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

NAUSEA ( 62 FDA reports)
DYSPNOEA ( 60 FDA reports)
ASTHENIA ( 59 FDA reports)
DIZZINESS ( 49 FDA reports)
FATIGUE ( 49 FDA reports)
HEADACHE ( 44 FDA reports)
HYPOTENSION ( 42 FDA reports)
DIARRHOEA ( 41 FDA reports)
PAIN ( 38 FDA reports)
ANAEMIA ( 37 FDA reports)
CHEST PAIN ( 34 FDA reports)
PAIN IN EXTREMITY ( 33 FDA reports)
VOMITING ( 33 FDA reports)
ABDOMINAL PAIN ( 31 FDA reports)
FALL ( 31 FDA reports)
OEDEMA PERIPHERAL ( 30 FDA reports)
INJECTION SITE PAIN ( 29 FDA reports)
PYREXIA ( 29 FDA reports)
ATRIAL FIBRILLATION ( 28 FDA reports)
PNEUMONIA ( 28 FDA reports)
RENAL FAILURE ACUTE ( 24 FDA reports)
BACK PAIN ( 22 FDA reports)
DEATH ( 22 FDA reports)
HYPERHIDROSIS ( 22 FDA reports)
RESPIRATORY FAILURE ( 22 FDA reports)
PRURITUS ( 21 FDA reports)
SEPSIS ( 21 FDA reports)
ABDOMINAL PAIN UPPER ( 20 FDA reports)
RASH ( 20 FDA reports)
ARTHRALGIA ( 19 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 19 FDA reports)
COUGH ( 19 FDA reports)
DEHYDRATION ( 19 FDA reports)
MALAISE ( 19 FDA reports)
MYOCARDIAL INFARCTION ( 19 FDA reports)
SYNCOPE ( 19 FDA reports)
RENAL FAILURE ( 18 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 17 FDA reports)
ANXIETY ( 17 FDA reports)
CARDIAC ARREST ( 16 FDA reports)
CONSTIPATION ( 16 FDA reports)
INJECTION SITE HAEMATOMA ( 16 FDA reports)
BLOOD GLUCOSE INCREASED ( 15 FDA reports)
RENAL FAILURE CHRONIC ( 15 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 15 FDA reports)
ARRHYTHMIA ( 14 FDA reports)
CONTUSION ( 14 FDA reports)
DECREASED APPETITE ( 14 FDA reports)
DRUG INEFFECTIVE ( 14 FDA reports)
WEIGHT DECREASED ( 14 FDA reports)
CEREBROVASCULAR ACCIDENT ( 13 FDA reports)
DEEP VEIN THROMBOSIS ( 13 FDA reports)
DYSPEPSIA ( 13 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 13 FDA reports)
HYPOAESTHESIA ( 13 FDA reports)
INSOMNIA ( 13 FDA reports)
NASOPHARYNGITIS ( 13 FDA reports)
PARAESTHESIA ( 13 FDA reports)
THROMBOCYTOPENIA ( 13 FDA reports)
EPISTAXIS ( 12 FDA reports)
INJURY ( 12 FDA reports)
PLEURAL EFFUSION ( 12 FDA reports)
PULMONARY EMBOLISM ( 12 FDA reports)
CHEST DISCOMFORT ( 11 FDA reports)
CHILLS ( 11 FDA reports)
ERYTHEMA ( 11 FDA reports)
FEELING ABNORMAL ( 11 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 11 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 11 FDA reports)
INFECTION ( 11 FDA reports)
TREMOR ( 11 FDA reports)
URINARY TRACT INFECTION ( 11 FDA reports)
ABDOMINAL DISTENSION ( 10 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
BRONCHITIS ( 10 FDA reports)
CELLULITIS ( 10 FDA reports)
DEPRESSION ( 10 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 10 FDA reports)
HYPOKALAEMIA ( 10 FDA reports)
PALPITATIONS ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
TACHYCARDIA ( 10 FDA reports)
UNRESPONSIVE TO STIMULI ( 10 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 9 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
CONVULSION ( 9 FDA reports)
DEVICE MALFUNCTION ( 9 FDA reports)
HAEMATOMA ( 9 FDA reports)
NEUROPATHY PERIPHERAL ( 9 FDA reports)
SINUSITIS ( 9 FDA reports)
VISION BLURRED ( 9 FDA reports)
WHEEZING ( 9 FDA reports)
AMNESIA ( 8 FDA reports)
ARTERIOSCLEROSIS ( 8 FDA reports)
BLOOD CREATININE INCREASED ( 8 FDA reports)
BONE DISORDER ( 8 FDA reports)
BRADYCARDIA ( 8 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 8 FDA reports)
COGNITIVE DISORDER ( 8 FDA reports)
CORONARY ARTERY DISEASE ( 8 FDA reports)
EMOTIONAL DISTRESS ( 8 FDA reports)
FLUID OVERLOAD ( 8 FDA reports)
HAEMORRHAGE ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
IMPAIRED HEALING ( 8 FDA reports)
INCORRECT DOSE ADMINISTERED ( 8 FDA reports)
MENTAL STATUS CHANGES ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
OSTEONECROSIS OF JAW ( 8 FDA reports)
PAIN IN JAW ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
PSORIASIS ( 8 FDA reports)
STAPHYLOCOCCAL INFECTION ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
ABDOMINAL DISCOMFORT ( 7 FDA reports)
ANGINA PECTORIS ( 7 FDA reports)
ATELECTASIS ( 7 FDA reports)
BALANCE DISORDER ( 7 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
CATARACT ( 7 FDA reports)
DRY MOUTH ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
HYPOXIA ( 7 FDA reports)
INJECTION SITE HAEMORRHAGE ( 7 FDA reports)
MULTI-ORGAN FAILURE ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
OSTEOARTHRITIS ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
PULMONARY OEDEMA ( 7 FDA reports)
RASH ERYTHEMATOUS ( 7 FDA reports)
RECTAL HAEMORRHAGE ( 7 FDA reports)
RHINORRHOEA ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
VISUAL IMPAIRMENT ( 7 FDA reports)
ANHEDONIA ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
COLITIS ISCHAEMIC ( 6 FDA reports)
DEMENTIA ( 6 FDA reports)
DRUG DOSE OMISSION ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
HEPATOMEGALY ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
HYPERLIPIDAEMIA ( 6 FDA reports)
HYPOAESTHESIA FACIAL ( 6 FDA reports)
HYPOPHAGIA ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
JOINT SWELLING ( 6 FDA reports)
LEUKOCYTOSIS ( 6 FDA reports)
LOCAL SWELLING ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
MIGRAINE ( 6 FDA reports)
MITRAL VALVE INCOMPETENCE ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
NECK PAIN ( 6 FDA reports)
OSTEOMYELITIS ( 6 FDA reports)
PULMONARY HYPERTENSION ( 6 FDA reports)
RASH GENERALISED ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
SINUS CONGESTION ( 6 FDA reports)
SINUS TACHYCARDIA ( 6 FDA reports)
SPINAL OSTEOARTHRITIS ( 6 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
SWELLING ( 6 FDA reports)
THROMBOSIS ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
BLISTER ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 5 FDA reports)
CLOSTRIDIAL INFECTION ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HIATUS HERNIA ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
NEURALGIA ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
OROPHARYNGEAL PAIN ( 5 FDA reports)
PALLOR ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
RASH PRURITIC ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
SHOCK ( 5 FDA reports)
SKIN DISCOLOURATION ( 5 FDA reports)
SKIN EXFOLIATION ( 5 FDA reports)
SPINAL FRACTURE ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
VASCULITIS ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
ACCIDENT AT WORK ( 4 FDA reports)
AGITATION ( 4 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
ASPIRATION ( 4 FDA reports)
ATRIAL FLUTTER ( 4 FDA reports)
AZOTAEMIA ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
COLITIS ( 4 FDA reports)
COMA ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DEFORMITY ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DUODENAL PERFORATION ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
FAILURE TO THRIVE ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HEART VALVE INCOMPETENCE ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INJECTION SITE SWELLING ( 4 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 4 FDA reports)
JAW DISORDER ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
MOTOR DYSFUNCTION ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
ORGAN FAILURE ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PHYSICAL DISABILITY ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RASH PAPULAR ( 4 FDA reports)
RENAL CYST ( 4 FDA reports)
RENAL INJURY ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
SCAR ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SNEEZING ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
TONGUE INJURY ( 4 FDA reports)
TOOTHACHE ( 4 FDA reports)
TRISMUS ( 4 FDA reports)
TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ACIDOSIS ( 3 FDA reports)
ACNE ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BONE SWELLING ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
DECREASED INTEREST ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSAESTHESIA ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FEAR ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GANGRENE ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GINGIVITIS ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HODGKIN'S DISEASE ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
INJECTION SITE PAPULE ( 3 FDA reports)
LEFT ATRIAL DILATATION ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LIFE EXPECTANCY SHORTENED ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MASS ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MULTIPLE MYELOMA ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PURULENT DISCHARGE ( 3 FDA reports)
RECTAL ABSCESS ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
STRESS ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
TACHYARRHYTHMIA ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TOXIC ENCEPHALOPATHY ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
WOUND DEHISCENCE ( 3 FDA reports)
ABSCESS ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADMINISTRATION SITE INFECTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BENIGN BONE NEOPLASM ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE CYST ( 2 FDA reports)
BONE FRAGMENTATION ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
BULIMIA NERVOSA ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARDIAC PERFORATION ( 2 FDA reports)
CARDIAC VALVE ABSCESS ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CARTILAGE ATROPHY ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CERVICAL SPINAL STENOSIS ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CRYING ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EPIDIDYMITIS ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FRACTURED SACRUM ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE MASS ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOOSE BODY IN JOINT ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MASTICATION DISORDER ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
ORCHITIS ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
OSTEORADIONECROSIS ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PERICARDIAL HAEMORRHAGE ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PNEUMATOSIS ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
REACTION TO AZO-DYES ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL ISCHAEMIA ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY MUSCLE WEAKNESS ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUBACUTE ENDOCARDITIS ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
TESTICULAR PAIN ( 2 FDA reports)
TESTICULAR SWELLING ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TONGUE HAEMATOMA ( 2 FDA reports)
TOOTH EROSION ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
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