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adding test data

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frankknoll
2022-01-27 14:26:48 +01:00
parent 64a03231fa
commit f445a8b486
5 changed files with 13 additions and 1 deletions
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test/VAERS/2022VAERSData/2022VAERSDATA.csv Normal file
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VAERS_ID,RECVDATE,STATE,AGE_YRS,CAGE_YR,CAGE_MO,SEX,RPT_DATE,SYMPTOM_TEXT,DIED,DATEDIED,L_THREAT,ER_VISIT,HOSPITAL,HOSPDAYS,X_STAY,DISABLE,RECOVD,VAX_DATE,ONSET_DATE,NUMDAYS,LAB_DATA,V_ADMINBY,V_FUNDBY,OTHER_MEDS,CUR_ILL,HISTORY,PRIOR_VAX,SPLTTYPE,FORM_VERS,TODAYS_DATE,BIRTH_DEFECT,OFC_VISIT,ER_ED_VISIT,ALLERGIES
1996873,01/01/2022,CA,,,,U,,"This spontaneous report was received from a pharmacist referring to a patient of unknown age and gender. Information regarding the patient's medical history, concurrent conditions or concomitant medications was not provided. On15-DEC-2021, the patient was vaccinated with an expired hpv rl1 6 11 16 18 31 33 45 52 58 vlp vaccine (yeast) (GARDASIL 9) 0.5 mL injection, (lot #R017624, which was considered to be valid, expiration date: 17-MAR-2021), administered for prophylaxis (vaccination scheme frequency, anatomical location and route of administration were not provided) (expired vaccine administered). The reporter stated the vaccine did not experience any temperature excursion. No additional adverse event was reported.",,,,,,,,,U,12/15/2021,12/15/2021,0,,UNK,,,,,,US0095075132112USA007320,2,12/31/2021,,,,
1996874,01/01/2022,,,,,U,,"SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; This spontaneous potential legal report received from a patient concerned a patient of unspecified age and sex. Initial information was processed along with the additional information received from a regulatory authority on 30-DEC-2021. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (dose number in series: 1) (suspension for injection, route of admin not reported, batch number: Unknown and expiry: UNKNOWN) dose, start therapy date were not reported, administered 1 in total for prophylactic vaccination. The batch number was not reported. The Company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. It was reported that on an unspecified dates, the patient caught covid twice(coded as suspected covid-19 infection and suspected clinical vaccination failure) and reporter also stated that ""If anyone is doing a class action lawsuit against these clowns, hit me up. I want in"". The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the suspected covid-19 infection and suspected clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality complaint 90000209391. The suspected product quality complaint has been confirmed to be voided(did not meet RA criteria) (as reported complaint was covid with no symptoms and test performed therefore did not meet RA criteria, hence was confirmed as voided) based on the RA evaluation/investigation performed.; Sender's Comments: V0: 20211263430 -Covid-19 vaccine ad26.cov2.s-Suspected clinical Vaccination failure. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS",,,,,,,,Y,U,,,,,UNK,,,,,,USJNJFOC20211263430,2,01/01/2022,,,,
1 VAERS_ID RECVDATE STATE AGE_YRS CAGE_YR CAGE_MO SEX RPT_DATE SYMPTOM_TEXT DIED DATEDIED L_THREAT ER_VISIT HOSPITAL HOSPDAYS X_STAY DISABLE RECOVD VAX_DATE ONSET_DATE NUMDAYS LAB_DATA V_ADMINBY V_FUNDBY OTHER_MEDS CUR_ILL HISTORY PRIOR_VAX SPLTTYPE FORM_VERS TODAYS_DATE BIRTH_DEFECT OFC_VISIT ER_ED_VISIT ALLERGIES
2 1996873 01/01/2022 CA U This spontaneous report was received from a pharmacist referring to a patient of unknown age and gender. Information regarding the patient's medical history, concurrent conditions or concomitant medications was not provided. On15-DEC-2021, the patient was vaccinated with an expired hpv rl1 6 11 16 18 31 33 45 52 58 vlp vaccine (yeast) (GARDASIL 9) 0.5 mL injection, (lot #R017624, which was considered to be valid, expiration date: 17-MAR-2021), administered for prophylaxis (vaccination scheme frequency, anatomical location and route of administration were not provided) (expired vaccine administered). The reporter stated the vaccine did not experience any temperature excursion. No additional adverse event was reported. U 12/15/2021 12/15/2021 0 UNK US0095075132112USA007320 2 12/31/2021
3 1996874 01/01/2022 U SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; This spontaneous potential legal report received from a patient concerned a patient of unspecified age and sex. Initial information was processed along with the additional information received from a regulatory authority on 30-DEC-2021. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (dose number in series: 1) (suspension for injection, route of admin not reported, batch number: Unknown and expiry: UNKNOWN) dose, start therapy date were not reported, administered 1 in total for prophylactic vaccination. The batch number was not reported. The Company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. It was reported that on an unspecified dates, the patient caught covid twice(coded as suspected covid-19 infection and suspected clinical vaccination failure) and reporter also stated that "If anyone is doing a class action lawsuit against these clowns, hit me up. I want in". The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the suspected covid-19 infection and suspected clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality complaint 90000209391. The suspected product quality complaint has been confirmed to be voided(did not meet RA criteria) (as reported complaint was covid with no symptoms and test performed therefore did not meet RA criteria, hence was confirmed as voided) based on the RA evaluation/investigation performed.; Sender's Comments: V0: 20211263430 -Covid-19 vaccine ad26.cov2.s-Suspected clinical Vaccination failure. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS Y U UNK USJNJFOC20211263430 2 01/01/2022

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test/VAERS/2022VAERSData/2022VAERSVAX.csv Normal file
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VAERS_ID,VAX_TYPE,VAX_MANU,VAX_LOT,VAX_DOSE_SERIES,VAX_ROUTE,VAX_SITE,VAX_NAME
1996873,HPV9,MERCK & CO. INC.,R017624,UNK,,,HPV (GARDASIL 9)
1996874,COVID19,MODERNA,025L20A,1,OT,,COVID19 (COVID19 (JANSSEN))
1 VAERS_ID VAX_TYPE VAX_MANU VAX_LOT VAX_DOSE_SERIES VAX_ROUTE VAX_SITE VAX_NAME
2 1996873 HPV9 MERCK & CO. INC. R017624 UNK HPV (GARDASIL 9)
3 1996874 COVID19 MODERNA 025L20A 1 OT COVID19 (COVID19 (JANSSEN))