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

PYREXIA ( 13 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 11 FDA reports)
COUGH ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
DIARRHOEA ( 9 FDA reports)
DIZZINESS ( 9 FDA reports)
HAEMATOCRIT DECREASED ( 9 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
CONJUNCTIVITIS ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
SINUSITIS ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
TACHYARRHYTHMIA ( 6 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
INFECTION ( 5 FDA reports)
TACHYPNOEA ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
ABSCESS ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
APLASIA ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RELAPSING FEVER ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERYTHROBLAST COUNT DECREASED ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PAROPHTHALMIA ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)

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