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
122005516 12200551 6 F 20140828 20160627 20160322 20160702 PER PHEH2016US006541 SANDOZ 55.44 YR M Y 66.67000 KG 20160702 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
122005516 12200551 1 SS ZOFRAN ONDANSETRON HYDROCHLORIDE 1 Oral UNK Y 0
122005516 12200551 2 PS GABAPENTIN. GABAPENTIN 1 Oral Y 75539
122005516 12200551 3 SS NITROSTAT NITROGLYCERIN 1 Unknown 1 DF, UNK (UNDER TOUNGE) U 0 1 DF TABLET
122005516 12200551 4 SS NEURONTIN GABAPENTIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122005516 12200551 1 Nausea
122005516 12200551 2 Neuralgia
122005516 12200551 3 Product used for unknown indication
122005516 12200551 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122005516 12200551 Abdominal discomfort
122005516 12200551 Drug hypersensitivity
122005516 12200551 Rash
122005516 12200551 Vomiting

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

no results found

Therapies reported

no results found