Vectobac 12 AS

Primær information

  • Handelsnavn:
  • Vectobac 12 AS Flydende middel
  • INN (International Name):
  • H14
  • Lægemiddelform:
  • Flydende middel
  • Sammensætning:
  • 1200 ITU/mg Bacilus thuringiensis var. H14
  • Brugt til:
  • Planter
  • Medicin typen:
  • agrokemiske

Dokumenter

  • for den brede offentlighed:
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    Anmode informationsbrochure for offentligheden.

Lokation

  • Fås i:
  • Vectobac 12 AS Flydende middel
    Danmark
  • Sprog:
  • dansk

Andre oplysninger

Status

  • Kilde:
  • SEGES Landbrug & Fødevarer
  • Autorisation status:
  • Udgået
  • Autorisationsnummer:
  • Ingen afstandskrav.
  • Sidste ændring:
  • 23-07-2018

Produktresumé: dosering, interaktioner, bivirkninger

LEVERANDØRBRUGSANVISNING

(Sikkerhedsdatablad)

Udarbejdet efter Arbejdsministeriets bekendtgørelse nr 485 af 16. juni 1995 om stoffer og materialer, § 16, stk. 2.

VECTOBAC

12AS

1. Produktidentifikation

VECTOBAC

12AS

Produkttype:

Biologisk insektmiddel til bekæmpelse

af larver på planter

Leverandør:

Cillus A/S

Tlf.: 4491 6055

Kobbervej 8

Fax.: 4491 6575

2730

Herlev

Kontaktperson: E. Rubæk

2. Oplysning om indholdsstoffer:

Analyse:

VECTOBAC

12AS indeholder 1200

International Toxic Units pr. mg

(1,25%) af Bacillus thuringiensis H-14.

Resten inaktive fyldstoffer (98,75%).

3. Faredeklaration

For mennesker: Undgå kontakt med huden og øjnene.

4. Førstehjælp

Øjne:

Kommer stoffet i øjnene, skylles straks

med vand og læge kontaktes.

Hud:

Forurenet tøj fjernes straks, og forure-

net hud vaskes straks med vand og

sæbe.

Indånding:

Søg frisk luft og hvile

Indtagelse:

Skyl munden, drik rigeligt vand og søg

læge.

Forbrænding:

Ikke brændbart.

5. Forholdsregler ved brand

Produktet bør så vidt muligt fjernes fra brandstedet.

Sluk med pulver, skum eller vandtåge. Hold emballa-

gerne afkølet ved oversprøjtning med vand, hvis udsat

for stærk varme. Undgå indånding af røg og gasser, der

udvikles ved branden.

6. Forholdsregler ved spild

Må ikke hældes i afløb, vandløb eller på jorden.

Evt. spild opsamles med væskeabsorberende materiale,

og dette skal sammen med tom emballage og rester af-

leveres til den kommunale modtageordning.

7. Håndtering og opbevaring

Undgå spild. Brug ansigtsskærm eller beskyttelsesbril-

ler, handsker og forklæde ved udsprøjtning.

S2 -Opbevares utilgængeligt for børn.

S13 -Må ikke opbevares sammen med fødevarer, drik-

kevarer og foderstoffer.

8. Eksponeringskontrol/Personlige værnemidler

Undgå indånding af sprøjtetågen

Undgå kontakt med huden

Brug beskyttelseshandsker. Flerlagshandsker bør fore-

trækkes. Tilsmudset tøj skiftes straks.

Vask huden efter arbejdet.

Efter sprøjtning skal planterne være tørre på bladene,

inden håndtering påbegyndes.

Følg i øvrigt Arbejdstilsynets vejledning og regler om

arbejdstøj og personlige værnemidler.

9. Fysisk-kemiske egenskaber

Tilstandsform:

Vandig suspension

Farve:

Lysebrun

Lugt:

Fermenteringsagtig

Kogepunkt:

Frysepunkt:

Flammepunkt:

ikke brændbart

Opløselighed

i vand:

Opslemning

Vægtfylde:

1,05

ca. 5

10. Stabilitet og reaktivitet

Produktet er lagerfast i mindst 2 år i uåbnet emballage.

Undgå store temperaturudsving. Undgå direkte sollys.

11. Toksikologiske oplysninger

Akut LD-50:

Ved indtagelse > 5000 mg/kg

Ved hudkontakt > 5000 mg/kg

Akut LC-50:

Ved inhalering >5,34 mg/l

Indånding:

Kan give svag irritation.

Hudkontakt:

Kan give svag irritation ved langvarig

påvirkning.

Øjnene:

Stænk i øjnene giver svag irritation

(sviden)

VECTOBAC

12AS

29.04.04

Side 2 af 2

12. Miljøoplysninger

Såvel B.t. som fyldstofferne anses for ikke særlig ska-

delig for miljøet. Se i øvrigt punkt 6.

13. Bortskaffelse

Tom emballage må ikke genanvendes til andet formål.

Tom emballage og rester afleveres til den kommunale

modtageordning.

Rengjort emballage afleveres som dagrenovation.

14. Transportoplysninger

VECTOBAC

12AS er ikke underlagt ADR, hvorfor

der ikke er specielle regler for tranport.

15. Forholdsregler ved brug:

Opbevaring:

VECTOBAC

12AS opbevares frost-

frit.

Må ikke stå i direkte sollys.

Holdbar i uåbnet emballage i mindst 2

år.

Emballagen omrystes grundigt inden det afmålte

kvantum hældes i sprøjtebeholderen under moderat

omrøring.

Tømt og skyllet emballage bortskaffes med dagre-

novationen.

Kommer væsken i øjnene, skyl da omgående med

rigeligt vand

Undgå indånding af sprøjtevæsken.

Anvend ansigtsskærm, handsker og forklæde ved

udsprøjtning.

Planterne skal være tørre inden håndtering påbe-

gyndes.

Vask sprøjteudstyret straks efter arbejdets ophør.

Der kræves ingen særlig uddannelse, dog må unge

under 18 år ikke arbejde med produktet.

16. Brugsanvisning

VECTOBAC

12AS er et biologisk bekæmpelses-

middel, der anvendes mod larver af sørgemyg

(svampemyg) i væksthuse, samt filterfluer (møg-

fluer) i rensningsanlæg og stankelbenlarver på

græsarealer.

"

VECTOBAC

12AS anvendes erhvervsmæssigt

eller privat efter behov.

"

Der er ingen behandlingsfrist. Vask hænder og ud-

styr efter endt udsprøjtning.

"

VECTOBAC

12AS sprøjtevandes på borde, i

potter og på jorden under bordene. Der vandes så

de øverste 3-4 cm af voksemediet er gennemvædet

-ca 2 ltr. væske pr m

. Gennemvanding bør have

fundet sted, inden sprøjtevanding -ikke omvendt.

"

VECTOBAC

12AS optages af sørgemyggens

larver i jorden. Efter 1-2 dages forløb standser lar-

verne fødeoptagelsen og dør.

"

Doseringen er 0,125 - 0,25% styrke i 2 ltr. vand pr.

. Svarende til, at der anvendes 2½ - 5 ml

VECTOBAC

12AS pr m

. 1 ltr. VECTOBAC

12AS rækker således til 200 - 400 m

behandlet

areal.

"

Første behandling umiddelbart efter oppotning.

Behandlingen gentages med 5 - 7 dages interval, i

alt 3 gange. Brug gule limplader til at kontrollere

om flyvningen er holdt op. VECTOBAC

12AS

kan sprøjtevandes sammen med nematoder.

"

VECTOBAC

12AS må ikke blandes med gød-

ning eller lign., der kan neutralisere virkningen -

hverken ved tankblanding eller drypvanding.

Tålsomhed:

Mange plantearter har været prøvet

uden skade, når doseringen overholdes.

Når der skiftes fra en art/sort til en an-

den, eller kulturbetingelserne ændres,

anbefales det at prøve få planter, inden

et helt parti behandles.

VECTOBAC

12AS er anerkendt af

Danmarks Jordbrugsforskning til be-

handling mod larver af sørgemyg på

prydplanter i væksthus med 5 ml pr m

2

Larver af mosestankelben på græsarealer kan være et

problem. Især hvis der året efter skal sås andre afgrø-

der. En total bekæmpelse af mosestankelben er ikke

mulig, men en væsentlig reduktion af larvebestanden

kan forventes.

Tidspunkt:

I oktober måned vælges en mild og fugtig dag. Sprøjt

sidst på dagen når larverne kommer op til overfladen

for at æde af planterne.

Dosering:

2 -2½ ltr. VECTOBAC

12AS pr. ha i mindst 400 ltr.

vand, gerne mere. Evt. i let regnvejr.

Genbehandling:

Hvis klækning af larver sker over en lang periode, kan

behandlingen gentages - evt. næste forår, fortsat med

stor fugtighed i jordoverfladen og gerne i let regn.

Læs mere om bekæmpelse af mosestankelben i ”Mar-

kens sygdomme og skadedyr”.

Udarbejdet af E. Rubæk den 29.04.2004

  • Oplysningerne indlægssedlen for dette produkt er i øjeblikket ikke tilgængelig, kan du sende en anmodning til vores kundeservice, og vi vil give dig besked, så snart vi er i stand til at opnå det.

    Anmode informationsbrochure for offentligheden.



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14-12-2018


European Medicines Agency stakeholder interaction on the development of medicinal products for chronic non-infectious liver diseases (PBC, PSC, NASH), European Medicines Agency, London, UK, from 03/12/2018 to 03/12/2018

European Medicines Agency stakeholder interaction on the development of medicinal products for chronic non-infectious liver diseases (PBC, PSC, NASH), European Medicines Agency, London, UK, from 03/12/2018 to 03/12/2018

European Medicines Agency stakeholder interaction on the development of medicinal products for chronic non-infectious liver diseases (PBC, PSC, NASH), European Medicines Agency, London, UK, from 03/12/2018 to 03/12/2018

Europe - EMA - European Medicines Agency

13-2-2019


Orphan designation: Recombinant IgG degrading enzyme of Streptococcus pyogenes (imlifidase), Prevention of graft rejection following solid organ transplantation, 12/01/2017, Positive

Orphan designation: Recombinant IgG degrading enzyme of Streptococcus pyogenes (imlifidase), Prevention of graft rejection following solid organ transplantation, 12/01/2017, Positive

Orphan designation: Recombinant IgG degrading enzyme of Streptococcus pyogenes (imlifidase), Prevention of graft rejection following solid organ transplantation, 12/01/2017, Positive

Europe - EMA - European Medicines Agency

13-2-2019


Orphan designation: Agammaglobulinaemia tyrosine kinase, Treatment of pemphigus, 12/12/2017, Positive

Orphan designation: Agammaglobulinaemia tyrosine kinase, Treatment of pemphigus, 12/12/2017, Positive

Orphan designation: Agammaglobulinaemia tyrosine kinase, Treatment of pemphigus, 12/12/2017, Positive

Europe - EMA - European Medicines Agency

13-2-2019


Orphan designation: Humanised single-chain monoclonal antibody against CD37 (otlertuzumab), Treatment chronic lymphocytic leukaemia, 06/12/2012, Positive

Orphan designation: Humanised single-chain monoclonal antibody against CD37 (otlertuzumab), Treatment chronic lymphocytic leukaemia, 06/12/2012, Positive

Orphan designation: Humanised single-chain monoclonal antibody against CD37 (otlertuzumab), Treatment chronic lymphocytic leukaemia, 06/12/2012, Positive

Europe - EMA - European Medicines Agency

12-2-2019

Vaxxitek HVT + IBD (Merial)

Vaxxitek HVT + IBD (Merial)

Vaxxitek HVT + IBD (Active substance: Live vHVT013-69 recombinant virus) - Centralised - Yearly update - Commission Decision (2019)1098 of Tue, 12 Feb 2019

Europe -DG Health and Food Safety

12-2-2019

Halagon (Emdoka bvba)

Halagon (Emdoka bvba)

Halagon (Active substance: halofuginone) - Centralised - Yearly update - Commission Decision (2019)1095 of Tue, 12 Feb 2019

Europe -DG Health and Food Safety

12-2-2019

Helicobacter Test INFAI (INFAI GmbH)

Helicobacter Test INFAI (INFAI GmbH)

Helicobacter Test INFAI (Active substance: 13C - urea) - Centralised - Yearly update - Commission Decision (2019)1109 of Tue, 12 Feb 2019

Europe -DG Health and Food Safety

12-2-2019

Kriptazen (Virbac)

Kriptazen (Virbac)

Kriptazen (Active substance: halofuginone) - Centralised - Authorisation - Commission Decision (2019)1097 of Tue, 12 Feb 2019 European Medicines Agency (EMA) procedure number: EMEA/V/C/4868

Europe -DG Health and Food Safety

12-2-2019

Vectra Felis (Ceva SantE Animale)

Vectra Felis (Ceva SantE Animale)

Vectra Felis (Active substance: dinotefuran, pyriproxyfen) - Centralised - Renewal - Commission Decision (2019)1096 of Tue, 12 Feb 2019 European Medicines Agency (EMA) procedure number: EMEA/V/C/2746/R/08

Europe -DG Health and Food Safety

5-2-2019


Human medicines European public assessment report (EPAR): Bevespi Aerosphere, glycopyrronium / formoterol fumarate dihydrate, Pulmonary Disease, Chronic Obstructive, Date of authorisation: 18/12/2018, Status: Authorised

Human medicines European public assessment report (EPAR): Bevespi Aerosphere, glycopyrronium / formoterol fumarate dihydrate, Pulmonary Disease, Chronic Obstructive, Date of authorisation: 18/12/2018, Status: Authorised

Human medicines European public assessment report (EPAR): Bevespi Aerosphere, glycopyrronium / formoterol fumarate dihydrate, Pulmonary Disease, Chronic Obstructive, Date of authorisation: 18/12/2018, Status: Authorised

Europe - EMA - European Medicines Agency

4-2-2019

Memantine Accord (Accord Healthcare S.L.U.)

Memantine Accord (Accord Healthcare S.L.U.)

Memantine Accord (Active substance: memantine) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2019)844 of Mon, 04 Feb 2019 European Medicines Agency (EMA) procedure number: EMEA/H/C/2766/T/12

Europe -DG Health and Food Safety

4-2-2019

EU/3/12/1083 (Voisin Consulting S.A.R.L.)

EU/3/12/1083 (Voisin Consulting S.A.R.L.)

EU/3/12/1083 (Active substance: Humanised single chain monoclonal antibody against CD37) - Transfer of orphan designation - Commission Decision (2019)814 of Mon, 04 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000003624

Europe -DG Health and Food Safety

1-2-2019


Human medicines European public assessment report (EPAR): Namuscla, mexiletine hcl, Myotonic Disorders, Date of authorisation: 18/12/2018, Status: Authorised

Human medicines European public assessment report (EPAR): Namuscla, mexiletine hcl, Myotonic Disorders, Date of authorisation: 18/12/2018, Status: Authorised

Human medicines European public assessment report (EPAR): Namuscla, mexiletine hcl, Myotonic Disorders, Date of authorisation: 18/12/2018, Status: Authorised

Europe - EMA - European Medicines Agency

1-2-2019

EU/3/12/1068 (StEphane Gibaud)

EU/3/12/1068 (StEphane Gibaud)

EU/3/12/1068 (Active substance: Melarsoprol) - Transfer of orphan designation - Commission Decision (2019)813 of Fri, 01 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000003439

Europe -DG Health and Food Safety

1-2-2019


Withdrawn application: Cavoley, pegfilgrastim, Date of withdrawal: 20/12/2018, Initial authorisation

Withdrawn application: Cavoley, pegfilgrastim, Date of withdrawal: 20/12/2018, Initial authorisation

Withdrawn application: Cavoley, pegfilgrastim, Date of withdrawal: 20/12/2018, Initial authorisation

Europe - EMA - European Medicines Agency

1-2-2019


Withdrawn application: Efgratin, pegfilgrastim, Date of withdrawal: 20/12/2019, Initial authorisation

Withdrawn application: Efgratin, pegfilgrastim, Date of withdrawal: 20/12/2019, Initial authorisation

Withdrawn application: Efgratin, pegfilgrastim, Date of withdrawal: 20/12/2019, Initial authorisation

Europe - EMA - European Medicines Agency

16-1-2019

EU/3/12/1062 (EUSA Pharma (Netherlands) B.V.)

EU/3/12/1062 (EUSA Pharma (Netherlands) B.V.)

EU/3/12/1062 (Active substance: Chimeric monoclonal antibody against GD2) - Transfer of orphan designation - Commission Decision (2019)238 of Wed, 16 Jan 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000003198

Europe -DG Health and Food Safety

11-1-2019

Consultation: Good Clinical Practice Inspections Program

Consultation: Good Clinical Practice Inspections Program

The TGA is seeking comments from interested parties on a pilot Good Clinical Practice (GCP) Inspections Program of 12 months duration that will inform a routine GCP Inspections Program. Closing date: 22 February 2019

Therapeutic Goods Administration - Australia

20-12-2018

TGA presentations: CAPSIG Seminar, 12 September 2018

TGA presentations: CAPSIG Seminar, 12 September 2018

Overview of regulatory requirements introduced as part of PIC/s PE009-13 Guide to GMP and a summary of the new PI041-1 Data Integrity

Therapeutic Goods Administration - Australia

19-12-2018

On 12/12/18 GE Healthcare Recalled CareScape R860 Inspiratory Safety Guard Due to Risk of Disconnection from Breathing Circuit. @US_FDA has identified this as a Class I Recall, the most serious type recall. Read more about the recall:  https://go.usa.gov/

On 12/12/18 GE Healthcare Recalled CareScape R860 Inspiratory Safety Guard Due to Risk of Disconnection from Breathing Circuit. @US_FDA has identified this as a Class I Recall, the most serious type recall. Read more about the recall: https://go.usa.gov/

On 12/12/18 GE Healthcare Recalled CareScape R860 Inspiratory Safety Guard Due to Risk of Disconnection from Breathing Circuit. @US_FDA has identified this as a Class I Recall, the most serious type recall. Read more about the recall: https://go.usa.gov/xE383  #MedicalDevice #FDA pic.twitter.com/S2EbMdmwpe

FDA - U.S. Food and Drug Administration

19-12-2018

EU/3/12/1087 (Richardson Associates Regulatory Affairs Ltd)

EU/3/12/1087 (Richardson Associates Regulatory Affairs Ltd)

EU/3/12/1087 (Active substance: Recombinant modified human growth hormone) - Transfer of orphan designation - Commission Decision (2018)9014 of Wed, 19 Dec 2018 European Medicines Agency (EMA) procedure number: EMA/OD/0000002652

Europe -DG Health and Food Safety

18-12-2018


Human medicines European public assessment report (EPAR): Dengvaxia, dengue tetravalent vaccine (live, attenuated), Dengue, Date of authorisation: 12/12/2018, Status: Authorised

Human medicines European public assessment report (EPAR): Dengvaxia, dengue tetravalent vaccine (live, attenuated), Dengue, Date of authorisation: 12/12/2018, Status: Authorised

Human medicines European public assessment report (EPAR): Dengvaxia, dengue tetravalent vaccine (live, attenuated), Dengue, Date of authorisation: 12/12/2018, Status: Authorised

Europe - EMA - European Medicines Agency

18-12-2018

EU/3/12/963 (Helsinn Birex Pharmaceuticals Ltd)

EU/3/12/963 (Helsinn Birex Pharmaceuticals Ltd)

EU/3/12/963 (Active substance: Chlormethine) - Transfer of orphan designation - Commission Decision (2018)9016 of Tue, 18 Dec 2018 European Medicines Agency (EMA) procedure number: EMA/OD/0000002753

Europe -DG Health and Food Safety

18-12-2018

Consultation: Review of Therapeutic Goods Order 54 - Standards for Disinfectants; and associated guidance

Consultation: Review of Therapeutic Goods Order 54 - Standards for Disinfectants; and associated guidance

TGA is seeking comments on the expansion and amendment of TGO 54. Closing date: 12 February 2019

Therapeutic Goods Administration - Australia

17-12-2018


Orphan designation: Nanoliposomal irinotecan, Treatment of pancreatic cancer, 09/12/2011, Positive

Orphan designation: Nanoliposomal irinotecan, Treatment of pancreatic cancer, 09/12/2011, Positive

Orphan designation: Nanoliposomal irinotecan, Treatment of pancreatic cancer, 09/12/2011, Positive

Europe - EMA - European Medicines Agency

14-12-2018


Summary of opinion: Adcetris,brentuximab vedotin,  13/12/2018,  Positive

Summary of opinion: Adcetris,brentuximab vedotin, 13/12/2018, Positive

Summary of opinion: Adcetris,brentuximab vedotin, 13/12/2018, Positive

Europe - EMA - European Medicines Agency

14-12-2018


Summary of opinion: Trecondi,treosulfan,  13/12/2018,  Positive

Summary of opinion: Trecondi,treosulfan, 13/12/2018, Positive

Summary of opinion: Trecondi,treosulfan, 13/12/2018, Positive

Europe - EMA - European Medicines Agency

14-12-2018


Summary of opinion: Besremi,ropeginterferon alfa-2b,  13/12/2018,  Positive

Summary of opinion: Besremi,ropeginterferon alfa-2b, 13/12/2018, Positive

Summary of opinion: Besremi,ropeginterferon alfa-2b, 13/12/2018, Positive

Europe - EMA - European Medicines Agency

14-12-2018


Summary of opinion: Lusutrombopag Shionogi,lusutrombopag,  13/12/2018,  Positive

Summary of opinion: Lusutrombopag Shionogi,lusutrombopag, 13/12/2018, Positive

Summary of opinion: Lusutrombopag Shionogi,lusutrombopag, 13/12/2018, Positive

Europe - EMA - European Medicines Agency

14-12-2018


Summary of opinion: Rapiscan,regadenoson,  13/12/2018,  Positive

Summary of opinion: Rapiscan,regadenoson, 13/12/2018, Positive

Summary of opinion: Rapiscan,regadenoson, 13/12/2018, Positive

Europe - EMA - European Medicines Agency

14-12-2018


Referral: Fosfomycin-containing medicinal products, fosfomycin calcium, fosfomycin disodium, fosfomycin sodium, fosfomycin trometamol, Article 31 referrals, Procedure started, 13/12/2018

Referral: Fosfomycin-containing medicinal products, fosfomycin calcium, fosfomycin disodium, fosfomycin sodium, fosfomycin trometamol, Article 31 referrals, Procedure started, 13/12/2018

Referral: Fosfomycin-containing medicinal products, fosfomycin calcium, fosfomycin disodium, fosfomycin sodium, fosfomycin trometamol, Article 31 referrals, Procedure started, 13/12/2018

Europe - EMA - European Medicines Agency

14-12-2018


Summary of opinion: Miglustat Dipharma,miglustat,  13/12/2018,  Positive

Summary of opinion: Miglustat Dipharma,miglustat, 13/12/2018, Positive

Summary of opinion: Miglustat Dipharma,miglustat, 13/12/2018, Positive

Europe - EMA - European Medicines Agency

14-12-2018


Summary of opinion: Tobramycin PARI,tobramycin,  13/12/2018,  Positive

Summary of opinion: Tobramycin PARI,tobramycin, 13/12/2018, Positive

Summary of opinion: Tobramycin PARI,tobramycin, 13/12/2018, Positive

Europe - EMA - European Medicines Agency

14-12-2018


Withdrawn application: Fyzoclad, adalimumab, Date of withdrawal: 05/12/2018, Initial authorisation

Withdrawn application: Fyzoclad, adalimumab, Date of withdrawal: 05/12/2018, Initial authorisation

Withdrawn application: Fyzoclad, adalimumab, Date of withdrawal: 05/12/2018, Initial authorisation

Europe - EMA - European Medicines Agency

14-12-2018


Withdrawn application: Canakinumab Novartis, canakinumab, Date of withdrawal: 04/12/2018, Initial authorisation

Withdrawn application: Canakinumab Novartis, canakinumab, Date of withdrawal: 04/12/2018, Initial authorisation

Withdrawn application: Canakinumab Novartis, canakinumab, Date of withdrawal: 04/12/2018, Initial authorisation

Europe - EMA - European Medicines Agency

14-12-2018


Summary of opinion: Trimbow,beclometasone / formoterol / glycopyrronium bromide,  13/12/2018,  Positive

Summary of opinion: Trimbow,beclometasone / formoterol / glycopyrronium bromide, 13/12/2018, Positive

Summary of opinion: Trimbow,beclometasone / formoterol / glycopyrronium bromide, 13/12/2018, Positive

Europe - EMA - European Medicines Agency

14-12-2018


Summary of opinion: Simponi,golimumab,  13/12/2018,  Positive

Summary of opinion: Simponi,golimumab, 13/12/2018, Positive

Summary of opinion: Simponi,golimumab, 13/12/2018, Positive

Europe - EMA - European Medicines Agency