The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
7030380 8011044 I 7030380-2 20100910 20100921 20101001 EXP 2010US005221 ELSAI INC. 27 YR M N 76.9 KG 20100930 MD UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
7030380 1014841700 PS PALONOSETRON HYDROCHLORIDE 1 INTRAVENOUS 0.25 MG, SINGLE, INTRAVENOUS Y D 021372
7030380 1014939294 SS DEXAMETHASONE 1 INTRAVENOUS 20 MG, SINGLE, INTRAVENOUS Y D
7030380 1014939305 C EXTRA STRENGTH TYLENOL 1 021372
7030380 1014939308 C HYDROCHLOROTHIAZIDE 1 021372
7030380 1014939310 C OXYGEN (OXYGEN) 2
7030380 1014939297 C CARBOPLATIN 1
7030380 1014939309 C METOPROLOL TARTRATE 1
7030380 1014939296 SS COMPAZINE 1 ORAL 10 MG, TID, ORAL Y D
7030380 1014939295 SS PLACEBO 1 ORAL 125 MG, QD, ORAL, 8MG, QD, ORAL Y D
7030380 1014939307 C DILTIAZEM 1
7030380 1014939306 C KEFLEX 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
7030380 1014841700 PROPHYLAXIS OF NAUSEA AND VOMITING
7030380 1014939294 PROPHYLAXIS OF NAUSEA AND VOMITING
7030380 1014939296 PROPHYLAXIS OF NAUSEA AND VOMITING
7030380 1014939295 PROPHYLAXIS OF NAUSEA AND VOMITING

Outcome of event

Event ID OUTC COD
7030380 HO

Reactions reported

Event ID PT
7030380 DYSTONIA
7030380 DYSPNOEA
7030380 SWOLLEN TONGUE
7030380 SPEECH DISORDER

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

Event ID RPSR COD
7030380 SDY
7030380 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
7030380 1014841700 20100908 20100908
7030380 1014939294 20100908 20100908
7030380 1014939296 20100909 20100910
7030380 1014939295 20100908 20100908
7030380 1014939295 20100909 20100910