ID

33253

Description

Study ID: 107434 Clinical Study ID: NAP107434 Study Title: A randomised, double-blind, double-dummy, placebo controlled, three-way cross-over study to investigate the effect of single oral doses of 100 mg GW273225 (4030W92) and 325 mg LAMICTAL on resting motor threshold in healthy subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Study Link: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: GW273225 Trade Name: lamictal Study Indication: Bipolar Disorder This form contains information about the subjects history of dermatological drug reactions. It should be filled out at each visit after the screening visit. Complete the Dermatological Drug Reaction History pages for each drug reaction experienced. Screening Visit: 28 days prior to first dosing. Treatment Period: The day before dosing, until 48h after dosing. Follow-Up: 14-21 days after last dose

Mots-clés

Versions (2)
  1. 03/12/2018 03/12/2018 -
  2. 16/12/2018 16/12/2018 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

3 décembre 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
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Effect of Lamictal on Resting Motor Threshold

Anglais

Dermatological Drug Reaction History

1 Formulaires  
Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Screening number
Description

Subject Screening No.

Type de données

integer

Alias
UMLS CUI [1,1]
C0220908
UMLS CUI [1,2]
C0600091
Subject no.
Description

Subject Number

Type de données

integer

Alias
UMLS CUI [1]
C2348585
Date Information Collected
Description

Date Information Collected

Type de données

date

Alias
UMLS CUI [1,1]
C3244127
UMLS CUI [1,2]
C0011008
Dermatological Drug Reaction History
Description

Dermatological Drug Reaction History

Alias
UMLS CUI-1
C0262926
UMLS CUI-2
C0037274
UMLS CUI-3
C0041755
Has the subject experienced any type of physician diagnosed dermatologic reaction to any drug?
Description

History of Dermatologic Drug Reaction

Type de données

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0037274
UMLS CUI [1,3]
C0013182
Name of suspect drug implicated (trade name preferred)
Description

Drug Name

Type de données

text

Alias
UMLS CUI [1]
C2360065
Onset Date of Reaction
Description

Onset Date of Reaction

Type de données

date

Alias
UMLS CUI [1,1]
C0574845
UMLS CUI [1,2]
C1527304
During what time period after initiation of the drug did the rash occur?
Description

Tick one box only

Type de données

integer

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C2745955
UMLS CUI [1,3]
C0011008
Was the reaction considered severe?
Description

Severe Reaction

Type de données

text

Alias
UMLS CUI [1,1]
C1527304
UMLS CUI [1,2]
C0205082
Was the subject hospitlaised due to the reaction?
Description

Hospitalisation

Type de données

text

Was the drug discontinued?
Description

If Yes, did the reaction resolve when the drug was discontinued?

Type de données

text

Did the reaction reappear with rechallenge?
Description

Reaction Reappearance

Type de données

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0242656
Where other systemic symptoms seen?
Description

Other Systemic Symptoms

Type de données

text

Alias
UMLS CUI [1,1]
C2039684
UMLS CUI [1,2]
C0205394
Fever
Description

Fever

Type de données

boolean

Alias
UMLS CUI [1]
C0015967
Pharyngitis
Description

Pharyngitis

Type de données

boolean

Alias
UMLS CUI [1]
C0031350
Rhabdomyolysis
Description

Rhabdomyolysis

Type de données

boolean

Alias
UMLS CUI [1]
C0035410
Lymphadenopathy
Description

Lymphadenopathy

Type de données

boolean

Alias
UMLS CUI [1]
C0497156
Facial Swelling
Description

Facial Swelling

Type de données

boolean

Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0015450
Hepatic abnormalities
Description

Hepatic abnormalities

Type de données

boolean

Alias
UMLS CUI [1]
C0023895
Pulmonar abnormalities
Description

Pulmonar abnormalities

Type de données

boolean

Alias
UMLS CUI [1,1]
C1704258
UMLS CUI [1,2]
C0035237
Hematologic Abnormalities
Description

Hematologic Abnormalities

Type de données

boolean

Alias
UMLS CUI [1]
C0850715
Cardiac Abnormalities
Description

Cardiac Abnormalities

Type de données

boolean

Alias
UMLS CUI [1,1]
C0018787
UMLS CUI [1,2]
C1704258
Renal Abnormalities
Description

Renal Abnormalities

Type de données

boolean

Alias
UMLS CUI [1,1]
C0022646
UMLS CUI [1,2]
C1704258
Conjunctival Lesions
Description

Conjunctival Lesions

Type de données

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C0009758
Oral Mucosal Abnormalities
Description

Oral Mucosal Abnormalities

Type de données

boolean

Alias
UMLS CUI [1,1]
C0442027
UMLS CUI [1,2]
C0026724
UMLS CUI [1,3]
C1704258
Other Mucosal Abnormalities
Description

Other Mucosal Abnormalities

Type de données

boolean

Alias
UMLS CUI [1,1]
C0026724
UMLS CUI [1,2]
C1704258
UMLS CUI [1,3]
C0205394
Skin Pain
Description

Skin Pain

Type de données

boolean

Alias
UMLS CUI [1,1]
C1123023
UMLS CUI [1,2]
C0030193
Other Symptom
Description

Other Symptom

Type de données

boolean

Alias
UMLS CUI [1,1]
C0037088
UMLS CUI [1,2]
C0205394
Urticaria
Description

Urticaria

Type de données

boolean

Alias
UMLS CUI [1]
C0042109
Angioedema
Description

Angioedema

Type de données

boolean

Alias
UMLS CUI [1]
C0002994
Stevens-Johnson Syndrom
Description

Stevens-Johnson Syndrome

Type de données

boolean

Alias
UMLS CUI [1]
C0038325
Toxic Epidermal Necrolysis
Description

Toxic Epidermal Necrolysis

Type de données

boolean

Alias
UMLS CUI [1]
C0014518
Erythema Multiforme Major
Description

Erytherma Multiforme Major

Type de données

boolean

Alias
UMLS CUI [1]
C0014742
Photosensitivity
Description

Photosensitivity

Type de données

boolean

Alias
UMLS CUI [1]
C0031762
Hypersensitivity
Description

Hypersensitivity

Type de données

boolean

Alias
UMLS CUI [1]
C0020517
Morbiliform Rash
Description

Morbiliform Rash

Type de données

boolean

Alias
UMLS CUI [1]
C0015230
Unknown
Description

Unknown

Type de données

boolean

Alias
UMLS CUI [1]
C0439673
Other, specify
Description

Other

Type de données

text

Alias
UMLS CUI [1]
C0205394
Conclusion
Description

Conclusion

Alias
UMLS CUI-1
C1707478
Staff initials
Description

Staff initials

Type de données

text

Alias
UMLS CUI [1,1]
C2986440
UMLS CUI [1,2]
C1552089
Date
Description

Date

Type de données

date

Alias
UMLS CUI [1]
C0011008
Retour au début de la page

Similar models

Dermatological Drug Reaction History

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Subject Screening No.
Item
Subject Screening number
integer
C0220908 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Subject Number
Item
Subject no.
integer
C2348585 (UMLS CUI [1])
Date Information Collected
Item
Date Information Collected
date
C3244127 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item Group
Dermatological Drug Reaction History
C0262926 (UMLS CUI-1)
C0037274 (UMLS CUI-2)
C0041755 (UMLS CUI-3)
History of Dermatologic Drug Reaction
Item
Has the subject experienced any type of physician diagnosed dermatologic reaction to any drug?
boolean
C0262926 (UMLS CUI [1,1])
C0037274 (UMLS CUI [1,2])
C0013182 (UMLS CUI [1,3])
Drug Name
Item
Name of suspect drug implicated (trade name preferred)
text
C2360065 (UMLS CUI [1])
Onset Date of Reaction
Item
Onset Date of Reaction
date
C0574845 (UMLS CUI [1,1])
C1527304 (UMLS CUI [1,2])
Item
During what time period after initiation of the drug did the rash occur?
integer
C0877248 (UMLS CUI [1,1])
C2745955 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Time Period of Rash Occurance
Code List
During what time period after initiation of the drug did the rash occur?
CL Item
Within first 6 weeks (1)
CL Item
After the first 6 weeks (2)
Item
Was the reaction considered severe?
text
C1527304 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Severe Reaction
Code List
Was the reaction considered severe?
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
Item
Was the subject hospitlaised due to the reaction?
text
Hospitalisation
Code List
Was the subject hospitlaised due to the reaction?
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
Item
Was the drug discontinued?
text
Drug Discontinuation
Code List
Was the drug discontinued?
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
Item
Did the reaction reappear with rechallenge?
text
C0877248 (UMLS CUI [1,1])
C0242656 (UMLS CUI [1,2])
Reaction Reappearance
Code List
Did the reaction reappear with rechallenge?
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
Item
Where other systemic symptoms seen?
text
C2039684 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Other Systemic Symptoms
Code List
Where other systemic symptoms seen?
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
Fever
Item
Fever
boolean
C0015967 (UMLS CUI [1])
Pharyngitis
Item
Pharyngitis
boolean
C0031350 (UMLS CUI [1])
Rhabdomyolysis
Item
Rhabdomyolysis
boolean
C0035410 (UMLS CUI [1])
Lymphadenopathy
Item
Lymphadenopathy
boolean
C0497156 (UMLS CUI [1])
Facial Swelling
Item
Facial Swelling
boolean
C0038999 (UMLS CUI [1,1])
C0015450 (UMLS CUI [1,2])
Hepatic abnormalities
Item
Hepatic abnormalities
boolean
C0023895 (UMLS CUI [1])
Pulmonar abnormalities
Item
Pulmonar abnormalities
boolean
C1704258 (UMLS CUI [1,1])
C0035237 (UMLS CUI [1,2])
Hematologic Abnormalities
Item
Hematologic Abnormalities
boolean
C0850715 (UMLS CUI [1])
Cardiac Abnormalities
Item
Cardiac Abnormalities
boolean
C0018787 (UMLS CUI [1,1])
C1704258 (UMLS CUI [1,2])
Renal Abnormalities
Item
Renal Abnormalities
boolean
C0022646 (UMLS CUI [1,1])
C1704258 (UMLS CUI [1,2])
Conjunctival Lesions
Item
Conjunctival Lesions
boolean
C0221198 (UMLS CUI [1,1])
C0009758 (UMLS CUI [1,2])
Oral Mucosal Abnormalities
Item
Oral Mucosal Abnormalities
boolean
C0442027 (UMLS CUI [1,1])
C0026724 (UMLS CUI [1,2])
C1704258 (UMLS CUI [1,3])
Other Mucosal Abnormalities
Item
Other Mucosal Abnormalities
boolean
C0026724 (UMLS CUI [1,1])
C1704258 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
Skin Pain
Item
Skin Pain
boolean
C1123023 (UMLS CUI [1,1])
C0030193 (UMLS CUI [1,2])
Other Symptom
Item
Other Symptom
boolean
C0037088 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Urticaria
Item
Urticaria
boolean
C0042109 (UMLS CUI [1])
Angioedema
Item
Angioedema
boolean
C0002994 (UMLS CUI [1])
Stevens-Johnson Syndrome
Item
Stevens-Johnson Syndrom
boolean
C0038325 (UMLS CUI [1])
Toxic Epidermal Necrolysis
Item
Toxic Epidermal Necrolysis
boolean
C0014518 (UMLS CUI [1])
Erytherma Multiforme Major
Item
Erythema Multiforme Major
boolean
C0014742 (UMLS CUI [1])
Photosensitivity
Item
Photosensitivity
boolean
C0031762 (UMLS CUI [1])
Hypersensitivity
Item
Hypersensitivity
boolean
C0020517 (UMLS CUI [1])
Morbiliform Rash
Item
Morbiliform Rash
boolean
C0015230 (UMLS CUI [1])
Unknown
Item
Unknown
boolean
C0439673 (UMLS CUI [1])
Other
Item
Other, specify
text
C0205394 (UMLS CUI [1])
Item Group
Conclusion
C1707478 (UMLS CUI-1)
Staff initials
Item
Staff initials
text
C2986440 (UMLS CUI [1,1])
C1552089 (UMLS CUI [1,2])
Date
Item
Date
date
C0011008 (UMLS CUI [1])
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