Registered Tanzania · TMDA

MEHECO

Lactose (Lactose Monohydrate) 450 mg,Oxaliplatin 50 mg,Water for Injection 10 ml

TAN 25 HM 0254 Freeze dried powder for injection single dose 50 INN generic

What it does

Lactose is a sugar found in milk and dairy products. It is often used as an excipient in medications.

Commonly used for: lactose intolerance, as a filler in tablets and capsules

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.
TAN 25 HM 0254
Registration date
2025-05-23
Expiry date
2030-05-22
Status
Registered/Compliant
Active ingredient
Lactose (Lactose Monohydrate) 450 mg,Oxaliplatin 50 mg,Water for Injection 10 ml
Strength
50
Pack size
-
Therapeutic class
-
RxNorm RxCUI
6211
Manufacturer / MAH
Cisen Pharmaceutical Co.
Applicant / LTR
China Meheco Corporation
Country of origin
P.R. CHINA

Source: Tanzania Medicines and Medical Devices Authority · fetched 2026-03-11 23:39:34 · updated 2026-10-19 03:00:44

Disclaimer: This information is sourced from Tanzania Medicines and Medical Devices Authority (Tanzania). Always consult a qualified healthcare professional before using any medication.

About lactose

Lactose is a sugar found in milk and dairy products. It is often used as an excipient in medications.

What it treats

  • lactose intolerance
  • as a filler in tablets and capsules

How it works

Lactose helps improve the texture and stability of medications and is sometimes used as a sweetener.

Who it's for

Individuals who require lactose as part of their medication or those who consume dairy products.

Cautions

  • • May cause digestive issues in people with lactose intolerance.

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

About oxaliplatin

Oxaliplatin is a chemotherapy medication used to treat certain types of cancer.

What it treats

  • colorectal cancer
  • cancer of the large intestine

How it works

It works by stopping the growth of cancer cells in the body.

Who it's for

It is prescribed for patients diagnosed with colorectal cancer.

Cautions

  • • Be careful if you are taking medicines that can harm your kidneys.
  • • Avoid drugs that can affect your bone marrow.
  • • Use caution with medications that can affect your hearing.

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

Clinical monograph: lactose

BNF-referenced

Lactose is a disaccharide sugar composed of galactose and glucose, primarily found in milk and dairy products. It serves as a source of energy and is metabolized by the enzyme lactase. In individuals with lactase deficiency, lactose can lead to gastrointestinal symptoms such as bloating, diarrhea, and abdominal pain.

Indications

  • Lactose intolerance
  • As a filler or excipient in pharmaceutical formulations

Dosage

Children: Refer to the BNF for Children for specific dosing information based on age and clinical context.

Adults: Refer to the BNF for specific dosing information based on clinical context.

Mechanism of action

Lactose is metabolized in the intestine by the enzyme lactase into its constituent monosaccharides, glucose and galactose. In individuals with lactase deficiency, unabsorbed lactose passes into the colon, where it is fermented by bacteria, leading to gas production and osmotic effects that contribute to diarrhea.

Pharmacodynamics

The pharmacodynamics of lactose are primarily related to its effects on gastrointestinal function. In healthy individuals, lactose is effectively broken down into glucose and galactose, which are absorbed and utilized for energy. In individuals with lactose intolerance, the unabsorbed lactose can cause osmotic diarrhea and colonic fermentation, leading to discomfort and symptoms associated with lactose intolerance.

Pharmacokinetics

Lactose is not absorbed in the gastrointestinal tract until it is hydrolyzed into glucose and galactose by lactase. The absorption of glucose and galactose occurs in the small intestine. The half-life is not applicable as lactose is not typically administered as a medication but is rather ingested as a natural component of food. Its metabolism primarily occurs in the intestine.

Adverse effects

  • Bloating
  • Diarrhea
  • Abdominal pain
  • Flatulence

Precautions

  • Use with caution in patients with lactose intolerance.
  • Consider potential for gastrointestinal upset in sensitive individuals.

Pregnancy

Lactose is generally considered safe for use during pregnancy. However, consult a healthcare professional for individual advice.

Breast-feeding

Lactose is safe to use while breastfeeding, as it is a natural sugar present in breast milk.

Storage

Store in a cool, dry place, away from direct sunlight.

Formulations

  • Powder
  • Granules
  • Tablets
  • Syrup

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: Oxaliplatin

BNF-referenced

Oxaliplatin is a platinum-based antineoplastic agent used in the treatment of various malignancies, particularly metastatic colorectal cancer. It is often administered in combination with other chemotherapeutic agents such as fluorouracil and folinic acid. The drug is known for its ability to interfere with DNA synthesis, leading to cell death and the inhibition of tumor growth.

Indications

  • Treatment of metastatic colorectal cancer in combination with fluorouracil and folinic acid
  • Adjuvant treatment of colon cancer after resection of the primary tumor

Dosage

Children: Refer to the BNF for Children for appropriate dosing in the paediatric population, as specific doses for children are not provided in the BNF for Adults.

Adults: Consult product literature for specific dosing guidelines. The typical adult dose is often around 85 mg/m² administered intravenously every two weeks, but this may vary based on the specific regimen and patient condition.

Mechanism of action

Oxaliplatin exerts its cytotoxic effects by forming DNA cross-links, which inhibit DNA replication and transcription. The drug is converted within the body to reactive platinum species that bind to DNA, leading to the formation of interstrand cross-links and ultimately triggering apoptosis in rapidly dividing cancer cells. This mechanism is particularly effective in targeting cancerous tissues that are highly proliferative.

Pharmacodynamics

The pharmacodynamics of oxaliplatin involve its ability to induce apoptosis in cancer cells through DNA damage. This damage activates several cellular pathways, including the p53 pathway, which is critical for cell cycle regulation and apoptosis. Additionally, oxaliplatin's unique structure allows it to bypass some resistance mechanisms that cancer cells develop against other platinum compounds, making it a valuable option in chemotherapy regimens.

Pharmacokinetics

Oxaliplatin is administered intravenously and has a distribution volume of approximately 16 L/m². Its plasma protein binding is around 95%. The drug undergoes rapid biotransformation in the liver, resulting in several metabolites, with the active form being the platinum-DNA adducts. The elimination half-life is approximately 1-2 hours, and it is primarily excreted via the urine as metabolites and unchanged drug. Dose adjustments may be necessary in patients with hepatic impairment.

Contra-indications

  • Peripheral neuropathy with functional impairment

Adverse effects

  • Alopecia
  • Anaemia
  • Appetite decrease
  • Arthralgia
  • Asthenia
  • Chills
  • Conjunctivitis
  • Constipation
  • Cough
  • Decreased leukocytes
  • Dehydration
  • Depression
  • Diarrhoea
  • Dizziness
  • Dyspnoea
  • Electrolyte imbalance
  • Embolism
  • Thrombosis
  • Fever
  • Flushing
  • Gastrointestinal discomfort
  • Gastrointestinal disorders
  • Haemorrhage
  • Headache
  • Hiccups
  • Hyperglycaemia
  • Hyperhidrosis
  • Hypersensitivity
  • Hypertension
  • Increased risk of infection
  • Insomnia
  • Meningism
  • Mucositis
  • Nail disorders
  • Peripheral neuropathy
  • Skin reactions
  • Stomatitis
  • Taste alteration
  • Thrombocytopenia
  • Urinary disorders
  • Vision disorders
  • Vomiting
  • Weight changes

Pregnancy

Manufacturer advises to avoid due to toxicity in animal studies.

Breast-feeding

Discontinue breastfeeding.

Storage

Store below 25 degrees Celsius. Protect from light.

Formulations

  • Oxaliplatin 50mg/10ml concentrate for solution for infusion vials
  • Oxaliplatin 100mg/100ml solution for infusion vials
  • Oxaliplatin 200mg/40ml concentrate for solution for infusion vials
BNF 85 (British National Formulary) p.1031 PubChem / pathway

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

Molecular reference: lactose

PubChem CID 6134

Molecular formula: C12H22O11

Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.

Molecular reference: Oxaliplatin

PubChem CID 9887053

Molecular formula: C8H14N2O4Pt

Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.

This drug in other countries

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