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
123569254 12356925 4 F 201405 20160711 20160511 20160801 PER US-PFIZER INC-2016249798 PFIZER 51.00 YR F Y 0.00000 20160801 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
123569254 12356925 1 PS ADVIL IBUPROFEN 1 UNK, AS NEEDED (2 TABLETS TO 4 A DAY WHEN NEEDED) M31249 18989 TABLET
123569254 12356925 2 SS ADVIL IBUPROFEN 1 18989 TABLET
123569254 12356925 3 SS ADVIL IBUPROFEN 1 18989 TABLET
123569254 12356925 4 SS ADVIL IBUPROFEN 1 18989 TABLET
123569254 12356925 5 SS ESTRADIOL. ESTRADIOL 1 UNK, DAILY (2.5 YEARS AGO) N 20472
123569254 12356925 6 SS SODIUM LAURYL SULFOACETATE SODIUM LAURYL SULFOACETATE 1 UNK U 0
123569254 12356925 7 C BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 UNK, AS NEEDED 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123569254 12356925 1 Arthralgia
123569254 12356925 2 Pain in extremity
123569254 12356925 3 Headache
123569254 12356925 4 Myalgia
123569254 12356925 5 Hormone replacement therapy
123569254 12356925 7 Hypersensitivity

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123569254 12356925 Cough
123569254 12356925 Drug hypersensitivity
123569254 12356925 Peripheral swelling
123569254 12356925 Reaction to drug excipients

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

no results found

Therapies reported

no results found