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

DRUG INTERACTION ( 75 FDA reports)
DYSTONIA ( 56 FDA reports)
MYOTONIA ( 54 FDA reports)
RENAL IMPAIRMENT ( 42 FDA reports)
SINUS TACHYCARDIA ( 34 FDA reports)
AGITATION ( 32 FDA reports)
BACK PAIN ( 28 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 28 FDA reports)
CARDIAC ARREST ( 26 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 26 FDA reports)
INFECTION ( 26 FDA reports)
DRUG EFFECT DECREASED ( 24 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 24 FDA reports)
BRADYCARDIA ( 23 FDA reports)
MYOCLONUS ( 19 FDA reports)
STARING ( 19 FDA reports)
TACHYCARDIA ( 19 FDA reports)
ANAPHYLACTIC SHOCK ( 18 FDA reports)
DRUG TOXICITY ( 18 FDA reports)
HYPOTENSION ( 18 FDA reports)
MULTI-ORGAN FAILURE ( 17 FDA reports)
BRONCHOSPASM ( 16 FDA reports)
DEATH ( 16 FDA reports)
VENTRICULAR FIBRILLATION ( 16 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 15 FDA reports)
HEPATITIS ( 15 FDA reports)
OXYGEN SATURATION DECREASED ( 15 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 14 FDA reports)
PANIC REACTION ( 14 FDA reports)
RESTLESSNESS ( 14 FDA reports)
ABDOMINAL PAIN ( 13 FDA reports)
DRUG INEFFECTIVE ( 13 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 13 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 13 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 13 FDA reports)
ANAPHYLACTIC REACTION ( 12 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
HYPERHIDROSIS ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
OEDEMA PERIPHERAL ( 12 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
AGGRESSION ( 11 FDA reports)
COMA ( 11 FDA reports)
CYANOSIS ( 11 FDA reports)
ESCHERICHIA INFECTION ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 11 FDA reports)
SOMNOLENCE ( 11 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 10 FDA reports)
CONDITION AGGRAVATED ( 10 FDA reports)
DISEASE PROGRESSION ( 10 FDA reports)
FEELING ABNORMAL ( 10 FDA reports)
HYPERVENTILATION ( 10 FDA reports)
HYPOXIA ( 10 FDA reports)
PLEURAL EFFUSION ( 10 FDA reports)
ATRIAL FIBRILLATION ( 9 FDA reports)
CAESAREAN SECTION ( 9 FDA reports)
CATATONIA ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
HEPATIC FAILURE ( 9 FDA reports)
MYALGIA ( 9 FDA reports)
MYDRIASIS ( 9 FDA reports)
PILOERECTION ( 9 FDA reports)
POST PROCEDURAL COMPLICATION ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
SEROTONIN SYNDROME ( 9 FDA reports)
SPEECH DISORDER ( 9 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 8 FDA reports)
AKATHISIA ( 8 FDA reports)
ANAESTHETIC COMPLICATION ( 8 FDA reports)
BLOOD ALBUMIN DECREASED ( 8 FDA reports)
BLOOD BILIRUBIN INCREASED ( 8 FDA reports)
BLOOD CALCIUM INCREASED ( 8 FDA reports)
BRAIN OEDEMA ( 8 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 8 FDA reports)
LACERATION ( 8 FDA reports)
PNEUMONIA ( 8 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
BLISTER ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 7 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
HAEMATEMESIS ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
PARAESTHESIA ( 7 FDA reports)
PREMATURE LABOUR ( 7 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
SCLERODERMA ( 7 FDA reports)
SLEEP DISORDER ( 7 FDA reports)
VOMITING ( 7 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 6 FDA reports)
AMNESIA ( 6 FDA reports)
ASCITES INFECTION ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
ENTEROCOCCAL INFECTION ( 6 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
HYPOCOAGULABLE STATE ( 6 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
NO THERAPEUTIC RESPONSE ( 6 FDA reports)
PEMPHIGOID ( 6 FDA reports)
PROCEDURAL COMPLICATION ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
WOUND SECRETION ( 6 FDA reports)
ABDOMINAL SEPSIS ( 5 FDA reports)
APHASIA ( 5 FDA reports)
ASCITES ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 5 FDA reports)
FALL ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
HEMIPLEGIA ( 5 FDA reports)
HYPERPARATHYROIDISM ( 5 FDA reports)
HYPERREFLEXIA ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
HYPOTONIA ( 5 FDA reports)
ISCHAEMIC STROKE ( 5 FDA reports)
PROPOFOL INFUSION SYNDROME ( 5 FDA reports)
SCREAMING ( 5 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
TREMOR ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
ECTOPIC PREGNANCY ( 4 FDA reports)
FOETAL MALPRESENTATION ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
INJURY ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
LABILE BLOOD PRESSURE ( 4 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 4 FDA reports)
MELAENA ( 4 FDA reports)
MOTOR DYSFUNCTION ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
NEUTROPHILIA ( 4 FDA reports)
NO ADVERSE EVENT ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RESPIRATORY DEPRESSION ( 4 FDA reports)
RESUSCITATION ( 4 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
APALLIC SYNDROME ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSPHASIA ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FEAR ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MICROSTOMIA ( 3 FDA reports)
ORGAN FAILURE ( 3 FDA reports)
PAIN ( 3 FDA reports)
PANCREATIC ABSCESS ( 3 FDA reports)
PANCREATIC NECROSIS ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
RAYNAUD'S PHENOMENON ( 3 FDA reports)
RENAL INJURY ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SEX CHROMOSOME ABNORMALITY ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
VARICOSE VEIN OPERATION ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ANAESTHETIC COMPLICATION PULMONARY ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
COAGULATION FACTOR DECREASED ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG EFFECT PROLONGED ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENDOMETRITIS ( 2 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PREMATURE RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
RASH ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN TEST POSITIVE ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TRYPTASE INCREASED ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANAPHYLACTOID SYNDROME OF PREGNANCY ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN STEM AUDITORY EVOKED RESPONSE ABNORMAL ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FUNGAL ABSCESS CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HYDROMETRA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PERIPARTUM CARDIOMYOPATHY ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PLATELET COUNT ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RETAINED PRODUCTS OF CONCEPTION ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUPRAPUBIC CATHETER INSERTION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TETANY ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRANSVERSE PRESENTATION ( 1 FDA reports)
UNWANTED AWARENESS DURING ANAESTHESIA ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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