ID

35507

Description

Study ID: 111652 Clinical Study ID: 111652 Study Title: A Study to Evaluate GSK Biologicals' Candidate Formulations of Pneumococcal Vaccines (GSK2189241A) in Elderly Subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00756067 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: Pneumococcal vaccine GSK2189241A Trade Name: Pneumo 23™ Study Indication: Infections, Streptococcal

Keywords

  1. 3/6/19 3/6/19 -
Copyright Holder

GSK group of companies

Uploaded on

March 6, 2019

DOI

To request one please log in.

License

Creative Commons BY-NC 3.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Candidate Formulations of Pneumococcal Vaccines in Elderly Subjects - 111652

Visit 1 - Day 0 - Dose 1

Administrative data
Description

Administrative data

Subject Number
Description

Subject Number

Data type

integer

Visit Number
Description

Visit Number

Data type

text

Date of Visit
Description

Date of Visit

Data type

date

CHECK FOR STUDY CONTINUATION
Description

CHECK FOR STUDY CONTINUATION

Did the subject return for visit 1?
Description

Check for Study Continuation

Data type

boolean

If No, please record ONE most appropriate reason and skip the following forms of this visit.
Description

If No, please record ONE most appropriate reason and skip the following forms of this visit.

Data type

text

HEMATOLOGY / BIOCHEMISTRY
Description

HEMATOLOGY / BIOCHEMISTRY

Has a blood sample been taken for haematology/ biochemistry testing?
Description

Hematology / Biochemistry Question

Data type

text

Date
Description

Date

Data type

date

Laboratory Name
Description

Laboratory Name

Data type

text

Laboratory Code
Description

Laboratory Code

Data type

integer

HEMATOLOGY
Description

HEMATOLOGY

[HB] Hemoglobin
Description

Result

Data type

float

Measurement units
  • g/dL
g/dL
[RBC] Red Blood Cells
Description

Result below

Data type

integer

[PLA] Platelets
Description

Result below

Data type

text

[WBC] White Blood Cells
Description

White Blood Cells

Data type

text

[NEU] Neutrophils
Description

Result below

Data type

text

Measurement units
  • abs
abs
[LYM] Lymphocytes
Description

Result below

Data type

integer

Measurement units
  • /l
/l
[MON] Monocytes
Description

Result below

Data type

text

[EOS] Eosinophils
Description

Result below

Data type

text

[BAS] Basophils
Description

Result below

Data type

text

[RET] Reticulocytes
Description

Result below

Data type

text

BIOCHEMISTRY
Description

BIOCHEMISTRY

[BUN] BUN
Description

BUN

Data type

float

Measurement units
  • mg/dL
mg/dL
[CREA] Creatinine
Description

Result below

Data type

float

Measurement units
  • mg/dL
mg/dL
[AST] AST/SGOT
Description

Result below

Data type

float

Measurement units
  • U/L
U/L
[ALT] ALT/SGPT
Description

Result below

Data type

float

Measurement units
  • U/L
U/L
[CHOL] Cholesterol
Description

Cholesterol

Data type

float

[CPK] Creatine phosphokinase
Description

Creatine phosphokinase

Data type

float

[HAP] Serum Haptoglobin
Description

Serum Haptoglobin

Data type

float

Measurement units
  • mg/dL
mg/dL
[LDH] Lactate Dehydrogenase
Description

Please complete the following informationwith LDH isoenzymes if the grade 2 or greater LDH is observed (> 1.5 ULN)

Data type

text

LDH
Description

LDH

LD1
Description

Result

Data type

text

LD2
Description

Result

Data type

text

LD3
Description

Result

Data type

text

LD4
Description

Result

Data type

text

LD5
Description

Result

Data type

text

Has a blood sample been taken for immunogenicity assays?
Description

Blood Sample for Immunogenicity Assays

Data type

boolean

Date
Description

Date

Data type

date

URINALYSIS
Description

URINALYSIS

Has a urine sample been taken for dipstick?
Description

Urine Sample Question

Data type

boolean

Date
Description

Date

Data type

date

Urinalysis (Dipstick) Test
Description

Urinalysis (Dipstick) Test

pH (via dipstick)
Description

Result

Data type

integer

Proteins (via dipstick)
Description

Proteins (via dipstick)

Data type

text

Glucose (via dipstick)
Description

Glucose (via dipstick)

Data type

text

Ketones (via dipstick)
Description

Ketones (via dipstick)

Data type

text

Blood and myoglobin (via dipstick)
Description

Blood and myoglobin (via dipstick)

Data type

text

Bilirubin (via dipstick)
Description

Bilirubin (via dipstick)

Data type

text

Urobilinogen (via dipstick)
Description

Urobilinogen (via dipstick)

Data type

text

Nitrites (via dipstick)
Description

Nitrites (via dipstick)

Data type

text

Leukocyte esterase (via dipstick)
Description

Leukocyte esterase (via dipstick)

Data type

text

Has a urine sample been taken for development of diagnostic assay?
Description

Urina Sample for Diagnostic Sssay?

Data type

boolean

Date
Description

Date

Data type

date

RANDOMISATION / TREATMENT ALLOCATION
Description

RANDOMISATION / TREATMENT ALLOCATION

Record treatment number:
Description

Treatment Number

Data type

integer

VACCINE ADMINISTRATION
Description

VACCINE ADMINISTRATION

Date
Description

Date

Data type

boolean

Pre-Vaccination temperature:
Description

Pre-Vaccination temperature

Data type

float

Measurement units
  • °C
°C
Route:
Description

Temperature Route

Data type

text

VACCINE
Description

VACCINE

Administration data
Description

only one box must be ticked by vaccine

Data type

text

Replacement vial Number
Description

Replacement vial Number

Data type

integer

Side
Description

Protocol: Non-Dominant

Data type

text

Site
Description

Protocol: Deltoid

Data type

text

Route
Description

Protocol: I.M.

Data type

text

Comment
Description

Comment

Data type

text

Has the study vaccine been administered according to the Protocol?
Description

Has the study vaccine been administered according to the Protocol?

Data type

boolean

Side
Description

Please tick all items that apply and comment if necessary

Data type

text

Site
Description

Please tick all items that apply and comment if necessary

Data type

text

Route
Description

Please tick all items that apply and comment if necessary

Data type

text

Comment
Description

Comment

Data type

text

VACCINE NON-ADMINISTRATION
Description

VACCINE NON-ADMINISTRATION

Please tick the major reason for non administration.
Description

Reason for Non-Administration

Data type

text

In case of SAE, record SAE number
Description

SAE number

Data type

integer

In case of AE, record AE number
Description

AE number

Data type

integer

In Other cases, specify
Description

Specify Other

Data type

text

Please record who made the decision
Description

who made the decision

Data type

text

IMMEDIATE POST-VACCINATION OBSERVATION
Description

IMMEDIATE POST-VACCINATION OBSERVATION

If any adverse events occurred during the immediate post-vaccination time (30 minutes) please fill in the Solicited Adverse Events section, the Non-Serious Adverse Event section or a Serious Adverse Event report.
Description

Reminder AE

Data type

text

If any prophylactic medication has been administered in anticipation of study vaccine reaction, please complete the Medication section and tick prophylactic box.
Description

Reminder Concomitant Medication

Data type

text

Any other vaccines administered during the study period must be recorded in the Concomitant Vaccination section.
Description

Reminder Concomitant Vaccination

Data type

text

SOLICITED ADVERSE EVENTS – LOCAL SYMPTOMS
Description

SOLICITED ADVERSE EVENTS – LOCAL SYMPTOMS

Has the subject experienced any of the following signs/symptoms at the administration site during the solicited period?
Description

Solicited Adverse Events Question

Data type

text

Local Symptoms - Redness
Description

Local Symptoms - Redness

Redness
Description

Redness

Data type

boolean

Day
Description

Day

Data type

text

Size
Description

Size

Data type

integer

Measurement units
  • mm
mm
Ongoing after day 6?
Description

Ongoing after day 6?

Data type

boolean

Date of last day of symptoms
Description

Date of last day of symptoms

Data type

date

Medically attended visit?
Description

Medically attended visit

Data type

boolean

Medically attended visit
Description

Type of Medical Attention

Data type

text

Local Symptoms - Swelling
Description

Local Symptoms - Swelling

Swelling
Description

Swelling

Data type

boolean

Day
Description

Day

Data type

text

Size
Description

Size

Data type

integer

Measurement units
  • mm
mm
Ongoing after day 6?
Description

Ongoing after day 6?

Data type

boolean

Date of last day of symptoms
Description

Date of last day of symptoms

Data type

date

Medically attended visit
Description

Medically attended visit

Data type

boolean

Medically attended visit
Description

Type of Medical Attention

Data type

text

Local Symptoms - Pain
Description

Local Symptoms - Pain

Pain
Description

Pain

Data type

boolean

Day
Description

Day

Data type

text

intensity
Description

intensity

Data type

text

Ongoing after day 6?
Description

Ongoing after day 6?

Data type

boolean

Date of last day of symptoms
Description

Date of last day of symptoms

Data type

date

Medically attended visit
Description

Medically attended visit

Data type

boolean

Medically attended visit
Description

Type of Medical Attention

Data type

text

SOLICITED ADVERSE EVENTS - GENERAL SYMPTOMS
Description

SOLICITED ADVERSE EVENTS - GENERAL SYMPTOMS

Has the subject experienced any of the following signs/symptoms during the solicited period?
Description

Solicited Adverse Events Question

Data type

text

Temperature
Description

Temperature

Temperature
Description

ick Yes from following limits Axillary, Oral > 37.5 °C Rectal > 38 °C

Data type

boolean

Day
Description

Day

Data type

text

Description

Data type

float

Measurement units
  • °C
°C
Route
Description

Route

Data type

text

Ongoing after day 6?
Description

Ongoing after day 6?

Data type

boolean

Date of last day of symptoms
Description

Date of last day of symptoms

Data type

date

Causality?
Description

Causality?

Data type

boolean

Medically attended visit?
Description

Medically attended visit

Data type

boolean

Medically attended visit
Description

Type of Medical involvement

Data type

text

Fatigue
Description

Fatigue

Fatigue
Description

Fatigue

Data type

boolean

Day
Description

Day

Data type

integer

intensity:
Description

fatigue intensity

Data type

text

Ongoing after day 6?
Description

Ongoing after day 6?

Data type

boolean

Date of last day of symptoms
Description

Date of last day of symptoms

Data type

date

Causality?
Description

Causality?

Data type

boolean

Medically attended visit?
Description

Medically attended visit

Data type

boolean

Medically attended visit
Description

Type of Medical Attention

Data type

text

Headache
Description

Headache

Headache
Description

Headache

Data type

boolean

Day
Description

Day

Data type

text

Intensity
Description

Intensity

Data type

text

Ongoing after day 6?
Description

Ongoing after day 6?

Data type

boolean

Date of last day of symptoms
Description

Date of last day of symptoms

Data type

date

Causality?
Description

Causality?

Data type

boolean

Medically attended visit
Description

Medically attended visit

Data type

boolean

Medically attended visit
Description

Type of Medical Attention

Data type

text

Gastrointestinal symptoms
Description

Gastrointestinal symptoms

Gastrointestinal symptoms
Description

Gastrointestinal symptoms

Data type

boolean

Day
Description

Day

Data type

integer

Intensity
Description

Intensity

Data type

text

Ongoing after day 6?
Description

Ongoing after day 6?

Data type

boolean

Date of last day of symptoms
Description

Date of last day of symptoms

Data type

date

Causality?
Description

Causality?

Data type

boolean

Medically attended visit
Description

Medically attended visit

Data type

boolean

Medically attended visit
Description

Type of Medical Attention

Data type

text

Malaise
Description

Malaise

Malaise
Description

Malaise

Data type

boolean

Day
Description

Day

Data type

text

Intensity
Description

Intensity

Data type

text

Ongoing after day 6?
Description

Ongoing after day 6?

Data type

boolean

Date of last day of symptoms
Description

Date of last day of symptoms

Data type

date

Medically attended visit
Description

Medically attended visit

Data type

boolean

Medically attended visit
Description

Type of Medical Attention

Data type

text

Myalgia
Description

Myalgia

Myalgia
Description

Myalgia

Data type

boolean

Day
Description

Day

Data type

text

intensity
Description

intensity

Data type

text

Ongoing after day 6?
Description

Ongoing after day 6?

Data type

boolean

Date of last day of symptoms
Description

Date of last day of symptoms

Data type

date

Causality
Description

Causality

Data type

boolean

Medically attended visit
Description

Medically attended visit

Data type

boolean

Medically attended visit
Description

Type of Medical Attention

Data type

text

UNSOLICITED ADVERSE EVENTS
Description

UNSOLICITED ADVERSE EVENTS

Has the subject experienced any non-serious unsolicited adverse events within one month (minimum 30 days) post-vaccination or any serious adverse events or medically significant condition between dose 1 and dose 2 (Day 60)?
Description

Unsolicited Adverse Events Question

Data type

text

Similar models

Visit 1 - Day 0 - Dose 1

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative data
Subject Number
Item
Subject Number
integer
Visit Number
Item
Visit Number
text
Date of Visit
Item
Date of Visit
date
Item Group
CHECK FOR STUDY CONTINUATION
Check for Study Continuation
Item
Did the subject return for visit 1?
boolean
If No, please record ONE most appropriate reason and skip the following forms of this visit.
Item
If No, please record ONE most appropriate reason and skip the following forms of this visit.
text
Item Group
HEMATOLOGY / BIOCHEMISTRY
Item
Has a blood sample been taken for haematology/ biochemistry testing?
text
Code List
Has a blood sample been taken for haematology/ biochemistry testing?
CL Item
Yes (1)
CL Item
No (2)
CL Item
N/A (Only if Visit 1 occurred within 48 hours from blood sample taken at screening visit) (3)
Date
Item
Date
date
Laboratory Name
Item
Laboratory Name
text
Laboratory Code
Item
Laboratory Code
integer
Item Group
HEMATOLOGY
[HB] Hemoglobin
Item
[HB] Hemoglobin
float
Red Blood Cells
Item
[RBC] Red Blood Cells
integer
Platelets
Item
[PLA] Platelets
text
White Blood Cells
Item
[WBC] White Blood Cells
text
Neutrophils
Item
[NEU] Neutrophils
text
Lymphocytes
Item
[LYM] Lymphocytes
integer
Monocytes
Item
[MON] Monocytes
text
Eosinophils
Item
[EOS] Eosinophils
text
Basophils
Item
[BAS] Basophils
text
Reticulocytes
Item
[RET] Reticulocytes
text
Item Group
BIOCHEMISTRY
BUN
Item
[BUN] BUN
float
Creatinine
Item
[CREA] Creatinine
float
AST/SGOT
Item
[AST] AST/SGOT
float
ALT/SGPT
Item
[ALT] ALT/SGPT
float
Cholesterol
Item
[CHOL] Cholesterol
float
Creatine phosphokinase
Item
[CPK] Creatine phosphokinase
float
Serum Haptoglobin
Item
[HAP] Serum Haptoglobin
float
Lactate Dehydrogenase
Item
[LDH] Lactate Dehydrogenase
text
Item Group
LDH
LD1
Item
LD1
text
LD2
Item
LD2
text
LD3
Item
LD3
text
LD4
Item
LD4
text
LD5
Item
LD5
text
Blood Sample for Immunogenicity Assays
Item
Has a blood sample been taken for immunogenicity assays?
boolean
Date
Item
Date
date
Item Group
URINALYSIS
Urine Sample Question
Item
Has a urine sample been taken for dipstick?
boolean
Date
Item
Date
date
Item Group
Urinalysis (Dipstick) Test
pH (via dipstick)
Item
pH (via dipstick)
integer
Item
Proteins (via dipstick)
text
Code List
Proteins (via dipstick)
CL Item
negative  (1)
CL Item
1+ (2)
CL Item
2+ (3)
CL Item
3+ (4)
Item
Glucose (via dipstick)
text
Code List
Glucose (via dipstick)
CL Item
normal (1)
CL Item
1+ (2)
CL Item
2+ (3)
CL Item
3+ (4)
CL Item
4+ (5)
Item
Ketones (via dipstick)
text
Code List
Ketones (via dipstick)
CL Item
negative (1)
CL Item
1+ (2)
CL Item
2+ (3)
CL Item
3+ (4)
Item
Blood and myoglobin (via dipstick)
text
Code List
Blood and myoglobin (via dipstick)
CL Item
negative (1)
CL Item
1+ (2)
CL Item
2+ (3)
CL Item
3+ (4)
CL Item
4+ (5)
Item
Bilirubin (via dipstick)
text
Code List
Bilirubin (via dipstick)
CL Item
negative (1)
CL Item
1+ (2)
CL Item
2+ (3)
CL Item
3+ (4)
Item
Urobilinogen (via dipstick)
text
Code List
Urobilinogen (via dipstick)
CL Item
normal (1)
CL Item
1+ (2)
CL Item
2+ (3)
CL Item
3+ (4)
CL Item
4+ (5)
Item
Nitrites (via dipstick)
text
Code List
Nitrites (via dipstick)
CL Item
negative (1)
CL Item
positive (2)
Item
Leukocyte esterase (via dipstick)
text
Code List
Leukocyte esterase (via dipstick)
CL Item
negative (1)
CL Item
1+ (2)
CL Item
2+ (3)
CL Item
3+ (4)
Urina Sample for Diagnostic Sssay?
Item
Has a urine sample been taken for development of diagnostic assay?
boolean
Date
Item
Date
date
Item Group
RANDOMISATION / TREATMENT ALLOCATION
Treatment Number
Item
Record treatment number:
integer
Item Group
VACCINE ADMINISTRATION
Date
Item
Date
boolean
Pre-Vaccination temperature
Item
Pre-Vaccination temperature:
float
Item
Route:
text
Code List
Route:
CL Item
Axillary (1)
CL Item
Oral (2)
CL Item
Rectal (3)
Item Group
VACCINE
Item
Administration data
text
Code List
Administration data
CL Item
Study Vaccine (1)
CL Item
Replacement vial (2)
CL Item
Not administered (3)
Replacement vial Number
Item
Replacement vial Number
integer
Item
Side
text
Code List
Side
CL Item
Dominant (1)
CL Item
Non-dominant (2)
Item
Site
text
Code List
Site
CL Item
Deltoid (1)
CL Item
Thigh (2)
CL Item
Buttock (3)
Item
Route
text
Code List
Route
CL Item
I.M. (1)
CL Item
S.C. (2)
Comment
Item
Comment
text
Has the study vaccine been administered according to the Protocol?
Item
Has the study vaccine been administered according to the Protocol?
boolean
Item
Side
text
Code List
Side
CL Item
Dominant (1)
CL Item
Non-dominant (2)
Item
Site
text
Code List
Site
CL Item
Deltoid (1)
CL Item
Thigh (2)
CL Item
Buttock (3)
Item
Route
text
Code List
Route
CL Item
I.M. (1)
CL Item
S.C. (2)
Comment
Item
Comment
text
Item Group
VACCINE NON-ADMINISTRATION
Item
Please tick the major reason for non administration.
text
Code List
Please tick the major reason for non administration.
CL Item
Serious adverse event (1)
CL Item
Non-Serious adverse event (2)
CL Item
Other (3)
SAE number
Item
In case of SAE, record SAE number
integer
AE number
Item
In case of AE, record AE number
integer
Specify Other
Item
In Other cases, specify
text
Item
Please record who made the decision
text
Code List
Please record who made the decision
CL Item
Investigator (1)
CL Item
Subject (2)
Item Group
IMMEDIATE POST-VACCINATION OBSERVATION
Reminder AE
Item
If any adverse events occurred during the immediate post-vaccination time (30 minutes) please fill in the Solicited Adverse Events section, the Non-Serious Adverse Event section or a Serious Adverse Event report.
text
Reminder Concomitant Medication
Item
If any prophylactic medication has been administered in anticipation of study vaccine reaction, please complete the Medication section and tick prophylactic box.
text
Reminder Concomitant Vaccination
Item
Any other vaccines administered during the study period must be recorded in the Concomitant Vaccination section.
text
Item Group
SOLICITED ADVERSE EVENTS – LOCAL SYMPTOMS
Item
Has the subject experienced any of the following signs/symptoms at the administration site during the solicited period?
text
Code List
Has the subject experienced any of the following signs/symptoms at the administration site during the solicited period?
CL Item
Information not available (1)
CL Item
No vaccine administered (2)
CL Item
No (3)
CL Item
Yes, please record information for all symptoms (4)
Item Group
Local Symptoms - Redness
Redness
Item
Redness
boolean
Item
Day
text
Code List
Day
CL Item
Day 0 (1)
CL Item
Day 1 (2)
CL Item
Day 2 (3)
CL Item
Day 3 (4)
CL Item
Day 4 (5)
CL Item
Day 5 (6)
CL Item
Day 6 (7)
Size
Item
Size
integer
Ongoing after day 6?
Item
Ongoing after day 6?
boolean
Date of last day of symptoms
Item
Date of last day of symptoms
date
Medically attended visit
Item
Medically attended visit?
boolean
Item
Medically attended visit
text
Code List
Medically attended visit
CL Item
Hospitalization (1)
CL Item
Emergency Room (2)
CL Item
Medical Personnel (3)
Item Group
Local Symptoms - Swelling
Swelling
Item
Swelling
boolean
Item
Day
text
Code List
Day
CL Item
Day 0 (1)
CL Item
Day 1 (2)
CL Item
Day 2 (3)
CL Item
Day 3 (4)
CL Item
Day 4 (5)
CL Item
Day 5 (6)
CL Item
Day 6 (7)
Size
Item
Size
integer
Ongoing after day 6?
Item
Ongoing after day 6?
boolean
Date of last day of symptoms
Item
Date of last day of symptoms
date
Medically attended visit
Item
Medically attended visit
boolean
Item
Medically attended visit
text
Code List
Medically attended visit
CL Item
Hospitalization (1)
CL Item
Emergency Room (2)
CL Item
Medical Personnel (3)
Item Group
Local Symptoms - Pain
Pain
Item
Pain
boolean
Item
Day
text
Code List
Day
CL Item
Day 0 (1)
CL Item
Day 1 (2)
CL Item
Day 2 (3)
CL Item
Day 3 (4)
CL Item
Day 4 (5)
CL Item
Day 5 (6)
CL Item
Day 6 (7)
Item
intensity
text
Code List
intensity
CL Item
Absent (1)
CL Item
Painful on touch (2)
CL Item
Painful when limb is moved (3)
CL Item
Pain that prevents normal activity (4)
Ongoing after day 6?
Item
Ongoing after day 6?
boolean
Date of last day of symptoms
Item
Date of last day of symptoms
date
Medically attended visit
Item
Medically attended visit
boolean
Item
Medically attended visit
text
Code List
Medically attended visit
CL Item
Hospitalization (1)
CL Item
Emergency Room (2)
CL Item
Medical Personnel (3)
Item Group
SOLICITED ADVERSE EVENTS - GENERAL SYMPTOMS
Item
Has the subject experienced any of the following signs/symptoms during the solicited period?
text
Code List
Has the subject experienced any of the following signs/symptoms during the solicited period?
CL Item
Information not available (1)
CL Item
No vaccine administered (2)
CL Item
No (3)
CL Item
Yes, please record information for each symptom (4)
Item Group
Temperature
Temperature
Item
Temperature
boolean
Item
Day
text
Code List
Day
CL Item
Day 0 (1)
CL Item
Day 1 (2)
CL Item
Day 2 (3)
CL Item
Day 3 (4)
CL Item
Day 4 (5)
CL Item
Day 5 (6)
CL Item
Day 6 (7)
Item
float
Item
Route
text
Code List
Route
CL Item
Rectal (1)
CL Item
Oral (2)
CL Item
Axillary (3)
Ongoing after day 6?
Item
Ongoing after day 6?
boolean
Date of last day of symptoms
Item
Date of last day of symptoms
date
Causality?
Item
Causality?
boolean
Medically attended visit
Item
Medically attended visit?
boolean
Item
Medically attended visit
text
Code List
Medically attended visit
CL Item
Hospitalization (1)
CL Item
Emergency Room (2)
CL Item
Medical Personnel (3)
Item Group
Fatigue
Fatigue
Item
Fatigue
boolean
Item
Day
integer
Code List
Day
CL Item
Day 0 (1)
CL Item
Day 1 (2)
CL Item
Day 2 (3)
CL Item
Day 3 (4)
CL Item
Day 4 (5)
CL Item
Day 5 (6)
CL Item
Day 6 (7)
Item
intensity:
text
Code List
intensity:
CL Item
Normal (1)
CL Item
Fatigue that is easily tolerated (2)
CL Item
Fatigue that interferes with normal activity (3)
CL Item
Fatigue that prevents normal activity (4)
Ongoing after day 6?
Item
Ongoing after day 6?
boolean
Date of last day of symptoms
Item
Date of last day of symptoms
date
Causality?
Item
Causality?
boolean
Medically attended visit
Item
Medically attended visit?
boolean
Item
Medically attended visit
text
Code List
Medically attended visit
CL Item
Hospitalization (1)
CL Item
Emergency Room (2)
CL Item
Medical Personnel (3)
Item Group
Headache
Headache
Item
Headache
boolean
Item
Day
text
Code List
Day
CL Item
Day 0 (1)
CL Item
Day 1 (2)
CL Item
Day 2 (3)
CL Item
Day 3 (4)
CL Item
Day 4 (5)
CL Item
Day 5 (6)
CL Item
Day 6 (7)
Item
Intensity
text
Code List
Intensity
CL Item
Normal (1)
CL Item
Headache that is easily tolerated (2)
CL Item
Headache that interferes with normal activity (3)
CL Item
Headache that prevents normal activity (4)
Ongoing after day 6?
Item
Ongoing after day 6?
boolean
Date of last day of symptoms
Item
Date of last day of symptoms
date
Causality?
Item
Causality?
boolean
Medically attended visit
Item
Medically attended visit
boolean
Item
Medically attended visit
text
Code List
Medically attended visit
CL Item
Hospitalization (1)
CL Item
Emergency Room (2)
CL Item
Medical Personnel (3)
Item Group
Gastrointestinal symptoms
Gastrointestinal symptoms
Item
Gastrointestinal symptoms
boolean
Item
Day
integer
Code List
Day
CL Item
Day 0 (1)
CL Item
Day 1 (2)
CL Item
Day 2 (3)
CL Item
Day 3 (4)
CL Item
Day 4 (5)
CL Item
Day 5 (6)
CL Item
Day 6 (7)
Item
Intensity
text
Code List
Intensity
CL Item
Normal (1)
CL Item
Gastrointestinal symptoms that are easily tolerated (2)
CL Item
Gastrointestinal symptoms that interfere with normal activity (3)
CL Item
Gastrointestinal symptoms that prevent normal activity (4)
Ongoing after day 6?
Item
Ongoing after day 6?
boolean
Date of last day of symptoms
Item
Date of last day of symptoms
date
Causality?
Item
Causality?
boolean
Medically attended visit
Item
Medically attended visit
boolean
Item
Medically attended visit
text
Code List
Medically attended visit
CL Item
Hospitalization (1)
CL Item
Emergency Room (2)
CL Item
Medical Personnel (3)
Item Group
Malaise
Malaise
Item
Malaise
boolean
Item
Day
text
Code List
Day
CL Item
Day 0 (1)
CL Item
Day 1 (2)
CL Item
Day 2 (3)
CL Item
Day 3 (4)
CL Item
Day 4 (5)
CL Item
Day 5 (6)
CL Item
Day 6 (7)
Item
Intensity
text
Code List
Intensity
CL Item
Normal (1)
CL Item
Malaise that is easily tolerated (2)
CL Item
Malaise that interferes with normal activity (3)
CL Item
Malaise that prevents normal activity (4)
Ongoing after day 6?
Item
Ongoing after day 6?
boolean
Date of last day of symptoms
Item
Date of last day of symptoms
date
Medically attended visit
Item
Medically attended visit
boolean
Item
Medically attended visit
text
Code List
Medically attended visit
CL Item
Hospitalization (1)
CL Item
Emergency Room (2)
CL Item
Medical Personnel (3)
Item Group
Myalgia
Myalgia
Item
Myalgia
boolean
Item
Day
text
Code List
Day
CL Item
Day 0 (1)
CL Item
Day 1 (2)
CL Item
Day 2 (3)
CL Item
Day 3 (4)
CL Item
Day 4 (5)
CL Item
Day 5 (6)
CL Item
Day 6 (7)
Item
intensity
text
Code List
intensity
CL Item
Normal (1)
CL Item
Myalgia that is easily tolerated (2)
CL Item
Myalgia that interferes with normal activity (3)
CL Item
Myalgia that prevents normal activity (4)
Ongoing after day 6?
Item
Ongoing after day 6?
boolean
Date of last day of symptoms
Item
Date of last day of symptoms
date
Causality
Item
Causality
boolean
Medically attended visit
Item
Medically attended visit
boolean
Item
Medically attended visit
text
Code List
Medically attended visit
CL Item
Hospitalization (1)
CL Item
Emergency Room (2)
CL Item
Medical Personnel (3)
Item Group
UNSOLICITED ADVERSE EVENTS
Item
Has the subject experienced any non-serious unsolicited adverse events within one month (minimum 30 days) post-vaccination or any serious adverse events or medically significant condition between dose 1 and dose 2 (Day 60)?
text
Code List
Has the subject experienced any non-serious unsolicited adverse events within one month (minimum 30 days) post-vaccination or any serious adverse events or medically significant condition between dose 1 and dose 2 (Day 60)?
CL Item
Information not available (1)
CL Item
No vaccine administered (2)
CL Item
No (3)
CL Item
Yes (4)

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial