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
6025170 6870947 F 6025170-3 20081031 20081222 20081231 EXP GB-ABBOTT-08P-167-0488723-00 ABBOTT LABORATORIES 72 F Y 58 KG 20081231 MD 20081031 UNITED KINGDOM

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
6025170 1010942243 PS ZEMPLAR 1 ORAL UNKNOWN 021606
6025170 1010942244 C DIALYSIS 2
6025170 1010942245 C LITHIUM 2 ORAL
6025170 1010942246 C LEVOTHYROXINE 2 ORAL
6025170 1010942247 C OMEPRAZOLE 1 ORAL
6025170 1010942248 C MIRTAZAPINE 2 ORAL
6025170 1010942249 C SIMVASTATIN 1 ORAL
6025170 1010942250 C DARBEPOETIN ALFA 2 SUBCUTANEOUS

Indications of drugs used

Event ID DRUG SEQ INDI PT
6025170 1010942243 HYPERPARATHYROIDISM TERTIARY
6025170 1010942244 DRUG USE FOR UNKNOWN INDICATION
6025170 1010942245 BIPOLAR DISORDER
6025170 1010942246 HYPOTHYROIDISM
6025170 1010942247 GASTROOESOPHAGEAL REFLUX DISEASE
6025170 1010942248 BIPOLAR DISORDER
6025170 1010942249 HYPERCHOLESTEROLAEMIA
6025170 1010942250 NEPHROGENIC ANAEMIA

Outcome of event

Event ID OUTC COD
6025170 DE

Reactions reported

Event ID PT
6025170 DRUG INEFFECTIVE
6025170 THERAPY CESSATION

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6025170 1010942243 20080820 20081018