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

PYREXIA ( 16 FDA reports)
VOMITING ( 15 FDA reports)
DIARRHOEA ( 13 FDA reports)
PNEUMONIA ( 13 FDA reports)
NAUSEA ( 10 FDA reports)
RENAL FAILURE ACUTE ( 9 FDA reports)
FATIGUE ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
HEPATOTOXICITY ( 8 FDA reports)
INFLAMMATION ( 8 FDA reports)
OROPHARYNGEAL PAIN ( 8 FDA reports)
VIRAL INFECTION ( 8 FDA reports)
ARTHRITIS ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
APNOEA ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
COUGH ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 6 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 6 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 6 FDA reports)
MYOCARDITIS ( 6 FDA reports)
PULSE ABSENT ( 6 FDA reports)
RESPIRATORY TRACT CONGESTION ( 6 FDA reports)
SERUM FERRITIN INCREASED ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
TACHYPNOEA ( 6 FDA reports)
WEIGHT INCREASED ( 6 FDA reports)
WHEEZING ( 6 FDA reports)
BACK PAIN ( 5 FDA reports)
BLISTER ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
FIBRIN D DIMER INCREASED ( 5 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 5 FDA reports)
RASH ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
RHEUMATOID ARTHRITIS ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ARM AMPUTATION ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
EPIDURAL LIPOMATOSIS ( 4 FDA reports)
HEPATOCELLULAR INJURY ( 4 FDA reports)
INFECTION ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
MALIGNANT NEOPLASM OF PLEURA ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
PAPILLOEDEMA ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
STREPTOCOCCAL SEPSIS ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BEHCET'S SYNDROME ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
HODGKIN'S DISEASE ( 3 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
LIVER ABSCESS ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
MALAISE ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SUBACUTE ENDOCARDITIS ( 3 FDA reports)
T-CELL LYMPHOMA ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
AUTOINFLAMMATORY DISEASE ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GOUT ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HYPOPYON ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENINGITIS TUBERCULOUS ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN FRAGILITY ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
TOOTH INJURY ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC INFANTILE NEUROLOGICAL CUTANEOUS AND ARTICULAR SYNDROME ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COMA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALLOPIAN TUBE CANCER STAGE III ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL STOMA NECROSIS ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
IRITIS ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JOINT TUBERCULOSIS ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOHISTIOCYTOSIS ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYELOID MATURATION ARREST ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PUNCTURE SITE PAIN ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)
RALES ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SEPTIC ARTHRITIS STREPTOCOCCAL ( 1 FDA reports)
SHOULDER ARTHROPLASTY ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TIC ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
VITAMIN D ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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