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
126303121 12630312 1 I 20150811 20160808 20160808 PER US-ACTAVIS-2015-17077 ACTAVIS 0.00 F Y 73.00000 KG 20160808 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
126303121 12630312 1 PS FIORICET ACETAMINOPHENBUTALBITALCAFFEINE 1 Oral UNK UNK, UNKNOWN U UNKNOWN 88616 TABLET
126303121 12630312 2 SS IMITREX SUMATRIPTAN SUCCINATE 1 Oral 50 MG, BID U 27-JUL-2016 0 50 MG BID
126303121 12630312 3 C ATORVASTATIN ATORVASTATIN 1 Unknown UNK, UNKNOWN UNKNOWN 0
126303121 12630312 4 C XANAX ALPRAZOLAM 1 Unknown UNK, UNKNOWN UNKNOWN 0
126303121 12630312 5 C PAXIL PAROXETINE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126303121 12630312 1 Migraine
126303121 12630312 2 Migraine
126303121 12630312 3 Product used for unknown indication
126303121 12630312 4 Product used for unknown indication
126303121 12630312 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126303121 12630312 Drug ineffective
126303121 12630312 Medication overuse headache

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

no results found

Therapies reported

no results found