Serious adverse events in Norplant users reported to the Food and Drug Administration's MedWatch Spontaneous Reporting System. [electronic resource]
Producer: 19950425Description: 538-42 p. digitalISSN:- 0029-7844
- Adolescent
- Adult
- Adverse Drug Reaction Reporting Systems -- statistics & numerical data
- Anti-Bacterial Agents -- therapeutic use
- Cerebrovascular Disorders -- chemically induced
- Combined Modality Therapy
- Debridement
- Drainage
- Drug Implants
- Female
- Hospitalization -- statistics & numerical data
- Humans
- Levonorgestrel -- adverse effects
- Plasmapheresis
- Pseudotumor Cerebri -- chemically induced
- Purpura, Thrombotic Thrombocytopenic -- chemically induced
- Surgical Wound Infection -- diagnosis
- United States
- United States Food and Drug Administration
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Publication Type: Journal Article
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