01 4ANAKINRA
02 1AVATROMBOPAG (AVATROMBOPAG MALEATE)
03 13Anakinra
04 3Avatrombopag
05 2Avatrombopag Maleate
06 3Avatrombopagmaleat
07 1Avatrombopagum
08 1Collagenase Clostridium Histolyticum
09 1Collagenase, Clostridium Histolyticum
10 14Efanesoctocog Alfa
11 7Efanesoctocog Alpha
12 7Efanesoctocog alfa
13 7Efanesoktokog alfa
14 26Efmoroctocog Alfa
15 8Efmoroctocog alfa
16 10Eftrenonacog Alfa
17 5Eftrenonacog alfa
18 5Eftrenonacogum Alfa
19 2Interferon Alpha (Leukocyte-derived)
20 1Loncastuximab Tesirine
21 1Loncastuximab tesirine
22 1Lonkastuximabtesirin
23 10NITISINONE
24 10Nitisinon
25 17Nitisinone
26 1Olezarsen
27 1PACRITINIB CITRATE
28 1PALIFERMIN
29 2PALIVIZUMAB
30 1PEGCETACOPLAN
31 1Palifermin
32 11Pegcetacoplan
33 1Pegcetacoplanum
34 2Sodium 4-Phenylbutyrate
35 8efmoroctocog alfa
36 5eftrenonacog alfa
01 4BIOVITRUM AB
02 1SOBI
03 7SWEDISH ORPHAN
04 6SWEDISH ORPHAN BIOVITR.INT.AB
05 8SWEDISH ORPHAN BIOVITRUM AB (PUBL)
06 2SWEDISH ORPHAN BIOVITRUM AB(PU
07 4SWEDISH ORPHAN BIOVITRUM INTERNATIONAL AB
08 7Swedish Orphan Biovitrum AB
09 3Swedish Orphan Biovitrum AB (1)
10 81Swedish Orphan Biovitrum Ab (Publ)
11 22Swedish Orphan Biovitrum Ag
12 17Swedish Orphan Biovitrum International AB
13 16Swedish Orphan Biovitrum International Ab
14 12Swedish Orphan Biovitrum Pty Ltd
15 3Swedish Orphan International AB
16 1Swedish Orphan International Ab
01 2Anakinra 100Mg 0.67 Ml 7 Joined The Parenteral Use
02 4CAPSULE
03 5CAPSULE;ORAL
04 12Capsule
05 1Collagenase Clostridium Histolyticum 0,9Mg 1 Units Use Intralesional
06 6Film Coated Tablet
07 1Film-Coated Tablet
08 4Hard Capsule
09 3Hard Capsule For Oral Use
10 1Hard Capsule Oral Use Hdpe
11 1INJECTABLE; INJECTION
12 2Infusion Solution
13 3Injectable Solution
14 1Injectable Solution In Pre-Filled Pen
15 3Injectable Solution In Pre-Filled Syringe
16 1Nitisinone 10Mg 60 Units Oral Use
17 1Nitisinone 2Mg 60 Units Oral Use
18 1Nitisinone 5Mg 60 Units Oral Use
19 4Oral Suspension
20 20Powder And Solvent For Injectable Solution
21 1Powder For Concentrate For Infusion Solution
22 2Powder For Concentrate For Solution For Infusion
23 1Powder For Solution For Injection
24 2SOLUTION
25 1SUSPENSION
26 1SUSPENSION;ORAL
27 1Sodium Phenylbutyrate 266G 940Mg/G Oral Use
28 1Sodium Phenylbutyrate 500Mg 250 Unita' Oral Use
29 3Solution For Infusion
30 86Solution For Injection
31 1Solution For Perfusion
32 1TABLET
33 2VIAL
34 3VIAL; SUBCUTANEOUS
35 2injection
36 10Blank
01 10.9mg
02 11 vial groun 0.9 mg + 1 vial solv
03 110 mg
04 2100 mg/0.67 mL
05 31000IE
06 111000IU
07 11000IU/5ml
08 3100MG
09 1100MG/VIAL
10 2100mg
11 3100mg/0.67ml
12 11080MG
13 11080MG/20ML
14 11080mg
15 11080mg/20ml
16 410MG
17 110MIU/VIAL
18 510mg
19 114400IU
20 51500IU
21 1150MG/ML
22 1150mg/ml
23 118MIU/VIAL
24 12 mg
25 120 mg
26 32000IE
27 112000IU
28 12000IU/5ml
29 520MG
30 920mg
31 1250 CPR 500 mg bottle
32 3250IE
33 11250IU
34 1250IU/5ml
35 125MIU/VIAL
36 32MG
37 32mg
38 133000IU
39 13000IU/5ml
40 13millionIU
41 14 000 IU
42 14000IE
43 84000IU
44 14MG
45 24MG/ML
46 34mg/ml
47 15 mg
48 15000IE
49 14500IU
50 1500IU/5ml
51 150MG/VIAL
52 154mg/ml
53 35MG
54 25mg
55 16.25mg
56 160 cps 10 mg vial
57 160 cps 2 mg bottle
58 160 cps 5 mg bottle
59 16000IU
60 160MCG/KG/DAY
61 16millionIU/ml
62 27 Syringes SC 100 mg 0,67 ml
63 1750IE
64 9750IU
65 180MG
66 1EQ 100MG BASE
67 1os granulate for suspension 266 g 940 mg/g
68 11Blank
01 12Australia
02 8Canada
03 29Estonia
04 12Italy
05 30Norway
06 32Spain
07 37Sweden
08 22Switzerland
09 12USA
Regulatory Info :
Registration Country : USA
Dosage Form : VIAL; SUBCUTANEOUS
Brand Name : KINERET
Dosage Strength : 10MIU/VIAL
Packaging :
Approval Date :
Application Number : 103950
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : VIAL; SUBCUTANEOUS
Brand Name : KINERET
Dosage Strength : 18MIU/VIAL
Packaging :
Approval Date :
Application Number : 103950
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : VIAL; SUBCUTANEOUS
Brand Name : KINERET
Dosage Strength : 25MIU/VIAL
Packaging :
Approval Date :
Application Number : 103950
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : Italy
Dosage Form : Anakinra 100Mg 0.67 Ml 7...
Brand Name : Kineret
Dosage Strength : 7 Syringes SC 100 mg 0...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Anakinra 100Mg 0.67 Ml 7...
Brand Name : Kineret
Dosage Strength : 7 Syringes SC 100 mg 0...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Solution For Injection
Brand Name : Kineret
Dosage Strength : 100mg/0.67ml
Packaging :
Approval Date : 15/11/2013
Application Number : 20121129000048
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Injectable Solution
Brand Name : Kineret
Dosage Strength : 100mg
Packaging :
Approval Date : 08/03/2002
Application Number : 20020308000025
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Solution For Injection
Brand Name : Kineret
Dosage Strength : 100mg
Packaging :
Approval Date : 08/03/2002
Application Number : 20020308000018
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Schedule D
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : KINERET
Dosage Strength : 150MG/ML
Packaging : 0.67 ML
Approval Date :
Application Number : 2245913
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info :
Registration Country : Australia
Dosage Form : injection
Brand Name : Kineret
Dosage Strength : 100 mg/0.67 mL
Packaging : 28
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
