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

DIARRHOEA ( 14 FDA reports)
ANAEMIA ( 13 FDA reports)
DYSPNOEA ( 13 FDA reports)
VOMITING ( 12 FDA reports)
SEPSIS ( 10 FDA reports)
DEHYDRATION ( 9 FDA reports)
DIZZINESS ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
ACUTE HEPATIC FAILURE ( 7 FDA reports)
BLOOD URINE PRESENT ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
METABOLIC ACIDOSIS ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
SLUGGISHNESS ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ASCITES ( 5 FDA reports)
CARDIOMYOPATHY ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
HYPOTHYROIDISM ( 5 FDA reports)
JOINT SWELLING ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
ORTHOSTATIC HYPOTENSION ( 5 FDA reports)
PAIN ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
IMMOBILE ( 4 FDA reports)
JOINT LOCK ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
MALAISE ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
THERMOHYPERAESTHESIA ( 4 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
TROPICAL SPRUE ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CYST ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)

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