000 01628 a2200433 4500
005 20250513051030.0
264 0 _c19950425
008 199504s 0 0 eng d
022 _a0029-7844
024 7 _a10.1016/0029-7844(94)00457-O
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWysowski, D K
245 0 0 _aSerious adverse events in Norplant users reported to the Food and Drug Administration's MedWatch Spontaneous Reporting System.
_h[electronic resource]
260 _bObstetrics and gynecology
_cApr 1995
300 _a538-42 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAdverse Drug Reaction Reporting Systems
_xstatistics & numerical data
650 0 4 _aAnti-Bacterial Agents
_xtherapeutic use
650 0 4 _aCerebrovascular Disorders
_xchemically induced
650 0 4 _aCombined Modality Therapy
650 0 4 _aDebridement
650 0 4 _aDrainage
650 0 4 _aDrug Implants
650 0 4 _aFemale
650 0 4 _aHospitalization
_xstatistics & numerical data
650 0 4 _aHumans
650 0 4 _aLevonorgestrel
_xadverse effects
650 0 4 _aPlasmapheresis
650 0 4 _aPseudotumor Cerebri
_xchemically induced
650 0 4 _aPurpura, Thrombotic Thrombocytopenic
_xchemically induced
650 0 4 _aSurgical Wound Infection
_xdiagnosis
650 0 4 _aUnited States
650 0 4 _aUnited States Food and Drug Administration
700 1 _aGreen, L
773 0 _tObstetrics and gynecology
_gvol. 85
_gno. 4
_gp. 538-42
856 4 0 _uhttps://doi.org/10.1016/0029-7844(94)00457-O
_zAvailable from publisher's website
999 _c7898163
_d7898163