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

DIARRHOEA ( 9 FDA reports)
HAEMOLYTIC ANAEMIA ( 8 FDA reports)
ASTHENIA ( 7 FDA reports)
VISUAL ACUITY REDUCED ( 7 FDA reports)
VOMITING ( 7 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
DEATH ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
SMALL FOR DATES BABY ( 6 FDA reports)
STILLBIRTH ( 6 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
PREMATURE BABY ( 5 FDA reports)
DEATH NEONATAL ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
MANIA ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AGITATION ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
COLD AGGLUTININS POSITIVE ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
FALL ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MALARIA ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PROLONGED LABOUR ( 2 FDA reports)
PULSE ABNORMAL ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SKIN TURGOR DECREASED ( 2 FDA reports)
TETANY ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OBSTRUCTED LABOUR ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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