The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
124717532 12471753 2 F 20160608 20160720 20160616 20160907 PER US-JNJFOC-20160610227 JANSSEN 37.88 YR A F Y 0.00000 20160907 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
124717532 12471753 1 PS FENTANYL TRANSDERMAL SYSTEM FENTANYL 1 Transdermal N UNKNOWN 19813 MATRIX PATCH
124717532 12471753 2 C CLARITIN LORATADINE 1 Oral 0 CAPSULE
124717532 12471753 3 C LYRICA PREGABALIN 1 Oral 0 CAPSULE
124717532 12471753 4 C NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 Oral UP TO 6 TABLETS 0 10 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124717532 12471753 1 Neuralgia
124717532 12471753 2 Multiple allergies
124717532 12471753 3 Neuralgia
124717532 12471753 4 Neuralgia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124717532 12471753 Abdominal pain upper
124717532 12471753 Neuralgia
124717532 12471753 Product quality issue
124717532 12471753 Withdrawal syndrome
124717532 12471753 Wrong technique in product usage process

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
124717532 12471753 1 2016 0
124717532 12471753 3 201601 0