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

BLOOD PRESSURE DECREASED ( 64 FDA reports)
DIARRHOEA ( 48 FDA reports)
NAUSEA ( 48 FDA reports)
RESPIRATORY FAILURE ( 44 FDA reports)
BRADYCARDIA ( 40 FDA reports)
PYREXIA ( 40 FDA reports)
RENAL FAILURE ACUTE ( 40 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 36 FDA reports)
ANAPHYLACTIC SHOCK ( 34 FDA reports)
ANXIETY ( 34 FDA reports)
RENAL FAILURE ( 34 FDA reports)
RHABDOMYOLYSIS ( 34 FDA reports)
PLATELET COUNT DECREASED ( 33 FDA reports)
PULMONARY OEDEMA ( 33 FDA reports)
HYPOTENSION ( 32 FDA reports)
DYSPNOEA ( 31 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 30 FDA reports)
LOSS OF CONSCIOUSNESS ( 30 FDA reports)
VENTRICULAR TACHYCARDIA ( 30 FDA reports)
BLOOD BILIRUBIN INCREASED ( 29 FDA reports)
FALL ( 29 FDA reports)
VOMITING ( 29 FDA reports)
ATRIAL FIBRILLATION ( 28 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 28 FDA reports)
MULTI-ORGAN FAILURE ( 28 FDA reports)
POST PROCEDURAL COMPLICATION ( 28 FDA reports)
CARDIAC ARREST ( 27 FDA reports)
PAIN ( 27 FDA reports)
DEPRESSION ( 26 FDA reports)
CHEST PAIN ( 25 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 25 FDA reports)
HYPERTENSION ( 24 FDA reports)
NEUROPATHY PERIPHERAL ( 24 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 23 FDA reports)
ASTHENIA ( 23 FDA reports)
CONVULSION ( 23 FDA reports)
TACHYCARDIA ( 23 FDA reports)
CARDIOMEGALY ( 22 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 22 FDA reports)
OEDEMA PERIPHERAL ( 22 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 22 FDA reports)
ARTERIOSPASM CORONARY ( 21 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 21 FDA reports)
BLOOD POTASSIUM DECREASED ( 21 FDA reports)
DEHYDRATION ( 21 FDA reports)
GAIT DISTURBANCE ( 21 FDA reports)
INSOMNIA ( 21 FDA reports)
PAIN IN EXTREMITY ( 21 FDA reports)
PNEUMONIA ( 21 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 20 FDA reports)
GASTRITIS ( 20 FDA reports)
OXYGEN SATURATION DECREASED ( 20 FDA reports)
PROCEDURAL COMPLICATION ( 20 FDA reports)
VENTRICULAR FIBRILLATION ( 20 FDA reports)
ANAEMIA ( 19 FDA reports)
CONDITION AGGRAVATED ( 19 FDA reports)
CONSTIPATION ( 19 FDA reports)
DRUG INEFFECTIVE ( 19 FDA reports)
LIVER DISORDER ( 19 FDA reports)
BLOOD PRESSURE INCREASED ( 18 FDA reports)
COUGH ( 18 FDA reports)
LUNG NEOPLASM MALIGNANT ( 18 FDA reports)
METABOLIC ACIDOSIS ( 18 FDA reports)
RASH ( 18 FDA reports)
SOMNOLENCE ( 18 FDA reports)
ATELECTASIS ( 17 FDA reports)
HYPOXIA ( 17 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 16 FDA reports)
ANAESTHETIC COMPLICATION ( 16 FDA reports)
DRUG INTERACTION ( 16 FDA reports)
EMPYEMA ( 16 FDA reports)
FIBULA FRACTURE ( 16 FDA reports)
HAEMOGLOBIN DECREASED ( 16 FDA reports)
HEADACHE ( 16 FDA reports)
HYPERTHERMIA MALIGNANT ( 16 FDA reports)
HYPOAESTHESIA ( 16 FDA reports)
INJURY ( 16 FDA reports)
RIB FRACTURE ( 16 FDA reports)
SHOCK ( 16 FDA reports)
WHEEZING ( 16 FDA reports)
ABDOMINAL PAIN UPPER ( 15 FDA reports)
ABSCESS ( 15 FDA reports)
CEREBRAL INFARCTION ( 15 FDA reports)
CYANOSIS ( 15 FDA reports)
DEATH ( 15 FDA reports)
EMPHYSEMA ( 15 FDA reports)
HEART RATE DECREASED ( 15 FDA reports)
NASOPHARYNGITIS ( 15 FDA reports)
PULMONARY FIBROSIS ( 15 FDA reports)
RESPIRATORY ARREST ( 15 FDA reports)
URINARY INCONTINENCE ( 15 FDA reports)
ANHEDONIA ( 14 FDA reports)
BACTERIAL DISEASE CARRIER ( 14 FDA reports)
BRONCHOPLEURAL FISTULA ( 14 FDA reports)
CEREBROVASCULAR DISORDER ( 14 FDA reports)
CERVICAL SPINAL STENOSIS ( 14 FDA reports)
CHONDROMALACIA ( 14 FDA reports)
COAGULOPATHY ( 14 FDA reports)
CONFUSIONAL STATE ( 14 FDA reports)
CYST ( 14 FDA reports)
EYE DISCHARGE ( 14 FDA reports)
FAECAL INCONTINENCE ( 14 FDA reports)
FOOT DEFORMITY ( 14 FDA reports)
FOOT FRACTURE ( 14 FDA reports)
HAEMODIALYSIS ( 14 FDA reports)
HAEMORRHAGE ( 14 FDA reports)
HEART RATE INCREASED ( 14 FDA reports)
HYDROPNEUMOTHORAX ( 14 FDA reports)
ILEUS PARALYTIC ( 14 FDA reports)
INJURY CORNEAL ( 14 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 14 FDA reports)
LIP DISCOLOURATION ( 14 FDA reports)
LUNG INFECTION ( 14 FDA reports)
MALAISE ( 14 FDA reports)
MASTICATION DISORDER ( 14 FDA reports)
MENOPAUSE ( 14 FDA reports)
MENTAL STATUS CHANGES ( 14 FDA reports)
MYOCARDIAL ISCHAEMIA ( 14 FDA reports)
OSTEOARTHRITIS ( 14 FDA reports)
OSTEOPENIA ( 14 FDA reports)
OSTEORADIONECROSIS ( 14 FDA reports)
PNEUMOTHORAX ( 14 FDA reports)
PULMONARY AIR LEAKAGE ( 14 FDA reports)
RENAL IMPAIRMENT ( 14 FDA reports)
RETCHING ( 14 FDA reports)
ROTATOR CUFF SYNDROME ( 14 FDA reports)
SINUS BRADYCARDIA ( 14 FDA reports)
SINUSITIS ( 14 FDA reports)
TIBIA FRACTURE ( 14 FDA reports)
TOOTH DISORDER ( 14 FDA reports)
TOOTH FRACTURE ( 14 FDA reports)
TOOTHACHE ( 14 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 14 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 14 FDA reports)
BACK PAIN ( 13 FDA reports)
CHROMATURIA ( 13 FDA reports)
DYSPNOEA EXERTIONAL ( 13 FDA reports)
MEDICATION ERROR ( 13 FDA reports)
PULMONARY EMBOLISM ( 13 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 13 FDA reports)
BLOOD CALCIUM DECREASED ( 12 FDA reports)
CHEST DISCOMFORT ( 12 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 12 FDA reports)
COLONIC POLYP ( 12 FDA reports)
DECREASED APPETITE ( 12 FDA reports)
DIZZINESS ( 12 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 12 FDA reports)
HAEMATOMA ( 12 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 12 FDA reports)
METASTASES TO LYMPH NODES ( 12 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 12 FDA reports)
OSTEONECROSIS OF JAW ( 12 FDA reports)
PARAESTHESIA ( 12 FDA reports)
RHINITIS ( 12 FDA reports)
SEPSIS ( 12 FDA reports)
SPINAL OSTEOARTHRITIS ( 12 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 12 FDA reports)
BLISTER ( 11 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 11 FDA reports)
CARDIAC FAILURE ( 11 FDA reports)
DIVERTICULUM INTESTINAL ( 11 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 11 FDA reports)
ERYTHEMA ( 11 FDA reports)
MELAENA ( 11 FDA reports)
MYDRIASIS ( 11 FDA reports)
OSTEOPOROSIS ( 11 FDA reports)
PNEUMONIA ASPIRATION ( 11 FDA reports)
RECTAL POLYP ( 11 FDA reports)
STRESS CARDIOMYOPATHY ( 11 FDA reports)
AGITATION ( 10 FDA reports)
APNOEA ( 10 FDA reports)
ASCITES ( 10 FDA reports)
ATRIOVENTRICULAR BLOCK ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 10 FDA reports)
BREAST CALCIFICATIONS ( 10 FDA reports)
CARDIO-RESPIRATORY ARREST ( 10 FDA reports)
CHILLS ( 10 FDA reports)
HAEMATOCRIT DECREASED ( 10 FDA reports)
HAEMATURIA ( 10 FDA reports)
INFECTION ( 10 FDA reports)
LACERATION ( 10 FDA reports)
LARYNGEAL OEDEMA ( 10 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 10 FDA reports)
MUSCULAR WEAKNESS ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
PLEURAL EFFUSION ( 10 FDA reports)
PLEURAL FIBROSIS ( 10 FDA reports)
RESTLESSNESS ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
TENDON RUPTURE ( 10 FDA reports)
VISION BLURRED ( 10 FDA reports)
ANGINA PECTORIS ( 9 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 9 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 9 FDA reports)
BLOOD MAGNESIUM DECREASED ( 9 FDA reports)
CONTUSION ( 9 FDA reports)
CORONARY ARTERY STENOSIS ( 9 FDA reports)
EPISTAXIS ( 9 FDA reports)
GASTROENTERITIS ( 9 FDA reports)
HYPONATRAEMIA ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 9 FDA reports)
RESPIRATORY DISTRESS ( 9 FDA reports)
SINUS TACHYCARDIA ( 9 FDA reports)
URINARY TRACT INFECTION ( 9 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 9 FDA reports)
ACCIDENTAL OVERDOSE ( 8 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 8 FDA reports)
BLOOD UREA INCREASED ( 8 FDA reports)
BODY TEMPERATURE INCREASED ( 8 FDA reports)
BRONCHOSPASM ( 8 FDA reports)
CARDIOVASCULAR DISORDER ( 8 FDA reports)
CIRCULATORY COLLAPSE ( 8 FDA reports)
DRUG ERUPTION ( 8 FDA reports)
DRUG HYPERSENSITIVITY ( 8 FDA reports)
DYSARTHRIA ( 8 FDA reports)
ENDOPHTHALMITIS ( 8 FDA reports)
FLUSHING ( 8 FDA reports)
HYPOKALAEMIA ( 8 FDA reports)
HYPOVENTILATION ( 8 FDA reports)
INJECTION SITE ULCER ( 8 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 8 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 8 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 8 FDA reports)
RESPIRATORY ACIDOSIS ( 8 FDA reports)
SINOATRIAL BLOCK ( 8 FDA reports)
SINUS ARRHYTHMIA ( 8 FDA reports)
SPEECH DISORDER ( 8 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 8 FDA reports)
TREMOR ( 8 FDA reports)
ANAPHYLACTIC REACTION ( 7 FDA reports)
ANEURYSM RUPTURED ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
CATHETERISATION CARDIAC ( 7 FDA reports)
CORONARY ANGIOPLASTY ( 7 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 7 FDA reports)
CORONARY ARTERY DISEASE ( 7 FDA reports)
DECUBITUS ULCER ( 7 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 7 FDA reports)
EXERCISE TEST ABNORMAL ( 7 FDA reports)
GINGIVAL SWELLING ( 7 FDA reports)
HAEMATEMESIS ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
HYPERAESTHESIA ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 7 FDA reports)
IRRITABLE BOWEL SYNDROME ( 7 FDA reports)
LUNG DISORDER ( 7 FDA reports)
MOUTH ULCERATION ( 7 FDA reports)
NECK PAIN ( 7 FDA reports)
OLIGURIA ( 7 FDA reports)
ORGANISING PNEUMONIA ( 7 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
ALLODYNIA ( 6 FDA reports)
BALANCE DISORDER ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
BRONCHITIS ( 6 FDA reports)
CANCER PAIN ( 6 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 6 FDA reports)
DELUSION ( 6 FDA reports)
DRY SKIN ( 6 FDA reports)
EMBOLISM ( 6 FDA reports)
EPIGLOTTIC OEDEMA ( 6 FDA reports)
GASTRIC ULCER ( 6 FDA reports)
GRAFT VERSUS HOST DISEASE ( 6 FDA reports)
HYDROCEPHALUS ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
HYPOVOLAEMIA ( 6 FDA reports)
INCREASED BRONCHIAL SECRETION ( 6 FDA reports)
INTERCOSTAL NEURALGIA ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
LARYNGOSPASM ( 6 FDA reports)
MYOGLOBINURIA ( 6 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 6 FDA reports)
PALLOR ( 6 FDA reports)
SEDATION ( 6 FDA reports)
SKIN LACERATION ( 6 FDA reports)
SKIN ULCER ( 6 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 6 FDA reports)
TENDERNESS ( 6 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 6 FDA reports)
URINE OUTPUT INCREASED ( 6 FDA reports)
VENOUS THROMBOSIS ( 6 FDA reports)
VENOUS THROMBOSIS LIMB ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ABDOMINAL PAIN LOWER ( 5 FDA reports)
ACIDOSIS ( 5 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 5 FDA reports)
ANAPHYLACTOID SHOCK ( 5 FDA reports)
APNOEIC ATTACK ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
ARTHROSCOPIC SURGERY ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CARDIORENAL SYNDROME ( 5 FDA reports)
CHEST TUBE INSERTION ( 5 FDA reports)
CHOLECYSTITIS CHRONIC ( 5 FDA reports)
DEBRIDEMENT ( 5 FDA reports)
DISEASE RECURRENCE ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
ENDODONTIC PROCEDURE ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
FEELING COLD ( 5 FDA reports)
GANGRENE ( 5 FDA reports)
GASTRITIS EROSIVE ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
HEPATOCELLULAR DAMAGE ( 5 FDA reports)
HERPES ZOSTER DISSEMINATED ( 5 FDA reports)
HYPERCAPNIA ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
HYPOPHAGIA ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
INTRACARDIAC THROMBUS ( 5 FDA reports)
LUNG OPERATION ( 5 FDA reports)
MAMMOPLASTY ( 5 FDA reports)
MUSCLE ATROPHY ( 5 FDA reports)
MUSCLE FLAP OPERATION ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 5 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 5 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
PULSE ABSENT ( 5 FDA reports)
RASH VESICULAR ( 5 FDA reports)
ROTATOR CUFF REPAIR ( 5 FDA reports)
SINUS OPERATION ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 5 FDA reports)
THORACOTOMY ( 5 FDA reports)
TONIC CONVULSION ( 5 FDA reports)
TORSADE DE POINTES ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
VIRAL DNA TEST POSITIVE ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ACNE ( 4 FDA reports)
ALVEOLAR PROTEINOSIS ( 4 FDA reports)
ANAPHYLACTOID REACTION ( 4 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 4 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 4 FDA reports)
ANURIA ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 4 FDA reports)
BRAIN OEDEMA ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CARDIAC ANEURYSM ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CEREBRAL HAEMATOMA ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 4 FDA reports)
CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
DEVICE FAILURE ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
DYSTROPHIA MYOTONICA ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
ENTEROBACTER PNEUMONIA ( 4 FDA reports)
ENTEROCOLITIS ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 4 FDA reports)
EYELID OEDEMA ( 4 FDA reports)
GINGIVAL ERYTHEMA ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HOFFMANN'S SIGN ( 4 FDA reports)
HORDEOLUM ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPERREFLEXIA ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 4 FDA reports)
INJECTION SITE INDURATION ( 4 FDA reports)
INJECTION SITE THROMBOSIS ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LIP OEDEMA ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
MIOSIS ( 4 FDA reports)
MORTON'S NEUROMA ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
NEUROBLASTOMA RECURRENT ( 4 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PARONYCHIA ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
PNEUMONIA KLEBSIELLA ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
PUPIL FIXED ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RESPIRATION ABNORMAL ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
T-CELL LYMPHOMA ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
VENTRICULAR HYPOKINESIA ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ADRENAL CORTEX NECROSIS ( 3 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
ANTICHOLINERGIC SYNDROME ( 3 FDA reports)
AORTIC CALCIFICATION ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ARTERIOVENOUS FISTULA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD PH DECREASED ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
CHOLINERGIC SYNDROME ( 3 FDA reports)
CLONIC CONVULSION ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 3 FDA reports)
CORNEAL DEPOSITS ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DEVICE BREAKAGE ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GINGIVITIS ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HEPATITIS C ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
ILEUS ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
KERATITIS BACTERIAL ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MONOPARESIS ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
NODAL RHYTHM ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PANCREATIC NECROSIS ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 3 FDA reports)
PRIAPISM ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SKIN TEST POSITIVE ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SUBILEUS ( 3 FDA reports)
SURGICAL PROCEDURE REPEATED ( 3 FDA reports)
SUTURE RUPTURE ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TACHYCARDIA PAROXYSMAL ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
VALVULOPLASTY CARDIAC ( 3 FDA reports)
VASCULAR INJURY ( 3 FDA reports)
VITAL CAPACITY DECREASED ( 3 FDA reports)
VULVAL OEDEMA ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
BLADDER TRABECULATION ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BRAIN INJURY ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
BUNION ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CATATONIA ( 2 FDA reports)
CATHETER REMOVAL ( 2 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COMA ( 2 FDA reports)
CORNEAL PERFORATION ( 2 FDA reports)
CORNEAL SCAR ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DACRYOCYSTITIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRUG EFFECT PROLONGED ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
ENCEPHALITIS TOXIC ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FAILURE TO ANASTOMOSE ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GLOSSECTOMY ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JUVENILE ARTHRITIS ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MESENTERIC OCCLUSION ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
MYOGLOBIN URINE PRESENT ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OVARIAN TORSION ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHOTOCOAGULATION ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
REACTION TO DRUG PRESERVATIVES ( 2 FDA reports)
RECTOSIGMOID CANCER ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
SENSE OF OPPRESSION ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SPLENIC ARTERY ANEURYSM ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SURGERY ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
THYMOMA MALIGNANT RECURRENT ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TRABECULECTOMY ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
ULCERATIVE KERATITIS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VOLUME BLOOD DECREASED ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACANTHAMOEBA INFECTION ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATROPHY OF GLOBE ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INSPIRATORY DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCIUM PHOSPHATE PRODUCT INCREASED ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CARDIOMYOPATHY NEONATAL ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CD4/CD8 RATIO DECREASED ( 1 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
END-TIDAL CO2 INCREASED ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFANTILE SPASMS ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
IRITIS ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGEAL DYSPNOEA ( 1 FDA reports)
LENS DISLOCATION ( 1 FDA reports)
LERICHE SYNDROME ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP HAEMATOMA ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METAMYELOCYTE COUNT ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYELOCYTE COUNT ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEONATAL TACHYCARDIA ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROBLASTOMA ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL HAEMATOMA ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
POISONING ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREGNANCY TEST POSITIVE ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYODERMA ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
REYE'S SYNDROME ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SMALL INTESTINE OPERATION ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
SYSTEMIC MASTOCYTOSIS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THYMOMA ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TRANSURETHRAL RESECTION SYNDROME ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UNWANTED AWARENESS DURING ANAESTHESIA ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VITREOUS OPACITIES ( 1 FDA reports)
VITREOUS PROLAPSE ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)

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