Atreon 0.5g (Injection)
Manufactured by: Square Pharmaceuticals Ltd.
Aztreonam Similar medicine
Atreon is indicated for
- Fibrosis quística
- peritonitis
- infecciones bacterianas
- ITU
- infecciones del tracto respiratorio inferior
- cistitis
- gonorrea
- septicemia
- infecciones de la piel y de sus estructuras
- endometritis
- celulitis pélvica
Precautions and warnings
Hipersensibilidad a otros betalactámicos, insuficiencia renal, mujeres embarazadas e insuficiencia hepática.
Side-effects
- IV: Flobitis y tromboflobitis. IM: dolor e hinchazón en el sitio de la inyección; diarrea
- náuseas
- vómitos
- alteración del gusto; ictericia
- hepatitis
- enzimas hepáticas elevadas; tiempo de protrombina prolongado
- tiempo de tromboplastina parcial; erupción
- urticaria
- eosinofilia. Potencialmente fatal: trombocitopenia
- neutropenia; crecimiento excesivo de organismos susceptibles; colitis pseudomembranosa.
Drug Interactions
El uso concomitante con anticoagulantes orales puede aumentar el tiempo de protrombina.
Contraindications
Hipersensibilidad de la lactancia.
Mode of actions
Aztreonam tiene una alta afinidad por la proteína transportadora de penicilina 3 (PBP-3) de las bacterias gramnegativas y, por lo tanto, tiene un efecto bactericida al bloquear la formación de la pared celular bacteriana. Es muy resistente a la hidrólisis de lactamasa. Enterobacteriaceae spp, E. coli, Klebsiella, Proteus, Providencia, Salmonella, Serratia, Shigella y Yersinia spp son todas susceptibles.
Dosage & Administration
Adultos: Infecciones GM-ve IV/IM 1-8 g/día en dosis divididas según la gravedad. Máximo: 8 g/día.
ITU 0,5-1 g 8-12 horas.
Cistitis IM; Gonorrea 1 g en dosis única.
Niños: y lactantes >1 semana: 30 mg/kg cada 6 u 8 horas; >2 años: 50 mg/kg cada 6 u 8 horas para infecciones graves. La dosis se puede administrar mediante una inyección IM profunda o una inyección o infusión IV lenta. Las dosis >1 g deben administrarse por vía intravenosa. Máx. (>2 años): 8 g/día.
Insuficiencia renal: Insuficiencia moderada a grave: Mismas dosis iniciales, ajustar las dosis de mantenimiento según el CrCl del paciente. Hemodiálisis: Se podrá administrar una dosis suplementaria de 1/8 de la dosis inicial después de cada sesión.
ClCr (ml/min)
10-30 Dosis de mantenimiento: La mitad de la dosis inicial.
Pregnancy & Lactation
Aunque los estudios de reproducción en animales han demostrado un efecto adverso, incluso a veces no pueden demostrar el riesgo para el feto y no existen estudios adecuados y bien controlados en mujeres embarazadas, durante el embarazo este medicamento se puede utilizar sólo cuando sea definitivamente necesario.
Hable con sus médicos y cuénteles sus comentarios sobre este medicamento.
No existe información específica sobre si este medicamento se transmite al bebé a través de la leche materna. Hable con su médico antes de amamantar.
Pack Size & Price
1's pack Price : ৳300
Similar medicine
Manufactured by: Incepta Pharmaceuticals Ltd.
Manufactured by: Square Pharmaceuticals Ltd.
Manufactured by: Square Pharmaceuticals Ltd.
Manufactured by: Square Pharmaceuticals Ltd.
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