PULMOCIS

This brand name is authorized in Austria, Croatia, Estonia, France, Hong Kong SAR China, Ireland, Malta, UK.

Active ingredients

The drug PULMOCIS contains one active pharmaceutical ingredient (API):

1
UNII ZIF514RVZR - ALBUMIN HUMAN
 

Technetium ⁹⁹ᵐTc macrosalb is for diagnostic use only. It is used for pulmonary perfusion scintigraphy and radionuclide venography. When administered in usual doses, technetium [99mTc] macrosalb injection shows no pharmacodynamic effects detectable clinically or/and analytically.

 
Read more about Technetium ⁹⁹ᵐTc macrosalb

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 PULMOCIS Kit for radiopharmaceutical preparation MPI, EU: SmPC Health Products Regulatory Authority (IE)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
V09EB01 Technetium (99mTc) macrosalb V Various → V09 Diagnostic radiopharmaceuticals → V09E Respiratory system → V09EB Technetium (99mTc), particles for injection
Discover more medicines within V09EB01

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
EE Ravimiamet 1385232
FR Base de données publique des médicaments 67986283
GB Medicines & Healthcare Products Regulatory Agency 395330
HK Department of Health Drug Office 66231
HR Agencija za lijekove i medicinske proizvode HR-H-430112868
MT Medicines Authority MA826/00502

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