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

DYSPNOEA ( 127 FDA reports)
FEMUR FRACTURE ( 99 FDA reports)
VOMITING ( 88 FDA reports)
NAUSEA ( 81 FDA reports)
FATIGUE ( 79 FDA reports)
DIZZINESS ( 77 FDA reports)
FALL ( 77 FDA reports)
DIARRHOEA ( 73 FDA reports)
DRUG INTERACTION ( 66 FDA reports)
ABDOMINAL PAIN ( 65 FDA reports)
CEREBROVASCULAR ACCIDENT ( 65 FDA reports)
PNEUMONIA ( 60 FDA reports)
MALAISE ( 59 FDA reports)
DEATH ( 51 FDA reports)
ANAEMIA ( 50 FDA reports)
SEPSIS ( 50 FDA reports)
SYNCOPE ( 50 FDA reports)
CONDITION AGGRAVATED ( 48 FDA reports)
PAIN ( 45 FDA reports)
RENAL FAILURE ACUTE ( 45 FDA reports)
CONFUSIONAL STATE ( 43 FDA reports)
RENAL FAILURE ( 43 FDA reports)
ASTHENIA ( 42 FDA reports)
PYREXIA ( 42 FDA reports)
ARTHRALGIA ( 39 FDA reports)
COUGH ( 38 FDA reports)
HEADACHE ( 37 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 37 FDA reports)
OEDEMA PERIPHERAL ( 36 FDA reports)
ATRIAL FIBRILLATION ( 35 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 35 FDA reports)
DRUG INEFFECTIVE ( 34 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 34 FDA reports)
PULMONARY EMBOLISM ( 34 FDA reports)
DEHYDRATION ( 33 FDA reports)
PAIN IN EXTREMITY ( 33 FDA reports)
AMNESIA ( 31 FDA reports)
BACK PAIN ( 31 FDA reports)
OSTEOPOROSIS ( 30 FDA reports)
RESPIRATORY FAILURE ( 30 FDA reports)
CARDIAC ARREST ( 29 FDA reports)
CHEST PAIN ( 29 FDA reports)
HYPONATRAEMIA ( 29 FDA reports)
RASH ( 29 FDA reports)
BONE DISORDER ( 28 FDA reports)
MYALGIA ( 28 FDA reports)
RHEUMATOID ARTHRITIS ( 28 FDA reports)
ASTHMA ( 26 FDA reports)
OSTEONECROSIS ( 26 FDA reports)
RECTAL HAEMORRHAGE ( 26 FDA reports)
INFECTION ( 25 FDA reports)
WEIGHT DECREASED ( 25 FDA reports)
PLEURAL EFFUSION ( 24 FDA reports)
URINARY TRACT INFECTION ( 24 FDA reports)
ABDOMINAL PAIN UPPER ( 23 FDA reports)
CONSTIPATION ( 23 FDA reports)
DEPRESSION ( 23 FDA reports)
THROMBOCYTOPENIA ( 23 FDA reports)
CIRCULATORY COLLAPSE ( 22 FDA reports)
HYPOTENSION ( 22 FDA reports)
PARAESTHESIA ( 22 FDA reports)
VISION BLURRED ( 22 FDA reports)
PANCYTOPENIA ( 21 FDA reports)
TREMOR ( 21 FDA reports)
ERYTHEMA ( 20 FDA reports)
HYPERTENSION ( 20 FDA reports)
IMPAIRED HEALING ( 20 FDA reports)
LOSS OF CONSCIOUSNESS ( 20 FDA reports)
NEUTROPENIA ( 20 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 19 FDA reports)
CARDIAC FAILURE ( 19 FDA reports)
DECREASED APPETITE ( 19 FDA reports)
GAIT DISTURBANCE ( 19 FDA reports)
HAEMATOCHEZIA ( 19 FDA reports)
HAEMOGLOBIN DECREASED ( 19 FDA reports)
SOMNOLENCE ( 19 FDA reports)
WEIGHT INCREASED ( 19 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 18 FDA reports)
CHILLS ( 18 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 18 FDA reports)
EPISTAXIS ( 18 FDA reports)
LOW TURNOVER OSTEOPATHY ( 18 FDA reports)
MULTI-ORGAN FAILURE ( 18 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 18 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 18 FDA reports)
UROSEPSIS ( 18 FDA reports)
ANXIETY ( 17 FDA reports)
CLEFT LIP AND PALATE ( 17 FDA reports)
MUSCULAR WEAKNESS ( 17 FDA reports)
HYPERSENSITIVITY ( 16 FDA reports)
LIVER DISORDER ( 16 FDA reports)
MYOCARDIAL INFARCTION ( 16 FDA reports)
RENAL IMPAIRMENT ( 16 FDA reports)
AGGRESSION ( 15 FDA reports)
BLOOD CREATININE INCREASED ( 15 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 15 FDA reports)
DIVERTICULITIS ( 15 FDA reports)
HALLUCINATION ( 15 FDA reports)
JAUNDICE ( 15 FDA reports)
MELAENA ( 15 FDA reports)
PNEUMONITIS ( 15 FDA reports)
PULMONARY FIBROSIS ( 15 FDA reports)
STRESS FRACTURE ( 15 FDA reports)
TACHYCARDIA ( 15 FDA reports)
VASCULITIS ( 15 FDA reports)
VERTIGO ( 15 FDA reports)
BRONCHOPNEUMONIA ( 14 FDA reports)
MOUTH ULCERATION ( 14 FDA reports)
OSTEONECROSIS OF JAW ( 14 FDA reports)
THROAT TIGHTNESS ( 14 FDA reports)
ANGIOEDEMA ( 13 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 13 FDA reports)
FEELING ABNORMAL ( 13 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 13 FDA reports)
SUICIDAL IDEATION ( 13 FDA reports)
TENDON RUPTURE ( 13 FDA reports)
VISUAL ACUITY REDUCED ( 13 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 12 FDA reports)
APHASIA ( 12 FDA reports)
COLITIS ISCHAEMIC ( 12 FDA reports)
GASTRITIS ( 12 FDA reports)
HEMIPARESIS ( 12 FDA reports)
HYPERHIDROSIS ( 12 FDA reports)
HYPOGLYCAEMIA ( 12 FDA reports)
HYPOKALAEMIA ( 12 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 12 FDA reports)
NEOPLASM MALIGNANT ( 12 FDA reports)
PULMONARY TUBERCULOSIS ( 12 FDA reports)
SKIN LESION ( 12 FDA reports)
TERATOGENICITY ( 12 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 12 FDA reports)
ABDOMINAL DISTENSION ( 11 FDA reports)
ARTHRITIS ( 11 FDA reports)
BASAL CELL CARCINOMA ( 11 FDA reports)
CANDIDIASIS ( 11 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 11 FDA reports)
CHEST DISCOMFORT ( 11 FDA reports)
CONVULSION ( 11 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 11 FDA reports)
HEAD INJURY ( 11 FDA reports)
HYPOXIA ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
INTERSTITIAL LUNG DISEASE ( 11 FDA reports)
JOINT SWELLING ( 11 FDA reports)
LETHARGY ( 11 FDA reports)
LEUKOPENIA ( 11 FDA reports)
NIGHTMARE ( 11 FDA reports)
RIB FRACTURE ( 11 FDA reports)
ANOREXIA ( 10 FDA reports)
BLISTER ( 10 FDA reports)
BRONCHOSPASM ( 10 FDA reports)
CELLULITIS ( 10 FDA reports)
DEEP VEIN THROMBOSIS ( 10 FDA reports)
DIABETES MELLITUS ( 10 FDA reports)
DYSPHAGIA ( 10 FDA reports)
EPILEPSY ( 10 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 10 FDA reports)
HYPERCALCAEMIA ( 10 FDA reports)
INFLUENZA ( 10 FDA reports)
INTENTIONAL DRUG MISUSE ( 10 FDA reports)
LUNG INFILTRATION ( 10 FDA reports)
MEMORY IMPAIRMENT ( 10 FDA reports)
MYOCARDIAL ISCHAEMIA ( 10 FDA reports)
OEDEMA ( 10 FDA reports)
OESOPHAGEAL CARCINOMA ( 10 FDA reports)
OESOPHAGITIS ( 10 FDA reports)
OSTEOMYELITIS ( 10 FDA reports)
OVERDOSE ( 10 FDA reports)
PALPITATIONS ( 10 FDA reports)
PATHOLOGICAL FRACTURE ( 10 FDA reports)
PLATELET COUNT DECREASED ( 10 FDA reports)
RENAL DISORDER ( 10 FDA reports)
SWELLING FACE ( 10 FDA reports)
ABDOMINAL SEPSIS ( 9 FDA reports)
ALOPECIA ( 9 FDA reports)
BALANCE DISORDER ( 9 FDA reports)
BLOOD SODIUM DECREASED ( 9 FDA reports)
DYSARTHRIA ( 9 FDA reports)
FEMORAL ARTERY EMBOLISM ( 9 FDA reports)
HAEMATEMESIS ( 9 FDA reports)
HEPATIC ENCEPHALOPATHY ( 9 FDA reports)
HYPOAESTHESIA ( 9 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 9 FDA reports)
METASTASES TO LIVER ( 9 FDA reports)
MOBILITY DECREASED ( 9 FDA reports)
MYOCLONUS ( 9 FDA reports)
PERIPHERAL ISCHAEMIA ( 9 FDA reports)
PURPURA ( 9 FDA reports)
VISUAL IMPAIRMENT ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 8 FDA reports)
BLOOD PRESSURE INCREASED ( 8 FDA reports)
CEREBRAL HAEMORRHAGE ( 8 FDA reports)
CHOLELITHIASIS ( 8 FDA reports)
CLOSTRIDIUM COLITIS ( 8 FDA reports)
CREPITATIONS ( 8 FDA reports)
DEVICE FAILURE ( 8 FDA reports)
DYSPHONIA ( 8 FDA reports)
ENTERITIS ( 8 FDA reports)
EYE DISORDER ( 8 FDA reports)
HAEMATOMA ( 8 FDA reports)
HOT FLUSH ( 8 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 8 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 8 FDA reports)
LIP SWELLING ( 8 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 8 FDA reports)
MULTIPLE FRACTURES ( 8 FDA reports)
NIGHT SWEATS ( 8 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 8 FDA reports)
PULMONARY OEDEMA ( 8 FDA reports)
RASH PUSTULAR ( 8 FDA reports)
RENAL FAILURE CHRONIC ( 8 FDA reports)
RESPIRATORY ARREST ( 8 FDA reports)
SKIN LACERATION ( 8 FDA reports)
STAPHYLOCOCCAL INFECTION ( 8 FDA reports)
TENDONITIS ( 8 FDA reports)
TINNITUS ( 8 FDA reports)
WITHDRAWAL SYNDROME ( 8 FDA reports)
ABNORMAL FAECES ( 7 FDA reports)
ABSCESS ( 7 FDA reports)
ACUTE HEPATIC FAILURE ( 7 FDA reports)
ALLERGY TO CHEMICALS ( 7 FDA reports)
ANAPHYLACTIC REACTION ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
BREAST CANCER ( 7 FDA reports)
BRONCHIECTASIS ( 7 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
CARDIAC PACEMAKER INSERTION ( 7 FDA reports)
CEREBRAL INFARCTION ( 7 FDA reports)
CHROMATURIA ( 7 FDA reports)
COLITIS ( 7 FDA reports)
DRUG ERUPTION ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
DYSSTASIA ( 7 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 7 FDA reports)
EMOTIONAL DISTRESS ( 7 FDA reports)
EMPHYSEMA ( 7 FDA reports)
ENCEPHALOPATHY ( 7 FDA reports)
ENDOTRACHEAL INTUBATION ( 7 FDA reports)
FAECALOMA ( 7 FDA reports)
HIATUS HERNIA ( 7 FDA reports)
HIP ARTHROPLASTY ( 7 FDA reports)
IRRITABILITY ( 7 FDA reports)
LUNG CANCER METASTATIC ( 7 FDA reports)
MENTAL STATUS CHANGES ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 7 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 7 FDA reports)
MYELODYSPLASTIC SYNDROME ( 7 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 7 FDA reports)
NEUROPATHY PERIPHERAL ( 7 FDA reports)
ORGANISING PNEUMONIA ( 7 FDA reports)
OSTEOSYNTHESIS ( 7 FDA reports)
PANCREATITIS ACUTE ( 7 FDA reports)
PANIC ATTACK ( 7 FDA reports)
PHARYNGEAL OEDEMA ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
PSORIATIC ARTHROPATHY ( 7 FDA reports)
PYELONEPHRITIS ACUTE ( 7 FDA reports)
SHOCK ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
SQUAMOUS CELL CARCINOMA ( 7 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
WHEEZING ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 7 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
AGRANULOCYTOSIS ( 6 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 6 FDA reports)
CLOSTRIDIAL INFECTION ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
DRY SKIN ( 6 FDA reports)
DUODENAL ULCER PERFORATION ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
ENCEPHALITIS ( 6 FDA reports)
ESCHERICHIA INFECTION ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
GRAND MAL CONVULSION ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HEMISENSORY NEGLECT ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
HEPATOCELLULAR INJURY ( 6 FDA reports)
HYPOPHOSPHATAEMIA ( 6 FDA reports)
HYPOTONIA ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 6 FDA reports)
INJURY ( 6 FDA reports)
INTESTINAL OBSTRUCTION ( 6 FDA reports)
INTESTINAL PERFORATION ( 6 FDA reports)
JOINT SPRAIN ( 6 FDA reports)
LEUKOENCEPHALOPATHY ( 6 FDA reports)
LOCALISED INFECTION ( 6 FDA reports)
LYMPHOPENIA ( 6 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 6 FDA reports)
MUCOSAL INFLAMMATION ( 6 FDA reports)
MUSCLE STRAIN ( 6 FDA reports)
MYOPATHY ( 6 FDA reports)
NASOPHARYNGITIS ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
PAIN IN JAW ( 6 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 6 FDA reports)
PANCREATITIS ( 6 FDA reports)
PELVIC FRACTURE ( 6 FDA reports)
PERITONEAL HAEMORRHAGE ( 6 FDA reports)
PNEUMOTHORAX ( 6 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 6 FDA reports)
SENSATION OF FOREIGN BODY ( 6 FDA reports)
SKIN EXFOLIATION ( 6 FDA reports)
SPINAL COMPRESSION FRACTURE ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
SWOLLEN TONGUE ( 6 FDA reports)
SYNOVIAL CYST ( 6 FDA reports)
TEMPORAL ARTERITIS ( 6 FDA reports)
TRANSAMINASES INCREASED ( 6 FDA reports)
WRIST FRACTURE ( 6 FDA reports)
ABDOMINAL TENDERNESS ( 5 FDA reports)
AORTIC CALCIFICATION ( 5 FDA reports)
B-CELL LYMPHOMA ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
CHOLESTASIS ( 5 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
DIPLOPIA ( 5 FDA reports)
DISEASE PROGRESSION ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
DIVERTICULUM INTESTINAL ( 5 FDA reports)
DRY MOUTH ( 5 FDA reports)
DUODENAL ULCER ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
ERYSIPELAS ( 5 FDA reports)
ESCHERICHIA BACTERAEMIA ( 5 FDA reports)
FACIAL PARESIS ( 5 FDA reports)
FAECES DISCOLOURED ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
HEPATIC STEATOSIS ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HERPES ZOSTER ( 5 FDA reports)
HYPERTONIA ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
JOINT DISLOCATION ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
MACULAR DEGENERATION ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
METASTASIS ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
NEUTROPENIC SEPSIS ( 5 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 5 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 5 FDA reports)
OESOPHAGEAL STENOSIS ( 5 FDA reports)
OESOPHAGEAL ULCER ( 5 FDA reports)
ORAL PAIN ( 5 FDA reports)
PALLOR ( 5 FDA reports)
PHOTOPHOBIA ( 5 FDA reports)
POLYARTHRITIS ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
PULMONARY CONGESTION ( 5 FDA reports)
PULSE ABSENT ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
RASH PRURITIC ( 5 FDA reports)
RENAL CYST ( 5 FDA reports)
RENAL TUBULAR DISORDER ( 5 FDA reports)
RESPIRATORY DEPRESSION ( 5 FDA reports)
RETROPERITONEAL FIBROSIS ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
SCIATICA ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
SKIN DISORDER ( 5 FDA reports)
SLEEP DISORDER ( 5 FDA reports)
SOFT TISSUE INFECTION ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
TACHYARRHYTHMIA ( 5 FDA reports)
TIBIA FRACTURE ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ABNORMAL DREAMS ( 4 FDA reports)
ABSCESS JAW ( 4 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 4 FDA reports)
ADRENAL INSUFFICIENCY ( 4 FDA reports)
AGITATION ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
APLASTIC ANAEMIA ( 4 FDA reports)
ARTERIOSCLEROSIS ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 4 FDA reports)
BLEPHARITIS ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
BONE INFARCTION ( 4 FDA reports)
BOWEN'S DISEASE ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
BRONCHITIS CHRONIC ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
CUSHINGOID ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
DERMATITIS PSORIASIFORM ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DIVERTICULUM ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
ESCHERICHIA SEPSIS ( 4 FDA reports)
EXTRASYSTOLES ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FEELING OF DESPAIR ( 4 FDA reports)
FISTULA ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
FOOT FRACTURE ( 4 FDA reports)
GASTRIC CANCER STAGE IV ( 4 FDA reports)
GASTROENTERITIS BACTERIAL ( 4 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 4 FDA reports)
GASTROINTESTINAL PAIN ( 4 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 4 FDA reports)
GLYCOSURIA ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
GRANULOCYTE COUNT DECREASED ( 4 FDA reports)
HAEMANGIOMA ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HAEMODYNAMIC INSTABILITY ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HAEMORRHOIDS ( 4 FDA reports)
HAIR GROWTH ABNORMAL ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOAESTHESIA ORAL ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
INCONTINENCE ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
KLEBSIELLA SEPSIS ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
LEIOMYOMA ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
NEPHROTIC SYNDROME ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 4 FDA reports)
PURULENT DISCHARGE ( 4 FDA reports)
PYELONEPHRITIS ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
RHODOCOCCUS INFECTION ( 4 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
STENOTROPHOMONAS INFECTION ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VASCULITIS CEREBRAL ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
WOUND ( 4 FDA reports)
WOUND INFECTION ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ADENOCARCINOMA ( 3 FDA reports)
ADRENAL NEOPLASM ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ALVEOLITIS FIBROSING ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 3 FDA reports)
BILIARY DILATATION ( 3 FDA reports)
BLADDER CANCER ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BRONCHIAL CARCINOMA ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 3 FDA reports)
CARPAL TUNNEL SYNDROME ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
CYST ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DYSLIPIDAEMIA ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
EYE SWELLING ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
FRACTURE DELAYED UNION ( 3 FDA reports)
GANGLIONEUROMA ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 3 FDA reports)
GINGIVITIS ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEAD BANGING ( 3 FDA reports)
HEART TRANSPLANT REJECTION ( 3 FDA reports)
HELICOBACTER TEST POSITIVE ( 3 FDA reports)
HEPATITIS C ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERPYREXIA ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
INTENTIONAL SELF-INJURY ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
JAW FRACTURE ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
MALIGNANT MELANOMA ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
METASTASES TO LUNG ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NEPHROSTOMY ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
OSTEITIS ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
PARAPARESIS ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
RETCHING ( 3 FDA reports)
SCOLIOSIS ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SIGMOIDITIS ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SJOGREN'S SYNDROME ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
SUICIDAL BEHAVIOUR ( 3 FDA reports)
TETANY ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
TONGUE ULCERATION ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TOXOPLASMOSIS ( 3 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VASCULAR DEMENTIA ( 3 FDA reports)
VENOUS THROMBOSIS ( 3 FDA reports)
VITREOUS HAEMORRHAGE ( 3 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ACETABULUM FRACTURE ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
APATHY ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTERIAL STENOSIS LIMB ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATONIC SEIZURES ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BILE DUCT STENOSIS ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CORTISOL ABNORMAL ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BLOOD UREA ABNORMAL ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BONE DENSITY DECREASED ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
BONE METABOLISM DISORDER ( 2 FDA reports)
BRACHYCEPHALY ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BREAST CANCER METASTATIC ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CAMPTODACTYLY CONGENITAL ( 2 FDA reports)
CANDIDA TEST POSITIVE ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CLINODACTYLY ( 2 FDA reports)
COLOBOMA ( 2 FDA reports)
COLORECTAL CANCER METASTATIC ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CORNEAL DEPOSITS ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DIVERTICULITIS OESOPHAGEAL ( 2 FDA reports)
DIVERTICULUM GASTRIC ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 2 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FAILURE OF IMPLANT ( 2 FDA reports)
FANCONI SYNDROME ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRIC PH DECREASED ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HALO VISION ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPERTELORISM OF ORBIT ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPERTROPHY ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFLAMMATORY MARKER INCREASED ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
IRIDOCYCLITIS ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
JEALOUS DELUSION ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LAPAROTOMY ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOOSE TOOTH ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE 0 ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METASTATIC GASTRIC CANCER ( 2 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 2 FDA reports)
MICROTIA ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
MYXOEDEMA ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OESOPHAGEAL ATRESIA ( 2 FDA reports)
OESOPHAGEAL PERFORATION ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OPTIC DISC DISORDER ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL DISCHARGE ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OSTEOMA CUTIS ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROSTRATION ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 2 FDA reports)
PSYCHOTIC BEHAVIOUR ( 2 FDA reports)
PULMONARY GRANULOMA ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 2 FDA reports)
RENAL MASS ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RESORPTION BONE INCREASED ( 2 FDA reports)
RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETINAL VEIN THROMBOSIS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SCAR ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SERUM FERRITIN DECREASED ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN PAPILLOMA ( 2 FDA reports)
SKIN ULCER HAEMORRHAGE ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SPONDYLOLISTHESIS ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THIRST ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
TONGUE EXFOLIATION ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
ULCER ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
ULTRASOUND SCAN ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
URTICARIA LOCALISED ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VISUAL BRIGHTNESS ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AIDS ENCEPHALOPATHY ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES STAGE IV ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANOGENITAL DYSPLASIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTI-CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BASE EXCESS ABNORMAL ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD OESTROGEN DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BRONCHIAL INJURY ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CERVIX CARCINOMA STAGE III ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CINCHONISM ( 1 FDA reports)
CLOSTRIDIUM TEST ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONGENITAL CYST ( 1 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CRYING ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENEMA ADMINISTRATION ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
GALLBLADDER NECROSIS ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC CYST ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTROENTERITIS SHIGELLA ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HYDROXYPROLINE INCREASED ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERMAGNESAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERPHOSPHATURIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOURICAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERMEDIATE UVEITIS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRITIS ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT PROSTHESIS USER ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNGEAL INJURY ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUDWIG ANGINA ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENINGITIS NONINFECTIVE ( 1 FDA reports)
MENISCUS REMOVAL ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 1 FDA reports)
MICROGNATHIA ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
NAIL BED INFLAMMATION ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHRECTASIA ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL HYPERSEGMENTED MORPHOLOGY PRESENT ( 1 FDA reports)
NODULAR VASCULITIS ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OLFACTORY NERVE DISORDER ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
OOPHORECTOMY BILATERAL ( 1 FDA reports)
OPTIC NERVE HYPOPLASIA ( 1 FDA reports)
ORAL HAIRY LEUKOPLAKIA ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSA ATROPHY ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARASPINAL ABSCESS ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIODONTAL INFECTION ( 1 FDA reports)
PERIOSTITIS ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PH BODY FLUID INCREASED ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYPOIDAL CHOROIDAL VASCULOPATHY ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL ONCOCYTOMA ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETROGNATHIA ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SENSITISATION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN HYPOPLASIA ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOLAR URTICARIA ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBDURAL EMPYEMA ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THIRST DECREASED ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TRACHEAL INJURY ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ULTRASOUND UTERUS ABNORMAL ( 1 FDA reports)
URINE ELECTROLYTES INCREASED ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL PROLAPSE ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VULVAR DYSPLASIA ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WITHDRAWAL BLEED ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)

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