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
127824621 12782462 1 I 20160915 20160927 20160927 PER US-JNJFOC-20160916794 JANSSEN 0.00 E F Y 48.99000 KG 20160927 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
127824621 12782462 1 PS ULTRAM TRAMADOL HYDROCHLORIDE 1 Oral N U UNKNOWN 20281 TABLETS
127824621 12782462 2 SS TYLENOL WITH CODEINE ACETAMINOPHENCODEINE PHOSPHATE 1 Oral U U 0 TABLETS
127824621 12782462 3 C VITAMINS NOS VITAMINS 1 Unknown D 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127824621 12782462 1 Pain
127824621 12782462 2 Pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127824621 12782462 Abdominal pain upper
127824621 12782462 Adverse drug reaction
127824621 12782462 Aphasia
127824621 12782462 Drug ineffective
127824621 12782462 Dry throat
127824621 12782462 Heart rate increased
127824621 12782462 Malaise
127824621 12782462 Pain
127824621 12782462 Peripheral swelling
127824621 12782462 Spinal pain

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
127824621 12782462 1 20160423 201604 0