety Features
Monitoring for toxicity, supportive therapy for overdose
Clinical Trials
Limited Phase I and II trials in children
Efficacy Studies
Combination therapy for metastatic breast cancer
Chemical Composition
Gemcitabine
Patient Monitoring
Blood counts, renal function
Adverse Reactions
Anaemia, leukopenia, thrombocytopenia, hepatic abnormalities, gastrointestinal effects, genito-urinary effects, pulmonary effects, allergic reactions, neurotoxicity, alopecia
Dosage Reduction
Based on toxicity experienced by the patient
Aetiology
Of renal failure
Drug Class
Cytotoxic Chemotherapy
Storage Precautions
Do not refrigerate as crystallisation may occur
Child Safety
Keep out of the reach of children
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