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

NAUSEA ( 225 FDA reports)
PAIN ( 223 FDA reports)
DYSPNOEA ( 222 FDA reports)
VOMITING ( 210 FDA reports)
HEADACHE ( 192 FDA reports)
ANXIETY ( 166 FDA reports)
DIARRHOEA ( 158 FDA reports)
DIZZINESS ( 153 FDA reports)
FATIGUE ( 137 FDA reports)
FALL ( 136 FDA reports)
PNEUMONIA ( 129 FDA reports)
ABDOMINAL PAIN ( 126 FDA reports)
PYREXIA ( 125 FDA reports)
ASTHENIA ( 124 FDA reports)
MALAISE ( 124 FDA reports)
OEDEMA PERIPHERAL ( 119 FDA reports)
DEPRESSION ( 109 FDA reports)
CHEST PAIN ( 108 FDA reports)
WEIGHT DECREASED ( 107 FDA reports)
CONFUSIONAL STATE ( 103 FDA reports)
ARTHRALGIA ( 101 FDA reports)
HYPERTENSION ( 99 FDA reports)
PULMONARY EMBOLISM ( 96 FDA reports)
ANAEMIA ( 95 FDA reports)
EMOTIONAL DISTRESS ( 94 FDA reports)
PAIN IN EXTREMITY ( 89 FDA reports)
ABDOMINAL PAIN UPPER ( 84 FDA reports)
DRUG INEFFECTIVE ( 83 FDA reports)
RENAL FAILURE ACUTE ( 83 FDA reports)
COMPLETED SUICIDE ( 81 FDA reports)
DEHYDRATION ( 81 FDA reports)
PRURITUS ( 81 FDA reports)
OVERDOSE ( 79 FDA reports)
INJURY ( 78 FDA reports)
SOMNOLENCE ( 77 FDA reports)
DEATH ( 72 FDA reports)
CONVULSION ( 70 FDA reports)
DEEP VEIN THROMBOSIS ( 70 FDA reports)
BACK PAIN ( 69 FDA reports)
URINARY TRACT INFECTION ( 69 FDA reports)
CONSTIPATION ( 68 FDA reports)
PARAESTHESIA ( 68 FDA reports)
COUGH ( 67 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 67 FDA reports)
HAEMOGLOBIN DECREASED ( 67 FDA reports)
CONDITION AGGRAVATED ( 66 FDA reports)
INSOMNIA ( 65 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 64 FDA reports)
HYPOTENSION ( 64 FDA reports)
LOSS OF CONSCIOUSNESS ( 62 FDA reports)
DECREASED APPETITE ( 61 FDA reports)
MYALGIA ( 61 FDA reports)
RENAL FAILURE ( 61 FDA reports)
HYPOAESTHESIA ( 60 FDA reports)
DRUG INTERACTION ( 59 FDA reports)
HALLUCINATION ( 59 FDA reports)
SEPSIS ( 59 FDA reports)
PALPITATIONS ( 56 FDA reports)
MYOCARDIAL INFARCTION ( 54 FDA reports)
TREMOR ( 54 FDA reports)
HYPERHIDROSIS ( 52 FDA reports)
RASH ( 52 FDA reports)
AGITATION ( 51 FDA reports)
MUSCLE SPASMS ( 50 FDA reports)
HAEMATEMESIS ( 49 FDA reports)
INFECTION ( 49 FDA reports)
THROMBOCYTOPENIA ( 49 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 49 FDA reports)
HYPOKALAEMIA ( 48 FDA reports)
RHEUMATOID ARTHRITIS ( 48 FDA reports)
CARDIAC ARREST ( 47 FDA reports)
FEELING ABNORMAL ( 47 FDA reports)
CEREBROVASCULAR ACCIDENT ( 44 FDA reports)
GAIT DISTURBANCE ( 44 FDA reports)
RESPIRATORY FAILURE ( 44 FDA reports)
SYNCOPE ( 44 FDA reports)
ATRIAL FIBRILLATION ( 43 FDA reports)
BONE DISORDER ( 43 FDA reports)
CHOLELITHIASIS ( 43 FDA reports)
ERYTHEMA ( 43 FDA reports)
HYPERSENSITIVITY ( 43 FDA reports)
BALANCE DISORDER ( 42 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 42 FDA reports)
SWELLING FACE ( 42 FDA reports)
WEIGHT INCREASED ( 42 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 41 FDA reports)
LETHARGY ( 41 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 41 FDA reports)
SUICIDE ATTEMPT ( 41 FDA reports)
VISION BLURRED ( 40 FDA reports)
AMNESIA ( 39 FDA reports)
MULTIPLE DRUG OVERDOSE ( 39 FDA reports)
SWELLING ( 39 FDA reports)
CHOLECYSTITIS CHRONIC ( 38 FDA reports)
MIGRAINE ( 38 FDA reports)
OSTEONECROSIS OF JAW ( 38 FDA reports)
VISUAL IMPAIRMENT ( 38 FDA reports)
ABDOMINAL DISTENSION ( 37 FDA reports)
DYSPHAGIA ( 37 FDA reports)
LYMPHADENOPATHY ( 37 FDA reports)
OSTEOARTHRITIS ( 37 FDA reports)
JOINT SWELLING ( 36 FDA reports)
PLATELET COUNT DECREASED ( 36 FDA reports)
RESPIRATORY ARREST ( 36 FDA reports)
CHEST DISCOMFORT ( 35 FDA reports)
DECREASED INTEREST ( 35 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 35 FDA reports)
HYPOXIA ( 35 FDA reports)
PULMONARY OEDEMA ( 35 FDA reports)
SINUSITIS ( 35 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 34 FDA reports)
HAEMORRHAGE ( 34 FDA reports)
HYPONATRAEMIA ( 34 FDA reports)
ASTHMA ( 33 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 33 FDA reports)
HIATUS HERNIA ( 33 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 33 FDA reports)
RECTAL HAEMORRHAGE ( 33 FDA reports)
SUICIDAL IDEATION ( 33 FDA reports)
URTICARIA ( 33 FDA reports)
ALOPECIA ( 32 FDA reports)
DEFORMITY ( 32 FDA reports)
NEUTROPENIA ( 32 FDA reports)
CONTUSION ( 31 FDA reports)
DISORIENTATION ( 31 FDA reports)
DISTURBANCE IN ATTENTION ( 31 FDA reports)
GASTRIC ULCER ( 31 FDA reports)
MEMORY IMPAIRMENT ( 31 FDA reports)
MYOCARDIAL ISCHAEMIA ( 31 FDA reports)
RASH ERYTHEMATOUS ( 31 FDA reports)
VERTIGO ( 31 FDA reports)
VISUAL ACUITY REDUCED ( 31 FDA reports)
COMA ( 30 FDA reports)
DYSGEUSIA ( 30 FDA reports)
FLUSHING ( 30 FDA reports)
JAUNDICE ( 30 FDA reports)
MELAENA ( 30 FDA reports)
PANCREATITIS ( 30 FDA reports)
SEPTIC SHOCK ( 30 FDA reports)
TOOTH EXTRACTION ( 30 FDA reports)
BLOOD CREATININE INCREASED ( 29 FDA reports)
CELLULITIS ( 29 FDA reports)
DRUG TOXICITY ( 29 FDA reports)
DYSPEPSIA ( 29 FDA reports)
FEMUR FRACTURE ( 29 FDA reports)
HAEMATURIA ( 29 FDA reports)
INFLUENZA LIKE ILLNESS ( 29 FDA reports)
MUSCULAR WEAKNESS ( 29 FDA reports)
NIGHTMARE ( 29 FDA reports)
POLLAKIURIA ( 29 FDA reports)
TOOTH DISORDER ( 29 FDA reports)
ABASIA ( 28 FDA reports)
AGGRESSION ( 28 FDA reports)
BLOOD PRESSURE INCREASED ( 28 FDA reports)
CARDIAC FAILURE ( 28 FDA reports)
CARDIOMEGALY ( 28 FDA reports)
HYPERLIPIDAEMIA ( 28 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 28 FDA reports)
RENAL IMPAIRMENT ( 28 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 27 FDA reports)
EYE PAIN ( 27 FDA reports)
GALLBLADDER DISORDER ( 27 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 27 FDA reports)
MOBILITY DECREASED ( 27 FDA reports)
OSTEONECROSIS ( 27 FDA reports)
OSTEOPENIA ( 27 FDA reports)
PLEURAL EFFUSION ( 27 FDA reports)
PULMONARY FIBROSIS ( 27 FDA reports)
TACHYCARDIA ( 27 FDA reports)
ANHEDONIA ( 26 FDA reports)
BLOOD PRESSURE DECREASED ( 26 FDA reports)
BONE PAIN ( 26 FDA reports)
BRONCHOPNEUMONIA ( 26 FDA reports)
DRY MOUTH ( 26 FDA reports)
HEART RATE INCREASED ( 26 FDA reports)
MENTAL DISORDER ( 26 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 26 FDA reports)
NASOPHARYNGITIS ( 26 FDA reports)
OEDEMA ( 26 FDA reports)
OROPHARYNGEAL PAIN ( 26 FDA reports)
PAIN IN JAW ( 26 FDA reports)
SPINAL OSTEOARTHRITIS ( 26 FDA reports)
ARRHYTHMIA ( 25 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 25 FDA reports)
CORONARY ARTERY DISEASE ( 25 FDA reports)
DYSURIA ( 25 FDA reports)
EPISTAXIS ( 25 FDA reports)
MITRAL VALVE INCOMPETENCE ( 25 FDA reports)
MOUTH ULCERATION ( 25 FDA reports)
ANOREXIA ( 24 FDA reports)
BRADYCARDIA ( 24 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 24 FDA reports)
DYSPHONIA ( 24 FDA reports)
EXOSTOSIS ( 24 FDA reports)
RASH PRURITIC ( 24 FDA reports)
SCAR ( 24 FDA reports)
SLEEP DISORDER ( 24 FDA reports)
SURGERY ( 24 FDA reports)
CHILLS ( 23 FDA reports)
ENCEPHALOPATHY ( 23 FDA reports)
HAEMATOMA ( 23 FDA reports)
HEPATIC FAILURE ( 23 FDA reports)
IMPAIRED HEALING ( 23 FDA reports)
LUNG NEOPLASM MALIGNANT ( 23 FDA reports)
METABOLIC ACIDOSIS ( 23 FDA reports)
THROMBOSIS ( 23 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 22 FDA reports)
HEPATIC STEATOSIS ( 22 FDA reports)
HOT FLUSH ( 22 FDA reports)
INJECTION SITE PAIN ( 22 FDA reports)
MUSCULOSKELETAL PAIN ( 22 FDA reports)
OSTEOPOROSIS ( 22 FDA reports)
BLISTER ( 21 FDA reports)
BREAST CANCER ( 21 FDA reports)
CIRCULATORY COLLAPSE ( 21 FDA reports)
HAEMORRHOIDS ( 21 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 21 FDA reports)
MASS ( 21 FDA reports)
MOUTH HAEMORRHAGE ( 21 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 20 FDA reports)
ANGINA PECTORIS ( 20 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 20 FDA reports)
EYE SWELLING ( 20 FDA reports)
LIP SWELLING ( 20 FDA reports)
PNEUMONIA ASPIRATION ( 20 FDA reports)
UNRESPONSIVE TO STIMULI ( 20 FDA reports)
ANAPHYLACTIC REACTION ( 19 FDA reports)
BLOOD BILIRUBIN INCREASED ( 19 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 19 FDA reports)
CHOLECYSTITIS ( 19 FDA reports)
DISEASE PROGRESSION ( 19 FDA reports)
FACE OEDEMA ( 19 FDA reports)
GRAND MAL CONVULSION ( 19 FDA reports)
HYPOPHAGIA ( 19 FDA reports)
INTENTIONAL DRUG MISUSE ( 19 FDA reports)
IRRITABILITY ( 19 FDA reports)
LIFE EXPECTANCY SHORTENED ( 19 FDA reports)
LUNG DISORDER ( 19 FDA reports)
OSTEOMYELITIS ( 19 FDA reports)
PALLOR ( 19 FDA reports)
PANIC ATTACK ( 19 FDA reports)
RESPIRATORY DISTRESS ( 19 FDA reports)
SLEEP APNOEA SYNDROME ( 19 FDA reports)
SPEECH DISORDER ( 19 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 19 FDA reports)
URINARY INCONTINENCE ( 19 FDA reports)
APHTHOUS STOMATITIS ( 18 FDA reports)
BURNING SENSATION ( 18 FDA reports)
CARDIO-RESPIRATORY ARREST ( 18 FDA reports)
DEPRESSED MOOD ( 18 FDA reports)
DYSARTHRIA ( 18 FDA reports)
FAECES DISCOLOURED ( 18 FDA reports)
HYPOKINESIA ( 18 FDA reports)
METASTASES TO LIVER ( 18 FDA reports)
METASTASES TO LUNG ( 18 FDA reports)
MULTIPLE MYELOMA ( 18 FDA reports)
ONYCHOMYCOSIS ( 18 FDA reports)
PANCREATITIS ACUTE ( 18 FDA reports)
RENAL DISORDER ( 18 FDA reports)
TENDERNESS ( 18 FDA reports)
TOOTH ABSCESS ( 18 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 18 FDA reports)
ANGER ( 17 FDA reports)
ATELECTASIS ( 17 FDA reports)
BRONCHITIS ( 17 FDA reports)
DEPENDENCE ( 17 FDA reports)
DIVERTICULITIS ( 17 FDA reports)
DIVERTICULUM ( 17 FDA reports)
FEELING HOT ( 17 FDA reports)
GASTRITIS ( 17 FDA reports)
HAEMODIALYSIS ( 17 FDA reports)
HERPES ZOSTER ( 17 FDA reports)
METASTASES TO BONE ( 17 FDA reports)
PHOTOPSIA ( 17 FDA reports)
PRODUCTIVE COUGH ( 17 FDA reports)
SKIN DISCOLOURATION ( 17 FDA reports)
SWOLLEN TONGUE ( 17 FDA reports)
ARTHRITIS ( 16 FDA reports)
BLOOD GLUCOSE INCREASED ( 16 FDA reports)
CATARACT ( 16 FDA reports)
DEAFNESS ( 16 FDA reports)
DRUG ABUSE ( 16 FDA reports)
DYSPNOEA EXERTIONAL ( 16 FDA reports)
HEPATIC ENZYME INCREASED ( 16 FDA reports)
HYPOGLYCAEMIA ( 16 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 16 FDA reports)
LACTIC ACIDOSIS ( 16 FDA reports)
LEFT VENTRICULAR FAILURE ( 16 FDA reports)
LEUKOPENIA ( 16 FDA reports)
LOOSE TOOTH ( 16 FDA reports)
NEUROPATHY PERIPHERAL ( 16 FDA reports)
ORTHOPNOEA ( 16 FDA reports)
RHABDOMYOLYSIS ( 16 FDA reports)
RHINORRHOEA ( 16 FDA reports)
SKIN EXFOLIATION ( 16 FDA reports)
SKIN PAPILLOMA ( 16 FDA reports)
SPONDYLOLISTHESIS ( 16 FDA reports)
TOOTHACHE ( 16 FDA reports)
URINARY RETENTION ( 16 FDA reports)
WHEEZING ( 16 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 16 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 15 FDA reports)
APHASIA ( 15 FDA reports)
CYSTITIS ( 15 FDA reports)
DELIRIUM ( 15 FDA reports)
DISCOMFORT ( 15 FDA reports)
HYPERKALAEMIA ( 15 FDA reports)
HYPOCALCAEMIA ( 15 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 15 FDA reports)
INTESTINAL ISCHAEMIA ( 15 FDA reports)
JOINT STIFFNESS ( 15 FDA reports)
LIPASE INCREASED ( 15 FDA reports)
MEDICATION ERROR ( 15 FDA reports)
MOOD SWINGS ( 15 FDA reports)
OBESITY ( 15 FDA reports)
OSTEORADIONECROSIS ( 15 FDA reports)
PARALYSIS ( 15 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 15 FDA reports)
PRURITUS GENERALISED ( 15 FDA reports)
PSORIASIS ( 15 FDA reports)
RESPIRATORY DEPRESSION ( 15 FDA reports)
ROAD TRAFFIC ACCIDENT ( 15 FDA reports)
SCIATICA ( 15 FDA reports)
SEROTONIN SYNDROME ( 15 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 15 FDA reports)
VITREOUS FLOATERS ( 15 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 14 FDA reports)
AORTIC VALVE INCOMPETENCE ( 14 FDA reports)
ARTERIOSCLEROSIS ( 14 FDA reports)
ARTHROPATHY ( 14 FDA reports)
BLOOD UREA INCREASED ( 14 FDA reports)
BODY TEMPERATURE INCREASED ( 14 FDA reports)
CEREBRAL HAEMORRHAGE ( 14 FDA reports)
COGNITIVE DISORDER ( 14 FDA reports)
DRUG LEVEL INCREASED ( 14 FDA reports)
DUODENAL ULCER ( 14 FDA reports)
FEBRILE NEUTROPENIA ( 14 FDA reports)
FOOT DEFORMITY ( 14 FDA reports)
GLAUCOMA ( 14 FDA reports)
HALLUCINATION, VISUAL ( 14 FDA reports)
HEART RATE IRREGULAR ( 14 FDA reports)
HYPOVOLAEMIA ( 14 FDA reports)
MUCOSAL INFLAMMATION ( 14 FDA reports)
MULTI-ORGAN FAILURE ( 14 FDA reports)
NECK PAIN ( 14 FDA reports)
NEOPLASM MALIGNANT ( 14 FDA reports)
NEPHROLITHIASIS ( 14 FDA reports)
NERVOUS SYSTEM DISORDER ( 14 FDA reports)
NOCTURIA ( 14 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 14 FDA reports)
ORAL CAVITY FISTULA ( 14 FDA reports)
ORAL INTAKE REDUCED ( 14 FDA reports)
ORAL PAIN ( 14 FDA reports)
PARANOIA ( 14 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 14 FDA reports)
POISONING ( 14 FDA reports)
PULMONARY HYPERTENSION ( 14 FDA reports)
RENAL CYST ( 14 FDA reports)
RHINITIS ALLERGIC ( 14 FDA reports)
SECONDARY SEQUESTRUM ( 14 FDA reports)
SENSITIVITY OF TEETH ( 14 FDA reports)
SINUS TACHYCARDIA ( 14 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 14 FDA reports)
VENTRICULAR TACHYCARDIA ( 14 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 13 FDA reports)
ADRENAL MASS ( 13 FDA reports)
ANGIOEDEMA ( 13 FDA reports)
BEDRIDDEN ( 13 FDA reports)
CEREBRAL INFARCTION ( 13 FDA reports)
CRYING ( 13 FDA reports)
DIPLOPIA ( 13 FDA reports)
DRUG EFFECT DECREASED ( 13 FDA reports)
DYSKINESIA ( 13 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 13 FDA reports)
HAEMATOCRIT DECREASED ( 13 FDA reports)
HYPERKERATOSIS ( 13 FDA reports)
HYPOMAGNESAEMIA ( 13 FDA reports)
ILL-DEFINED DISORDER ( 13 FDA reports)
INTERSTITIAL LUNG DISEASE ( 13 FDA reports)
METASTATIC NEOPLASM ( 13 FDA reports)
OESOPHAGITIS ( 13 FDA reports)
PHARYNGITIS ( 13 FDA reports)
PULMONARY HAEMORRHAGE ( 13 FDA reports)
PURULENCE ( 13 FDA reports)
RESTLESSNESS ( 13 FDA reports)
TREATMENT NONCOMPLIANCE ( 13 FDA reports)
UNEVALUABLE EVENT ( 13 FDA reports)
VENTRICULAR HYPERTROPHY ( 13 FDA reports)
ACUTE HEPATIC FAILURE ( 12 FDA reports)
BLINDNESS ( 12 FDA reports)
CARDIAC MURMUR ( 12 FDA reports)
COAGULOPATHY ( 12 FDA reports)
DIABETES MELLITUS ( 12 FDA reports)
DRY SKIN ( 12 FDA reports)
EAR INFECTION ( 12 FDA reports)
EPILEPSY ( 12 FDA reports)
ESCHERICHIA INFECTION ( 12 FDA reports)
FAECAL INCONTINENCE ( 12 FDA reports)
FEAR ( 12 FDA reports)
FEMORAL NECK FRACTURE ( 12 FDA reports)
FLUID RETENTION ( 12 FDA reports)
GOUT ( 12 FDA reports)
HAEMOLYTIC ANAEMIA ( 12 FDA reports)
HEPATOTOXICITY ( 12 FDA reports)
HYPERTONIC BLADDER ( 12 FDA reports)
INFLUENZA ( 12 FDA reports)
MIOSIS ( 12 FDA reports)
NEPHROTIC SYNDROME ( 12 FDA reports)
NIGHT SWEATS ( 12 FDA reports)
OFF LABEL USE ( 12 FDA reports)
ORAL DISORDER ( 12 FDA reports)
PAROSMIA ( 12 FDA reports)
PATHOLOGICAL FRACTURE ( 12 FDA reports)
PERICARDIAL EFFUSION ( 12 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 12 FDA reports)
RASH GENERALISED ( 12 FDA reports)
SINUS DISORDER ( 12 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 12 FDA reports)
TUBERCULOSIS ( 12 FDA reports)
VASCULITIS ( 12 FDA reports)
ABNORMAL BEHAVIOUR ( 11 FDA reports)
ACCIDENTAL OVERDOSE ( 11 FDA reports)
BLADDER CANCER ( 11 FDA reports)
BLOOD POTASSIUM INCREASED ( 11 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 11 FDA reports)
CHANGE OF BOWEL HABIT ( 11 FDA reports)
CHROMATURIA ( 11 FDA reports)
CRYSTALLURIA ( 11 FDA reports)
DENTAL CARIES ( 11 FDA reports)
EAR PAIN ( 11 FDA reports)
FISTULA ( 11 FDA reports)
GYNAECOMASTIA ( 11 FDA reports)
HEART RATE DECREASED ( 11 FDA reports)
HEPATIC CIRRHOSIS ( 11 FDA reports)
HEPATITIS ACUTE ( 11 FDA reports)
HIP FRACTURE ( 11 FDA reports)
HYPERGLYCAEMIA ( 11 FDA reports)
HYPOPHOSPHATAEMIA ( 11 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 11 FDA reports)
INJECTION SITE ERYTHEMA ( 11 FDA reports)
LACRIMATION INCREASED ( 11 FDA reports)
LUNG INFILTRATION ( 11 FDA reports)
LUNG NEOPLASM ( 11 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 11 FDA reports)
MENTAL STATUS CHANGES ( 11 FDA reports)
NEUTROPENIC SEPSIS ( 11 FDA reports)
PRODUCT QUALITY ISSUE ( 11 FDA reports)
PULMONARY CONGESTION ( 11 FDA reports)
SCOLIOSIS ( 11 FDA reports)
SINUS BRADYCARDIA ( 11 FDA reports)
TACHYPNOEA ( 11 FDA reports)
TINNITUS ( 11 FDA reports)
TOOTH LOSS ( 11 FDA reports)
TYPE 2 DIABETES MELLITUS ( 11 FDA reports)
WALKING AID USER ( 11 FDA reports)
WITHDRAWAL SYNDROME ( 11 FDA reports)
ABDOMINAL DISCOMFORT ( 10 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 10 FDA reports)
BIOPSY GINGIVAL ( 10 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 10 FDA reports)
CHRONIC SINUSITIS ( 10 FDA reports)
DEVICE RELATED INFECTION ( 10 FDA reports)
DRUG DEPENDENCE ( 10 FDA reports)
EMOTIONAL DISORDER ( 10 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 10 FDA reports)
ENTEROVESICAL FISTULA ( 10 FDA reports)
EYELID OEDEMA ( 10 FDA reports)
GALLBLADDER INJURY ( 10 FDA reports)
GINGIVAL BLEEDING ( 10 FDA reports)
GINGIVAL DISORDER ( 10 FDA reports)
GINGIVAL OEDEMA ( 10 FDA reports)
GINGIVITIS ( 10 FDA reports)
HAEMOPTYSIS ( 10 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 10 FDA reports)
HEPATORENAL SYNDROME ( 10 FDA reports)
IMPAIRED DRIVING ABILITY ( 10 FDA reports)
INJECTION SITE REACTION ( 10 FDA reports)
INTENTIONAL OVERDOSE ( 10 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 10 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 10 FDA reports)
MOTOR DYSFUNCTION ( 10 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 10 FDA reports)
MYOSITIS ( 10 FDA reports)
NERVOUSNESS ( 10 FDA reports)
ORTHOSTATIC HYPOTENSION ( 10 FDA reports)
PLASMACYTOSIS ( 10 FDA reports)
POST PROCEDURAL COMPLICATION ( 10 FDA reports)
PRESBYOPIA ( 10 FDA reports)
PROTHROMBIN TIME PROLONGED ( 10 FDA reports)
RASH MACULO-PAPULAR ( 10 FDA reports)
SKIN CANDIDA ( 10 FDA reports)
SKIN ODOUR ABNORMAL ( 10 FDA reports)
SPLENOMEGALY ( 10 FDA reports)
STAPHYLOCOCCAL INFECTION ( 10 FDA reports)
SUDDEN DEATH ( 10 FDA reports)
TEARFULNESS ( 10 FDA reports)
TENSION ( 10 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 10 FDA reports)
VAGINAL INFECTION ( 10 FDA reports)
VIRAL INFECTION ( 10 FDA reports)
ABORTION INDUCED ( 9 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 9 FDA reports)
BLOOD POTASSIUM DECREASED ( 9 FDA reports)
BONE SWELLING ( 9 FDA reports)
BREAST CANCER RECURRENT ( 9 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 9 FDA reports)
CHOLESTASIS ( 9 FDA reports)
CLOSTRIDIAL INFECTION ( 9 FDA reports)
COLONIC POLYP ( 9 FDA reports)
DISABILITY ( 9 FDA reports)
EATING DISORDER ( 9 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 9 FDA reports)
ENDODONTIC PROCEDURE ( 9 FDA reports)
EYE DISORDER ( 9 FDA reports)
HEPATITIS C ( 9 FDA reports)
HERNIA REPAIR ( 9 FDA reports)
IMPAIRED WORK ABILITY ( 9 FDA reports)
INCOHERENT ( 9 FDA reports)
INFUSION RELATED REACTION ( 9 FDA reports)
INJECTION SITE PRURITUS ( 9 FDA reports)
LYMPHOEDEMA ( 9 FDA reports)
MENISCUS LESION ( 9 FDA reports)
MENTAL IMPAIRMENT ( 9 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 9 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 9 FDA reports)
PERFORATED ULCER ( 9 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 9 FDA reports)
PHOTOPHOBIA ( 9 FDA reports)
PRESYNCOPE ( 9 FDA reports)
PROTEINURIA ( 9 FDA reports)
RESPIRATORY DISORDER ( 9 FDA reports)
SPINAL COMPRESSION FRACTURE ( 9 FDA reports)
STRESS ( 9 FDA reports)
THINKING ABNORMAL ( 9 FDA reports)
THIRST ( 9 FDA reports)
VENTRICULAR FIBRILLATION ( 9 FDA reports)
VISUAL DISTURBANCE ( 9 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 9 FDA reports)
ABSCESS ( 8 FDA reports)
ACIDOSIS ( 8 FDA reports)
APNOEA ( 8 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 8 FDA reports)
BLOOD SODIUM DECREASED ( 8 FDA reports)
BONE DEBRIDEMENT ( 8 FDA reports)
BREAST PAIN ( 8 FDA reports)
BRONCHOSPASM ( 8 FDA reports)
CAESAREAN SECTION ( 8 FDA reports)
COLITIS ( 8 FDA reports)
CROHN'S DISEASE ( 8 FDA reports)
DENTAL IMPLANTATION ( 8 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 8 FDA reports)
DRUG HYPERSENSITIVITY ( 8 FDA reports)
ECONOMIC PROBLEM ( 8 FDA reports)
ECZEMA ( 8 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 8 FDA reports)
EMPHYSEMA ( 8 FDA reports)
FIBROSIS ( 8 FDA reports)
FLANK PAIN ( 8 FDA reports)
GASTROINTESTINAL DISORDER ( 8 FDA reports)
HEPATIC CYST ( 8 FDA reports)
HEPATIC NECROSIS ( 8 FDA reports)
HODGKIN'S DISEASE ( 8 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 8 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 8 FDA reports)
INJECTION SITE BURNING ( 8 FDA reports)
INTENTIONAL SELF-INJURY ( 8 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 8 FDA reports)
JAW DISORDER ( 8 FDA reports)
JOINT EFFUSION ( 8 FDA reports)
LABILE BLOOD PRESSURE ( 8 FDA reports)
LOCALISED INFECTION ( 8 FDA reports)
MEDICAL DEVICE REMOVAL ( 8 FDA reports)
MUSCLE DISORDER ( 8 FDA reports)
MUSCLE STRAIN ( 8 FDA reports)
MUSCLE TWITCHING ( 8 FDA reports)
MYOCLONUS ( 8 FDA reports)
NEUTROPHIL COUNT DECREASED ( 8 FDA reports)
OCULAR HYPERAEMIA ( 8 FDA reports)
OSTEOLYSIS ( 8 FDA reports)
OXYGEN SATURATION DECREASED ( 8 FDA reports)
PANCREATIC CYST ( 8 FDA reports)
PHOTOSENSITIVITY REACTION ( 8 FDA reports)
PROSTATITIS ( 8 FDA reports)
RADICULITIS ( 8 FDA reports)
RALES ( 8 FDA reports)
RASH PAPULAR ( 8 FDA reports)
SENSORY DISTURBANCE ( 8 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 8 FDA reports)
SPINAL DISORDER ( 8 FDA reports)
STEVENS-JOHNSON SYNDROME ( 8 FDA reports)
TARDIVE DYSKINESIA ( 8 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 8 FDA reports)
ABORTION SPONTANEOUS ( 7 FDA reports)
ACCIDENTAL EXPOSURE ( 7 FDA reports)
ADVERSE DRUG REACTION ( 7 FDA reports)
ANGIONEUROTIC OEDEMA ( 7 FDA reports)
ARTHRITIS BACTERIAL ( 7 FDA reports)
ARTHRITIS INFECTIVE ( 7 FDA reports)
AZOTAEMIA ( 7 FDA reports)
BACK DISORDER ( 7 FDA reports)
BLOOD GLUCOSE DECREASED ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 7 FDA reports)
BODY HEIGHT DECREASED ( 7 FDA reports)
BONE MARROW FAILURE ( 7 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 7 FDA reports)
CARDIOVASCULAR DISORDER ( 7 FDA reports)
CEREBRAL ATROPHY ( 7 FDA reports)
DEVICE DISLOCATION ( 7 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 7 FDA reports)
DRUG SCREEN POSITIVE ( 7 FDA reports)
DUODENITIS ( 7 FDA reports)
DYSAESTHESIA ( 7 FDA reports)
DYSSTASIA ( 7 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 7 FDA reports)
FACIAL PALSY ( 7 FDA reports)
GASTROENTERITIS ( 7 FDA reports)
GLOSSODYNIA ( 7 FDA reports)
HEPATIC CONGESTION ( 7 FDA reports)
HERNIA ( 7 FDA reports)
HYPOTHYROIDISM ( 7 FDA reports)
JOINT CONTRACTURE ( 7 FDA reports)
JOINT INJURY ( 7 FDA reports)
KNEE ARTHROPLASTY ( 7 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 7 FDA reports)
LIVEDO RETICULARIS ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
LOBAR PNEUMONIA ( 7 FDA reports)
LYMPHOPENIA ( 7 FDA reports)
METASTASES TO SPINE ( 7 FDA reports)
MOVEMENT DISORDER ( 7 FDA reports)
NO THERAPEUTIC RESPONSE ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
PERIPHERAL ISCHAEMIA ( 7 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 7 FDA reports)
PERITONITIS ( 7 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 7 FDA reports)
POISONING DELIBERATE ( 7 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 7 FDA reports)
SEDATION ( 7 FDA reports)
SKIN TURGOR DECREASED ( 7 FDA reports)
STOMATITIS ( 7 FDA reports)
STRIDOR ( 7 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 7 FDA reports)
UPPER LIMB FRACTURE ( 7 FDA reports)
WOUND INFECTION ( 7 FDA reports)
ABDOMINAL TENDERNESS ( 6 FDA reports)
ALVEOLITIS ( 6 FDA reports)
AMENORRHOEA ( 6 FDA reports)
ANGINA UNSTABLE ( 6 FDA reports)
ANURIA ( 6 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 6 FDA reports)
BACTERIAL DISEASE CARRIER ( 6 FDA reports)
BILIARY DYSKINESIA ( 6 FDA reports)
BLOOD COUNT ABNORMAL ( 6 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 6 FDA reports)
BRAIN NEOPLASM ( 6 FDA reports)
BREAKTHROUGH PAIN ( 6 FDA reports)
CALCULUS BLADDER ( 6 FDA reports)
CANDIDIASIS ( 6 FDA reports)
CARDIAC PACEMAKER INSERTION ( 6 FDA reports)
CARDIAC VALVE DISEASE ( 6 FDA reports)
CHOLANGITIS ( 6 FDA reports)
CHOLECYSTITIS ACUTE ( 6 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 6 FDA reports)
CYST ( 6 FDA reports)
DELUSION ( 6 FDA reports)
DILATATION VENTRICULAR ( 6 FDA reports)
DRUG ABUSER ( 6 FDA reports)
DRUG DOSE OMISSION ( 6 FDA reports)
DRY EYE ( 6 FDA reports)
DUODENAL ULCER PERFORATION ( 6 FDA reports)
ENCEPHALITIS ( 6 FDA reports)
ENTEROCUTANEOUS FISTULA ( 6 FDA reports)
EOSINOPHILIA ( 6 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 6 FDA reports)
ERECTILE DYSFUNCTION ( 6 FDA reports)
ESSENTIAL HYPERTENSION ( 6 FDA reports)
FACET JOINT SYNDROME ( 6 FDA reports)
FANCONI SYNDROME ( 6 FDA reports)
FEELING COLD ( 6 FDA reports)
FEELING DRUNK ( 6 FDA reports)
FIBROUS HISTIOCYTOMA ( 6 FDA reports)
FLATULENCE ( 6 FDA reports)
FOOD POISONING ( 6 FDA reports)
GASTRIC HAEMORRHAGE ( 6 FDA reports)
HEAD INJURY ( 6 FDA reports)
HEPATIC INFARCTION ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
HOSPITALISATION ( 6 FDA reports)
HYPERAESTHESIA ( 6 FDA reports)
HYPERCALCAEMIA ( 6 FDA reports)
HYPOAESTHESIA FACIAL ( 6 FDA reports)
HYPOVENTILATION ( 6 FDA reports)
ILLUSION ( 6 FDA reports)
INCONTINENCE ( 6 FDA reports)
INCORRECT DOSE ADMINISTERED ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
INJECTION SITE RASH ( 6 FDA reports)
INTESTINAL PERFORATION ( 6 FDA reports)
IRON DEFICIENCY ( 6 FDA reports)
LIMB INJURY ( 6 FDA reports)
LOSS OF LIBIDO ( 6 FDA reports)
MANIA ( 6 FDA reports)
MASTECTOMY ( 6 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 6 FDA reports)
METASTASES TO PELVIS ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME ( 6 FDA reports)
NEUROLOGICAL SYMPTOM ( 6 FDA reports)
NEUROTOXICITY ( 6 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 6 FDA reports)
OSTEOSCLEROSIS ( 6 FDA reports)
PARKINSON'S DISEASE ( 6 FDA reports)
PERSONALITY CHANGE ( 6 FDA reports)
PHARYNGEAL OEDEMA ( 6 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 6 FDA reports)
PIGMENTATION DISORDER ( 6 FDA reports)
PNEUMONITIS ( 6 FDA reports)
POLYCYTHAEMIA ( 6 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 6 FDA reports)
PROCEDURAL PAIN ( 6 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 6 FDA reports)
PSYCHOTIC DISORDER ( 6 FDA reports)
PULMONARY GRANULOMA ( 6 FDA reports)
PURPURA ( 6 FDA reports)
RECTAL ULCER ( 6 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
RENAL FAILURE CHRONIC ( 6 FDA reports)
RETINAL HAEMORRHAGE ( 6 FDA reports)
SKIN HYPERTROPHY ( 6 FDA reports)
SKIN TIGHTNESS ( 6 FDA reports)
SKIN ULCER ( 6 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 6 FDA reports)
SUBCUTANEOUS NODULE ( 6 FDA reports)
TENDON RUPTURE ( 6 FDA reports)
TOXIC OPTIC NEUROPATHY ( 6 FDA reports)
ULCER ( 6 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 6 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 6 FDA reports)
WOUND DRAINAGE ( 6 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ADHESION ( 5 FDA reports)
AGEUSIA ( 5 FDA reports)
ANAPHYLACTOID REACTION ( 5 FDA reports)
APATHY ( 5 FDA reports)
APLASIA PURE RED CELL ( 5 FDA reports)
ARTERIOSPASM CORONARY ( 5 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 5 FDA reports)
BILE DUCT CANCER ( 5 FDA reports)
BLADDER OPERATION ( 5 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 5 FDA reports)
BODY TEMPERATURE DECREASED ( 5 FDA reports)
BREAST MASS ( 5 FDA reports)
BREATH SOUNDS ABNORMAL ( 5 FDA reports)
CARDIAC FIBRILLATION ( 5 FDA reports)
CARDIOGENIC SHOCK ( 5 FDA reports)
CARDIOMYOPATHY ( 5 FDA reports)
CHEST X-RAY ABNORMAL ( 5 FDA reports)
CHOKING ( 5 FDA reports)
COLD SWEAT ( 5 FDA reports)
COLITIS ISCHAEMIC ( 5 FDA reports)
COLON OPERATION ( 5 FDA reports)
DEAFNESS NEUROSENSORY ( 5 FDA reports)
DEBRIDEMENT ( 5 FDA reports)
DEMENTIA ( 5 FDA reports)
DEVICE FAILURE ( 5 FDA reports)
DIALYSIS ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
DROOLING ( 5 FDA reports)
DRUG ADMINISTRATION ERROR ( 5 FDA reports)
ECCHYMOSIS ( 5 FDA reports)
EJECTION FRACTION DECREASED ( 5 FDA reports)
ENTEROCOLITIS ( 5 FDA reports)
ERUCTATION ( 5 FDA reports)
ESCHERICHIA SEPSIS ( 5 FDA reports)
EYE HAEMORRHAGE ( 5 FDA reports)
EYE MOVEMENT DISORDER ( 5 FDA reports)
EYE PRURITUS ( 5 FDA reports)
FAECALOMA ( 5 FDA reports)
FIBROMYALGIA ( 5 FDA reports)
GASTROENTERITIS VIRAL ( 5 FDA reports)
GENERALISED OEDEMA ( 5 FDA reports)
GINGIVAL PAIN ( 5 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 5 FDA reports)
HAEMATOCHEZIA ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
HEPATOCELLULAR DAMAGE ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HYSTERECTOMY ( 5 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 5 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 5 FDA reports)
INTESTINAL OBSTRUCTION ( 5 FDA reports)
JAW OPERATION ( 5 FDA reports)
JOINT ARTHROPLASTY ( 5 FDA reports)
JOINT DISLOCATION ( 5 FDA reports)
LACERATION ( 5 FDA reports)
LARYNGOSPASM ( 5 FDA reports)
LIPOMA ( 5 FDA reports)
LIVER TRANSPLANT ( 5 FDA reports)
LOCAL SWELLING ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
MACROCYTOSIS ( 5 FDA reports)
MALNUTRITION ( 5 FDA reports)
MAXILLOFACIAL OPERATION ( 5 FDA reports)
METRORRHAGIA ( 5 FDA reports)
MIDDLE INSOMNIA ( 5 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 5 FDA reports)
MYOPATHY ( 5 FDA reports)
NASAL OBSTRUCTION ( 5 FDA reports)
NOCTURNAL DYSPNOEA ( 5 FDA reports)
NON-CARDIAC CHEST PAIN ( 5 FDA reports)
OCCULT BLOOD POSITIVE ( 5 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 5 FDA reports)
PANCREATIC ENZYMES INCREASED ( 5 FDA reports)
PANCREATITIS CHRONIC ( 5 FDA reports)
PAPILLOEDEMA ( 5 FDA reports)
PARKINSONISM ( 5 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 5 FDA reports)
PERSONALITY DISORDER ( 5 FDA reports)
PHARYNGEAL ULCERATION ( 5 FDA reports)
PLATELET COUNT INCREASED ( 5 FDA reports)
POLYP ( 5 FDA reports)
POST POLIO SYNDROME ( 5 FDA reports)
PSORIATIC ARTHROPATHY ( 5 FDA reports)
PULMONARY INFARCTION ( 5 FDA reports)
PULMONARY VASCULAR DISORDER ( 5 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 5 FDA reports)
REFLUX OESOPHAGITIS ( 5 FDA reports)
RESTLESS LEGS SYNDROME ( 5 FDA reports)
RETCHING ( 5 FDA reports)
RETROPERITONEAL FIBROSIS ( 5 FDA reports)
RIB FRACTURE ( 5 FDA reports)
SELF-INJURIOUS IDEATION ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
SERUM SICKNESS ( 5 FDA reports)
SHOCK ( 5 FDA reports)
SKIN BURNING SENSATION ( 5 FDA reports)
SKIN DISORDER ( 5 FDA reports)
SKIN LACERATION ( 5 FDA reports)
SKIN LESION ( 5 FDA reports)
STOMACH DISCOMFORT ( 5 FDA reports)
SUBDURAL HAEMATOMA ( 5 FDA reports)
SUBDURAL HAEMORRHAGE ( 5 FDA reports)
TENSION HEADACHE ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
VAGINAL HAEMORRHAGE ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
WOUND ( 5 FDA reports)
WRIST FRACTURE ( 5 FDA reports)
ABDOMINAL MASS ( 4 FDA reports)
ABDOMINAL RIGIDITY ( 4 FDA reports)
ABNORMAL DREAMS ( 4 FDA reports)
ABSCESS NECK ( 4 FDA reports)
ACUTE ABDOMEN ( 4 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
AMPUTATION ( 4 FDA reports)
ANAL HAEMORRHAGE ( 4 FDA reports)
ANEURYSM ( 4 FDA reports)
ANORGASMIA ( 4 FDA reports)
AORTIC ANEURYSM REPAIR ( 4 FDA reports)
APLASIA ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 4 FDA reports)
BILE DUCT STONE ( 4 FDA reports)
BILIARY COLIC ( 4 FDA reports)
BIPOLAR DISORDER ( 4 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
BLOOD ALBUMIN INCREASED ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
BONE CYST ( 4 FDA reports)
BONE DENSITY INCREASED ( 4 FDA reports)
BRAIN OEDEMA ( 4 FDA reports)
BREAST FEEDING ( 4 FDA reports)
BRUXISM ( 4 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 4 FDA reports)
BURKITT'S LYMPHOMA ( 4 FDA reports)
CARDIAC ANEURYSM ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CATHETER RELATED COMPLICATION ( 4 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 4 FDA reports)
CERUMEN IMPACTION ( 4 FDA reports)
CHOKING SENSATION ( 4 FDA reports)
CHOLECYSTECTOMY ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 4 FDA reports)
COLLAPSE OF LUNG ( 4 FDA reports)
COLON NEOPLASM ( 4 FDA reports)
COMA SCALE ABNORMAL ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DEPRESSIVE SYMPTOM ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DISSOCIATION ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
DRUG RESISTANCE ( 4 FDA reports)
DUPUYTREN'S CONTRACTURE ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
ENDOCARDITIS ( 4 FDA reports)
ENTERITIS ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
FACE LIFT ( 4 FDA reports)
FASCIAL INFECTION ( 4 FDA reports)
GALLBLADDER OBSTRUCTION ( 4 FDA reports)
GASTRITIS HAEMORRHAGIC ( 4 FDA reports)
GLOSSITIS ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HALLUCINATION, AUDITORY ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HYPERAEMIA ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
IMMUNE SYSTEM DISORDER ( 4 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 4 FDA reports)
INJECTION SITE IRRITATION ( 4 FDA reports)
INJECTION SITE SWELLING ( 4 FDA reports)
INJECTION SITE WARMTH ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 4 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 4 FDA reports)
INTESTINAL RESECTION ( 4 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 4 FDA reports)
INTRACRANIAL HYPOTENSION ( 4 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
LARGE INTESTINE PERFORATION ( 4 FDA reports)
LEG AMPUTATION ( 4 FDA reports)
LIBIDO DECREASED ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
MACULAR OEDEMA ( 4 FDA reports)
MAJOR DEPRESSION ( 4 FDA reports)
MALIGNANT MELANOMA ( 4 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 4 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
NASAL DRYNESS ( 4 FDA reports)
NEONATAL DISORDER ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEPHROPATHY TOXIC ( 4 FDA reports)
NEURALGIA ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
ODYNOPHAGIA ( 4 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 4 FDA reports)
OPTIC NEUROPATHY ( 4 FDA reports)
OVARIAN CANCER ( 4 FDA reports)
PAROTITIS ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
PERIPHERAL EMBOLISM ( 4 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 4 FDA reports)
PERITONEAL HAEMORRHAGE ( 4 FDA reports)
PETECHIAE ( 4 FDA reports)
PINGUECULA ( 4 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 4 FDA reports)
POLYARTHRITIS ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 4 FDA reports)
POSTPARTUM DEPRESSION ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PREMATURE LABOUR ( 4 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 4 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 4 FDA reports)
PROSTATE CANCER ( 4 FDA reports)
PROSTATE CANCER METASTATIC ( 4 FDA reports)
RENAL INJURY ( 4 FDA reports)
RENAL TUBULAR NECROSIS ( 4 FDA reports)
RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
RHEUMATOID NODULE ( 4 FDA reports)
SALIVARY HYPERSECRETION ( 4 FDA reports)
SARCOIDOSIS ( 4 FDA reports)
SEASONAL ALLERGY ( 4 FDA reports)
SELF ESTEEM DECREASED ( 4 FDA reports)
SELF-MEDICATION ( 4 FDA reports)
SENSATION OF HEAVINESS ( 4 FDA reports)
SENSATION OF PRESSURE ( 4 FDA reports)
SEQUESTRECTOMY ( 4 FDA reports)
SKIN WARM ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
SYNOVITIS ( 4 FDA reports)
TALIPES ( 4 FDA reports)
TENDON DISORDER ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 4 FDA reports)
THROMBOSIS IN DEVICE ( 4 FDA reports)
TOE OPERATION ( 4 FDA reports)
TONGUE PARALYSIS ( 4 FDA reports)
TONSIL CANCER ( 4 FDA reports)
TONSILLITIS ( 4 FDA reports)
TRIGEMINAL NEURALGIA ( 4 FDA reports)
TRISMUS ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 4 FDA reports)
TUMOUR PAIN ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
UROSEPSIS ( 4 FDA reports)
UTERINE MASS ( 4 FDA reports)
VENTRICULAR HYPOKINESIA ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
ABDOMINAL NEOPLASM ( 3 FDA reports)
ABDOMINAL WALL ABSCESS ( 3 FDA reports)
ACNE ( 3 FDA reports)
ACTINIC KERATOSIS ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
AKINESIA ( 3 FDA reports)
ALCOHOLISM ( 3 FDA reports)
ALVEOLITIS FIBROSING ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANAL FISTULA ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
AORTIC DISORDER ( 3 FDA reports)
APHONIA ( 3 FDA reports)
APPETITE DISORDER ( 3 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
ATROPHY ( 3 FDA reports)
AXONAL NEUROPATHY ( 3 FDA reports)
B-CELL LYMPHOMA ( 3 FDA reports)
BILIARY DILATATION ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BLOOD ALCOHOL INCREASED ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 3 FDA reports)
BLOOD PRESSURE ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
BRAIN INJURY ( 3 FDA reports)
BREAST CANCER IN SITU ( 3 FDA reports)
BREAST RECONSTRUCTION ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
CARDIAC ASTHMA ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CARPAL TUNNEL SYNDROME ( 3 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 3 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 3 FDA reports)
COGAN'S SYNDROME ( 3 FDA reports)
COLOSTOMY ( 3 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
COR PULMONALE ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DIABETIC COMA ( 3 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 3 FDA reports)
DISSEMINATED TUBERCULOSIS ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
DYSAESTHESIA PHARYNX ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
ELDERLY ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 3 FDA reports)
ERYTHRODERMIC PSORIASIS ( 3 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
FACIAL BONES FRACTURE ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FAT INTOLERANCE ( 3 FDA reports)
FLUID INTAKE RESTRICTION ( 3 FDA reports)
FOOD INTOLERANCE ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
GALLBLADDER ENLARGEMENT ( 3 FDA reports)
GANGRENE ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTRIC POLYPS ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
GASTROINTESTINAL PERFORATION ( 3 FDA reports)
GASTROINTESTINAL TOXICITY ( 3 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 3 FDA reports)
GINGIVAL INFECTION ( 3 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HAEMOCHROMATOSIS ( 3 FDA reports)
HAEMOGLOBIN ABNORMAL ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HAEMORRHOID OPERATION ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HIP ARTHROPLASTY ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPERREFLEXIA ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
INCREASED TENDENCY TO BRUISE ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INTERMITTENT CLAUDICATION ( 3 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 3 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 3 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
INVESTIGATION ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
JAUNDICE NEONATAL ( 3 FDA reports)
KIDNEY ENLARGEMENT ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LASER THERAPY ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LUNG OPERATION ( 3 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
LYMPHANGITIS ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
METASTASES TO ABDOMINAL WALL ( 3 FDA reports)
MICROCYTIC ANAEMIA ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
MOEBIUS II SYNDROME ( 3 FDA reports)
MORBID THOUGHTS ( 3 FDA reports)
MULTI-ORGAN DISORDER ( 3 FDA reports)
MURPHY'S SIGN POSITIVE ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MYRINGITIS ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NASAL NEOPLASM ( 3 FDA reports)
NASAL SINUS CANCER ( 3 FDA reports)
NEGATIVE THOUGHTS ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NEUTROPENIC COLITIS ( 3 FDA reports)
NEUTROPHILIA ( 3 FDA reports)
NOCARDIOSIS ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
OESOPHAGEAL NEOPLASM ( 3 FDA reports)
ONYCHOCLASIS ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
OPTIC ATROPHY ( 3 FDA reports)
OPTIC NERVE INJURY ( 3 FDA reports)
OROPHARYNGEAL BLISTERING ( 3 FDA reports)
OSTEITIS ( 3 FDA reports)
OSTEITIS DEFORMANS ( 3 FDA reports)
OTITIS MEDIA ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
OVERWEIGHT ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PELVIC ABSCESS ( 3 FDA reports)
PERINEPHRIC COLLECTION ( 3 FDA reports)
PERIORBITAL HAEMATOMA ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PERSECUTORY DELUSION ( 3 FDA reports)
PHARYNGEAL ERYTHEMA ( 3 FDA reports)
PHYSICAL ASSAULT ( 3 FDA reports)
PITTING OEDEMA ( 3 FDA reports)
PLANTAR FASCIITIS ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
PLEURISY VIRAL ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 3 FDA reports)
POLAND'S SYNDROME ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
POST THROMBOTIC SYNDROME ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 3 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RECTAL CANCER ( 3 FDA reports)
RESPIRATORY RATE DECREASED ( 3 FDA reports)
RESUSCITATION ( 3 FDA reports)
RETINAL DETACHMENT ( 3 FDA reports)
RETINAL OEDEMA ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
SALMONELLOSIS ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SCLERODERMA RENAL CRISIS ( 3 FDA reports)
SCOTOMA ( 3 FDA reports)
SCRATCH ( 3 FDA reports)
SEBORRHOEIC KERATOSIS ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SIGMOIDECTOMY ( 3 FDA reports)
SINUS HEADACHE ( 3 FDA reports)
SKIN HYPERPIGMENTATION ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SKIN NODULE ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
SNORING ( 3 FDA reports)
SOMNAMBULISM ( 3 FDA reports)
SOPOR ( 3 FDA reports)
SPINAL CORD COMPRESSION ( 3 FDA reports)
SPLINTER HAEMORRHAGES ( 3 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
TONGUE BITING ( 3 FDA reports)
TONGUE DISORDER ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
TONGUE ULCERATION ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
UNDERDOSE ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
VARICOSE VEIN ( 3 FDA reports)
VASCULAR BYPASS GRAFT ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VENOUS OCCLUSION ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
WOUND HAEMORRHAGE ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACID BASE BALANCE ABNORMAL ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ALVEOLAR SOFT PART SARCOMA METASTATIC ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANASTOMOTIC ULCER ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANKLE OPERATION ( 2 FDA reports)
ANORECTAL CELLULITIS ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APPARENT LIFE THREATENING EVENT ( 2 FDA reports)
APPENDICITIS PERFORATED ( 2 FDA reports)
ARM AMPUTATION ( 2 FDA reports)
ARRHYTHMIA NEONATAL ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATHETOSIS ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BIOPSY LYMPH GLAND ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 2 FDA reports)
BLAST CELLS PRESENT ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CALCIUM ABNORMAL ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CREATINE DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLUNTED AFFECT ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BREAST LUMP REMOVAL ( 2 FDA reports)
BRONCHIAL CARCINOMA ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BUNION OPERATION ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CERULOPLASMIN DECREASED ( 2 FDA reports)
CERVIX CARCINOMA ( 2 FDA reports)
CHLORACNE ( 2 FDA reports)
CHLOROMA ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
CLAUSTROPHOBIA ( 2 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COLORECTAL CANCER METASTATIC ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGENITAL ABSENCE OF CRANIAL VAULT ( 2 FDA reports)
CONGENITAL HAND MALFORMATION ( 2 FDA reports)
CONGENITAL MULTIPLEX ARTHROGRYPOSIS ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 2 FDA reports)
COR PULMONALE ACUTE ( 2 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 2 FDA reports)
CORNEAL ULCER ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CRANIAL NERVE PARALYSIS ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CRYOGLOBULINAEMIA ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
DELUSION OF GRANDEUR ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DERMATITIS HERPETIFORMIS ( 2 FDA reports)
DEVICE DAMAGE ( 2 FDA reports)
DEXTROCARDIA ( 2 FDA reports)
DIAGNOSTIC PROCEDURE ( 2 FDA reports)
DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY ( 2 FDA reports)
DISLOCATION OF VERTEBRA ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG INTERACTION POTENTIATION ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSMORPHISM ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
EAR PRURITUS ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
EMOTIONAL POVERTY ( 2 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENURESIS ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOETAL HEART RATE ABNORMAL ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
FRACTURE DELAYED UNION ( 2 FDA reports)
FRACTURE DISPLACEMENT ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 2 FDA reports)
FUNGAL RASH ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GINGIVAL ERYTHEMA ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
GLIOBLASTOMA ( 2 FDA reports)
H1N1 INFLUENZA ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HEART RATE ABNORMAL ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC ISCHAEMIA ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERSPLENISM ACQUIRED ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOLIPIDAEMIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
ILEAL STENOSIS ( 2 FDA reports)
ILEOCOLECTOMY ( 2 FDA reports)
ILEUS ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LARYNGEAL CANCER ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIMB OPERATION ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LISTERIA SEPSIS ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
LYMPHATIC DISORDER ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
MATERNAL DISTRESS DURING LABOUR ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MENINGITIS TUBERCULOUS ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MYELOPATHY ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
MYRINGOTOMY ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEUROFIBROMATOSIS ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
NODULE ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OCULAR RETROBULBAR HAEMORRHAGE ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL FISTULA ( 2 FDA reports)
ONYCHOMADESIS ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
OSTEOCHONDROSIS ( 2 FDA reports)
OVERGROWTH BACTERIAL ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PAPILLARY THYROID CANCER ( 2 FDA reports)
PARAPROTEINAEMIA ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERIPHERAL NERVE LESION ( 2 FDA reports)
PERITONSILLAR ABSCESS ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL ABSCESS ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PHONOPHOBIA ( 2 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PLASTIC SURGERY TO THE FACE ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POOR VENOUS ACCESS ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
POST PROCEDURAL FISTULA ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
POSTURING ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PREGNANCY WITH CONTRACEPTIVE PATCH ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROCTITIS ULCERATIVE ( 2 FDA reports)
PRODUCT ADHESION ISSUE ( 2 FDA reports)
PROTEIN S DEFICIENCY ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
PULPITIS DENTAL ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
PYLORUS DILATATION ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RECTAL NEOPLASM ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL ISCHAEMIA ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RHEUMATIC HEART DISEASE ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SCAB ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SENSATION OF PRESSURE IN EAR ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SKIN ULCER HAEMORRHAGE ( 2 FDA reports)
SLEEP-RELATED EATING DISORDER ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
SPINAL DECOMPRESSION ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SPONDYLOLYSIS ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 2 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
SYNDACTYLY ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
SYSTOLIC DYSFUNCTION ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TENDON SHEATH INCISION ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYMUS ENLARGEMENT ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TONGUE HAEMORRHAGE ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
UMBILICAL CORD AROUND NECK ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
VAGINAL PAIN ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VISUAL PATHWAY DISORDER ( 2 FDA reports)
VITAMIN B12 DECREASED ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WOUND INFECTION BACTERIAL ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC VALVE REPAIR ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPLICATION SITE DISCHARGE ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARRESTED LABOUR ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATYPICAL FEMUR FRACTURE ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AVERSION ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CARBON MONOXIDE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE MARROW BASOPHILIC LEUKOCYTE COUNT INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC MALPOSITION ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LEUKAEMIA ( 1 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL VASOCONSTRICTION ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CERUMEN REMOVAL ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CLEFT LIP ( 1 FDA reports)
CLONAL EVOLUTION ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONTRACEPTIVE DEVICE COMPLICATION ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CRYSTAL URINE ABSENT ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DENTAL CARE ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG ADDICT ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
ECHOCARDIOGRAM ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELBOW OPERATION ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENOPHTHALMOS ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
EPIDEMIC POLYARTHRITIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOMA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEMORAL HERNIA ( 1 FDA reports)
FEMORAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FORCEPS DELIVERY ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLBLADDER NECROSIS ( 1 FDA reports)
GAMMA RADIATION THERAPY TO PROSTATE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTRITIS VIRAL ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION, OLFACTORY ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY STAGE UNSPECIFIED ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPERPROLACTINAEMIA ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCISION SITE BLISTER ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLAMMATION LOCALISED ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE STINGING ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INTESTINAL CONGESTION ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JOINT IRRIGATION ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LABELLED DRUG-DISEASE INTERACTION MEDICATION ERROR ( 1 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARYNGEAL HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
MACULE ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MALIGNANT NEOPLASM OF EYELID ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MEDICAL OBSERVATION ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE OEDEMA ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NAIL PSORIASIS ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROTISING SCLERITIS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NERVE STIMULATION TEST ABNORMAL ( 1 FDA reports)
NEUROBLASTOMA ( 1 FDA reports)
NEUROMYELITIS OPTICA ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE II ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE III ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OCULAR NEOPLASM ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OILY SKIN ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OSMOLAR GAP ABNORMAL ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PANCREATIC PHLEGMON ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PERIPORTAL SINUS DILATATION ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURAL MESOTHELIOMA MALIGNANT ( 1 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PO2 ABNORMAL ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PORTAL VEIN OCCLUSION ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREGNANCY TEST POSITIVE ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PYELECTASIA ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCLERAL BUCKLING SURGERY ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL CORD HAEMORRHAGE ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPINE MALFORMATION ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STARING ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TESTICULAR CYST ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TIC ( 1 FDA reports)
TONGUE ABSCESS ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
ULNAR NEURITIS ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY BLADDER RUPTURE ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL PERFORATION ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VENOUS PRESSURE INCREASED ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENOUS THROMBOSIS IN PREGNANCY ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VERTEBROPLASTY ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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