Composition : Lenvatinib
Strength availability : 4mg
Pack : Pack of 20 Capsules.
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Lenvima 4mg is also known as tyrosine kinase inhibitor.
Lenvima 4mg targets something to the cancer cells.
Lenvima 4mg is well absorbed. In which Food does not affect the range of absorption but lower the rate.
Lenvima 4mg which is a prescription drug used under proper guidance of medical oncologist.
• Indicated For the treatment of thyroid cancer which cannot be treated with radioactiveiodine.
• Indicated By combined with everolimus to treat the advanced renal carcinoma in which other drugs failed to be effective.
• Indicated For the treatment of hepatocellular primary liver cancer
The recommended dose of differentiated thyroid cancer is Lenvima 4mg, it administers by two 10mg and one 4 mg capsules taken orally, once in a day along with or without food.
The recommended dose of renal cell carcinomas is Lenvima 4mg 18 mg, given as one 10mg capsule and two 4 mg capsules administrated in combination with 5mg everolimus orally taken once in a day with or without food.
The recommended dose of first-line treatment of unresectable hepatocellular carcinoma is based on actual body weight
If < 60 kg then 8mg PO qDay
If ≥ 60 kg then 12mg PO qDay
• Lenvima 4mg capsule must take at same time each day
• Follow the drug till disease progression.
• Lenvima 4mg capsules must swallowed whole.
• In a small glass of liquid dissolved the capsules
• In 1 tablespoon apple juice or water and embed the capsules into the liquid without breaking or crushing them.
• Dip the capsules in the liquid for at least 10 minutes.
• The liquid is agitated for at least 3 minutes. Drink the mixture.
• Add 1 tablespoon of water or apple juice to the glass after drinking the mixture
• Mix up the contents a few times and swallow the additional liquid.
OVERDOSAGE: Lenvima 4mg has no individual antitoxin for overdose. Since high plasma protein binding. Lenvima 4mg is not expected to be dialyzable. Take the patients to emergency medical department or call poison control helpline.
Lenvima 4mg called as targeted therapy. In which it aims something particular to the cancer cells, hence reduces side effects caused by repairing to the healthy cells. Lenvima 4mg mechanism by inhibiting two processes which allow cancer cells to develop
• Prevention of a protein that promotes cell division
• Stopping the VEGF receptor, which is necessary for angiogenesis, or the growth of a blood supply to the tumor. This discard the tumor's source of nutrients.
Maximum plasma concentration is 1 to 4 hours post dose.
Effect with food is low to the extent of absorption.
Human plasma proteins bounding about 98% to 99%.
Metabolized in CYP3A and aldehyde oxidase. Lenvima 4mg metabolic pathway is identified as enzymatic and non-enzymatic processes.
The drug excreted via 64% feces and 25% urine,
The terminal half-life of Lenvima 4mg is 28 hours.
• When using Lenvima 4mg Hypertension reslted in 73% of Lenvima 4mg-treated patients in clinical trials (grade 3 hypertension was 44%); regulate blood pressure before to treatment; check blood pressure after 1 week, then q2weeks for the first 2 months.
• Lenvima 4mg causes Arterial thromboembolic events occurred in 5% of treated patients; stop drug following a thromboembolic event; forever stop treatment following an arterial thrombotic event.
• When using of Lenvima 4mg capsules will occurs Gastrointestinal perforation or fistula (2%); stop if patient experience a GI perforation or life-threatening fistula; permanently stop therapy in patients who have gastrointestinal perforation of any serious or Grade 3 or 4 fistula.
• While on treatment will reported Serious complications of poorly controlled hypertension.
• Discuss with the doctor if you are breastfeeding or plan to breastfeed. Avoid breastfeed during Lenvima 4mg treatment.
The dose of drug is missed, and then takes the dose as you remember earlier. If time to next dose reaches, then swap the missed dose and continue the routine schedule. Avoid taking 2 doses at one time. Please consult your doctor for further clarification
Store the drug at 2 ℃ – 8 ℃
Avoid freezing or shake
Protect from light
Common side effects :
• Weight reduced
• Palmar-plantar erythrodysesthesia
• Protein urea
• Hand-foot syndrome
• Loss of appetite
• Difficulty speaking
• Blood pressure increased
• Muscle aches
• Mouth sores
• Dental & oral infection
• Taste changes
• Nose bleed
• Urinary tract infection
• Hair loss
• Taste changes