The Safety Rates Drug Report

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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
127102311 12710231 1 I 20160822 20160902 20160902 PER US-ASTRAZENECA-2016SE90046 ASTRAZENECA 86.00 YR F Y 0.00000 20160902 MD 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
127102311 12710231 1 PS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral UNK U 21153
127102311 12710231 2 SS BIAXIN CLARITHROMYCIN 1 Unknown UNK U 0
127102311 12710231 3 SS FENTANYL. FENTANYL 1 Unknown UNK U 0
127102311 12710231 4 SS NORVASC AMLODIPINE BESYLATE 1 Unknown UNK U 0
127102311 12710231 5 SS TETRACYCLINE HCL TETRACYCLINE HYDROCHLORIDE 1 Unknown UNK U 0
127102311 12710231 6 SS CLINORIL SULINDAC 1 Unknown UNK U 0
127102311 12710231 7 SS NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 Unknown UNK U 0
127102311 12710231 8 SS SULFUR. SULFUR 1 Unknown UNK U 0
127102311 12710231 9 SS VERSED MIDAZOLAM HYDROCHLORIDE 1 Unknown UNK U 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127102311 12710231 Drug hypersensitivity

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

no results found

Therapies reported

no results found