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Inj.

Dimi-Vet

Composition: Sulphadimidine sodium BP 333.3mg/ml

Drug Class: Antibiotic

Manufacturer: Square Pharmaceuticals Ltd.

Basic information

Generic Drug

Route of Administration

IM/IV/SC/IP

Strength / Concentration

333.3 mg/ml

Presentation and price

100 ml vial

115 Taka

30 ml vial

35 Taka

Dose and dosage

Cattle

First day: 1ml/2-3kg body weight 

From 2nd day: 1ml/4-6kg body weight for 4 days.

Buffalo

First day: 1ml/2-3kg body weight 

From 2nd day: 1ml/4-6kg body weight for 4 days.

Horse

First day: 1ml/2-3kg body weight 

From 2nd day: 1ml/4-6kg body weight for 4 days.

Goat

First day: 1ml/2-3kg body weight 

From 2nd day: 1ml/4-6kg body weight for 4 days.

Sheep

First day: 1ml/2-3kg body weight 

From 2nd day: 1ml/4-6kg body weight for 4 days.

Dog

First day: 1ml/2-3kg body weight 

From 2nd day: 1ml/4-6kg body weight for 4 days.

Cat

First day: 1ml/2-3kg body weight 

From 2nd day: 1ml/4-6kg body weight for 4 days.

Rabbit

First day: 1ml/2-3kg body weight 

From 2nd day: 1ml/4-6kg body weight for 4 days.


Applications:
  • Pneumonia
  • bronchitis
  • Hemorrhagic Septicemia
  • Actinobacillosis
  • infection of urogenital system
  • Metritis
  • Retention of placenta
  • Abscess
  • Gastrointestinal infection
  • Diarrhea
  • Dysentery
  • Enteritis
  • salmonellosis
  • Septicemia
Indication Notes:

Prevention of secondary bacterial infection

Avoid In:
  • Hypersensitivity
Contraindication Notes:

N/A

Sulfadimidine is a short-acting sulfonamide. It interferes with the synthesis of nucleic acids in sensitive organisms by blocking the conversion of p-aminobenzoic acid (PABA) to the co-enzyme dihydrofolic acid.

Nausea, vomiting, anorexia, diarrhoea, hypersensitivity reactions, SLE, serum sickness-like syndrome, liver necrosis and hepatomegaly, myocarditis, pulmonary eosinophilia and fibrosing alveolitis, vasculitis, hypoglycaemia, hypothyroidism, neurological reactions, jaundice and kernicterus in premature neonates

Sulfadimidine has been assigned to pregnancy category C by the FDA. Sulfonamides cross the placenta. Animal studies with high oral doses of some sulfonamides have revealed an increased incidence of cleft palate and other bony abnormalities.

Because sulfonamides compete with bilirubin for binding to serum albumin, free bilirubin levels rise in the presence of sulfonamides. Neonates are, therefore, at risk for hyperbilirubinemia, jaundice, and kernicterus when sulfonamides are administered to the mother near term

Meat: 7 days

Milk: 3 days