Polypleurisin APX Plus IM Formulation:  Each mL (dose) contains:  Actinobacillus pleuropneumoniae Serotype 2 and 9 …………………..≥ 1 RP  Bordetella bronchiseptica Serotype 9 …………………..≥ 1 RP  Pasteurella multocida Serotype 625/A and 115/D…………………..≥ 1 RP  Actinobacillus pleuropneumoniae (Apx I, II and III Toxin)…………………..≥ 1 RP       RP Relative Potency Emulsion for Injection  (IM) Philippines - anglais - FDA (Food And Drug Administration)

polypleurisin apx plus im formulation: each ml (dose) contains: actinobacillus pleuropneumoniae serotype 2 and 9 …………………..≥ 1 rp bordetella bronchiseptica serotype 9 …………………..≥ 1 rp pasteurella multocida serotype 625/a and 115/d…………………..≥ 1 rp actinobacillus pleuropneumoniae (apx i, ii and iii toxin)…………………..≥ 1 rp rp relative potency emulsion for injection (im)

broadchem philippines biopharma corporation - inactivated actinobacillus pleuropneumoniae , bordetella bronchiseptica , pasteurella multocida , actinobacillus pleuropneumoniae toxoid vaccine (vet.) - emulsion for injection (im) - formulation: each ml (dose) contains: actinobacillus pleuropneumoniae serotype 2 and 9 …………………..≥ 1 rp bordetella bronchiseptica serotype 9 …………………..≥ 1 rp pasteurella multocida serotype 625/a and 115/d…………………..≥ 1 rp actinobacillus pleuropneumoniae (apx i, ii and iii toxin)…………………..≥ 1 rp rp relative potency

Izovac FC Formulation:   Each 0.5 mL (dose) contains:   Pasteurella multocida, Serotypes 1, 3 and 4   SAT - Serum Agglutination Test   ≥ 7.3 log2 SAT Emulsion for Injection (SC) Philippines - anglais - FDA (Food And Drug Administration)

izovac fc formulation: each 0.5 ml (dose) contains: pasteurella multocida, serotypes 1, 3 and 4 sat - serum agglutination test ≥ 7.3 log2 sat emulsion for injection (sc)

farmline agriventures, inc.; distributor: farmline agriventures, inc. - inactivated pasteurella multocida vaccine (vet.) - emulsion for injection (sc) - formulation: each 0.5 ml (dose) contains: pasteurella multocida, serotypes 1, 3 and 4 sat - serum agglutination test ≥ 7.3 log2 sat

RISPOVAL PASTEURELLA Irlande - anglais - HPRA (Health Products Regulatory Authority)

rispoval pasteurella

pfizer healthcare ireland - pasteurella haemolytica type a1 strain nl 1009 - lyophilisate and solvent for emulsion for injection - bovine - immunological - inactivated vaccine

Bovilis Bovipast RSP suspension for injection for cattle Irlande - anglais - HPRA (Health Products Regulatory Authority)

bovilis bovipast rsp suspension for injection for cattle

intervet ireland limited - inactivated bovine respiratory syncytial virus strain ev908; inactivated parainfluenza-3-virus, strain sf-4 reisinger; inactivated mannheimia (pasteurella) haemolyticaa1, strain m4/1 - suspension for injection - . - bovine parainfluenza virus + bovine respiratory syncytial virus + pasteurella - cattle - immunological - inactivated vaccine

Poulvac Pabac IV Vaccine (Inactivated) Nouvelle-Zélande - anglais - Ministry for Primary Industries

poulvac pabac iv vaccine (inactivated)

zoetis new zealand limited - pasteurella multocida (inactivated) - pasteurella multocida (inactivated) 0 vaccine - vaccine

LINEZOLID- linezolid tablet, film coated États-Unis - anglais - NLM (National Library of Medicine)

linezolid- linezolid tablet, film coated

teva pharmaceuticals usa inc - linezolid (unii: isq9i6j12j) (linezolid - unii:isq9i6j12j) - linezolid 600 mg - linezolid is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions listed below. linezolid is not indicated for the treatment of gram-negative infections. it is critical that specific gram-negative therapy be initiated immediately if a concomitant gram-negative pathogen is documented or suspected [see warnings and precautions (5.4) ]. nosocomial pneumonia caused by staphylococcus aureus (methicillin-susceptible and -resistant isolates) or streptococcus pneumoniae [see clinical studies (14) ]. community-acquired pneumonia caused by streptococcus pneumoniae , including cases with concurrent bacteremia, or staphylococcus aureus (methicillin-susceptible isolates only) [see clinical studies (14) ]. complicated skin and skin structure infections, including diabetic foot infections, without concomitant osteomyelitis , caused by staphylococcus aureus (methicillin-susceptible and -resistant isolates), streptococcus pyogenes , or strept

CIPROFLOXACIN tablet, film coated États-Unis - anglais - NLM (National Library of Medicine)

ciprofloxacin tablet, film coated

aphena pharma solutions - tennessee, llc - ciprofloxacin hydrochloride (unii: 4ba73m5e37) (ciprofloxacin - unii:5e8k9i0o4u) - ciprofloxacin 500 mg - ciprofloxacin tablets are indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the conditions and patient populations listed below. please see dosage and administration  for specific recommendations. urinary tract infections caused by escherichia coli, klebsiella pneumoniae, enterobacter cloacae, serratia marcescens, proteus mirabilis, providencia rettgeri, morganella morganii, citrobacter diversus, citrobacter freundii, pseudomonas aeruginosa, methicillin-susceptible staphylococcus epidermidis, staphylococcus saprophyticus, or enterococcus faecalis. acute uncomplicated cystitis in females caused by escherichia coli or staphylococcus saprophyticus. chronic bacterial prostatitis caused by escherichia coli or proteus mirabilis. lower respiratory tract infections caused by escherichia coli, klebsiella pneumoniae, enterobacter cloacae, proteus mirabilis, pseudomonas aeruginosa, haemophilus influenzae, haemophilus parainfluenzae, or penicillin-suscept

Porcilis AR-T inj. emuls. i.m. Belgique - anglais - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

porcilis ar-t inj. emuls. i.m.

intervet international b.v. - bordetella bronchiseptica (inactivated) ; pasteurella multocida d0 protein - emulsion for injection - pasteurella multocida; bordetella bronchiseptica - bordetella + pasteurella - pig

Porcilis AR-T inj. emuls. i.m. Belgique - anglais - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

porcilis ar-t inj. emuls. i.m.

intervet international - bordetella bronchiseptica (inactivated) = 8,0 log2/do agglutiantietiter; pasteurella multocida d0 protein = 4,0 log2/dose toxin-neutralising antibody titre - emulsion for injection - pasteurella multocida anatoxine; pasteurella multocida; bordetella bronchiseptica - bordetella + pasteurella - pig