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

THROMBOCYTOPENIA ( 28 FDA reports)
BLOOD URINE PRESENT ( 17 FDA reports)
HAEMOLYTIC ANAEMIA ( 15 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 15 FDA reports)
MYCOSIS FUNGOIDES ( 8 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
TRANSPLANT REJECTION ( 7 FDA reports)
DRUG TOXICITY ( 6 FDA reports)
HAEMOLYSIS ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
DIZZINESS ( 5 FDA reports)
PETECHIAE ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
BONE MARROW DEPRESSION ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
COLON CANCER ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
PAIN ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
INFECTION ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FALL ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LYMPHOCYTOSIS ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SIMPLE PARTIAL SEIZURES ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CRYPTOCOCCAL CUTANEOUS INFECTION ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHOMATOID PAPULOSIS ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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