Wysowski, D K <br/><br/>
Serious adverse events in Norplant users reported to the Food and Drug Administration's MedWatch Spontaneous Reporting System.  [electronic resource] 

 -  Obstetrics and gynecology  Apr 1995 
 - 538-42 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0029-7844 
<br/><br/><label>Standard No.: </label>10.1016/0029-7844(94)00457-O  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Adverse Drug Reaction Reporting Systems--statistics & numerical data<br/>Anti-Bacterial Agents--therapeutic use<br/>Cerebrovascular Disorders--chemically induced<br/>Combined Modality Therapy<br/>Debridement<br/>Drainage<br/>Drug Implants<br/>Female<br/>Hospitalization--statistics & numerical data<br/>Humans<br/>Levonorgestrel--adverse effects<br/>Plasmapheresis<br/>Pseudotumor Cerebri--chemically induced<br/>Purpura, Thrombotic Thrombocytopenic--chemically induced<br/>Surgical Wound Infection--diagnosis<br/>United States<br/>United States Food and Drug Administration