Please choose an event type to view the corresponding MedsFacts report:

POST PROCEDURAL INFECTION ( 13 FDA reports)
INFECTION ( 10 FDA reports)
SERRATIA INFECTION ( 6 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 5 FDA reports)
SEROMA ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
WOUND DEHISCENCE ( 4 FDA reports)
PSEUDOMONAS INFECTION ( 4 FDA reports)
CULTURE POSITIVE ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
BREAST INFECTION ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
FAILURE OF IMPLANT ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
IMPLANT TISSUE NECROSIS ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
SKIN GRAFT INFECTION ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
BREAST DISORDER FEMALE ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)

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