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

FATIGUE ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
BACK PAIN ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
ALOPECIA ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
TREMOR ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN WRINKLING ( 2 FDA reports)
STRESS ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
APATHY ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD HOMOCYSTEINE DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use