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

PAIN ( 725 FDA reports)
NAUSEA ( 702 FDA reports)
DYSPNOEA ( 608 FDA reports)
VOMITING ( 560 FDA reports)
PYREXIA ( 546 FDA reports)
DIARRHOEA ( 483 FDA reports)
ABDOMINAL PAIN ( 441 FDA reports)
FATIGUE ( 428 FDA reports)
ANXIETY ( 425 FDA reports)
DIZZINESS ( 401 FDA reports)
PNEUMONIA ( 399 FDA reports)
PULMONARY EMBOLISM ( 376 FDA reports)
HEADACHE ( 357 FDA reports)
MALAISE ( 345 FDA reports)
ASTHENIA ( 328 FDA reports)
CHOLELITHIASIS ( 322 FDA reports)
ABDOMINAL PAIN UPPER ( 314 FDA reports)
CHEST PAIN ( 313 FDA reports)
WEIGHT DECREASED ( 304 FDA reports)
INJURY ( 302 FDA reports)
OEDEMA PERIPHERAL ( 297 FDA reports)
ANAEMIA ( 294 FDA reports)
CROHN'S DISEASE ( 292 FDA reports)
DRUG INEFFECTIVE ( 291 FDA reports)
DEEP VEIN THROMBOSIS ( 287 FDA reports)
CHOLECYSTITIS CHRONIC ( 282 FDA reports)
PAIN IN EXTREMITY ( 282 FDA reports)
URINARY TRACT INFECTION ( 278 FDA reports)
HYPOTENSION ( 263 FDA reports)
INFECTION ( 249 FDA reports)
SEPSIS ( 241 FDA reports)
ARTHRALGIA ( 240 FDA reports)
BACK PAIN ( 234 FDA reports)
GALLBLADDER DISORDER ( 229 FDA reports)
RASH ( 226 FDA reports)
FALL ( 221 FDA reports)
DEHYDRATION ( 207 FDA reports)
DEATH ( 194 FDA reports)
COUGH ( 187 FDA reports)
RENAL FAILURE ( 186 FDA reports)
ERYTHEMA ( 185 FDA reports)
CONSTIPATION ( 180 FDA reports)
HYPOAESTHESIA ( 180 FDA reports)
DECREASED APPETITE ( 179 FDA reports)
HYPERTENSION ( 179 FDA reports)
INSOMNIA ( 179 FDA reports)
CONFUSIONAL STATE ( 175 FDA reports)
DEPRESSION ( 169 FDA reports)
OSTEOMYELITIS ( 167 FDA reports)
BRONCHITIS ( 166 FDA reports)
CONVULSION ( 166 FDA reports)
EMOTIONAL DISTRESS ( 160 FDA reports)
PLATELET COUNT DECREASED ( 159 FDA reports)
RESPIRATORY FAILURE ( 159 FDA reports)
PAIN IN JAW ( 158 FDA reports)
PLEURAL EFFUSION ( 158 FDA reports)
OSTEONECROSIS OF JAW ( 157 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 155 FDA reports)
LOSS OF CONSCIOUSNESS ( 154 FDA reports)
PRURITUS ( 149 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 147 FDA reports)
GAIT DISTURBANCE ( 147 FDA reports)
SINUSITIS ( 142 FDA reports)
PARAESTHESIA ( 139 FDA reports)
RENAL FAILURE ACUTE ( 139 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 135 FDA reports)
THROMBOSIS ( 134 FDA reports)
CELLULITIS ( 132 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 130 FDA reports)
MUSCLE SPASMS ( 130 FDA reports)
CHILLS ( 129 FDA reports)
ASTHMA ( 128 FDA reports)
BONE DISORDER ( 128 FDA reports)
CARDIAC DISORDER ( 127 FDA reports)
MUSCULAR WEAKNESS ( 127 FDA reports)
OSTEOARTHRITIS ( 125 FDA reports)
THROMBOCYTOPENIA ( 125 FDA reports)
HYPERHIDROSIS ( 124 FDA reports)
SYNCOPE ( 124 FDA reports)
SEPTIC SHOCK ( 121 FDA reports)
IMPAIRED HEALING ( 120 FDA reports)
DYSPHAGIA ( 119 FDA reports)
FEELING ABNORMAL ( 117 FDA reports)
HYPERSENSITIVITY ( 117 FDA reports)
BLOOD PRESSURE INCREASED ( 116 FDA reports)
DRUG INTERACTION ( 116 FDA reports)
HAEMOGLOBIN DECREASED ( 116 FDA reports)
MULTI-ORGAN FAILURE ( 116 FDA reports)
BLOOD GLUCOSE INCREASED ( 114 FDA reports)
MYOCARDIAL INFARCTION ( 113 FDA reports)
STAPHYLOCOCCAL INFECTION ( 113 FDA reports)
ABDOMINAL DISTENSION ( 110 FDA reports)
NEUTROPENIA ( 110 FDA reports)
SWELLING ( 109 FDA reports)
ABDOMINAL DISCOMFORT ( 108 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 106 FDA reports)
CONDITION AGGRAVATED ( 106 FDA reports)
PANCYTOPENIA ( 106 FDA reports)
ATRIAL FIBRILLATION ( 105 FDA reports)
DYSPEPSIA ( 105 FDA reports)
OSTEONECROSIS ( 104 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 103 FDA reports)
CEREBROVASCULAR ACCIDENT ( 102 FDA reports)
HEART RATE INCREASED ( 100 FDA reports)
PALPITATIONS ( 99 FDA reports)
BLOOD PRESSURE DECREASED ( 98 FDA reports)
BONE PAIN ( 96 FDA reports)
WEIGHT INCREASED ( 96 FDA reports)
CARDIAC ARREST ( 95 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 95 FDA reports)
TACHYCARDIA ( 95 FDA reports)
CHEST DISCOMFORT ( 94 FDA reports)
SOMNOLENCE ( 94 FDA reports)
TREMOR ( 94 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 94 FDA reports)
ANHEDONIA ( 93 FDA reports)
VISION BLURRED ( 93 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 92 FDA reports)
CHOLECYSTITIS ( 91 FDA reports)
MEMORY IMPAIRMENT ( 88 FDA reports)
HAEMORRHAGE ( 87 FDA reports)
TOOTH EXTRACTION ( 87 FDA reports)
MYALGIA ( 86 FDA reports)
MUSCULOSKELETAL PAIN ( 85 FDA reports)
PANCREATITIS ( 84 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 84 FDA reports)
CATARACT ( 82 FDA reports)
CONTUSION ( 82 FDA reports)
ARTHRITIS ( 81 FDA reports)
INJECTION SITE PAIN ( 81 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 80 FDA reports)
JOINT SWELLING ( 79 FDA reports)
NEPHROLITHIASIS ( 79 FDA reports)
STRESS ( 79 FDA reports)
INFLAMMATION ( 77 FDA reports)
JAUNDICE ( 77 FDA reports)
OVERDOSE ( 77 FDA reports)
HYPOKALAEMIA ( 75 FDA reports)
MIGRAINE ( 75 FDA reports)
FISTULA ( 73 FDA reports)
MITRAL VALVE INCOMPETENCE ( 73 FDA reports)
NEUROPATHY PERIPHERAL ( 73 FDA reports)
RENAL FAILURE CHRONIC ( 73 FDA reports)
ABSCESS ( 72 FDA reports)
DYSURIA ( 72 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 72 FDA reports)
SPINAL OSTEOARTHRITIS ( 72 FDA reports)
SWELLING FACE ( 72 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 72 FDA reports)
RENAL IMPAIRMENT ( 71 FDA reports)
BLOOD CREATININE INCREASED ( 70 FDA reports)
NASOPHARYNGITIS ( 69 FDA reports)
BILIARY DYSKINESIA ( 68 FDA reports)
PULMONARY OEDEMA ( 68 FDA reports)
CARDIO-RESPIRATORY ARREST ( 67 FDA reports)
FLUSHING ( 67 FDA reports)
CYSTITIS ( 66 FDA reports)
SKIN DISCOLOURATION ( 66 FDA reports)
VERTIGO ( 66 FDA reports)
MENTAL DISORDER ( 65 FDA reports)
SCAR ( 65 FDA reports)
TOOTH DISORDER ( 65 FDA reports)
UNRESPONSIVE TO STIMULI ( 65 FDA reports)
BALANCE DISORDER ( 64 FDA reports)
NECK PAIN ( 64 FDA reports)
OEDEMA ( 64 FDA reports)
OFF LABEL USE ( 64 FDA reports)
VISUAL IMPAIRMENT ( 64 FDA reports)
ALOPECIA ( 63 FDA reports)
DEAFNESS ( 63 FDA reports)
GASTRITIS ( 63 FDA reports)
MENTAL STATUS CHANGES ( 63 FDA reports)
ABASIA ( 62 FDA reports)
FEBRILE NEUTROPENIA ( 62 FDA reports)
HAEMATURIA ( 62 FDA reports)
TOOTHACHE ( 62 FDA reports)
ARRHYTHMIA ( 61 FDA reports)
BLOOD BILIRUBIN INCREASED ( 61 FDA reports)
DEFORMITY ( 61 FDA reports)
OROPHARYNGEAL PAIN ( 61 FDA reports)
LUNG DISORDER ( 60 FDA reports)
CHOLECYSTECTOMY ( 59 FDA reports)
MOBILITY DECREASED ( 59 FDA reports)
AMNESIA ( 58 FDA reports)
COLITIS ( 58 FDA reports)
FUNGAL INFECTION ( 58 FDA reports)
HALLUCINATION ( 58 FDA reports)
LUNG NEOPLASM ( 58 FDA reports)
DIABETES MELLITUS ( 57 FDA reports)
HEPATIC FAILURE ( 57 FDA reports)
LYMPHADENOPATHY ( 57 FDA reports)
SPEECH DISORDER ( 57 FDA reports)
BILIARY COLIC ( 56 FDA reports)
CANDIDIASIS ( 56 FDA reports)
FEAR ( 56 FDA reports)
URTICARIA ( 56 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 55 FDA reports)
DEVICE RELATED INFECTION ( 55 FDA reports)
FLANK PAIN ( 55 FDA reports)
LETHARGY ( 55 FDA reports)
OXYGEN SATURATION DECREASED ( 55 FDA reports)
RESPIRATORY DISTRESS ( 55 FDA reports)
CARDIAC FAILURE ( 54 FDA reports)
DRUG DOSE OMISSION ( 54 FDA reports)
HYPOXIA ( 54 FDA reports)
INFLUENZA ( 54 FDA reports)
AGITATION ( 53 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 53 FDA reports)
LEUKOCYTOSIS ( 53 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 52 FDA reports)
BLISTER ( 52 FDA reports)
BURNING SENSATION ( 52 FDA reports)
FLATULENCE ( 52 FDA reports)
LUNG INFILTRATION ( 52 FDA reports)
MASS ( 52 FDA reports)
BURSITIS ( 51 FDA reports)
CLOSTRIDIAL INFECTION ( 51 FDA reports)
DYSPNOEA EXERTIONAL ( 51 FDA reports)
HEPATIC ENZYME INCREASED ( 51 FDA reports)
NEUTROPHIL COUNT DECREASED ( 51 FDA reports)
ATELECTASIS ( 50 FDA reports)
DRUG HYPERSENSITIVITY ( 50 FDA reports)
JOINT STIFFNESS ( 50 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 50 FDA reports)
POLLAKIURIA ( 50 FDA reports)
SHOCK ( 50 FDA reports)
APHASIA ( 49 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 49 FDA reports)
DRY SKIN ( 49 FDA reports)
EPISTAXIS ( 49 FDA reports)
HEPATITIS ( 49 FDA reports)
HYPERGLYCAEMIA ( 49 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 49 FDA reports)
INTERSTITIAL LUNG DISEASE ( 49 FDA reports)
LOCALISED INFECTION ( 49 FDA reports)
TOOTH INFECTION ( 49 FDA reports)
INFLUENZA LIKE ILLNESS ( 48 FDA reports)
SURGERY ( 48 FDA reports)
TOOTH FRACTURE ( 48 FDA reports)
URINARY INCONTINENCE ( 48 FDA reports)
CARDIOMEGALY ( 47 FDA reports)
CHOLECYSTITIS ACUTE ( 47 FDA reports)
COGNITIVE DISORDER ( 47 FDA reports)
EYE DISORDER ( 47 FDA reports)
HEART RATE IRREGULAR ( 46 FDA reports)
HYPOPHAGIA ( 46 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 46 FDA reports)
LIVER DISORDER ( 46 FDA reports)
METASTASES TO BONE ( 46 FDA reports)
PHARYNGEAL OEDEMA ( 46 FDA reports)
TINNITUS ( 46 FDA reports)
BRADYCARDIA ( 45 FDA reports)
DISEASE PROGRESSION ( 45 FDA reports)
IRON DEFICIENCY ANAEMIA ( 45 FDA reports)
TOOTH LOSS ( 45 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 44 FDA reports)
DISCOMFORT ( 44 FDA reports)
HAEMATOCHEZIA ( 44 FDA reports)
HOT FLUSH ( 44 FDA reports)
COAGULOPATHY ( 43 FDA reports)
GALLBLADDER INJURY ( 43 FDA reports)
HERPES ZOSTER ( 43 FDA reports)
SCOLIOSIS ( 43 FDA reports)
BLOOD URINE PRESENT ( 42 FDA reports)
CARDIAC MURMUR ( 42 FDA reports)
DYSGEUSIA ( 42 FDA reports)
NEOPLASM MALIGNANT ( 42 FDA reports)
PRODUCT QUALITY ISSUE ( 42 FDA reports)
TOOTH ABSCESS ( 42 FDA reports)
ARTERIOSCLEROSIS ( 41 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 41 FDA reports)
GINGIVITIS ( 41 FDA reports)
HYPONATRAEMIA ( 41 FDA reports)
ORAL PAIN ( 41 FDA reports)
PREMATURE BABY ( 41 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 40 FDA reports)
GASTROINTESTINAL DISORDER ( 40 FDA reports)
MASTICATION DISORDER ( 40 FDA reports)
PULMONARY HYPERTENSION ( 40 FDA reports)
RENAL DISORDER ( 40 FDA reports)
RESTLESSNESS ( 40 FDA reports)
ARTHROPATHY ( 39 FDA reports)
BONE MARROW FAILURE ( 39 FDA reports)
CORONARY ARTERY DISEASE ( 39 FDA reports)
DIVERTICULUM ( 39 FDA reports)
GINGIVAL SWELLING ( 39 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 39 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 39 FDA reports)
PERICARDIAL EFFUSION ( 39 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 39 FDA reports)
RECTAL HAEMORRHAGE ( 39 FDA reports)
STOMATITIS ( 39 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 38 FDA reports)
GLAUCOMA ( 38 FDA reports)
NASAL CONGESTION ( 38 FDA reports)
ABNORMAL BEHAVIOUR ( 37 FDA reports)
ANAL FISTULA ( 37 FDA reports)
BACTERIAL INFECTION ( 37 FDA reports)
CIRCULATORY COLLAPSE ( 37 FDA reports)
COMA ( 37 FDA reports)
EATING DISORDER ( 37 FDA reports)
INJECTION SITE ERYTHEMA ( 37 FDA reports)
LEUKOPENIA ( 37 FDA reports)
PERITONITIS ( 37 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 37 FDA reports)
VAGINAL HAEMORRHAGE ( 37 FDA reports)
BONE DEBRIDEMENT ( 36 FDA reports)
CARDIOMYOPATHY ( 36 FDA reports)
CEREBRAL ATROPHY ( 36 FDA reports)
CHROMATURIA ( 36 FDA reports)
DEPRESSED MOOD ( 36 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 36 FDA reports)
ECZEMA ( 36 FDA reports)
MOUTH ULCERATION ( 36 FDA reports)
OSTEITIS ( 36 FDA reports)
OSTEOPENIA ( 36 FDA reports)
PURULENT DISCHARGE ( 36 FDA reports)
SLEEP DISORDER ( 36 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 36 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 35 FDA reports)
ADVERSE EVENT ( 35 FDA reports)
ANGINA PECTORIS ( 35 FDA reports)
ANOREXIA ( 35 FDA reports)
DYSPHONIA ( 35 FDA reports)
FACIAL PAIN ( 35 FDA reports)
GASTROENTERITIS ( 35 FDA reports)
GOUT ( 35 FDA reports)
JOINT EFFUSION ( 35 FDA reports)
OSTEOLYSIS ( 35 FDA reports)
PROCEDURAL PAIN ( 35 FDA reports)
SINUS DISORDER ( 35 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 35 FDA reports)
WHEEZING ( 35 FDA reports)
ABDOMINAL PAIN LOWER ( 34 FDA reports)
CAESAREAN SECTION ( 34 FDA reports)
CEREBRAL INFARCTION ( 34 FDA reports)
COMPRESSION FRACTURE ( 34 FDA reports)
DISORIENTATION ( 34 FDA reports)
EAR PAIN ( 34 FDA reports)
INTESTINAL OBSTRUCTION ( 34 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 34 FDA reports)
MUCOSAL INFLAMMATION ( 34 FDA reports)
SKIN DISORDER ( 34 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 34 FDA reports)
TREATMENT NONCOMPLIANCE ( 34 FDA reports)
URINARY RETENTION ( 34 FDA reports)
CEREBRAL HAEMORRHAGE ( 33 FDA reports)
CYST ( 33 FDA reports)
DRUG TOXICITY ( 33 FDA reports)
DRY MOUTH ( 33 FDA reports)
DYSARTHRIA ( 33 FDA reports)
EAR INFECTION ( 33 FDA reports)
JAW DISORDER ( 33 FDA reports)
KIDNEY INFECTION ( 33 FDA reports)
METABOLIC ACIDOSIS ( 33 FDA reports)
OPEN WOUND ( 33 FDA reports)
PULMONARY HAEMORRHAGE ( 33 FDA reports)
UNEVALUABLE EVENT ( 33 FDA reports)
VIRAL INFECTION ( 33 FDA reports)
ASCITES ( 32 FDA reports)
DECUBITUS ULCER ( 32 FDA reports)
GINGIVAL DISORDER ( 32 FDA reports)
HYPOTHYROIDISM ( 32 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 32 FDA reports)
MALNUTRITION ( 32 FDA reports)
MOVEMENT DISORDER ( 32 FDA reports)
NEUTROPHIL COUNT INCREASED ( 32 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 32 FDA reports)
VISUAL ACUITY REDUCED ( 32 FDA reports)
ABNORMAL DREAMS ( 31 FDA reports)
ABORTION SPONTANEOUS ( 31 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 31 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 31 FDA reports)
BLOOD GLUCOSE DECREASED ( 31 FDA reports)
BLOOD UREA INCREASED ( 31 FDA reports)
DIVERTICULITIS ( 31 FDA reports)
FEELING HOT ( 31 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 31 FDA reports)
PNEUMONIA ASPIRATION ( 31 FDA reports)
PNEUMOTHORAX ( 31 FDA reports)
POST PROCEDURAL COMPLICATION ( 31 FDA reports)
SKIN ULCER ( 31 FDA reports)
SPINAL COLUMN STENOSIS ( 31 FDA reports)
STEVENS-JOHNSON SYNDROME ( 31 FDA reports)
TENDERNESS ( 31 FDA reports)
AORTIC ANEURYSM ( 30 FDA reports)
ENCEPHALOPATHY ( 30 FDA reports)
FLUID RETENTION ( 30 FDA reports)
INCORRECT DOSE ADMINISTERED ( 30 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 30 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 30 FDA reports)
PREGNANCY ( 30 FDA reports)
RASH GENERALISED ( 30 FDA reports)
SKIN HYPERTROPHY ( 30 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 29 FDA reports)
BRAIN OEDEMA ( 29 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 29 FDA reports)
FEELING COLD ( 29 FDA reports)
HEAD INJURY ( 29 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 29 FDA reports)
HYDRONEPHROSIS ( 29 FDA reports)
INJECTION SITE HAEMATOMA ( 29 FDA reports)
LARGE INTESTINE PERFORATION ( 29 FDA reports)
LARYNGITIS ( 29 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 29 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 29 FDA reports)
ORAL DISORDER ( 29 FDA reports)
PALLOR ( 29 FDA reports)
PANIC ATTACK ( 29 FDA reports)
PELVIC PAIN ( 29 FDA reports)
RASH MACULAR ( 29 FDA reports)
TENDONITIS ( 29 FDA reports)
VENTRICULAR TACHYCARDIA ( 29 FDA reports)
ANGIOEDEMA ( 28 FDA reports)
BILE DUCT STONE ( 28 FDA reports)
CAROTID ARTERY STENOSIS ( 28 FDA reports)
DELIRIUM ( 28 FDA reports)
DENTAL CARIES ( 28 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 28 FDA reports)
GASTRIC DISORDER ( 28 FDA reports)
HAEMATOCRIT DECREASED ( 28 FDA reports)
ILEUS ( 28 FDA reports)
LUMBAR RADICULOPATHY ( 28 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 28 FDA reports)
OSTEOPOROSIS ( 28 FDA reports)
PHARYNGITIS ( 28 FDA reports)
PYELONEPHRITIS ( 28 FDA reports)
ROAD TRAFFIC ACCIDENT ( 28 FDA reports)
SKIN EXFOLIATION ( 28 FDA reports)
SLEEP APNOEA SYNDROME ( 28 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 27 FDA reports)
BACTERAEMIA ( 27 FDA reports)
CONJUNCTIVITIS ( 27 FDA reports)
DEBRIDEMENT ( 27 FDA reports)
EYE PAIN ( 27 FDA reports)
GASTRIC ULCER ( 27 FDA reports)
HYPERKALAEMIA ( 27 FDA reports)
HYPOGLYCAEMIA ( 27 FDA reports)
LUNG INFECTION ( 27 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 27 FDA reports)
NERVOUSNESS ( 27 FDA reports)
ORAL INFECTION ( 27 FDA reports)
PANCREATITIS ACUTE ( 27 FDA reports)
PARANOIA ( 27 FDA reports)
RIB FRACTURE ( 27 FDA reports)
SCIATICA ( 27 FDA reports)
SEQUESTRECTOMY ( 27 FDA reports)
SICK SINUS SYNDROME ( 27 FDA reports)
SKIN TIGHTNESS ( 27 FDA reports)
WOUND ( 27 FDA reports)
ABSCESS JAW ( 26 FDA reports)
ANAL ABSCESS ( 26 FDA reports)
BODY TEMPERATURE INCREASED ( 26 FDA reports)
DRUG ADMINISTRATION ERROR ( 26 FDA reports)
ECONOMIC PROBLEM ( 26 FDA reports)
EMOTIONAL DISORDER ( 26 FDA reports)
EMPHYSEMA ( 26 FDA reports)
HYPERCHOLESTEROLAEMIA ( 26 FDA reports)
OEDEMA MOUTH ( 26 FDA reports)
OESOPHAGEAL DISORDER ( 26 FDA reports)
OTITIS MEDIA ( 26 FDA reports)
RENAL CYST ( 26 FDA reports)
RHABDOMYOLYSIS ( 26 FDA reports)
RHINITIS ( 26 FDA reports)
SKIN INDURATION ( 26 FDA reports)
AMENORRHOEA ( 25 FDA reports)
DISTURBANCE IN ATTENTION ( 25 FDA reports)
DYSKINESIA ( 25 FDA reports)
EXPOSED BONE IN JAW ( 25 FDA reports)
GINGIVAL INFECTION ( 25 FDA reports)
GRAFT VERSUS HOST DISEASE ( 25 FDA reports)
GROIN PAIN ( 25 FDA reports)
HEART RATE DECREASED ( 25 FDA reports)
HYPOCALCAEMIA ( 25 FDA reports)
ILL-DEFINED DISORDER ( 25 FDA reports)
IRRITABILITY ( 25 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 25 FDA reports)
LIMB INJURY ( 25 FDA reports)
NIGHT SWEATS ( 25 FDA reports)
ORGAN FAILURE ( 25 FDA reports)
PSEUDOMONAS INFECTION ( 25 FDA reports)
PSORIASIS ( 25 FDA reports)
PURULENCE ( 25 FDA reports)
RESPIRATORY ARREST ( 25 FDA reports)
SEDATION ( 25 FDA reports)
SENSORY DISTURBANCE ( 25 FDA reports)
SERRATIA INFECTION ( 25 FDA reports)
TACHYPNOEA ( 25 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 24 FDA reports)
ACUTE RESPIRATORY FAILURE ( 24 FDA reports)
APHAGIA ( 24 FDA reports)
BACK DISORDER ( 24 FDA reports)
CHOLESTASIS ( 24 FDA reports)
CHRONIC SINUSITIS ( 24 FDA reports)
COLON CANCER ( 24 FDA reports)
DENTURE WEARER ( 24 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 24 FDA reports)
HOSPITALISATION ( 24 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 24 FDA reports)
LIMB DISCOMFORT ( 24 FDA reports)
MECHANICAL VENTILATION ( 24 FDA reports)
MENORRHAGIA ( 24 FDA reports)
PATHOLOGICAL FRACTURE ( 24 FDA reports)
PEPTIC ULCER ( 24 FDA reports)
RETCHING ( 24 FDA reports)
ROTATOR CUFF SYNDROME ( 24 FDA reports)
SPINAL DISORDER ( 24 FDA reports)
SPINAL FRACTURE ( 24 FDA reports)
ACNE ( 23 FDA reports)
BONE FRAGMENTATION ( 23 FDA reports)
CHOLESTEROSIS ( 23 FDA reports)
DERMATITIS ( 23 FDA reports)
DILATATION VENTRICULAR ( 23 FDA reports)
DIPLOPIA ( 23 FDA reports)
ENDODONTIC PROCEDURE ( 23 FDA reports)
GINGIVAL PAIN ( 23 FDA reports)
GLOSSODYNIA ( 23 FDA reports)
HAEMOPTYSIS ( 23 FDA reports)
HEMIPARESIS ( 23 FDA reports)
INTENTIONAL DRUG MISUSE ( 23 FDA reports)
LOCAL SWELLING ( 23 FDA reports)
MYELODYSPLASTIC SYNDROME ( 23 FDA reports)
PHYSICAL DISABILITY ( 23 FDA reports)
PIGMENTATION DISORDER ( 23 FDA reports)
PREMATURE LABOUR ( 23 FDA reports)
PRODUCTIVE COUGH ( 23 FDA reports)
PRURITUS GENERALISED ( 23 FDA reports)
RASH PRURITIC ( 23 FDA reports)
SWOLLEN TONGUE ( 23 FDA reports)
ABDOMINAL ABSCESS ( 22 FDA reports)
ANAPHYLACTIC REACTION ( 22 FDA reports)
APPENDICITIS ( 22 FDA reports)
ASPERGILLOSIS ( 22 FDA reports)
BLOOD SODIUM DECREASED ( 22 FDA reports)
CYANOSIS ( 22 FDA reports)
DIALYSIS ( 22 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 22 FDA reports)
DRY EYE ( 22 FDA reports)
FACE OEDEMA ( 22 FDA reports)
GYNAECOMASTIA ( 22 FDA reports)
HYPOTONIA ( 22 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 22 FDA reports)
MEAN CELL VOLUME DECREASED ( 22 FDA reports)
METRORRHAGIA ( 22 FDA reports)
NIGHTMARE ( 22 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 22 FDA reports)
RESPIRATORY TRACT INFECTION ( 22 FDA reports)
SINUS TACHYCARDIA ( 22 FDA reports)
SUICIDAL IDEATION ( 22 FDA reports)
ULCER ( 22 FDA reports)
URINE OUTPUT DECREASED ( 22 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 22 FDA reports)
WOUND DEHISCENCE ( 22 FDA reports)
ABSCESS INTESTINAL ( 21 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 21 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 21 FDA reports)
DEVELOPMENTAL DELAY ( 21 FDA reports)
DYSSTASIA ( 21 FDA reports)
EJECTION FRACTION DECREASED ( 21 FDA reports)
ESCHERICHIA INFECTION ( 21 FDA reports)
FIBROMYALGIA ( 21 FDA reports)
HAEMATEMESIS ( 21 FDA reports)
HAEMORRHOIDS ( 21 FDA reports)
HEPATIC STEATOSIS ( 21 FDA reports)
INJECTION SITE REACTION ( 21 FDA reports)
LEFT ATRIAL DILATATION ( 21 FDA reports)
MITRAL VALVE CALCIFICATION ( 21 FDA reports)
PELVIC FRACTURE ( 21 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 21 FDA reports)
RHEUMATOID ARTHRITIS ( 21 FDA reports)
RHINORRHOEA ( 21 FDA reports)
SKIN WARM ( 21 FDA reports)
SOFT TISSUE DISORDER ( 21 FDA reports)
BONE LESION ( 20 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 20 FDA reports)
COLITIS ULCERATIVE ( 20 FDA reports)
COLON ADENOMA ( 20 FDA reports)
ENTEROCOCCAL INFECTION ( 20 FDA reports)
FEEDING DISORDER NEONATAL ( 20 FDA reports)
HAEMATOMA ( 20 FDA reports)
HYPOVOLAEMIA ( 20 FDA reports)
INTESTINAL PERFORATION ( 20 FDA reports)
JOINT INJURY ( 20 FDA reports)
LUMBAR SPINE FLATTENING ( 20 FDA reports)
MELANOCYTIC NAEVUS ( 20 FDA reports)
NECROSIS ( 20 FDA reports)
NEURALGIA ( 20 FDA reports)
PNEUMONITIS ( 20 FDA reports)
POOR QUALITY SLEEP ( 20 FDA reports)
PRESYNCOPE ( 20 FDA reports)
PSYCHOTIC DISORDER ( 20 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 20 FDA reports)
SPLENOMEGALY ( 20 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 20 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 19 FDA reports)
BRUXISM ( 19 FDA reports)
DISABILITY ( 19 FDA reports)
INJECTION SITE HAEMORRHAGE ( 19 FDA reports)
INJECTION SITE SWELLING ( 19 FDA reports)
INTRACRANIAL ANEURYSM ( 19 FDA reports)
KYPHOSIS ( 19 FDA reports)
LACRIMATION INCREASED ( 19 FDA reports)
MELAENA ( 19 FDA reports)
MENINGITIS ( 19 FDA reports)
METASTASES TO SPINE ( 19 FDA reports)
MOUTH HAEMORRHAGE ( 19 FDA reports)
NERVOUS SYSTEM DISORDER ( 19 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 19 FDA reports)
OVARIAN CYST ( 19 FDA reports)
PARAESTHESIA ORAL ( 19 FDA reports)
RENAL INJURY ( 19 FDA reports)
RESPIRATORY DISORDER ( 19 FDA reports)
SINUS OPERATION ( 19 FDA reports)
THIRST ( 19 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 19 FDA reports)
VASCULAR CALCIFICATION ( 19 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 18 FDA reports)
AFFECTIVE DISORDER ( 18 FDA reports)
BLOOD POTASSIUM DECREASED ( 18 FDA reports)
BONE NEOPLASM MALIGNANT ( 18 FDA reports)
BREAST CANCER ( 18 FDA reports)
CEREBRAL ISCHAEMIA ( 18 FDA reports)
DEVICE MALFUNCTION ( 18 FDA reports)
EAR DISORDER ( 18 FDA reports)
HAEMODYNAMIC INSTABILITY ( 18 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 18 FDA reports)
HYPERLIPIDAEMIA ( 18 FDA reports)
HYPOACUSIS ( 18 FDA reports)
ILEAL STENOSIS ( 18 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 18 FDA reports)
MENTAL IMPAIRMENT ( 18 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 18 FDA reports)
NO THERAPEUTIC RESPONSE ( 18 FDA reports)
PHLEBITIS ( 18 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 18 FDA reports)
PROCEDURAL COMPLICATION ( 18 FDA reports)
PROCTALGIA ( 18 FDA reports)
PULMONARY INFARCTION ( 18 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 18 FDA reports)
THROAT TIGHTNESS ( 18 FDA reports)
TIC ( 18 FDA reports)
TINEA PEDIS ( 18 FDA reports)
TONGUE DISCOLOURATION ( 18 FDA reports)
UPPER LIMB FRACTURE ( 18 FDA reports)
WOUND INFECTION ( 18 FDA reports)
ABDOMINAL TENDERNESS ( 17 FDA reports)
ACCIDENTAL OVERDOSE ( 17 FDA reports)
AGGRESSION ( 17 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 17 FDA reports)
CARDIAC PACEMAKER INSERTION ( 17 FDA reports)
CHOLANGITIS ( 17 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 17 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 17 FDA reports)
DILATATION ATRIAL ( 17 FDA reports)
ELECTROLYTE IMBALANCE ( 17 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 17 FDA reports)
HAEMODIALYSIS ( 17 FDA reports)
HIATUS HERNIA ( 17 FDA reports)
INTESTINAL ISCHAEMIA ( 17 FDA reports)
IRRITABLE BOWEL SYNDROME ( 17 FDA reports)
LUMBAR SPINAL STENOSIS ( 17 FDA reports)
MACROGLOSSIA ( 17 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 17 FDA reports)
MENSTRUATION IRREGULAR ( 17 FDA reports)
METASTASES TO MENINGES ( 17 FDA reports)
ORAL CANDIDIASIS ( 17 FDA reports)
PARALYSIS ( 17 FDA reports)
PERIODONTAL DISEASE ( 17 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 17 FDA reports)
PRIMARY SEQUESTRUM ( 17 FDA reports)
RESPIRATORY RATE INCREASED ( 17 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 17 FDA reports)
SYNOVIAL CYST ( 17 FDA reports)
SYNOVITIS ( 17 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 17 FDA reports)
ACIDOSIS ( 16 FDA reports)
ALLERGIC COLITIS ( 16 FDA reports)
APHONIA ( 16 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 16 FDA reports)
AUTISM SPECTRUM DISORDER ( 16 FDA reports)
BLINDNESS ( 16 FDA reports)
BLOOD CALCIUM DECREASED ( 16 FDA reports)
BLOOD POTASSIUM INCREASED ( 16 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 16 FDA reports)
BRAIN INJURY ( 16 FDA reports)
BRONCHOSPASM ( 16 FDA reports)
COLD SWEAT ( 16 FDA reports)
COLLAPSE OF LUNG ( 16 FDA reports)
DEAFNESS NEUROSENSORY ( 16 FDA reports)
DISEASE RECURRENCE ( 16 FDA reports)
DRUG EFFECT DECREASED ( 16 FDA reports)
DYSTONIA ( 16 FDA reports)
FAILURE TO THRIVE ( 16 FDA reports)
FEMUR FRACTURE ( 16 FDA reports)
FUNGAL SEPSIS ( 16 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 16 FDA reports)
GASTROENTERITIS VIRAL ( 16 FDA reports)
HYPOAESTHESIA ORAL ( 16 FDA reports)
ISCHAEMIA ( 16 FDA reports)
JAW FRACTURE ( 16 FDA reports)
LOOSE TOOTH ( 16 FDA reports)
MOOD SWINGS ( 16 FDA reports)
MULTIPLE MYELOMA ( 16 FDA reports)
MUSCLE TIGHTNESS ( 16 FDA reports)
NEOPLASM PROGRESSION ( 16 FDA reports)
NOCTURIA ( 16 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 16 FDA reports)
PHOTOPHOBIA ( 16 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 16 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 16 FDA reports)
PROTEIN URINE PRESENT ( 16 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 16 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 16 FDA reports)
VENTRICULAR FIBRILLATION ( 16 FDA reports)
WOUND SECRETION ( 16 FDA reports)
ABDOMINAL INFECTION ( 15 FDA reports)
AGEUSIA ( 15 FDA reports)
APNOEA ( 15 FDA reports)
AUTISM ( 15 FDA reports)
BIRTH TRAUMA ( 15 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 15 FDA reports)
CACHEXIA ( 15 FDA reports)
CHARLES BONNET SYNDROME ( 15 FDA reports)
DENTAL FISTULA ( 15 FDA reports)
DIVERTICULUM INTESTINAL ( 15 FDA reports)
DRUG PRESCRIBING ERROR ( 15 FDA reports)
EAR NEOPLASM ( 15 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 15 FDA reports)
ENTHESOPATHY ( 15 FDA reports)
EXTRASYSTOLES ( 15 FDA reports)
GANGRENE ( 15 FDA reports)
GINGIVAL ULCERATION ( 15 FDA reports)
GRAND MAL CONVULSION ( 15 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 15 FDA reports)
HALLUCINATION, VISUAL ( 15 FDA reports)
HERNIA ( 15 FDA reports)
HIP FRACTURE ( 15 FDA reports)
HYPOTHERMIA NEONATAL ( 15 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 15 FDA reports)
KLEBSIELLA INFECTION ( 15 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 15 FDA reports)
PERIODONTITIS ( 15 FDA reports)
PERIPHERAL COLDNESS ( 15 FDA reports)
PERONEAL NERVE PALSY ( 15 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 15 FDA reports)
PULSE ABSENT ( 15 FDA reports)
RESPIRATORY DEPRESSION ( 15 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 15 FDA reports)
SINUS BRADYCARDIA ( 15 FDA reports)
SKIN LESION ( 15 FDA reports)
SKIN NODULE ( 15 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 15 FDA reports)
THYROID DISORDER ( 15 FDA reports)
VARICOSE VEIN ( 15 FDA reports)
ABORTION INDUCED ( 14 FDA reports)
ADVERSE DRUG REACTION ( 14 FDA reports)
AGRANULOCYTOSIS ( 14 FDA reports)
APHTHOUS STOMATITIS ( 14 FDA reports)
BLINDNESS UNILATERAL ( 14 FDA reports)
BLOOD DISORDER ( 14 FDA reports)
BONE EROSION ( 14 FDA reports)
BRONCHOPNEUMONIA ( 14 FDA reports)
CEREBRAL THROMBOSIS ( 14 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 14 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 14 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 14 FDA reports)
EXOSTOSIS ( 14 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 14 FDA reports)
FIBROMA ( 14 FDA reports)
FIBROSIS ( 14 FDA reports)
GINGIVAL BLEEDING ( 14 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 14 FDA reports)
HYPOMAGNESAEMIA ( 14 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 14 FDA reports)
INCONTINENCE ( 14 FDA reports)
INFUSION RELATED REACTION ( 14 FDA reports)
INJECTION SITE MASS ( 14 FDA reports)
JAW OPERATION ( 14 FDA reports)
MEDICATION ERROR ( 14 FDA reports)
MUSCLE RIGIDITY ( 14 FDA reports)
MYOCARDIAL ISCHAEMIA ( 14 FDA reports)
OESOPHAGITIS ( 14 FDA reports)
OSTEORADIONECROSIS ( 14 FDA reports)
PANIC DISORDER ( 14 FDA reports)
PERICARDITIS ( 14 FDA reports)
PROSTATE CANCER METASTATIC ( 14 FDA reports)
QUALITY OF LIFE DECREASED ( 14 FDA reports)
RENAL TUBULAR NECROSIS ( 14 FDA reports)
RESTLESS LEGS SYNDROME ( 14 FDA reports)
SKIN INFECTION ( 14 FDA reports)
SPINAL COMPRESSION FRACTURE ( 14 FDA reports)
TARDIVE DYSKINESIA ( 14 FDA reports)
TENSION ( 14 FDA reports)
THERAPY NON-RESPONDER ( 14 FDA reports)
TYPE 2 DIABETES MELLITUS ( 14 FDA reports)
VASCULITIS ( 14 FDA reports)
WOUND COMPLICATION ( 14 FDA reports)
WOUND DRAINAGE ( 14 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 13 FDA reports)
AORTIC VALVE INCOMPETENCE ( 13 FDA reports)
ATRIAL SEPTAL DEFECT ( 13 FDA reports)
AZOTAEMIA ( 13 FDA reports)
BACTERIAL DISEASE CARRIER ( 13 FDA reports)
BONE MARROW TRANSPLANT ( 13 FDA reports)
BREAST MASS ( 13 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 13 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 13 FDA reports)
CONGENITAL KNEE DEFORMITY ( 13 FDA reports)
CORONARY ARTERY BYPASS ( 13 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 13 FDA reports)
ENDOTRACHEAL INTUBATION ( 13 FDA reports)
ERECTILE DYSFUNCTION ( 13 FDA reports)
FLUID OVERLOAD ( 13 FDA reports)
HEPATOTOXICITY ( 13 FDA reports)
IMPULSIVE BEHAVIOUR ( 13 FDA reports)
INTENTIONAL OVERDOSE ( 13 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 13 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 13 FDA reports)
LYMPH GLAND INFECTION ( 13 FDA reports)
MALIGNANT MELANOMA ( 13 FDA reports)
MIDDLE INSOMNIA ( 13 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 13 FDA reports)
NEUROTOXICITY ( 13 FDA reports)
OBESITY ( 13 FDA reports)
OLIGURIA ( 13 FDA reports)
ORAL SURGERY ( 13 FDA reports)
ORTHOSTATIC HYPOTENSION ( 13 FDA reports)
OSTEOCHONDROSIS ( 13 FDA reports)
PHOTOSENSITIVITY REACTION ( 13 FDA reports)
PLATELET COUNT INCREASED ( 13 FDA reports)
PLEURISY ( 13 FDA reports)
POLYMYALGIA RHEUMATICA ( 13 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 13 FDA reports)
PSYCHOLOGICAL TRAUMA ( 13 FDA reports)
PULMONARY CALCIFICATION ( 13 FDA reports)
PULMONARY CONGESTION ( 13 FDA reports)
PULMONARY FIBROSIS ( 13 FDA reports)
PULMONARY GRANULOMA ( 13 FDA reports)
PULMONARY TOXICITY ( 13 FDA reports)
RASH ERYTHEMATOUS ( 13 FDA reports)
RASH PUSTULAR ( 13 FDA reports)
RESPIRATORY TRACT CONGESTION ( 13 FDA reports)
SKIN HYPERPIGMENTATION ( 13 FDA reports)
SQUAMOUS CELL CARCINOMA ( 13 FDA reports)
STATUS EPILEPTICUS ( 13 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 13 FDA reports)
TUMOUR LYSIS SYNDROME ( 13 FDA reports)
UNINTENDED PREGNANCY ( 13 FDA reports)
VAGINAL DISCHARGE ( 13 FDA reports)
VARICELLA ( 13 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 13 FDA reports)
WALKING AID USER ( 13 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 13 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 12 FDA reports)
ADJUSTMENT DISORDER ( 12 FDA reports)
ANAPHYLACTIC SHOCK ( 12 FDA reports)
AORTIC STENOSIS ( 12 FDA reports)
ASPIRATION ( 12 FDA reports)
ATRIAL FLUTTER ( 12 FDA reports)
BACTERIAL TEST ( 12 FDA reports)
BLADDER DISORDER ( 12 FDA reports)
BONE DENSITY DECREASED ( 12 FDA reports)
BREAST TENDERNESS ( 12 FDA reports)
CARDIOVASCULAR DISORDER ( 12 FDA reports)
CHOKING ( 12 FDA reports)
CRYING ( 12 FDA reports)
DIZZINESS POSTURAL ( 12 FDA reports)
DRUG DEPENDENCE ( 12 FDA reports)
EYE SWELLING ( 12 FDA reports)
GALLBLADDER ENLARGEMENT ( 12 FDA reports)
HEPATIC ENCEPHALOPATHY ( 12 FDA reports)
HODGKIN'S DISEASE ( 12 FDA reports)
HYPERKERATOSIS ( 12 FDA reports)
HYPOALBUMINAEMIA ( 12 FDA reports)
HYPOKINESIA ( 12 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 12 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 12 FDA reports)
INJECTION SITE NECROSIS ( 12 FDA reports)
LOWER LIMB FRACTURE ( 12 FDA reports)
LYMPHOEDEMA ( 12 FDA reports)
MULTIPLE INJURIES ( 12 FDA reports)
NO ADVERSE EVENT ( 12 FDA reports)
ONYCHOMYCOSIS ( 12 FDA reports)
OSTEOMYELITIS CHRONIC ( 12 FDA reports)
OVARIAN MASS ( 12 FDA reports)
PAIN OF SKIN ( 12 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 12 FDA reports)
PERIRECTAL ABSCESS ( 12 FDA reports)
PERITONITIS BACTERIAL ( 12 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 12 FDA reports)
POLYNEUROPATHY ( 12 FDA reports)
POLYP ( 12 FDA reports)
PORTAL VEIN THROMBOSIS ( 12 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 12 FDA reports)
REACTIVE PSYCHOSIS ( 12 FDA reports)
SECRETION DISCHARGE ( 12 FDA reports)
SERUM FERRITIN INCREASED ( 12 FDA reports)
SKIN LACERATION ( 12 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 12 FDA reports)
SUBCUTANEOUS NODULE ( 12 FDA reports)
THROAT IRRITATION ( 12 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 12 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 12 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 12 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 12 FDA reports)
YELLOW SKIN ( 12 FDA reports)
ACTINOMYCOSIS ( 11 FDA reports)
ANGER ( 11 FDA reports)
ANOXIC ENCEPHALOPATHY ( 11 FDA reports)
ANURIA ( 11 FDA reports)
APPENDICECTOMY ( 11 FDA reports)
ARTERIAL DISORDER ( 11 FDA reports)
ARTHRITIS BACTERIAL ( 11 FDA reports)
BILIARY DILATATION ( 11 FDA reports)
BLEPHARITIS ( 11 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 11 FDA reports)
BONE OPERATION ( 11 FDA reports)
BRAIN ABSCESS ( 11 FDA reports)
BREATH ODOUR ( 11 FDA reports)
BREATH SOUNDS ABNORMAL ( 11 FDA reports)
CARDIOPULMONARY FAILURE ( 11 FDA reports)
COLECTOMY ( 11 FDA reports)
COLITIS ISCHAEMIC ( 11 FDA reports)
COMPLETED SUICIDE ( 11 FDA reports)
CORONARY ARTERY OCCLUSION ( 11 FDA reports)
DEVICE EXPULSION ( 11 FDA reports)
DEVICE FAILURE ( 11 FDA reports)
DRUG ERUPTION ( 11 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 11 FDA reports)
DYSLIPIDAEMIA ( 11 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 11 FDA reports)
ENCEPHALITIS ( 11 FDA reports)
EPILEPSY ( 11 FDA reports)
ERYTHEMA MULTIFORME ( 11 FDA reports)
FISTULA REPAIR ( 11 FDA reports)
FOOD INTOLERANCE ( 11 FDA reports)
GALLBLADDER PAIN ( 11 FDA reports)
GINGIVAL EROSION ( 11 FDA reports)
HYPERBILIRUBINAEMIA ( 11 FDA reports)
INJECTION SITE ABSCESS ( 11 FDA reports)
LIPOMA ( 11 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 11 FDA reports)
MULTIPLE SCLEROSIS ( 11 FDA reports)
NEPHROPATHY ( 11 FDA reports)
OCULAR HYPERAEMIA ( 11 FDA reports)
PANIC REACTION ( 11 FDA reports)
PLEURITIC PAIN ( 11 FDA reports)
PNEUMONIA BACTERIAL ( 11 FDA reports)
POSTOPERATIVE ILEUS ( 11 FDA reports)
PROTEINURIA ( 11 FDA reports)
PROTHROMBIN TIME PROLONGED ( 11 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 11 FDA reports)
PYELOCALIECTASIS ( 11 FDA reports)
RALES ( 11 FDA reports)
RASH MACULO-PAPULAR ( 11 FDA reports)
RECTAL ABSCESS ( 11 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 11 FDA reports)
SKELETAL INJURY ( 11 FDA reports)
SKIN INJURY ( 11 FDA reports)
SPONDYLOLISTHESIS ( 11 FDA reports)
STREPTOCOCCAL INFECTION ( 11 FDA reports)
SUICIDE ATTEMPT ( 11 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 11 FDA reports)
VISUAL DISTURBANCE ( 11 FDA reports)
WITHDRAWAL SYNDROME ( 11 FDA reports)
ACCIDENTAL EXPOSURE ( 10 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 10 FDA reports)
AKINESIA ( 10 FDA reports)
APATHY ( 10 FDA reports)
BEDRIDDEN ( 10 FDA reports)
BLOOD CALCIUM INCREASED ( 10 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 10 FDA reports)
BLOOD TEST ABNORMAL ( 10 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 10 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 10 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 10 FDA reports)
DENTAL OPERATION ( 10 FDA reports)
DRUG LEVEL INCREASED ( 10 FDA reports)
DRUG SCREEN POSITIVE ( 10 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 10 FDA reports)
FURUNCLE ( 10 FDA reports)
HAEMANGIOMA OF LIVER ( 10 FDA reports)
HAEMOLYSIS ( 10 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 10 FDA reports)
HAEMORRHAGIC ANAEMIA ( 10 FDA reports)
HEPATOMEGALY ( 10 FDA reports)
HYDROCEPHALUS ( 10 FDA reports)
HYPERNATRAEMIA ( 10 FDA reports)
IMMUNE SYSTEM DISORDER ( 10 FDA reports)
INJECTION SITE DISCOLOURATION ( 10 FDA reports)
INTESTINAL STENOSIS ( 10 FDA reports)
LACERATION ( 10 FDA reports)
LOBAR PNEUMONIA ( 10 FDA reports)
LYMPHOMA ( 10 FDA reports)
MUSCLE ATROPHY ( 10 FDA reports)
MYELOID LEUKAEMIA ( 10 FDA reports)
PANCREATITIS NECROTISING ( 10 FDA reports)
PAROSMIA ( 10 FDA reports)
PAROTID GLAND ENLARGEMENT ( 10 FDA reports)
PLATELET DISORDER ( 10 FDA reports)
POST THROMBOTIC SYNDROME ( 10 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 10 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 10 FDA reports)
RIGHT ATRIAL DILATATION ( 10 FDA reports)
SCREAMING ( 10 FDA reports)
SENSORY LOSS ( 10 FDA reports)
SEROTONIN SYNDROME ( 10 FDA reports)
SKIN ODOUR ABNORMAL ( 10 FDA reports)
SKIN REACTION ( 10 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 10 FDA reports)
TRANSAMINASES INCREASED ( 10 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 10 FDA reports)
VAGINAL INFECTION ( 10 FDA reports)
VENA CAVA FILTER INSERTION ( 10 FDA reports)
ABDOMINAL ADHESIONS ( 9 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 9 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 9 FDA reports)
ADRENAL INSUFFICIENCY ( 9 FDA reports)
APPENDICITIS PERFORATED ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK ( 9 FDA reports)
B-CELL LYMPHOMA ( 9 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 9 FDA reports)
BONE CYST ( 9 FDA reports)
BRONCHIECTASIS ( 9 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 9 FDA reports)
CHOLECYSTITIS INFECTIVE ( 9 FDA reports)
COLONIC POLYP ( 9 FDA reports)
COLONIC STENOSIS ( 9 FDA reports)
CUSHINGOID ( 9 FDA reports)
DENTAL IMPRESSION PROCEDURE ( 9 FDA reports)
DERMATITIS BULLOUS ( 9 FDA reports)
DERMATITIS EXFOLIATIVE ( 9 FDA reports)
DEVICE BREAKAGE ( 9 FDA reports)
DIABETIC NEPHROPATHY ( 9 FDA reports)
DRUG ABUSER ( 9 FDA reports)
DYSPLASIA ( 9 FDA reports)
ECCHYMOSIS ( 9 FDA reports)
ENCEPHALITIS FUNGAL ( 9 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 9 FDA reports)
EYE IRRITATION ( 9 FDA reports)
FOOT FRACTURE ( 9 FDA reports)
GENITAL HAEMORRHAGE ( 9 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 9 FDA reports)
HALLUCINATION, AUDITORY ( 9 FDA reports)
HEMIANOPIA ( 9 FDA reports)
HEPATIC NECROSIS ( 9 FDA reports)
HERPES SIMPLEX ( 9 FDA reports)
HIP SURGERY ( 9 FDA reports)
HUNGER ( 9 FDA reports)
HYPERAESTHESIA ( 9 FDA reports)
HYPERTHERMIA ( 9 FDA reports)
HYSTERECTOMY ( 9 FDA reports)
ILEUS PARALYTIC ( 9 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 9 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 9 FDA reports)
JOINT DISLOCATION ( 9 FDA reports)
JOINT INSTABILITY ( 9 FDA reports)
LABORATORY TEST ABNORMAL ( 9 FDA reports)
LABYRINTHITIS ( 9 FDA reports)
LIP SWELLING ( 9 FDA reports)
LIVER INJURY ( 9 FDA reports)
MACULAR OEDEMA ( 9 FDA reports)
MEDICAL DEVICE COMPLICATION ( 9 FDA reports)
METABOLIC ENCEPHALOPATHY ( 9 FDA reports)
MICTURITION URGENCY ( 9 FDA reports)
MULTIPLE DRUG OVERDOSE ( 9 FDA reports)
MUSCLE SWELLING ( 9 FDA reports)
MYOSITIS ( 9 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 9 FDA reports)
NEUTROPENIC SEPSIS ( 9 FDA reports)
OCULAR ICTERUS ( 9 FDA reports)
ORAL INTAKE REDUCED ( 9 FDA reports)
OSTEOMALACIA ( 9 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 9 FDA reports)
PEAU D'ORANGE ( 9 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 9 FDA reports)
PROCTITIS ( 9 FDA reports)
PROSTATOMEGALY ( 9 FDA reports)
PURPURA ( 9 FDA reports)
QUADRIPLEGIA ( 9 FDA reports)
RASH PAPULAR ( 9 FDA reports)
REFLUX GASTRITIS ( 9 FDA reports)
RETINAL HAEMORRHAGE ( 9 FDA reports)
RETROPERITONEAL ABSCESS ( 9 FDA reports)
SALIVARY HYPERSECRETION ( 9 FDA reports)
SEBORRHOEIC KERATOSIS ( 9 FDA reports)
SKIN FIBROSIS ( 9 FDA reports)
SKIN NECROSIS ( 9 FDA reports)
SKIN SWELLING ( 9 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 9 FDA reports)
SUBDURAL HAEMATOMA ( 9 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 9 FDA reports)
TEMPERATURE INTOLERANCE ( 9 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 9 FDA reports)
TRANSFUSION ( 9 FDA reports)
TRANSFUSION REACTION ( 9 FDA reports)
TRANSPLANT REJECTION ( 9 FDA reports)
UTERINE POLYP ( 9 FDA reports)
VESTIBULAR DISORDER ( 9 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 9 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 9 FDA reports)
ABDOMINAL HERNIA ( 8 FDA reports)
ANGIOPATHY ( 8 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 8 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 8 FDA reports)
ARTHRITIS INFECTIVE ( 8 FDA reports)
ASTHENOPIA ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 8 FDA reports)
AXILLARY PAIN ( 8 FDA reports)
BLINDNESS TRANSIENT ( 8 FDA reports)
BLOOD AMYLASE INCREASED ( 8 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 8 FDA reports)
BONE LOSS ( 8 FDA reports)
CALCIPHYLAXIS ( 8 FDA reports)
CARDIOGENIC SHOCK ( 8 FDA reports)
CAROTID BRUIT ( 8 FDA reports)
CARPAL TUNNEL SYNDROME ( 8 FDA reports)
CATHETERISATION CARDIAC ( 8 FDA reports)
CHONDROCALCINOSIS ( 8 FDA reports)
CLONUS ( 8 FDA reports)
CORONARY ARTERY STENOSIS ( 8 FDA reports)
DEAFNESS UNILATERAL ( 8 FDA reports)
DEMENTIA ( 8 FDA reports)
DENTAL PLAQUE ( 8 FDA reports)
DENTAL TREATMENT ( 8 FDA reports)
DIABETES INSIPIDUS ( 8 FDA reports)
DIABETIC RETINOPATHY ( 8 FDA reports)
DRUG INTOLERANCE ( 8 FDA reports)
DUODENAL ULCER ( 8 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 8 FDA reports)
EROSIVE OESOPHAGITIS ( 8 FDA reports)
ERUCTATION ( 8 FDA reports)
EUPHORIC MOOD ( 8 FDA reports)
EXCORIATION ( 8 FDA reports)
FACIAL PALSY ( 8 FDA reports)
FAECES DISCOLOURED ( 8 FDA reports)
FAT INTOLERANCE ( 8 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 8 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 8 FDA reports)
GALLBLADDER OEDEMA ( 8 FDA reports)
GASTROINTESTINAL INFECTION ( 8 FDA reports)
GENERALISED OEDEMA ( 8 FDA reports)
HAND FRACTURE ( 8 FDA reports)
HEARING IMPAIRED ( 8 FDA reports)
HEART VALVE INCOMPETENCE ( 8 FDA reports)
HEPATIC CIRRHOSIS ( 8 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 8 FDA reports)
HYPERCAPNIA ( 8 FDA reports)
HYPERSOMNIA ( 8 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 8 FDA reports)
IMPAIRED DRIVING ABILITY ( 8 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 8 FDA reports)
INJECTION SITE CELLULITIS ( 8 FDA reports)
ISCHAEMIC STROKE ( 8 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 8 FDA reports)
KNEE ARTHROPLASTY ( 8 FDA reports)
LIBIDO DECREASED ( 8 FDA reports)
LIVER ABSCESS ( 8 FDA reports)
LUNG ABSCESS ( 8 FDA reports)
LYME DISEASE ( 8 FDA reports)
MENSTRUATION DELAYED ( 8 FDA reports)
METASTASES TO LIVER ( 8 FDA reports)
MIOSIS ( 8 FDA reports)
MURPHY'S SIGN POSITIVE ( 8 FDA reports)
MUSCLE STRAIN ( 8 FDA reports)
MUSCULOSKELETAL DISORDER ( 8 FDA reports)
MYDRIASIS ( 8 FDA reports)
MYOPATHY ( 8 FDA reports)
NEPHROPATHY TOXIC ( 8 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 8 FDA reports)
OBSTRUCTION ( 8 FDA reports)
OPTIC NEURITIS ( 8 FDA reports)
PANCREATIC ENZYMES INCREASED ( 8 FDA reports)
PERIPHERAL ISCHAEMIA ( 8 FDA reports)
PHARYNGEAL ERYTHEMA ( 8 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 8 FDA reports)
PNEUMONIA VIRAL ( 8 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 8 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 8 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 8 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 8 FDA reports)
SCROTAL OEDEMA ( 8 FDA reports)
SCROTAL SWELLING ( 8 FDA reports)
SLUGGISHNESS ( 8 FDA reports)
SNEEZING ( 8 FDA reports)
STENT PLACEMENT ( 8 FDA reports)
STILLBIRTH ( 8 FDA reports)
SUDDEN DEATH ( 8 FDA reports)
TONSILLITIS ( 8 FDA reports)
UNDERDOSE ( 8 FDA reports)
UTERINE HAEMORRHAGE ( 8 FDA reports)
VENTRICULAR DYSFUNCTION ( 8 FDA reports)
ABDOMINAL RIGIDITY ( 7 FDA reports)
ACNE PUSTULAR ( 7 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 7 FDA reports)
ANAPHYLACTOID REACTION ( 7 FDA reports)
APPLICATION SITE RASH ( 7 FDA reports)
ASPIRATION JOINT ( 7 FDA reports)
ASTIGMATISM ( 7 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 7 FDA reports)
BACTERIAL SEPSIS ( 7 FDA reports)
BILE DUCT OBSTRUCTION ( 7 FDA reports)
BLOOD ALBUMIN DECREASED ( 7 FDA reports)
BODY HEIGHT DECREASED ( 7 FDA reports)
BODY TEMPERATURE DECREASED ( 7 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 7 FDA reports)
BREAST CANCER STAGE I ( 7 FDA reports)
BULLOUS LUNG DISEASE ( 7 FDA reports)
CALCULUS URETHRAL ( 7 FDA reports)
CARDIAC VALVE DISEASE ( 7 FDA reports)
CLEFT LIP AND PALATE ( 7 FDA reports)
CLOSTRIDIUM COLITIS ( 7 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 7 FDA reports)
CONVERSION DISORDER ( 7 FDA reports)
COORDINATION ABNORMAL ( 7 FDA reports)
CREPITATIONS ( 7 FDA reports)
DERMAL CYST ( 7 FDA reports)
DEVICE DISLOCATION ( 7 FDA reports)
DIASTOLIC DYSFUNCTION ( 7 FDA reports)
DRUG ABUSE ( 7 FDA reports)
DRY THROAT ( 7 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 7 FDA reports)
EMBOLISM ( 7 FDA reports)
ERYTHEMA OF EYELID ( 7 FDA reports)
EXOPHTHALMOS ( 7 FDA reports)
EYELID OEDEMA ( 7 FDA reports)
FACE INJURY ( 7 FDA reports)
FAECAL INCONTINENCE ( 7 FDA reports)
FALLOT'S TETRALOGY ( 7 FDA reports)
FAMILY STRESS ( 7 FDA reports)
FIBRIN D DIMER INCREASED ( 7 FDA reports)
FUNGAL SKIN INFECTION ( 7 FDA reports)
GALLBLADDER OPERATION ( 7 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 7 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 7 FDA reports)
GUILLAIN-BARRE SYNDROME ( 7 FDA reports)
HEART SOUNDS ABNORMAL ( 7 FDA reports)
HEPATITIS ACUTE ( 7 FDA reports)
HERNIA REPAIR ( 7 FDA reports)
HIRSUTISM ( 7 FDA reports)
HYPERCALCAEMIA ( 7 FDA reports)
HYPOAESTHESIA FACIAL ( 7 FDA reports)
ILEITIS ( 7 FDA reports)
ILEOSTOMY ( 7 FDA reports)
IMPAIRED WORK ABILITY ( 7 FDA reports)
INADEQUATE ANALGESIA ( 7 FDA reports)
INCISION SITE HAEMORRHAGE ( 7 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 7 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 7 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 7 FDA reports)
INJECTION SITE INDURATION ( 7 FDA reports)
INJECTION SITE OEDEMA ( 7 FDA reports)
INJECTION SITE SCAB ( 7 FDA reports)
INTESTINAL INFARCTION ( 7 FDA reports)
IUCD COMPLICATION ( 7 FDA reports)
JAUNDICE NEONATAL ( 7 FDA reports)
LACTIC ACIDOSIS ( 7 FDA reports)
LEARNING DISABILITY ( 7 FDA reports)
LEARNING DISORDER ( 7 FDA reports)
LIPASE INCREASED ( 7 FDA reports)
MASTOIDITIS ( 7 FDA reports)
MEGACOLON ( 7 FDA reports)
MENISCUS LESION ( 7 FDA reports)
MENSTRUAL DISORDER ( 7 FDA reports)
METASTASES TO LARGE INTESTINE ( 7 FDA reports)
MOTOR DYSFUNCTION ( 7 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 7 FDA reports)
MUSCLE TWITCHING ( 7 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 7 FDA reports)
NOSOCOMIAL INFECTION ( 7 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 7 FDA reports)
ONYCHOMADESIS ( 7 FDA reports)
OROPHARYNGEAL BLISTERING ( 7 FDA reports)
OSTEOSCLEROSIS ( 7 FDA reports)
PANCREATITIS RELAPSING ( 7 FDA reports)
PELVIC ABSCESS ( 7 FDA reports)
PERIOSTITIS ( 7 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 7 FDA reports)
PNEUMONIA FUNGAL ( 7 FDA reports)
POLYURIA ( 7 FDA reports)
POST PROCEDURAL INFECTION ( 7 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 7 FDA reports)
PSORIATIC ARTHROPATHY ( 7 FDA reports)
PSYCHIATRIC SYMPTOM ( 7 FDA reports)
PULMONARY TUBERCULOSIS ( 7 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 7 FDA reports)
RHONCHI ( 7 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 7 FDA reports)
SKIN ATROPHY ( 7 FDA reports)
STEM CELL TRANSPLANT ( 7 FDA reports)
STRESS FRACTURE ( 7 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 7 FDA reports)
TEARFULNESS ( 7 FDA reports)
TOE AMPUTATION ( 7 FDA reports)
TONGUE DISORDER ( 7 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 7 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 7 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 7 FDA reports)
TREATMENT FAILURE ( 7 FDA reports)
TUBERCULOSIS ( 7 FDA reports)
URINARY HESITATION ( 7 FDA reports)
VENOOCCLUSIVE DISEASE ( 7 FDA reports)
VENTRICULAR HYPERTROPHY ( 7 FDA reports)
VENTRICULAR HYPOKINESIA ( 7 FDA reports)
VIITH NERVE PARALYSIS ( 7 FDA reports)
VITAMIN D DECREASED ( 7 FDA reports)
VITH NERVE PARALYSIS ( 7 FDA reports)
VOCAL CORD PARALYSIS ( 7 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 7 FDA reports)
YAWNING ( 7 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 6 FDA reports)
ANAL FISSURE ( 6 FDA reports)
ANAL STENOSIS ( 6 FDA reports)
ANOSMIA ( 6 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 6 FDA reports)
ARTHROPOD BITE ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 6 FDA reports)
AUTOIMMUNE DISORDER ( 6 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 6 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 6 FDA reports)
BIOPSY PROSTATE ( 6 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 6 FDA reports)
BONE MARROW DISORDER ( 6 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 6 FDA reports)
BREAST OEDEMA ( 6 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 6 FDA reports)
CAECITIS ( 6 FDA reports)
CALCULUS URETERIC ( 6 FDA reports)
CHEST X-RAY ABNORMAL ( 6 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 6 FDA reports)
DECREASED ACTIVITY ( 6 FDA reports)
DELUSION ( 6 FDA reports)
DENTAL DISCOMFORT ( 6 FDA reports)
DEPRESSIVE SYMPTOM ( 6 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 6 FDA reports)
DIABETIC KETOACIDOSIS ( 6 FDA reports)
DIABETIC NEUROPATHY ( 6 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 6 FDA reports)
DRUG RESISTANCE ( 6 FDA reports)
ENCEPHALOMALACIA ( 6 FDA reports)
ENDOCARDITIS ( 6 FDA reports)
ENDOMETRIOSIS ( 6 FDA reports)
ENTEROBACTER INFECTION ( 6 FDA reports)
EOSINOPHIL COUNT INCREASED ( 6 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 6 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 6 FDA reports)
ERYSIPELAS ( 6 FDA reports)
ESCHERICHIA SEPSIS ( 6 FDA reports)
EXOMPHALOS ( 6 FDA reports)
EXTRADURAL ABSCESS ( 6 FDA reports)
EYE HAEMORRHAGE ( 6 FDA reports)
EYE PRURITUS ( 6 FDA reports)
FAECALOMA ( 6 FDA reports)
FEEDING DISORDER ( 6 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 6 FDA reports)
FINGER AMPUTATION ( 6 FDA reports)
FOOT AMPUTATION ( 6 FDA reports)
FUSOBACTERIUM INFECTION ( 6 FDA reports)
GENERALISED ERYTHEMA ( 6 FDA reports)
GENITAL HERPES ( 6 FDA reports)
HAEMATOTOXICITY ( 6 FDA reports)
HEPATIC NEOPLASM ( 6 FDA reports)
HIP ARTHROPLASTY ( 6 FDA reports)
HORMONE LEVEL ABNORMAL ( 6 FDA reports)
HYPERMETABOLISM ( 6 FDA reports)
HYPERPARATHYROIDISM ( 6 FDA reports)
HYPERTONIA ( 6 FDA reports)
HYPERVENTILATION ( 6 FDA reports)
HYPOVOLAEMIC SHOCK ( 6 FDA reports)
INCISION SITE COMPLICATION ( 6 FDA reports)
INFANTILE SPITTING UP ( 6 FDA reports)
INGUINAL HERNIA ( 6 FDA reports)
INJECTION SITE PRURITUS ( 6 FDA reports)
INJECTION SITE WARMTH ( 6 FDA reports)
JOINT CONTRACTURE ( 6 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 6 FDA reports)
KETOACIDOSIS ( 6 FDA reports)
KLEBSIELLA SEPSIS ( 6 FDA reports)
LEG AMPUTATION ( 6 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 6 FDA reports)
LIFE EXPECTANCY SHORTENED ( 6 FDA reports)
LIPID METABOLISM DISORDER ( 6 FDA reports)
LISTLESS ( 6 FDA reports)
LIVEDO RETICULARIS ( 6 FDA reports)
LOCALISED OEDEMA ( 6 FDA reports)
LOSS OF CONTROL OF LEGS ( 6 FDA reports)
LUDWIG ANGINA ( 6 FDA reports)
LUNG NEOPLASM MALIGNANT ( 6 FDA reports)
LYMPHOCYTOSIS ( 6 FDA reports)
MENOPAUSE ( 6 FDA reports)
METASTASES TO LUNG ( 6 FDA reports)
MULTIPLE ALLERGIES ( 6 FDA reports)
MUSCLE CONTRACTURE ( 6 FDA reports)
NASAL TURBINATE ABNORMALITY ( 6 FDA reports)
NASAL ULCER ( 6 FDA reports)
NECROTISING FASCIITIS ( 6 FDA reports)
NERVE INJURY ( 6 FDA reports)
NON-CARDIAC CHEST PAIN ( 6 FDA reports)
NORMAL NEWBORN ( 6 FDA reports)
NYSTAGMUS ( 6 FDA reports)
OCCULT BLOOD ( 6 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 6 FDA reports)
OPHTHALMOPLEGIA ( 6 FDA reports)
ORAL DISCOMFORT ( 6 FDA reports)
ORAL FUNGAL INFECTION ( 6 FDA reports)
OVARIAN ADENOMA ( 6 FDA reports)
PANCREATIC ATROPHY ( 6 FDA reports)
PENILE SWELLING ( 6 FDA reports)
PEPTIC ULCER PERFORATION ( 6 FDA reports)
PORTAL HYPERTENSION ( 6 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 6 FDA reports)
PRE-ECLAMPSIA ( 6 FDA reports)
PROSTATIC OPERATION ( 6 FDA reports)
PULMONARY THROMBOSIS ( 6 FDA reports)
PULMONARY VALVE STENOSIS ( 6 FDA reports)
PULSE PRESSURE DECREASED ( 6 FDA reports)
PUPIL FIXED ( 6 FDA reports)
RASH VESICULAR ( 6 FDA reports)
RENAL HYPERTROPHY ( 6 FDA reports)
RESORPTION BONE INCREASED ( 6 FDA reports)
SCRATCH ( 6 FDA reports)
SEPTIC EMBOLUS ( 6 FDA reports)
SINUS CONGESTION ( 6 FDA reports)
SKIN BURNING SENSATION ( 6 FDA reports)
SKIN CANCER ( 6 FDA reports)
SKIN HAEMORRHAGE ( 6 FDA reports)
SMALL FOR DATES BABY ( 6 FDA reports)
SMALL INTESTINAL PERFORATION ( 6 FDA reports)
SOFT TISSUE INFECTION ( 6 FDA reports)
SOFT TISSUE INJURY ( 6 FDA reports)
SPONDYLOLYSIS ( 6 FDA reports)
STUPOR ( 6 FDA reports)
TALIPES ( 6 FDA reports)
TOBACCO USER ( 6 FDA reports)
TRACHEOMALACIA ( 6 FDA reports)
TRAUMATIC HAEMATOMA ( 6 FDA reports)
TYPE 1 DIABETES MELLITUS ( 6 FDA reports)
ULCER HAEMORRHAGE ( 6 FDA reports)
URETHRAL OBSTRUCTION ( 6 FDA reports)
URINE ABNORMALITY ( 6 FDA reports)
VAGINITIS BACTERIAL ( 6 FDA reports)
VARICES OESOPHAGEAL ( 6 FDA reports)
VOCAL CORD DISORDER ( 6 FDA reports)
ABDOMINAL OPERATION ( 5 FDA reports)
ABSCESS DRAINAGE ( 5 FDA reports)
ABSCESS MANAGEMENT ( 5 FDA reports)
ACCIDENT ( 5 FDA reports)
ADENOVIRUS INFECTION ( 5 FDA reports)
ADRENAL NEOPLASM ( 5 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
ANKLE FRACTURE ( 5 FDA reports)
ANOXIA ( 5 FDA reports)
APLASTIC ANAEMIA ( 5 FDA reports)
APPARENT DEATH ( 5 FDA reports)
APPLICATION SITE PRURITUS ( 5 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 5 FDA reports)
ASEPTIC NECROSIS BONE ( 5 FDA reports)
BILIARY TRACT DISORDER ( 5 FDA reports)
BLEEDING TIME PROLONGED ( 5 FDA reports)
BLOOD CHLORIDE DECREASED ( 5 FDA reports)
BLOOD COUNT ABNORMAL ( 5 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 5 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 5 FDA reports)
BLOOD PH DECREASED ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 5 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 5 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 5 FDA reports)
BONE SWELLING ( 5 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 5 FDA reports)
BRAIN SCAN ABNORMAL ( 5 FDA reports)
BREAST CANCER METASTATIC ( 5 FDA reports)
BRONCHITIS CHRONIC ( 5 FDA reports)
CALCULUS BLADDER ( 5 FDA reports)
CAPILLARY LEAK SYNDROME ( 5 FDA reports)
CARDIAC VALVE VEGETATION ( 5 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 5 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 5 FDA reports)
CEREBROSPINAL FLUID RESERVOIR PLACEMENT ( 5 FDA reports)
CHANGE OF BOWEL HABIT ( 5 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 5 FDA reports)
COELIAC DISEASE ( 5 FDA reports)
COLON OPERATION ( 5 FDA reports)
CONCUSSION ( 5 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 5 FDA reports)
DANDRUFF ( 5 FDA reports)
DECREASED INTEREST ( 5 FDA reports)
DERMATITIS CONTACT ( 5 FDA reports)
DEVICE OCCLUSION ( 5 FDA reports)
DIABETIC MICROANGIOPATHY ( 5 FDA reports)
DIFFICULTY IN WALKING ( 5 FDA reports)
DISBACTERIOSIS ( 5 FDA reports)
DRUG LEVEL DECREASED ( 5 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 5 FDA reports)
DYSMENORRHOEA ( 5 FDA reports)
ENTEROCOLITIS ( 5 FDA reports)
ENTEROCUTANEOUS FISTULA ( 5 FDA reports)
EOSINOPHIL COUNT DECREASED ( 5 FDA reports)
EOSINOPHILIA ( 5 FDA reports)
EPIGASTRIC DISCOMFORT ( 5 FDA reports)
ESCHERICHIA BACTERAEMIA ( 5 FDA reports)
ESSENTIAL HYPERTENSION ( 5 FDA reports)
EXANTHEM ( 5 FDA reports)
EXERCISE TOLERANCE DECREASED ( 5 FDA reports)
EXPIRED DRUG ADMINISTERED ( 5 FDA reports)
EYE DISCHARGE ( 5 FDA reports)
EYE INFECTION ( 5 FDA reports)
FAECES HARD ( 5 FDA reports)
FEELING DRUNK ( 5 FDA reports)
FEELING JITTERY ( 5 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 5 FDA reports)
FINGER DEFORMITY ( 5 FDA reports)
FLAT AFFECT ( 5 FDA reports)
FOETAL DISTRESS SYNDROME ( 5 FDA reports)
FOETAL GROWTH RESTRICTION ( 5 FDA reports)
GASTRITIS EROSIVE ( 5 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 5 FDA reports)
GINGIVAL CYST ( 5 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 5 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 5 FDA reports)
GUN SHOT WOUND ( 5 FDA reports)
HAEMOGLOBIN ABNORMAL ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HELICOBACTER INFECTION ( 5 FDA reports)
HEPATIC CONGESTION ( 5 FDA reports)
HEPATIC CYST ( 5 FDA reports)
HEPATOCELLULAR DAMAGE ( 5 FDA reports)
HEPATOSPLENOMEGALY ( 5 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 5 FDA reports)
HYPERCOAGULATION ( 5 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 5 FDA reports)
HYPERPHOSPHATAEMIA ( 5 FDA reports)
HYPOHIDROSIS ( 5 FDA reports)
HYPOPHOSPHATAEMIA ( 5 FDA reports)
HYPOTHERMIA ( 5 FDA reports)
HYPOVENTILATION ( 5 FDA reports)
IATROGENIC INJURY ( 5 FDA reports)
IMMUNOSUPPRESSION ( 5 FDA reports)
INAPPROPRIATE AFFECT ( 5 FDA reports)
INCISION SITE INFECTION ( 5 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 5 FDA reports)
INJECTION SITE INFECTION ( 5 FDA reports)
INJECTION SITE IRRITATION ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 5 FDA reports)
INTESTINAL MALROTATION ( 5 FDA reports)
JOINT SPRAIN ( 5 FDA reports)
JUGULAR VEIN THROMBOSIS ( 5 FDA reports)
KAPOSI'S SARCOMA ( 5 FDA reports)
LABILE BLOOD PRESSURE ( 5 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 5 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 5 FDA reports)
MACROCEPHALY ( 5 FDA reports)
MASTITIS ( 5 FDA reports)
MEDICAL DIET ( 5 FDA reports)
MELANOMA RECURRENT ( 5 FDA reports)
METASTATIC PAIN ( 5 FDA reports)
MICROPHTHALMOS ( 5 FDA reports)
MICROTIA ( 5 FDA reports)
MITRAL VALVE DISEASE ( 5 FDA reports)
MULTIPLE FRACTURES ( 5 FDA reports)
MUSCLE INJURY ( 5 FDA reports)
MYASTHENIA GRAVIS ( 5 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 5 FDA reports)
NASAL SEPTUM DEVIATION ( 5 FDA reports)
NEPHROTIC SYNDROME ( 5 FDA reports)
NIPPLE PAIN ( 5 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 5 FDA reports)
ODYNOPHAGIA ( 5 FDA reports)
OESOPHAGEAL PAIN ( 5 FDA reports)
ORAL CAVITY FISTULA ( 5 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 5 FDA reports)
PANCREATIC PSEUDOCYST ( 5 FDA reports)
PATHOGEN RESISTANCE ( 5 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 5 FDA reports)
PELVIC HAEMATOMA ( 5 FDA reports)
PEMPHIGOID ( 5 FDA reports)
PENILE HAEMORRHAGE ( 5 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 5 FDA reports)
PERIPROCTITIS ( 5 FDA reports)
PERITONSILLAR ABSCESS ( 5 FDA reports)
PNEUMATOSIS INTESTINALIS ( 5 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 5 FDA reports)
POLYMENORRHOEA ( 5 FDA reports)
POOR VENOUS ACCESS ( 5 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 5 FDA reports)
POSTOPERATIVE THROMBOSIS ( 5 FDA reports)
POSTPARTUM DEPRESSION ( 5 FDA reports)
PRIAPISM ( 5 FDA reports)
PROTEUS INFECTION ( 5 FDA reports)
PULMONARY MASS ( 5 FDA reports)
PYODERMA GANGRENOSUM ( 5 FDA reports)
RADIATION INJURY ( 5 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 5 FDA reports)
RENAL CANCER ( 5 FDA reports)
RENAL CORTICAL NECROSIS ( 5 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 5 FDA reports)
RHINITIS ALLERGIC ( 5 FDA reports)
RHINITIS SEASONAL ( 5 FDA reports)
RIGHT VENTRICULAR FAILURE ( 5 FDA reports)
SENSATION OF HEAVINESS ( 5 FDA reports)
SEROMA ( 5 FDA reports)
SINUS ARRHYTHMIA ( 5 FDA reports)
SINUS POLYP ( 5 FDA reports)
SKIN TURGOR DECREASED ( 5 FDA reports)
SOCIAL PROBLEM ( 5 FDA reports)
SPHEROCYTIC ANAEMIA ( 5 FDA reports)
STOMACH DISCOMFORT ( 5 FDA reports)
STRONGYLOIDIASIS ( 5 FDA reports)
SUICIDAL BEHAVIOUR ( 5 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 5 FDA reports)
SYSTOLIC DYSFUNCTION ( 5 FDA reports)
THINKING ABNORMAL ( 5 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
TOBACCO ABUSE ( 5 FDA reports)
TONGUE BLISTERING ( 5 FDA reports)
TONSILLAR DISORDER ( 5 FDA reports)
TOXIC SKIN ERUPTION ( 5 FDA reports)
TRANSPLANT FAILURE ( 5 FDA reports)
TRAUMATIC LUNG INJURY ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
TUMOUR INVASION ( 5 FDA reports)
URINARY TRACT DISORDER ( 5 FDA reports)
URINE ODOUR ABNORMAL ( 5 FDA reports)
UROSEPSIS ( 5 FDA reports)
UTERINE CANCER ( 5 FDA reports)
VAGINAL CONTRACEPTIVE DEVICE EXPELLED ( 5 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 5 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
VITAMIN B12 DECREASED ( 5 FDA reports)
VULVOVAGINITIS ( 5 FDA reports)
WEIGHT BEARING DIFFICULTY ( 5 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 5 FDA reports)
WHITE CLOT SYNDROME ( 5 FDA reports)
WRONG DRUG ADMINISTERED ( 5 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ABORTION INCOMPLETE ( 4 FDA reports)
ACUTE ABDOMEN ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 4 FDA reports)
ACUTE PRERENAL FAILURE ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 4 FDA reports)
ADDISON'S DISEASE ( 4 FDA reports)
ADENOCARCINOMA ( 4 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 4 FDA reports)
ALVEOLITIS ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 4 FDA reports)
ANAEMIA MACROCYTIC ( 4 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 4 FDA reports)
ANASTOMOTIC LEAK ( 4 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
AORTIC VALVE CALCIFICATION ( 4 FDA reports)
AORTIC VALVE SCLEROSIS ( 4 FDA reports)
APGAR SCORE LOW ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ATAXIA ( 4 FDA reports)
ATROPHIC VULVOVAGINITIS ( 4 FDA reports)
BACTERIAL FOOD POISONING ( 4 FDA reports)
BILIARY CYST ( 4 FDA reports)
BIPOLAR DISORDER ( 4 FDA reports)
BLADDER HYPERTROPHY ( 4 FDA reports)
BLADDER INJURY ( 4 FDA reports)
BLADDER PAIN ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 4 FDA reports)
BLOOD CREATININE ABNORMAL ( 4 FDA reports)
BLOOD CULTURE POSITIVE ( 4 FDA reports)
BLOOD FOLATE DECREASED ( 4 FDA reports)
BLOOD PRESSURE ABNORMAL ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 4 FDA reports)
BLUNTED AFFECT ( 4 FDA reports)
BODY MASS INDEX INCREASED ( 4 FDA reports)
BONE INFARCTION ( 4 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 4 FDA reports)
BRADYPHRENIA ( 4 FDA reports)
BREAST CANCER FEMALE ( 4 FDA reports)
CARDIAC TAMPONADE ( 4 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 4 FDA reports)
CAROTID ARTERY OCCLUSION ( 4 FDA reports)
CATARACT OPERATION ( 4 FDA reports)
CATHETER RELATED INFECTION ( 4 FDA reports)
CATHETER REMOVAL ( 4 FDA reports)
CEREBRAL DISORDER ( 4 FDA reports)
CEREBRAL HAEMATOMA ( 4 FDA reports)
CEREBRAL PALSY ( 4 FDA reports)
CERVICAL POLYP ( 4 FDA reports)
CHEMICAL PERITONITIS ( 4 FDA reports)
CHONDROPATHY ( 4 FDA reports)
CHRONIC HEPATITIS ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
COGWHEEL RIGIDITY ( 4 FDA reports)
COITAL BLEEDING ( 4 FDA reports)
COLON POLYPECTOMY ( 4 FDA reports)
COLOSTOMY ( 4 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 4 FDA reports)
COXSACKIE VIRUS TEST POSITIVE ( 4 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 4 FDA reports)
CREATININE URINE INCREASED ( 4 FDA reports)
CRYPTOCOCCOSIS ( 4 FDA reports)
CYSTITIS NONINFECTIVE ( 4 FDA reports)
CYTOGENETIC ABNORMALITY ( 4 FDA reports)
DEVICE INTOLERANCE ( 4 FDA reports)
DIALYSIS DISEQUILIBRIUM SYNDROME ( 4 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 4 FDA reports)
DISEASE COMPLICATION ( 4 FDA reports)
DIVERTICULAR PERFORATION ( 4 FDA reports)
DRUG DISPENSING ERROR ( 4 FDA reports)
DRUG TOLERANCE INCREASED ( 4 FDA reports)
DUODENITIS ( 4 FDA reports)
DYSAESTHESIA ( 4 FDA reports)
DYSPLASTIC NAEVUS ( 4 FDA reports)
EAR CONGESTION ( 4 FDA reports)
EAR DISCOMFORT ( 4 FDA reports)
ENGRAFTMENT SYNDROME ( 4 FDA reports)
ENTEROBACTER BACTERAEMIA ( 4 FDA reports)
ENZYME ABNORMALITY ( 4 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
FANCONI SYNDROME ( 4 FDA reports)
FEAR OF DEATH ( 4 FDA reports)
FEAR OF DISEASE ( 4 FDA reports)
FLUORESCENT IN SITU HYBRIDISATION ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
FRUSTRATION ( 4 FDA reports)
GASTRIC BYPASS ( 4 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 4 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 4 FDA reports)
GASTROINTESTINAL PAIN ( 4 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 4 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 4 FDA reports)
GINGIVAL ERYTHEMA ( 4 FDA reports)
GINGIVAL OEDEMA ( 4 FDA reports)
GOITRE ( 4 FDA reports)
HEAD AND NECK CANCER ( 4 FDA reports)
HEMIPLEGIA ( 4 FDA reports)
HEPATIC FIBROSIS ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 4 FDA reports)
HIDRADENITIS ( 4 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 4 FDA reports)
HOSTILITY ( 4 FDA reports)
HYPERACUSIS ( 4 FDA reports)
HYPERTENSIVE CRISIS ( 4 FDA reports)
HYPERTHYROIDISM ( 4 FDA reports)
HYPERURICAEMIA ( 4 FDA reports)
HYPOPROTEINAEMIA ( 4 FDA reports)
IMMUNODEFICIENCY ( 4 FDA reports)
IMPLANT SITE INFECTION ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
INCISION SITE PAIN ( 4 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 4 FDA reports)
INFECTIOUS PERITONITIS ( 4 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 4 FDA reports)
INFUSION SITE SWELLING ( 4 FDA reports)
INJECTION SITE ULCER ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 4 FDA reports)
INTERVERTEBRAL DISCITIS ( 4 FDA reports)
INTESTINAL FISTULA ( 4 FDA reports)
INTESTINAL MASS ( 4 FDA reports)
INTESTINAL STOMA ( 4 FDA reports)
INTESTINAL ULCER ( 4 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 4 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
JUGULAR VEIN DISTENSION ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LIFE SUPPORT ( 4 FDA reports)
LIVER TRANSPLANT ( 4 FDA reports)
LOWER EXTREMITY MASS ( 4 FDA reports)
LUPUS NEPHRITIS ( 4 FDA reports)
LYMPHADENECTOMY ( 4 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 4 FDA reports)
MACULAR DEGENERATION ( 4 FDA reports)
MALABSORPTION ( 4 FDA reports)
METABOLIC SYNDROME ( 4 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 4 FDA reports)
METASTASIS ( 4 FDA reports)
METASTATIC NEOPLASM ( 4 FDA reports)
MICROALBUMINURIA ( 4 FDA reports)
MICTURITION DISORDER ( 4 FDA reports)
MONONUCLEOSIS SYNDROME ( 4 FDA reports)
MONOPLEGIA ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
MOUTH CYST ( 4 FDA reports)
MUSCLE HAEMORRHAGE ( 4 FDA reports)
MUSCLE SPASTICITY ( 4 FDA reports)
MUTISM ( 4 FDA reports)
MYCOPLASMA INFECTION ( 4 FDA reports)
MYELOPATHY ( 4 FDA reports)
MYOCLONUS ( 4 FDA reports)
NASAL DISCOMFORT ( 4 FDA reports)
NECROTISING COLITIS ( 4 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 4 FDA reports)
NEURODERMATITIS ( 4 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 4 FDA reports)
NODULE ( 4 FDA reports)
OCULOGYRIC CRISIS ( 4 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
OLIGOMENORRHOEA ( 4 FDA reports)
OPPORTUNISTIC INFECTION ( 4 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 4 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 4 FDA reports)
ORTHOPNOEA ( 4 FDA reports)
OVARIAN CANCER ( 4 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 4 FDA reports)
PALLIATIVE CARE ( 4 FDA reports)
PARESIS ( 4 FDA reports)
PAROTITIS ( 4 FDA reports)
PERFORMANCE STATUS DECREASED ( 4 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 4 FDA reports)
PERIPHERAL NERVE INJURY ( 4 FDA reports)
PERITONEAL HAEMORRHAGE ( 4 FDA reports)
PHONOPHOBIA ( 4 FDA reports)
PLAGIOCEPHALY ( 4 FDA reports)
PLEURAL FIBROSIS ( 4 FDA reports)
PNEUMONIA KLEBSIELLA ( 4 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 4 FDA reports)
POLYARTHRITIS ( 4 FDA reports)
POSTOPERATIVE INFECTION ( 4 FDA reports)
PROCEDURAL HYPOTENSION ( 4 FDA reports)
PROSTATE CANCER ( 4 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 4 FDA reports)
RECTAL DISCHARGE ( 4 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
RENAL CELL CARCINOMA ( 4 FDA reports)
RENAL COLIC ( 4 FDA reports)
RENAL INFARCT ( 4 FDA reports)
RESPIRATORY ACIDOSIS ( 4 FDA reports)
RESPIRATORY ALKALOSIS ( 4 FDA reports)
RESPIRATORY RATE DECREASED ( 4 FDA reports)
RIB DEFORMITY ( 4 FDA reports)
ROTAVIRUS INFECTION ( 4 FDA reports)
SACROILIITIS ( 4 FDA reports)
SCAB ( 4 FDA reports)
SEXUAL DYSFUNCTION ( 4 FDA reports)
SINUS HEADACHE ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SKIN INFLAMMATION ( 4 FDA reports)
SKIN IRRITATION ( 4 FDA reports)
SOMNAMBULISM ( 4 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 4 FDA reports)
SPINAL ANAESTHESIA ( 4 FDA reports)
SPINAL CORD INFARCTION ( 4 FDA reports)
SPINAL FUSION SURGERY ( 4 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 4 FDA reports)
STRIDOR ( 4 FDA reports)
SUDDEN HEARING LOSS ( 4 FDA reports)
SUDDEN VISUAL LOSS ( 4 FDA reports)
TENSION HEADACHE ( 4 FDA reports)
THROMBOPHLEBITIS ( 4 FDA reports)
THYROID NEOPLASM ( 4 FDA reports)
TRANSPLANT ( 4 FDA reports)
UMBILICAL HERNIA ( 4 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
UNDERWEIGHT ( 4 FDA reports)
URETHRAL DILATATION ( 4 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 4 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 4 FDA reports)
VENOUS INSUFFICIENCY ( 4 FDA reports)
VENOUS THROMBOSIS ( 4 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 4 FDA reports)
VITAMIN B12 DEFICIENCY ( 4 FDA reports)
VITILIGO ( 4 FDA reports)
VITREOUS OPACITIES ( 4 FDA reports)
VULVAL ABSCESS ( 4 FDA reports)
VULVAL ULCERATION ( 4 FDA reports)
WOUND HAEMORRHAGE ( 4 FDA reports)
WOUND TREATMENT ( 4 FDA reports)
ACANTHOSIS NIGRICANS ( 3 FDA reports)
ACCIDENT AT WORK ( 3 FDA reports)
ACUTE TONSILLITIS ( 3 FDA reports)
ADHESION ( 3 FDA reports)
AEROMONA INFECTION ( 3 FDA reports)
AKATHISIA ( 3 FDA reports)
ANAL HAEMORRHAGE ( 3 FDA reports)
ANGIOPLASTY ( 3 FDA reports)
ANORECTAL DISCOMFORT ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
AORTIC CALCIFICATION ( 3 FDA reports)
AORTIC VALVE REPAIR ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
APPENDIX DISORDER ( 3 FDA reports)
APPLICATION SITE BURN ( 3 FDA reports)
APPLICATION SITE DERMATITIS ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
APPLICATION SITE PAIN ( 3 FDA reports)
APPLICATION SITE SWELLING ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
ATRIAL THROMBOSIS ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
BARRETT'S OESOPHAGUS ( 3 FDA reports)
BARTHOLIN'S ABSCESS ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BINGE EATING ( 3 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 3 FDA reports)
BK VIRUS INFECTION ( 3 FDA reports)
BLADDER CANCER ( 3 FDA reports)
BLADDER DISCOMFORT ( 3 FDA reports)
BLADDER IRRITATION ( 3 FDA reports)
BLADDER PERFORATION ( 3 FDA reports)
BLADDER SPASM ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD BICARBONATE INCREASED ( 3 FDA reports)
BLOOD CORTISOL DECREASED ( 3 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 3 FDA reports)
BLOOD OSMOLARITY INCREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 3 FDA reports)
BODY TINEA ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
BONE MARROW TOXICITY ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BRAIN STEM HAEMORRHAGE ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
BUNDLE BRANCH BLOCK ( 3 FDA reports)
CALCINOSIS ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIAC STRESS TEST ( 3 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 3 FDA reports)
CASTLEMAN'S DISEASE ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
CAUSTIC INJURY ( 3 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 3 FDA reports)
CELLULITIS ORBITAL ( 3 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 3 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 3 FDA reports)
CEREBRAL ARTERY STENOSIS ( 3 FDA reports)
CEREBROVASCULAR SPASM ( 3 FDA reports)
CERVICAL SPINAL STENOSIS ( 3 FDA reports)
CHEILITIS ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHOLANGITIS ACUTE ( 3 FDA reports)
CHOLESTATIC LIVER INJURY ( 3 FDA reports)
COARCTATION OF THE AORTA ( 3 FDA reports)
COLONOSCOPY ABNORMAL ( 3 FDA reports)
COMPARTMENT SYNDROME ( 3 FDA reports)
COMPLEX PARTIAL SEIZURES ( 3 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 3 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
CSF PROTEIN INCREASED ( 3 FDA reports)
CULTURE POSITIVE ( 3 FDA reports)
CUSHING'S SYNDROME ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
CYTOKINE RELEASE SYNDROME ( 3 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 3 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 3 FDA reports)
DEPRESSION SUICIDAL ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DEVICE LEAKAGE ( 3 FDA reports)
DIABETIC EYE DISEASE ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 3 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 3 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 3 FDA reports)
DYSMORPHISM ( 3 FDA reports)
EARLY SATIETY ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
ENDOMETRIAL ABLATION ( 3 FDA reports)
ENTEROBACTER TEST POSITIVE ( 3 FDA reports)
ENTEROVESICAL FISTULA ( 3 FDA reports)
ENURESIS ( 3 FDA reports)
EPITHELIOID SARCOMA ( 3 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 3 FDA reports)
EUSTACHIAN TUBE DISORDER ( 3 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 3 FDA reports)
EXFOLIATIVE RASH ( 3 FDA reports)
FACIAL BONES FRACTURE ( 3 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 3 FDA reports)
FAECAL VOLUME INCREASED ( 3 FDA reports)
FAT NECROSIS ( 3 FDA reports)
FEMORAL ARTERY OCCLUSION ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
FIBRIN INCREASED ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
FOOD ALLERGY ( 3 FDA reports)
FOOD CRAVING ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTRIC POLYPS ( 3 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 3 FDA reports)
GASTROINTESTINAL PERFORATION ( 3 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 3 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HEART INJURY ( 3 FDA reports)
HELICOBACTER TEST POSITIVE ( 3 FDA reports)
HEPATITIS C ( 3 FDA reports)
HERPES ZOSTER DISSEMINATED ( 3 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 3 FDA reports)
HICCUPS ( 3 FDA reports)
HISTOLOGY ABNORMAL ( 3 FDA reports)
HORSESHOE KIDNEY ( 3 FDA reports)
HUMAN CHORIONIC GONADOTROPIN NEGATIVE ( 3 FDA reports)
HYDROCELE ( 3 FDA reports)
HYPERCHLORHYDRIA ( 3 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 3 FDA reports)
HYPOTONIA NEONATAL ( 3 FDA reports)
IMMOBILE ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 3 FDA reports)
INCISIONAL DRAINAGE ( 3 FDA reports)
INCOHERENT ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
INCREASED TENDENCY TO BRUISE ( 3 FDA reports)
INFECTED SKIN ULCER ( 3 FDA reports)
INFERTILITY ( 3 FDA reports)
INJECTION SITE CYST ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INTENTIONAL SELF-INJURY ( 3 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 3 FDA reports)
INTESTINAL HAEMORRHAGE ( 3 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
INTRACRANIAL HYPOTENSION ( 3 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 3 FDA reports)
INTRASPINAL ABSCESS ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 3 FDA reports)
ISCHAEMIC HEPATITIS ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
KELOID SCAR ( 3 FDA reports)
KIDNEY ENLARGEMENT ( 3 FDA reports)
LARGE FOR DATES BABY ( 3 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LEUKOENCEPHALOPATHY ( 3 FDA reports)
LICHENOID KERATOSIS ( 3 FDA reports)
LIGAMENT RUPTURE ( 3 FDA reports)
LIGAMENT SPRAIN ( 3 FDA reports)
LIMB OPERATION ( 3 FDA reports)
LIP DISORDER ( 3 FDA reports)
LIP HAEMORRHAGE ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LOSS OF LIBIDO ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
LUNG TRANSPLANT REJECTION ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MALIGNANT HYPERTENSION ( 3 FDA reports)
MANIA ( 3 FDA reports)
MENIERE'S DISEASE ( 3 FDA reports)
MESENTERIC ARTERY STENOSIS ( 3 FDA reports)
MESENTERIC OCCLUSION ( 3 FDA reports)
METAMORPHOPSIA ( 3 FDA reports)
METAPNEUMOVIRUS INFECTION ( 3 FDA reports)
MITRAL VALVE STENOSIS ( 3 FDA reports)
MORAXELLA INFECTION ( 3 FDA reports)
MUCOUS STOOLS ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
MYOPIA ( 3 FDA reports)
NAIL DISORDER ( 3 FDA reports)
NASAL POLYPS ( 3 FDA reports)
NECK INJURY ( 3 FDA reports)
NECROTISING SCLERITIS ( 3 FDA reports)
NEONATAL DISORDER ( 3 FDA reports)
NEOVASCULARISATION ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 3 FDA reports)
NERVE COMPRESSION ( 3 FDA reports)
NEURODEGENERATIVE DISORDER ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NEUROPATHY ( 3 FDA reports)
NEUTROPENIC COLITIS ( 3 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 3 FDA reports)
OCCULT BLOOD POSITIVE ( 3 FDA reports)
ORAL HERPES ( 3 FDA reports)
OVERGROWTH BACTERIAL ( 3 FDA reports)
PAINFUL RESPIRATION ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PAPILLOMA VIRAL INFECTION ( 3 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PARTIAL SEIZURES ( 3 FDA reports)
PERIODONTAL INFECTION ( 3 FDA reports)
PERIORBITAL HAEMATOMA ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PHARYNGEAL DISORDER ( 3 FDA reports)
PHLEBOLITH ( 3 FDA reports)
PLACENTAL DISORDER ( 3 FDA reports)
PLASMACYTOMA ( 3 FDA reports)
PNEUMATOSIS ( 3 FDA reports)
PNEUMOCONIOSIS ( 3 FDA reports)
POLYCYSTIC OVARIES ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
POOR SUCKING REFLEX ( 3 FDA reports)
PORTAL VENOUS GAS ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 3 FDA reports)
PROSTATITIS ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 3 FDA reports)
PRURITUS GENITAL ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 3 FDA reports)
PULMONARY NECROSIS ( 3 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 3 FDA reports)
PULSE ABNORMAL ( 3 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
PYLORIC STENOSIS ( 3 FDA reports)
RADIUS FRACTURE ( 3 FDA reports)
RAYNAUD'S PHENOMENON ( 3 FDA reports)
REGURGITATION ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
RETICULOCYTE COUNT DECREASED ( 3 FDA reports)
RETINOPATHY ( 3 FDA reports)
SCINTIGRAPHY ( 3 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 3 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 3 FDA reports)
SENSATION OF FOREIGN BODY ( 3 FDA reports)
SERUM SICKNESS ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SHOCK HYPOGLYCAEMIC ( 3 FDA reports)
SINUS ARREST ( 3 FDA reports)
SKIN CHAPPED ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN WRINKLING ( 3 FDA reports)
SLEEP TALKING ( 3 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 3 FDA reports)
SPASTIC DIPLEGIA ( 3 FDA reports)
SPINAL CORD COMPRESSION ( 3 FDA reports)
SPLEEN DISORDER ( 3 FDA reports)
SPLENIC INFARCTION ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
STRABISMUS ( 3 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 3 FDA reports)
STREPTOCOCCAL SEPSIS ( 3 FDA reports)
SUBCUTANEOUS ABSCESS ( 3 FDA reports)
SUTURE RUPTURE ( 3 FDA reports)
TACHYARRHYTHMIA ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
TERMINAL STATE ( 3 FDA reports)
TESTICULAR PAIN ( 3 FDA reports)
THROMBOCYTOSIS ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
TIBIA FRACTURE ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
TOOTH EROSION ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
TOXIC ENCEPHALOPATHY ( 3 FDA reports)
TRACHEAL HAEMORRHAGE ( 3 FDA reports)
TRACHEAL NEOPLASM ( 3 FDA reports)
TRAUMATIC BRAIN INJURY ( 3 FDA reports)
TROPONIN I INCREASED ( 3 FDA reports)
TUBERCULOUS PLEURISY ( 3 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 3 FDA reports)
URETERAL STENT INSERTION ( 3 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VAGINAL SWELLING ( 3 FDA reports)
VANISHING BILE DUCT SYNDROME ( 3 FDA reports)
VEIN PAIN ( 3 FDA reports)
VENA CAVA THROMBOSIS ( 3 FDA reports)
VENOUS STASIS ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
VENTRICULAR HYPOPLASIA ( 3 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
WEIGHT FLUCTUATION ( 3 FDA reports)
WISDOM TEETH REMOVAL ( 3 FDA reports)
WRIST FRACTURE ( 3 FDA reports)
ZYGOMYCOSIS ( 3 FDA reports)
5Q MINUS SYNDROME ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ABULIA ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
ADENOMYOSIS ( 2 FDA reports)
ADNEXA UTERI PAIN ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 2 FDA reports)
AMNIOTIC CAVITY INFECTION ( 2 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 2 FDA reports)
AMPULLA OF VATER STENOSIS ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
ANAEMIA NEONATAL ( 2 FDA reports)
ANAL CANCER ( 2 FDA reports)
ANASTOMOTIC STENOSIS ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANEURYSM RUPTURED ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
APPLICATION SITE VESICLES ( 2 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 2 FDA reports)
ARTIFICIAL ANUS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASPERGILLUS TEST POSITIVE ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
ATYPICAL FEMUR FRACTURE ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
AUTONOMIC NEUROPATHY ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
BACTERIAL PYELONEPHRITIS ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
BILE DUCT NECROSIS ( 2 FDA reports)
BILE DUCT STENOSIS ( 2 FDA reports)
BILIARY DRAINAGE ( 2 FDA reports)
BILIARY SPHINCTEROTOMY ( 2 FDA reports)
BIOPSY BONE MARROW ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BLADDER DYSFUNCTION ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
BLOOD ALCOHOL ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN DECREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID DECREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BLOOD PRESSURE AMBULATORY INCREASED ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 2 FDA reports)
BLOODY DISCHARGE ( 2 FDA reports)
BONE SARCOMA ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
BREECH PRESENTATION ( 2 FDA reports)
BRONCHIAL INJURY ( 2 FDA reports)
BRONCHIAL SECRETION RETENTION ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
BRONCHITIS BACTERIAL ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CARBON DIOXIDE ABNORMAL ( 2 FDA reports)
CARBOXYHAEMOGLOBINAEMIA ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIAC DISCOMFORT ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIAC MYXOMA ( 2 FDA reports)
CARDIAC SEPTAL DEFECT ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CARDIOSPASM ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CAROTID ARTERY DISEASE ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CATHETER PLACEMENT ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CEREBRAL ASPERGILLOSIS ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CERUMEN IMPACTION ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CERVICITIS ( 2 FDA reports)
CHEMICAL INJURY ( 2 FDA reports)
CHLAMYDIAL INFECTION ( 2 FDA reports)
CHOLANGITIS SUPPURATIVE ( 2 FDA reports)
CHONDROLYSIS ( 2 FDA reports)
CHORIOAMNIONITIS ( 2 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONJUNCTIVAL OEDEMA ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
COW'S MILK INTOLERANCE ( 2 FDA reports)
CRANIAL NERVE DISORDER ( 2 FDA reports)
CRYPTORCHISM ( 2 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 2 FDA reports)
CRYSTALLURIA ( 2 FDA reports)
CSF PRESSURE INCREASED ( 2 FDA reports)
CSF TEST ABNORMAL ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
CYSTOID MACULAR OEDEMA ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 2 FDA reports)
DEAFNESS CONGENITAL ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DELAYED ENGRAFTMENT ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DENTAL IMPLANTATION ( 2 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DESMOID TUMOUR ( 2 FDA reports)
DIABETIC FOETOPATHY ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 2 FDA reports)
EATING DISORDER SYMPTOM ( 2 FDA reports)
ECTOPIC PREGNANCY ( 2 FDA reports)
EJACULATION DISORDER ( 2 FDA reports)
EJECTION FRACTION ABNORMAL ( 2 FDA reports)
ELBOW OPERATION ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
EMBOLIA CUTIS MEDICAMENTOSA ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
EMBOLISM ARTERIAL ( 2 FDA reports)
ENDOCARDITIS BACTERIAL ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
EPIDERMOLYSIS BULLOSA ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
EXPOSURE VIA FATHER ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EYE INFECTION FUNGAL ( 2 FDA reports)
EYE INFECTION TOXOPLASMAL ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
FACTOR VIII INHIBITION ( 2 FDA reports)
FASCIITIS ( 2 FDA reports)
FEAR OF FALLING ( 2 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 2 FDA reports)
FEMALE GENITAL-DIGESTIVE TRACT FISTULA ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
FLASHBACK ( 2 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III RECURRENT ( 2 FDA reports)
FOOD AVERSION ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FORCED EXPIRATORY VOLUME INCREASED ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GASTRIC CYST ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTRIC LAVAGE ABNORMAL ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTRIC PH DECREASED ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
GENITAL DISORDER FEMALE ( 2 FDA reports)
GENITAL PAIN ( 2 FDA reports)
GENITAL RASH ( 2 FDA reports)
GENITAL SWELLING ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GILBERT'S SYNDROME ( 2 FDA reports)
GINGIVAL DISCOLOURATION ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GLUCAGONOMA ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GRAFT COMPLICATION ( 2 FDA reports)
GRAFT LOSS ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
GROWING PAINS ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMATOMA INFECTION ( 2 FDA reports)
HAEMOBILIA ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HEART RATE ABNORMAL ( 2 FDA reports)
HEPATIC ARTERY OCCLUSION ( 2 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATITIS B ANTIBODY ( 2 FDA reports)
HEPATITIS B DNA INCREASED ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 2 FDA reports)
HERNIA PAIN ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HORDEOLUM ( 2 FDA reports)
HORNER'S SYNDROME ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERCHLORAEMIA ( 2 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOPERFUSION ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 2 FDA reports)
IMPLANT SITE INFLAMMATION ( 2 FDA reports)
INCISION SITE ABSCESS ( 2 FDA reports)
INCISION SITE ERYTHEMA ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INFILTRATION ANAESTHESIA ( 2 FDA reports)
INFUSION SITE INFECTION ( 2 FDA reports)
INGROWN HAIR ( 2 FDA reports)
INGUINAL MASS ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INJECTION SITE DISCHARGE ( 2 FDA reports)
INJECTION SITE DRYNESS ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE INJURY ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 2 FDA reports)
INTERCOSTAL RETRACTION ( 2 FDA reports)
INTERNAL HERNIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
LACRIMATION DECREASED ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LENS DISCOLOURATION ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHATIC DISORDER ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MACULE ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MECONIUM STAIN ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 2 FDA reports)
MEDICAL DEVICE REMOVAL ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENINGITIS LISTERIA ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MOANING ( 2 FDA reports)
MONOCYTOSIS ( 2 FDA reports)
MUCOSAL INFECTION ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MYASTHENIC SYNDROME ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYELITIS TRANSVERSE ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
MYRINGOTOMY ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEPHROGENIC ANAEMIA ( 2 FDA reports)
NERVE ROOT INJURY ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OLFACTORY NERVE DISORDER ( 2 FDA reports)
OLIGODIPSIA ( 2 FDA reports)
OOPHORECTOMY ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 2 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 2 FDA reports)
ORAL PUSTULE ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OSTEITIS DEFORMANS ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
OVULATION PAIN ( 2 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PAGET-SCHROETTER SYNDROME ( 2 FDA reports)
PALPABLE PURPURA ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCREATIC PHLEGMON ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PANOPHTHALMITIS ( 2 FDA reports)
PARANOID PERSONALITY DISORDER ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 2 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 2 FDA reports)
PEDAL PULSE ABNORMAL ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 2 FDA reports)
PERICARDIAL DISEASE ( 2 FDA reports)
PERICARDIAL DRAINAGE ( 2 FDA reports)
PERINEURIAL CYST ( 2 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 2 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PEYRONIE'S DISEASE ( 2 FDA reports)
PHARYNGEAL STENOSIS ( 2 FDA reports)
PHLEBITIS SUPERFICIAL ( 2 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 2 FDA reports)
PILONIDAL CYST ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONECTOMY ( 2 FDA reports)
PNEUMONIA HAEMOPHILUS ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 2 FDA reports)
PO2 ABNORMAL ( 2 FDA reports)
POISONING ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
PORTAL TRIADITIS ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
POST PROCEDURAL BILE LEAK ( 2 FDA reports)
POST PROCEDURAL DIARRHOEA ( 2 FDA reports)
POST PROCEDURAL DISCHARGE ( 2 FDA reports)
POST PROCEDURAL DISCOMFORT ( 2 FDA reports)
POST PROCEDURAL OEDEMA ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
POSTOPERATIVE ADHESION ( 2 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 2 FDA reports)
POSTURING ( 2 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 2 FDA reports)
PRESBYOPIA ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PROPOFOL INFUSION SYNDROME ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROSTATE INFECTION ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROSTHESIS IMPLANTATION ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
PULMONARY SEPSIS ( 2 FDA reports)
RADICULAR PAIN ( 2 FDA reports)
RADICULOPATHY ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RECURRING SKIN BOILS ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENAL MASS ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RESECTION OF RECTUM ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
RESPIRATORY TRACT OEDEMA ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RETINAL OEDEMA ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
RHEUMATOID FACTOR INCREASED ( 2 FDA reports)
RICHTER'S SYNDROME ( 2 FDA reports)
ROSACEA ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SARCOMA ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 2 FDA reports)
SHOULDER OPERATION ( 2 FDA reports)
SINUSITIS BACTERIAL ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
SKIN ULCER HAEMORRHAGE ( 2 FDA reports)
SKULL FRACTURE ( 2 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SMALL INTESTINE GANGRENE ( 2 FDA reports)
SNORING ( 2 FDA reports)
SOPOR ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SPLENIC CYST ( 2 FDA reports)
SPLENIC HAEMATOMA ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
STEAL SYNDROME ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STRESS ULCER ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SUPERFICIAL VEIN PROMINENCE ( 2 FDA reports)
SUPERINFECTION VIRAL ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SUTURE INSERTION ( 2 FDA reports)
TEETH BRITTLE ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TERMINAL DRIBBLING ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THORACIC OUTLET SYNDROME ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
TOE DEFORMITY ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TOOTH HYPOPLASIA ( 2 FDA reports)
TOOTH INJURY ( 2 FDA reports)
TOXIC NEUROPATHY ( 2 FDA reports)
TOXOPLASMOSIS ( 2 FDA reports)
TRACHEITIS ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRICHIASIS ( 2 FDA reports)
TRICHOSPORON INFECTION ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
TUMOUR COMPRESSION ( 2 FDA reports)
TUMOUR FLARE ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
TWIN PREGNANCY ( 2 FDA reports)
ULTRASOUND BILIARY TRACT ABNORMAL ( 2 FDA reports)
UMBILICAL CORD AROUND NECK ( 2 FDA reports)
UMBILICAL HERNIA PERFORATION ( 2 FDA reports)
UPPER EXTREMITY MASS ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VAGINAL BURNING SENSATION ( 2 FDA reports)
VAGINAL CYST ( 2 FDA reports)
VAGINAL DISORDER ( 2 FDA reports)
VAGINAL FISTULA ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VAGUS NERVE DISORDER ( 2 FDA reports)
VASCULAR GRAFT ( 2 FDA reports)
VEILLONELLA INFECTION ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENOUS PRESSURE INCREASED ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
WEIGHT GAIN POOR ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WOUND DEBRIDEMENT ( 2 FDA reports)
WOUND INFECTION BACTERIAL ( 2 FDA reports)
X-RAY LIMB ABNORMAL ( 2 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABNORMAL WITHDRAWAL BLEEDING ( 1 FDA reports)
ABO HAEMOLYTIC DISEASE OF NEWBORN ( 1 FDA reports)
ABO INCOMPATIBILITY ( 1 FDA reports)
ABORTED PREGNANCY ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABORTION THREATENED ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ABSCESS NECK ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
ACROCHORDON ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE PHASE REACTION ( 1 FDA reports)
ADENOID CYSTIC CARCINOMA ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADMINISTRATION SITE REACTION ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
ALBINISM ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALOPECIA TOTALIS ( 1 FDA reports)
ALOPECIA UNIVERSALIS ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
ALVEOLAR OSTEITIS ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
ALVEOLOPLASTY ( 1 FDA reports)
AMIMIA ( 1 FDA reports)
AMINO ACID METABOLISM DISORDER ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA OF PREGNANCY ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APOPTOSIS ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE DRYNESS ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE NODULE ( 1 FDA reports)
APPLICATION SITE PUSTULES ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE SCAR ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 1 FDA reports)
ASBESTOSIS ( 1 FDA reports)
ASPIRATION JOINT ABNORMAL ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATHERECTOMY ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA STAGE IV ( 1 FDA reports)
B-LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
BABESIOSIS ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BARIUM SWALLOW ABNORMAL ( 1 FDA reports)
BARTHOLINITIS ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY BILE DUCT ABNORMAL ( 1 FDA reports)
BIOPSY BRONCHUS ABNORMAL ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY ABNORMAL ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BONE DENSITY INCREASED ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BONE FISTULA ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW NECROSIS ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BORDETELLA INFECTION ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BRACHIAL PLEXOPATHY ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHITIS FUNGAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
BULLOUS IMPETIGO ( 1 FDA reports)
BURN OF INTERNAL ORGANS ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CARNITINE DECREASED ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CAROTIDYNIA ( 1 FDA reports)
CATARACT CONGENITAL ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE NECROSIS ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLESTEATOMA ( 1 FDA reports)
CHONDROMALACIA ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CHRONIC TONSILLITIS ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR XI LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR XII LEVEL DECREASED ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COLOBOMA ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON INJURY ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED PANCREAS ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL AORTIC VALVE STENOSIS ( 1 FDA reports)
CONGENITAL GENITAL MALFORMATION ( 1 FDA reports)
CONGENITAL GENITAL MALFORMATION MALE ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 1 FDA reports)
CONGENITAL INGUINAL HERNIA ( 1 FDA reports)
CONGENITAL MEGAURETER ( 1 FDA reports)
CONGENITAL NOSE MALFORMATION ( 1 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 1 FDA reports)
CONGENITAL RENAL CYST ( 1 FDA reports)
CONGENITAL TORTICOLLIS ( 1 FDA reports)
CONJUNCTIVAL ABRASION ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
CONVULSIONS LOCAL ( 1 FDA reports)
COR TRIATRIATUM ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CSF BACTERIA IDENTIFIED ( 1 FDA reports)
CSF CULTURE POSITIVE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYSTITIS BACTERIAL ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DACRYOCYSTITIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DEVELOPMENTAL GLAUCOMA ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DEVICE SHAPE ALTERATION ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
DIGEORGE'S SYNDROME ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DISTAL ILEAL OBSTRUCTION SYNDROME ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DOUBLE URETER ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 1 FDA reports)
DRY SOCKET ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DYSKINESIA OESOPHAGEAL ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
EAR INFECTION BACTERIAL ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
ECTOPIC ACTH SYNDROME ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENCEPHALITIS TOXIC ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOMETRITIS ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENTEROCOLONIC FISTULA ( 1 FDA reports)
EOSINOPHILIC PUSTULAR FOLLICULITIS ( 1 FDA reports)
EPENDYMITIS ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
ETHMOID SINUS SURGERY ( 1 FDA reports)
EXCESSIVE SKIN ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYE OPERATION COMPLICATION ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACTOR V INHIBITION ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FAHR'S DISEASE ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA DIFFUSE SMALL CELL LYMPHOMA ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE IV ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FRONTAL SINUS OPERATION ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
FUNGAL ENDOCARDITIS ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUSARIUM INFECTION ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC BANDING ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS ADENOVIRUS ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROOESOPHAGEAL CANCER ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL INFECTION ( 1 FDA reports)
GENITAL INFECTION FEMALE ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GENITALIA EXTERNAL PAINFUL ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GINGIVAL INJURY ( 1 FDA reports)
GINGIVAL OPERATION ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULONEPHROPATHY ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRADENIGO'S SYNDROME ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATOMETRA ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOGLOBIN S INCREASED ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMOPERFUSION ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HBV DNA INCREASED ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEART BLOCK CONGENITAL ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HELMINTHIC INFECTION ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC ADENOMA ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC INFECTION FUNGAL ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOMANS' SIGN ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUMAN HERPESVIRUS 7 INFECTION ( 1 FDA reports)
HUMAN IMMUNODEFICIENCY VIRUS TRANSMISSION ( 1 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERTELORISM OF ORBIT ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTONIA NEONATAL ( 1 FDA reports)
HYPERVITAMINOSIS ( 1 FDA reports)
HYPOCOMPLEMENTAEMIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOPARATHYROIDISM ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
IATROGENIC INFECTION ( 1 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANT SITE ULCER ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INFECTED DERMAL CYST ( 1 FDA reports)
INFECTION PROTOZOAL ( 1 FDA reports)
INFECTIVE TENOSYNOVITIS ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFLAMMATORY MYOFIBROBLASTIC TUMOUR ( 1 FDA reports)
INFUSION SITE CELLULITIS ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INFUSION SITE OEDEMA ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INFUSION SITE THROMBOSIS ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INNER EAR INFLAMMATION ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 1 FDA reports)
KARNOFSKY SCALE WORSENED ( 1 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LACTATION INHIBITION THERAPY ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LARYNGEAL GRANULOMA ( 1 FDA reports)
LARYNGITIS FUNGAL ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKAEMOID REACTION ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIGHT ANAESTHESIA ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOOSE BODY IN JOINT ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MAMMOPLASTY ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MANTLE CELL LYMPHOMA RECURRENT ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MEDIASTINAL SHIFT ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEDICAL OBSERVATION ABNORMAL ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS HAEMOPHILUS ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO PELVIS ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICROSPORIDIA INFECTION ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 1 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
MYCOPLASMA TEST POSITIVE ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYOCARDITIS POST INFECTION ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL ABSCESS ( 1 FDA reports)
NASAL CAVITY MASS ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL DISCHARGE DISCOLOURATION ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEONATAL ASPHYXIA ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEONATAL RESPIRATORY ACIDOSIS ( 1 FDA reports)
NEONATAL TACHYPNOEA ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NERVE STIMULATION TEST ABNORMAL ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NORMAL DELIVERY ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSTRUCTED LABOUR ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
OCCUPATIONAL THERAPY ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OEDEMATOUS PANCREATITIS ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL IRRITATION ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
OPHTHALMIA NEONATORUM ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORCHITIS NONINFECTIVE ( 1 FDA reports)
OROANTRAL FISTULA ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOPEDIC EXAMINATION ( 1 FDA reports)
OSTEOGENESIS IMPERFECTA ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OSTEOSYNTHESIS ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PALINDROMIC RHEUMATISM ( 1 FDA reports)
PANCREATECTOMY ( 1 FDA reports)
PANCREATIC ABSCESS ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC INJURY ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PANTOEA AGGLOMERANS INFECTION ( 1 FDA reports)
PAPILLARY MUSCLE RUPTURE ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARASITE BLOOD TEST POSITIVE ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PAROPHTHALMIA ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PELVIC DISCOMFORT ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE NECROSIS ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIHEPATIC ABSCESS ( 1 FDA reports)
PERIODONTAL OPERATION ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PHARYNGEAL CANDIDIASIS ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBITIS INFECTIVE ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PHYSIOTHERAPY ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMONIA BLASTOMYCES ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYCYSTIC LIVER DISEASE ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PORPHYRIA ACUTE ( 1 FDA reports)
PORTAL VEIN PHLEBITIS ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 1 FDA reports)
POST LAMINECTOMY SYNDROME ( 1 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST TRANSPLANT DISTAL LIMB SYNDROME ( 1 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
POST-TUSSIVE VOMITING ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROCTOCOLECTOMY ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROTEIN ALBUMIN RATIO INCREASED ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSEUDOPOLYP ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY HYPERTENSIVE CRISIS ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PULMONARY MALFORMATION ( 1 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PURULENT PERICARDITIS ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
PYODERMA ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADIATION MUCOSITIS ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RADIOTHERAPY TO BONE ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RECTAL FISTULA REPAIR ( 1 FDA reports)
RECTAL STENOSIS ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RELAPSING FEVER ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RESPIRATORY DEPTH DECREASED ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETICULOCYTOPENIA ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL INFILTRATES ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETINAL NEOVASCULARISATION ( 1 FDA reports)
RETINOPATHY OF PREMATURITY ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 1 FDA reports)
RETROPHARYNGEAL ABSCESS ( 1 FDA reports)
RETROPLACENTAL HAEMATOMA ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALIVARY GLAND DISORDER ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCROTAL VARICOSE VEINS ( 1 FDA reports)
SEBORRHOEA ( 1 FDA reports)
SECONDARY HYPOTHYROIDISM ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SHONE COMPLEX ( 1 FDA reports)
SHOULDER ARTHROPLASTY ( 1 FDA reports)
SIALOCELE ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SIGNET-RING CELL CARCINOMA ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SINUS ANTROSTOMY ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKIN GRAFT FAILURE ( 1 FDA reports)
SKIN GRAFT INFECTION ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINE OPERATION ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SPEECH REHABILITATION ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CORD HAEMORRHAGE ( 1 FDA reports)
SPINAL CORD INFECTION ( 1 FDA reports)
SPINAL CORD ISCHAEMIA ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SPLENIC INJURY ( 1 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 1 FDA reports)
SPLENIC VEIN OCCLUSION ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STARING ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STENT REMOVAL ( 1 FDA reports)
STIFF-MAN SYNDROME ( 1 FDA reports)
STREPTOCOCCAL ABSCESS ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SWEAT GLAND INFECTION ( 1 FDA reports)
SYMBLEPHARON ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TABLET ISSUE ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
THALASSAEMIA BETA ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THORACOTOMY ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THROMBOSED VARICOSE VEIN ( 1 FDA reports)
THYMECTOMY ( 1 FDA reports)
THYMOMA ( 1 FDA reports)
THYROID CYST ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSILLAR INFLAMMATION ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH IMPACTED ( 1 FDA reports)
TOOTH REPAIR ( 1 FDA reports)
TOURETTE'S DISORDER ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHOMA ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 1 FDA reports)
UHTHOFF'S PHENOMENON ( 1 FDA reports)
ULNAR NERVE PALSY ( 1 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
UMBILICAL CORD ABNORMALITY ( 1 FDA reports)
UMBILICAL HERNIA REPAIR ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETHRAL CANCER ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY GLYCOSAMINOGLYCANS INCREASED ( 1 FDA reports)
URINARY TRACT INFLAMMATION ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE CALCIUM/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
URINOMA ( 1 FDA reports)
UROGENITAL HAEMORRHAGE ( 1 FDA reports)
URTICARIA CHRONIC ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE INFECTION ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
VAGINAL CANCER STAGE 0 ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VARICELLA POST VACCINE ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASCULAR SKIN DISORDER ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENIPUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VERTEBROPLASTY ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VIRAL DNA TEST POSITIVE ( 1 FDA reports)
VIRAL MUTATION IDENTIFIED ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VIRUS CULTURE POSITIVE ( 1 FDA reports)
VISCERAL LEISHMANIASIS ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITAMIN A INCREASED ( 1 FDA reports)
VOCAL CORD CYST ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VOLVULUS OF SMALL BOWEL ( 1 FDA reports)
VOMITING NEONATAL ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VULVAL OEDEMA ( 1 FDA reports)
VULVOVAGINAL ADHESION ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
VULVOVAGINAL RASH ( 1 FDA reports)
VULVOVAGINAL SWELLING ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WITHDRAWAL BLEED ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
X-LINKED CHROMOSOMAL DISORDER ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
XANTHOCHROMIA ( 1 FDA reports)

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