ID

35523

Descripción

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

Palabras clave

  1. 7/3/19 7/3/19 -
Titular de derechos de autor

GSK group of companies

Subido en

7 de marzo de 2019

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0

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Candidate Formulations of Pneumococcal Vaccines in Elderly Subjects - 111652

Visit 5 - Day 60 - Dose 2

Administrative data
Descripción

Administrative data

Subject Number
Descripción

Subject Number

Tipo de datos

integer

Visit Number
Descripción

Visit Number

Tipo de datos

text

Date of Visit
Descripción

Date of Visit

Tipo de datos

date

CHECK FOR STUDY CONTINUATION
Descripción

CHECK FOR STUDY CONTINUATION

Did the subject return for visit 1?
Descripción

Check for Study Continuation

Tipo de datos

boolean

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

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

Tipo de datos

text

HEMATOLOGY / BIOCHEMISTRY
Descripción

HEMATOLOGY / BIOCHEMISTRY

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

Hematology / Biochemistry Question

Tipo de datos

text

Date
Descripción

Date

Tipo de datos

date

Laboratory Name
Descripción

Laboratory Name

Tipo de datos

text

Laboratory Code
Descripción

Laboratory Code

Tipo de datos

integer

HEMATOLOGY
Descripción

HEMATOLOGY

[HB] Hemoglobin
Descripción

Result

Tipo de datos

float

Unidades de medida
  • g/dL
g/dL
[RBC] Red Blood Cells
Descripción

Result below

Tipo de datos

integer

[PLA] Platelets
Descripción

Result below

Tipo de datos

text

[WBC] White Blood Cells
Descripción

White Blood Cells

Tipo de datos

text

[NEU] Neutrophils
Descripción

Result below

Tipo de datos

text

Unidades de medida
  • abs
abs
[LYM] Lymphocytes
Descripción

Result below

Tipo de datos

integer

Unidades de medida
  • /l
/l
[MON] Monocytes
Descripción

Result below

Tipo de datos

text

[EOS] Eosinophils
Descripción

Result below

Tipo de datos

text

[BAS] Basophils
Descripción

Result below

Tipo de datos

text

[RET] Reticulocytes
Descripción

Result below

Tipo de datos

text

BIOCHEMISTRY
Descripción

BIOCHEMISTRY

[BUN] BUN
Descripción

BUN

Tipo de datos

float

Unidades de medida
  • mg/dL
mg/dL
[CREA] Creatinine
Descripción

Result below

Tipo de datos

float

Unidades de medida
  • mg/dL
mg/dL
[AST] AST/SGOT
Descripción

Result below

Tipo de datos

float

Unidades de medida
  • U/L
U/L
[ALT] ALT/SGPT
Descripción

Result below

Tipo de datos

float

Unidades de medida
  • U/L
U/L
[CHOL] Cholesterol
Descripción

Cholesterol

Tipo de datos

float

[CPK] Creatine phosphokinase
Descripción

Creatine phosphokinase

Tipo de datos

float

[HAP] Serum Haptoglobin
Descripción

Serum Haptoglobin

Tipo de datos

float

Unidades de medida
  • mg/dL
mg/dL
[LDH] Lactate Dehydrogenase
Descripción

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

Tipo de datos

text

LDH
Descripción

LDH

LD1
Descripción

Result

Tipo de datos

text

LD2
Descripción

Result

Tipo de datos

text

LD3
Descripción

Result

Tipo de datos

text

LD4
Descripción

Result

Tipo de datos

text

LD5
Descripción

Result

Tipo de datos

text

Has a blood sample been taken for immunogenicity assays?
Descripción

Blood Sample for Immunogenicity Assays

Tipo de datos

boolean

Date
Descripción

Date

Tipo de datos

date

URINALYSIS
Descripción

URINALYSIS

Has a urine sample been taken for dipstick?
Descripción

Urine Sample Question

Tipo de datos

boolean

Date
Descripción

Date

Tipo de datos

date

Urinalysis (Dipstick) Test
Descripción

Urinalysis (Dipstick) Test

pH (via dipstick)
Descripción

Result

Tipo de datos

integer

Proteins (via dipstick)
Descripción

Proteins (via dipstick)

Tipo de datos

text

Glucose (via dipstick)
Descripción

Glucose (via dipstick)

Tipo de datos

text

Ketones (via dipstick)
Descripción

Ketones (via dipstick)

Tipo de datos

text

Blood and myoglobin (via dipstick)
Descripción

Blood and myoglobin (via dipstick)

Tipo de datos

text

Bilirubin (via dipstick)
Descripción

Bilirubin (via dipstick)

Tipo de datos

text

Urobilinogen (via dipstick)
Descripción

Urobilinogen (via dipstick)

Tipo de datos

text

Nitrites (via dipstick)
Descripción

Nitrites (via dipstick)

Tipo de datos

text

Leukocyte esterase (via dipstick)
Descripción

Leukocyte esterase (via dipstick)

Tipo de datos

text

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

Urina Sample for Diagnostic Sssay?

Tipo de datos

boolean

Date
Descripción

Date

Tipo de datos

date

RANDOMISATION / TREATMENT ALLOCATION
Descripción

RANDOMISATION / TREATMENT ALLOCATION

Record treatment number:
Descripción

Treatment Number

Tipo de datos

integer

VACCINE ADMINISTRATION
Descripción

VACCINE ADMINISTRATION

Date
Descripción

Date

Tipo de datos

boolean

Pre-Vaccination temperature:
Descripción

Pre-Vaccination temperature

Tipo de datos

float

Unidades de medida
  • °C
°C
Route:
Descripción

Temperature Route

Tipo de datos

text

VACCINE
Descripción

VACCINE

Administration data
Descripción

only one box must be ticked by vaccine

Tipo de datos

text

Replacement vial Number
Descripción

Replacement vial Number

Tipo de datos

integer

Side
Descripción

Protocol: Non-Dominant

Tipo de datos

text

Site
Descripción

Protocol: Deltoid

Tipo de datos

text

Route
Descripción

Protocol: I.M.

Tipo de datos

text

Comment
Descripción

Comment

Tipo de datos

text

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

Has the study vaccine been administered according to the Protocol?

Tipo de datos

boolean

Side
Descripción

Please tick all items that apply and comment if necessary

Tipo de datos

text

Site
Descripción

Please tick all items that apply and comment if necessary

Tipo de datos

text

Route
Descripción

Please tick all items that apply and comment if necessary

Tipo de datos

text

Comment
Descripción

Comment

Tipo de datos

text

VACCINE NON-ADMINISTRATION
Descripción

VACCINE NON-ADMINISTRATION

Please tick the major reason for non administration.
Descripción

Reason for Non-Administration

Tipo de datos

text

In case of SAE, record SAE number
Descripción

SAE number

Tipo de datos

integer

In case of AE, record AE number
Descripción

AE number

Tipo de datos

integer

In Other cases, specify
Descripción

Specify Other

Tipo de datos

text

Please record who made the decision
Descripción

who made the decision

Tipo de datos

text

IMMEDIATE POST-VACCINATION OBSERVATION
Descripción

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.
Descripción

Reminder AE

Tipo de datos

text

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

Reminder Concomitant Medication

Tipo de datos

text

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

Reminder Concomitant Vaccination

Tipo de datos

text

SOLICITED ADVERSE EVENTS – LOCAL SYMPTOMS
Descripción

SOLICITED ADVERSE EVENTS – LOCAL SYMPTOMS

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

Solicited Adverse Events Question

Tipo de datos

text

Local Symptoms - Redness
Descripción

Local Symptoms - Redness

Redness
Descripción

Redness

Tipo de datos

boolean

Day
Descripción

Day

Tipo de datos

text

Size
Descripción

Size

Tipo de datos

integer

Unidades de medida
  • mm
mm
Ongoing after day 6?
Descripción

Ongoing after day 6?

Tipo de datos

boolean

Date of last day of symptoms
Descripción

Date of last day of symptoms

Tipo de datos

date

Medically attended visit?
Descripción

Medically attended visit

Tipo de datos

boolean

Medically attended visit
Descripción

Type of Medical Attention

Tipo de datos

text

Local Symptoms - Swelling
Descripción

Local Symptoms - Swelling

Swelling
Descripción

Swelling

Tipo de datos

boolean

Day
Descripción

Day

Tipo de datos

text

Size
Descripción

Size

Tipo de datos

integer

Unidades de medida
  • mm
mm
Ongoing after day 6?
Descripción

Ongoing after day 6?

Tipo de datos

boolean

Date of last day of symptoms
Descripción

Date of last day of symptoms

Tipo de datos

date

Medically attended visit
Descripción

Medically attended visit

Tipo de datos

boolean

Medically attended visit
Descripción

Type of Medical Attention

Tipo de datos

text

Local Symptoms - Pain
Descripción

Local Symptoms - Pain

Pain
Descripción

Pain

Tipo de datos

boolean

Day
Descripción

Day

Tipo de datos

text

intensity
Descripción

intensity

Tipo de datos

text

Ongoing after day 6?
Descripción

Ongoing after day 6?

Tipo de datos

boolean

Date of last day of symptoms
Descripción

Date of last day of symptoms

Tipo de datos

date

Medically attended visit
Descripción

Medically attended visit

Tipo de datos

boolean

Medically attended visit
Descripción

Type of Medical Attention

Tipo de datos

text

SOLICITED ADVERSE EVENTS - GENERAL SYMPTOMS
Descripción

SOLICITED ADVERSE EVENTS - GENERAL SYMPTOMS

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

Solicited Adverse Events Question

Tipo de datos

text

Temperature
Descripción

Temperature

Temperature
Descripción

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

Tipo de datos

boolean

Day
Descripción

Day

Tipo de datos

text

Descripción

Tipo de datos

float

Unidades de medida
  • °C
°C
Route
Descripción

Route

Tipo de datos

text

Ongoing after day 6?
Descripción

Ongoing after day 6?

Tipo de datos

boolean

Date of last day of symptoms
Descripción

Date of last day of symptoms

Tipo de datos

date

Causality?
Descripción

Causality?

Tipo de datos

boolean

Medically attended visit?
Descripción

Medically attended visit

Tipo de datos

boolean

Medically attended visit
Descripción

Type of Medical involvement

Tipo de datos

text

Fatigue
Descripción

Fatigue

Fatigue
Descripción

Fatigue

Tipo de datos

boolean

Day
Descripción

Day

Tipo de datos

integer

intensity:
Descripción

fatigue intensity

Tipo de datos

text

Ongoing after day 6?
Descripción

Ongoing after day 6?

Tipo de datos

boolean

Date of last day of symptoms
Descripción

Date of last day of symptoms

Tipo de datos

date

Causality?
Descripción

Causality?

Tipo de datos

boolean

Medically attended visit?
Descripción

Medically attended visit

Tipo de datos

boolean

Medically attended visit
Descripción

Type of Medical Attention

Tipo de datos

text

Headache
Descripción

Headache

Headache
Descripción

Headache

Tipo de datos

boolean

Day
Descripción

Day

Tipo de datos

text

Intensity
Descripción

Intensity

Tipo de datos

text

Ongoing after day 6?
Descripción

Ongoing after day 6?

Tipo de datos

boolean

Date of last day of symptoms
Descripción

Date of last day of symptoms

Tipo de datos

date

Causality?
Descripción

Causality?

Tipo de datos

boolean

Medically attended visit
Descripción

Medically attended visit

Tipo de datos

boolean

Medically attended visit
Descripción

Type of Medical Attention

Tipo de datos

text

Gastrointestinal symptoms
Descripción

Gastrointestinal symptoms

Gastrointestinal symptoms
Descripción

Gastrointestinal symptoms

Tipo de datos

boolean

Day
Descripción

Day

Tipo de datos

integer

Intensity
Descripción

Intensity

Tipo de datos

text

Ongoing after day 6?
Descripción

Ongoing after day 6?

Tipo de datos

boolean

Date of last day of symptoms
Descripción

Date of last day of symptoms

Tipo de datos

date

Causality?
Descripción

Causality?

Tipo de datos

boolean

Medically attended visit
Descripción

Medically attended visit

Tipo de datos

boolean

Medically attended visit
Descripción

Type of Medical Attention

Tipo de datos

text

Malaise
Descripción

Malaise

Malaise
Descripción

Malaise

Tipo de datos

boolean

Day
Descripción

Day

Tipo de datos

text

Intensity
Descripción

Intensity

Tipo de datos

text

Ongoing after day 6?
Descripción

Ongoing after day 6?

Tipo de datos

boolean

Date of last day of symptoms
Descripción

Date of last day of symptoms

Tipo de datos

date

Medically attended visit
Descripción

Medically attended visit

Tipo de datos

boolean

Medically attended visit
Descripción

Type of Medical Attention

Tipo de datos

text

Myalgia
Descripción

Myalgia

Myalgia
Descripción

Myalgia

Tipo de datos

boolean

Day
Descripción

Day

Tipo de datos

text

intensity
Descripción

intensity

Tipo de datos

text

Ongoing after day 6?
Descripción

Ongoing after day 6?

Tipo de datos

boolean

Date of last day of symptoms
Descripción

Date of last day of symptoms

Tipo de datos

date

Causality
Descripción

Causality

Tipo de datos

boolean

Medically attended visit
Descripción

Medically attended visit

Tipo de datos

boolean

Medically attended visit
Descripción

Type of Medical Attention

Tipo de datos

text

UNSOLICITED ADVERSE EVENTS
Descripción

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)?
Descripción

Unsolicited Adverse Events Question

Tipo de datos

text

Similar models

Visit 5 - Day 60 - Dose 2

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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)

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