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

CONFUSIONAL STATE ( 9 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
FALL ( 7 FDA reports)
GRAND MAL CONVULSION ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
COLITIS ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
TONGUE DISCOLOURATION ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
COMA ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INJURY ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PURPURA ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
TRACHEAL OEDEMA ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ACCIDENT ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 1 FDA reports)
DEATH ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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