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

ALANINE AMINOTRANSFERASE INCREASED ( 755 FDA reports)
DIARRHOEA ( 719 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 711 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 641 FDA reports)
PYREXIA ( 601 FDA reports)
NAUSEA ( 556 FDA reports)
ARTHRALGIA ( 530 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 491 FDA reports)
DYSPNOEA ( 484 FDA reports)
RHEUMATOID ARTHRITIS ( 476 FDA reports)
PNEUMONIA ( 444 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 432 FDA reports)
HYPERTENSION ( 432 FDA reports)
ASTHENIA ( 428 FDA reports)
FATIGUE ( 413 FDA reports)
HEADACHE ( 401 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 392 FDA reports)
VOMITING ( 386 FDA reports)
PAIN ( 380 FDA reports)
INJECTION SITE PAIN ( 376 FDA reports)
WEIGHT DECREASED ( 376 FDA reports)
DRUG INEFFECTIVE ( 356 FDA reports)
PAIN IN EXTREMITY ( 356 FDA reports)
ANAEMIA ( 351 FDA reports)
RASH ( 348 FDA reports)
DIZZINESS ( 283 FDA reports)
PRURITUS ( 277 FDA reports)
COUGH ( 272 FDA reports)
RENAL FAILURE ( 266 FDA reports)
ABDOMINAL PAIN ( 256 FDA reports)
MALAISE ( 256 FDA reports)
OEDEMA PERIPHERAL ( 250 FDA reports)
INJECTION SITE ERYTHEMA ( 243 FDA reports)
MYOCARDIAL INFARCTION ( 241 FDA reports)
INTERSTITIAL LUNG DISEASE ( 236 FDA reports)
CONDITION AGGRAVATED ( 231 FDA reports)
RESPIRATORY FAILURE ( 216 FDA reports)
CHEST PAIN ( 211 FDA reports)
FALL ( 211 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 211 FDA reports)
HAEMOGLOBIN DECREASED ( 209 FDA reports)
ALOPECIA ( 203 FDA reports)
SEPSIS ( 203 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 196 FDA reports)
CARDIAC FAILURE ( 191 FDA reports)
PLEURAL EFFUSION ( 191 FDA reports)
GAIT DISTURBANCE ( 190 FDA reports)
BACK PAIN ( 188 FDA reports)
HYPOAESTHESIA ( 186 FDA reports)
PARAESTHESIA ( 183 FDA reports)
DEATH ( 181 FDA reports)
BLOOD PRESSURE INCREASED ( 174 FDA reports)
URINARY TRACT INFECTION ( 172 FDA reports)
NASOPHARYNGITIS ( 171 FDA reports)
JOINT SWELLING ( 168 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 167 FDA reports)
HEPATIC ENZYME INCREASED ( 165 FDA reports)
LIVER DISORDER ( 162 FDA reports)
INFECTION ( 160 FDA reports)
DEPRESSION ( 159 FDA reports)
ERYTHEMA ( 158 FDA reports)
WEIGHT INCREASED ( 158 FDA reports)
PLATELET COUNT DECREASED ( 157 FDA reports)
INJECTION SITE PRURITUS ( 153 FDA reports)
BLOOD BILIRUBIN INCREASED ( 152 FDA reports)
ANOREXIA ( 151 FDA reports)
BRONCHITIS ( 151 FDA reports)
PANCYTOPENIA ( 149 FDA reports)
THROMBOCYTOPENIA ( 149 FDA reports)
BLOOD CREATININE INCREASED ( 143 FDA reports)
IMPAIRED HEALING ( 142 FDA reports)
ABDOMINAL PAIN UPPER ( 141 FDA reports)
RENAL FAILURE ACUTE ( 141 FDA reports)
DEHYDRATION ( 139 FDA reports)
PULMONARY EMBOLISM ( 137 FDA reports)
INJECTION SITE REACTION ( 136 FDA reports)
MULTI-ORGAN FAILURE ( 135 FDA reports)
STAPHYLOCOCCAL INFECTION ( 134 FDA reports)
ANXIETY ( 133 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 131 FDA reports)
SINUSITIS ( 131 FDA reports)
CHILLS ( 129 FDA reports)
ATRIAL FIBRILLATION ( 127 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 126 FDA reports)
HYPOTENSION ( 125 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 125 FDA reports)
HYPERSENSITIVITY ( 124 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 124 FDA reports)
CEREBROVASCULAR ACCIDENT ( 123 FDA reports)
TACHYCARDIA ( 123 FDA reports)
HEPATIC FAILURE ( 121 FDA reports)
JAUNDICE ( 117 FDA reports)
INJECTION SITE SWELLING ( 116 FDA reports)
LEUKOPENIA ( 116 FDA reports)
INFUSION RELATED REACTION ( 114 FDA reports)
INSOMNIA ( 114 FDA reports)
CELLULITIS ( 112 FDA reports)
OSTEOARTHRITIS ( 112 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 111 FDA reports)
ARTHROPATHY ( 110 FDA reports)
ARTHRITIS ( 109 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 109 FDA reports)
TRANSAMINASES INCREASED ( 108 FDA reports)
DECREASED APPETITE ( 106 FDA reports)
HEPATITIS ( 104 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 103 FDA reports)
BLOOD GLUCOSE INCREASED ( 103 FDA reports)
INJECTION SITE IRRITATION ( 103 FDA reports)
OEDEMA ( 102 FDA reports)
PSORIASIS ( 102 FDA reports)
SYNCOPE ( 102 FDA reports)
MUSCULAR WEAKNESS ( 101 FDA reports)
SEPTIC SHOCK ( 100 FDA reports)
DRUG INTERACTION ( 99 FDA reports)
LOSS OF CONSCIOUSNESS ( 99 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 97 FDA reports)
CONVULSION ( 96 FDA reports)
FEELING ABNORMAL ( 96 FDA reports)
CORONARY ARTERY DISEASE ( 95 FDA reports)
OSTEONECROSIS ( 95 FDA reports)
URTICARIA ( 95 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 94 FDA reports)
OSTEOMYELITIS ( 94 FDA reports)
INJECTION SITE HAEMATOMA ( 93 FDA reports)
HYPERHIDROSIS ( 92 FDA reports)
SWELLING ( 91 FDA reports)
BLOOD UREA INCREASED ( 90 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 90 FDA reports)
ABORTION SPONTANEOUS ( 89 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 89 FDA reports)
ABORTION INDUCED ( 88 FDA reports)
INFLAMMATION ( 88 FDA reports)
NEUROPATHY PERIPHERAL ( 87 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 87 FDA reports)
MYALGIA ( 86 FDA reports)
HERPES ZOSTER ( 84 FDA reports)
NEUTROPENIA ( 83 FDA reports)
BLOOD ALBUMIN DECREASED ( 82 FDA reports)
CATARACT ( 81 FDA reports)
TREMOR ( 79 FDA reports)
CONFUSIONAL STATE ( 78 FDA reports)
PNEUMONITIS ( 78 FDA reports)
DYSPHAGIA ( 77 FDA reports)
STOMATITIS ( 77 FDA reports)
ABDOMINAL DISTENSION ( 76 FDA reports)
BREAST CANCER ( 75 FDA reports)
DIABETES MELLITUS ( 75 FDA reports)
PREGNANCY ( 75 FDA reports)
PULMONARY OEDEMA ( 74 FDA reports)
CONTUSION ( 73 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 73 FDA reports)
LYMPHADENOPATHY ( 73 FDA reports)
PALPITATIONS ( 73 FDA reports)
DEEP VEIN THROMBOSIS ( 72 FDA reports)
HEPATIC STEATOSIS ( 72 FDA reports)
INFLUENZA ( 72 FDA reports)
MUSCLE SPASMS ( 72 FDA reports)
DIVERTICULITIS ( 71 FDA reports)
INJECTION SITE BRUISING ( 71 FDA reports)
ASTHMA ( 70 FDA reports)
CARDIAC ARREST ( 70 FDA reports)
GASTRIC ULCER ( 70 FDA reports)
OSTEOPOROSIS ( 70 FDA reports)
RASH PRURITIC ( 70 FDA reports)
TUBERCULOSIS ( 68 FDA reports)
MEDICATION ERROR ( 67 FDA reports)
CARDIAC DISORDER ( 66 FDA reports)
HYPOKALAEMIA ( 66 FDA reports)
MOBILITY DECREASED ( 66 FDA reports)
PULMONARY FIBROSIS ( 66 FDA reports)
SOMNOLENCE ( 66 FDA reports)
VISION BLURRED ( 66 FDA reports)
BURSITIS ( 65 FDA reports)
CHEST DISCOMFORT ( 65 FDA reports)
PANCREATITIS ( 65 FDA reports)
DYSPEPSIA ( 64 FDA reports)
GASTRITIS ( 64 FDA reports)
HYPOXIA ( 64 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 63 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 63 FDA reports)
LUNG DISORDER ( 63 FDA reports)
LUNG NEOPLASM ( 63 FDA reports)
MOUTH ULCERATION ( 63 FDA reports)
OFF LABEL USE ( 63 FDA reports)
ASCITES ( 62 FDA reports)
MUSCULOSKELETAL PAIN ( 61 FDA reports)
FEMUR FRACTURE ( 60 FDA reports)
HEART RATE INCREASED ( 60 FDA reports)
INJECTION SITE WARMTH ( 60 FDA reports)
RASH ERYTHEMATOUS ( 60 FDA reports)
HEPATOTOXICITY ( 59 FDA reports)
LOCALISED INFECTION ( 59 FDA reports)
STEVENS-JOHNSON SYNDROME ( 59 FDA reports)
DRUG HYPERSENSITIVITY ( 58 FDA reports)
HEPATOCELLULAR DAMAGE ( 58 FDA reports)
SKIN ULCER ( 58 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 57 FDA reports)
VIRAL INFECTION ( 57 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 56 FDA reports)
DYSGEUSIA ( 56 FDA reports)
PLEURISY ( 56 FDA reports)
GASTROINTESTINAL DISORDER ( 54 FDA reports)
HAEMATOCRIT DECREASED ( 54 FDA reports)
OROPHARYNGEAL PAIN ( 54 FDA reports)
PULMONARY HYPERTENSION ( 54 FDA reports)
INFLUENZA LIKE ILLNESS ( 53 FDA reports)
JOINT STIFFNESS ( 53 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 53 FDA reports)
MELAENA ( 53 FDA reports)
VASCULITIS ( 53 FDA reports)
VERTIGO ( 53 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 52 FDA reports)
PERICARDIAL EFFUSION ( 52 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 52 FDA reports)
SHOCK ( 52 FDA reports)
CONSTIPATION ( 51 FDA reports)
DRUG EFFECT DECREASED ( 51 FDA reports)
INJECTION SITE HAEMORRHAGE ( 51 FDA reports)
LABORATORY TEST ABNORMAL ( 51 FDA reports)
NECK PAIN ( 51 FDA reports)
PROTEIN TOTAL DECREASED ( 51 FDA reports)
AMNESIA ( 50 FDA reports)
ARTHRITIS BACTERIAL ( 50 FDA reports)
CHOLESTASIS ( 50 FDA reports)
CYST ( 50 FDA reports)
DIPLOPIA ( 50 FDA reports)
DYSPNOEA EXERTIONAL ( 50 FDA reports)
RENAL DISORDER ( 50 FDA reports)
VISUAL IMPAIRMENT ( 50 FDA reports)
ABDOMINAL DISCOMFORT ( 49 FDA reports)
BALANCE DISORDER ( 49 FDA reports)
CARDIO-RESPIRATORY ARREST ( 49 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 49 FDA reports)
NIGHT SWEATS ( 49 FDA reports)
RENAL IMPAIRMENT ( 49 FDA reports)
BLISTER ( 48 FDA reports)
DUODENAL ULCER ( 48 FDA reports)
GASTROENTERITIS ( 48 FDA reports)
PLATELET COUNT INCREASED ( 48 FDA reports)
SWELLING FACE ( 48 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 48 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 48 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 47 FDA reports)
BLOOD PRESSURE DECREASED ( 47 FDA reports)
KNEE ARTHROPLASTY ( 47 FDA reports)
ABASIA ( 46 FDA reports)
ANGINA PECTORIS ( 46 FDA reports)
CHOLELITHIASIS ( 46 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 46 FDA reports)
RECTAL HAEMORRHAGE ( 46 FDA reports)
THROMBOSIS ( 46 FDA reports)
BONE PAIN ( 45 FDA reports)
CARDIOMYOPATHY ( 45 FDA reports)
COMA ( 45 FDA reports)
CYTOLYTIC HEPATITIS ( 45 FDA reports)
PNEUMOTHORAX ( 45 FDA reports)
PSEUDOMONAS INFECTION ( 45 FDA reports)
SURGERY ( 45 FDA reports)
CARPAL TUNNEL SYNDROME ( 44 FDA reports)
COLITIS ( 44 FDA reports)
FEELING HOT ( 44 FDA reports)
FUNGAL INFECTION ( 44 FDA reports)
LUNG INFECTION ( 44 FDA reports)
LUNG NEOPLASM MALIGNANT ( 44 FDA reports)
PRODUCTIVE COUGH ( 44 FDA reports)
RHEUMATOID NODULE ( 44 FDA reports)
SYNOVITIS ( 44 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 44 FDA reports)
ARRHYTHMIA ( 43 FDA reports)
CHROMATURIA ( 43 FDA reports)
DRUG TOXICITY ( 43 FDA reports)
DRY MOUTH ( 43 FDA reports)
MIGRAINE ( 43 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 43 FDA reports)
PALLOR ( 43 FDA reports)
HAEMATEMESIS ( 42 FDA reports)
HALLUCINATION ( 42 FDA reports)
HEPATIC CIRRHOSIS ( 42 FDA reports)
PSORIATIC ARTHROPATHY ( 42 FDA reports)
COAGULOPATHY ( 41 FDA reports)
DRUG DOSE OMISSION ( 41 FDA reports)
HAEMORRHAGE ( 41 FDA reports)
HOT FLUSH ( 41 FDA reports)
LEUKOCYTOSIS ( 41 FDA reports)
LUNG INFILTRATION ( 41 FDA reports)
LUPUS-LIKE SYNDROME ( 41 FDA reports)
WOUND ( 41 FDA reports)
ABSCESS ( 40 FDA reports)
AGRANULOCYTOSIS ( 40 FDA reports)
BLOOD POTASSIUM DECREASED ( 40 FDA reports)
MALIGNANT MELANOMA ( 40 FDA reports)
RESPIRATORY DISORDER ( 40 FDA reports)
RESPIRATORY DISTRESS ( 40 FDA reports)
SKIN DISORDER ( 40 FDA reports)
SKIN EXFOLIATION ( 40 FDA reports)
ULCER ( 40 FDA reports)
CEREBRAL INFARCTION ( 39 FDA reports)
HAEMATURIA ( 39 FDA reports)
INJECTION SITE INDURATION ( 39 FDA reports)
SLEEP DISORDER ( 39 FDA reports)
VISUAL ACUITY REDUCED ( 39 FDA reports)
BURNING SENSATION ( 38 FDA reports)
EPISTAXIS ( 38 FDA reports)
PRURITUS GENERALISED ( 38 FDA reports)
SPINAL DISORDER ( 38 FDA reports)
URINARY INCONTINENCE ( 38 FDA reports)
BASAL CELL CARCINOMA ( 37 FDA reports)
BONE DISORDER ( 37 FDA reports)
DISORIENTATION ( 37 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 37 FDA reports)
HYPONATRAEMIA ( 37 FDA reports)
OXYGEN SATURATION DECREASED ( 37 FDA reports)
SKIN LESION ( 37 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 36 FDA reports)
BLADDER CANCER ( 36 FDA reports)
EOSINOPHILIA ( 36 FDA reports)
LUMBAR SPINAL STENOSIS ( 36 FDA reports)
NODULE ( 36 FDA reports)
RASH MACULAR ( 36 FDA reports)
SKIN DISCOLOURATION ( 36 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 36 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 35 FDA reports)
CANDIDIASIS ( 35 FDA reports)
FIBROMYALGIA ( 35 FDA reports)
GENERALISED OEDEMA ( 35 FDA reports)
HAEMATOMA ( 35 FDA reports)
HEMIPARESIS ( 35 FDA reports)
HYPERTENSIVE CRISIS ( 35 FDA reports)
POST PROCEDURAL COMPLICATION ( 35 FDA reports)
PURPURA ( 35 FDA reports)
BLINDNESS ( 34 FDA reports)
CARDIAC MURMUR ( 34 FDA reports)
EMPHYSEMA ( 34 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 34 FDA reports)
LABILE BLOOD PRESSURE ( 34 FDA reports)
PHARYNGITIS ( 34 FDA reports)
PHOTOSENSITIVITY REACTION ( 34 FDA reports)
PULMONARY TUBERCULOSIS ( 34 FDA reports)
RASH GENERALISED ( 34 FDA reports)
SPINAL OSTEOARTHRITIS ( 34 FDA reports)
WOUND INFECTION ( 34 FDA reports)
CHOLECYSTITIS ( 33 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 33 FDA reports)
HEPATOMEGALY ( 33 FDA reports)
LYMPHOMA ( 33 FDA reports)
PROTEINURIA ( 33 FDA reports)
ACUTE HEPATIC FAILURE ( 32 FDA reports)
APHTHOUS STOMATITIS ( 32 FDA reports)
DRUG ERUPTION ( 32 FDA reports)
HAEMORRHOIDS ( 32 FDA reports)
HYPOGLYCAEMIA ( 32 FDA reports)
INJURY ( 32 FDA reports)
PNEUMONIA BACTERIAL ( 32 FDA reports)
POLYNEUROPATHY ( 32 FDA reports)
PREMATURE BABY ( 32 FDA reports)
PROTEIN URINE PRESENT ( 32 FDA reports)
RENAL FAILURE CHRONIC ( 32 FDA reports)
RESPIRATORY TRACT INFECTION ( 32 FDA reports)
BLOOD SODIUM DECREASED ( 31 FDA reports)
CIRCULATORY COLLAPSE ( 31 FDA reports)
CORONARY ARTERY OCCLUSION ( 31 FDA reports)
DRY EYE ( 31 FDA reports)
HYPERCHOLESTEROLAEMIA ( 31 FDA reports)
HYPERGLYCAEMIA ( 31 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 31 FDA reports)
MENTAL STATUS CHANGES ( 31 FDA reports)
NASAL CONGESTION ( 31 FDA reports)
RASH MACULO-PAPULAR ( 31 FDA reports)
RHEUMATOID LUNG ( 31 FDA reports)
SKIN NECROSIS ( 31 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 31 FDA reports)
CARDIOMEGALY ( 30 FDA reports)
COLITIS ULCERATIVE ( 30 FDA reports)
FAECES DISCOLOURED ( 30 FDA reports)
HIATUS HERNIA ( 30 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 30 FDA reports)
MEMORY IMPAIRMENT ( 30 FDA reports)
MITRAL VALVE INCOMPETENCE ( 30 FDA reports)
OVARIAN CANCER ( 30 FDA reports)
RHABDOMYOLYSIS ( 30 FDA reports)
SCIATICA ( 30 FDA reports)
SINUS TACHYCARDIA ( 30 FDA reports)
TINNITUS ( 30 FDA reports)
WHEEZING ( 30 FDA reports)
CAESAREAN SECTION ( 29 FDA reports)
CYSTITIS ( 29 FDA reports)
MYOSITIS ( 29 FDA reports)
OESOPHAGITIS ( 29 FDA reports)
PANCREATITIS ACUTE ( 29 FDA reports)
PERITONITIS ( 29 FDA reports)
POLYMYOSITIS ( 29 FDA reports)
SLEEP APNOEA SYNDROME ( 29 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 29 FDA reports)
SWOLLEN TONGUE ( 29 FDA reports)
SYNOVIAL CYST ( 29 FDA reports)
THROAT IRRITATION ( 29 FDA reports)
VENTRICULAR TACHYCARDIA ( 29 FDA reports)
BLOOD URINE PRESENT ( 28 FDA reports)
BODY TEMPERATURE INCREASED ( 28 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 28 FDA reports)
DIALYSIS ( 28 FDA reports)
FLUSHING ( 28 FDA reports)
HAEMODIALYSIS ( 28 FDA reports)
HYPOALBUMINAEMIA ( 28 FDA reports)
INTENTIONAL DRUG MISUSE ( 28 FDA reports)
JOINT EFFUSION ( 28 FDA reports)
LOWER LIMB FRACTURE ( 28 FDA reports)
MALNUTRITION ( 28 FDA reports)
NEPHROLITHIASIS ( 28 FDA reports)
NERVOUSNESS ( 28 FDA reports)
STRESS ( 28 FDA reports)
TENDON RUPTURE ( 28 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 28 FDA reports)
ACUTE RESPIRATORY FAILURE ( 27 FDA reports)
BLOOD POTASSIUM INCREASED ( 27 FDA reports)
CYANOSIS ( 27 FDA reports)
FOOT FRACTURE ( 27 FDA reports)
GASTRIC CANCER ( 27 FDA reports)
HEPATITIS TOXIC ( 27 FDA reports)
INJECTION SITE RASH ( 27 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 27 FDA reports)
LUNG ABSCESS ( 27 FDA reports)
OVERDOSE ( 27 FDA reports)
PAIN IN JAW ( 27 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 27 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 27 FDA reports)
PYELONEPHRITIS ACUTE ( 27 FDA reports)
SKIN LACERATION ( 27 FDA reports)
TREATMENT NONCOMPLIANCE ( 27 FDA reports)
TYPE 2 DIABETES MELLITUS ( 27 FDA reports)
ABSCESS LIMB ( 26 FDA reports)
ADVERSE EVENT ( 26 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 26 FDA reports)
DISSEMINATED TUBERCULOSIS ( 26 FDA reports)
GLUCOSE URINE PRESENT ( 26 FDA reports)
HAEMATOCHEZIA ( 26 FDA reports)
INCORRECT DOSE ADMINISTERED ( 26 FDA reports)
NERVE COMPRESSION ( 26 FDA reports)
PANCREATIC CARCINOMA ( 26 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 26 FDA reports)
RASH PAPULAR ( 26 FDA reports)
RASH PUSTULAR ( 26 FDA reports)
SCAR ( 26 FDA reports)
UTERINE CANCER ( 26 FDA reports)
ANGIOEDEMA ( 25 FDA reports)
ATELECTASIS ( 25 FDA reports)
BONE MARROW DEPRESSION ( 25 FDA reports)
CROHN'S DISEASE ( 25 FDA reports)
DEAFNESS ( 25 FDA reports)
DYSPHONIA ( 25 FDA reports)
ERYSIPELAS ( 25 FDA reports)
GASTRIC DISORDER ( 25 FDA reports)
HYPERKERATOSIS ( 25 FDA reports)
HYPOPROTEINAEMIA ( 25 FDA reports)
JOINT INJURY ( 25 FDA reports)
NERVOUS SYSTEM DISORDER ( 25 FDA reports)
POLLAKIURIA ( 25 FDA reports)
RHINORRHOEA ( 25 FDA reports)
SPEECH DISORDER ( 25 FDA reports)
SPINAL COLUMN STENOSIS ( 25 FDA reports)
BRADYCARDIA ( 24 FDA reports)
CARDIOVASCULAR DISORDER ( 24 FDA reports)
CHEST X-RAY ABNORMAL ( 24 FDA reports)
DENTAL CARIES ( 24 FDA reports)
DERMATITIS ( 24 FDA reports)
DYSURIA ( 24 FDA reports)
EYE DISORDER ( 24 FDA reports)
GRANULOMA ( 24 FDA reports)
HYPOAESTHESIA ORAL ( 24 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 24 FDA reports)
INTESTINAL PERFORATION ( 24 FDA reports)
JAW FRACTURE ( 24 FDA reports)
LETHARGY ( 24 FDA reports)
NEPHROTIC SYNDROME ( 24 FDA reports)
OSTEOPENIA ( 24 FDA reports)
PERICARDITIS ( 24 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 24 FDA reports)
PROSTATE CANCER ( 24 FDA reports)
SQUAMOUS CELL CARCINOMA ( 24 FDA reports)
URETERIC STENOSIS ( 24 FDA reports)
ADVERSE DRUG REACTION ( 23 FDA reports)
ANKLE FRACTURE ( 23 FDA reports)
APHASIA ( 23 FDA reports)
ARTHRITIS INFECTIVE ( 23 FDA reports)
BRONCHOPNEUMONIA ( 23 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 23 FDA reports)
DYSARTHRIA ( 23 FDA reports)
ECZEMA ( 23 FDA reports)
GRAND MAL CONVULSION ( 23 FDA reports)
HEPATIC CONGESTION ( 23 FDA reports)
HIP ARTHROPLASTY ( 23 FDA reports)
IMMUNODEFICIENCY ( 23 FDA reports)
MYELODYSPLASTIC SYNDROME ( 23 FDA reports)
MYOCARDIAL ISCHAEMIA ( 23 FDA reports)
NECROSIS ( 23 FDA reports)
OCULAR HYPERAEMIA ( 23 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 23 FDA reports)
PULMONARY MASS ( 23 FDA reports)
PUSTULAR PSORIASIS ( 23 FDA reports)
ASPERGILLOSIS ( 22 FDA reports)
BONE MARROW FAILURE ( 22 FDA reports)
CARDIOGENIC SHOCK ( 22 FDA reports)
COLON CANCER ( 22 FDA reports)
DRY SKIN ( 22 FDA reports)
FURUNCLE ( 22 FDA reports)
HIP FRACTURE ( 22 FDA reports)
HYPERTHERMIA ( 22 FDA reports)
HYPOTHYROIDISM ( 22 FDA reports)
INJECTION SITE URTICARIA ( 22 FDA reports)
LIMB INJURY ( 22 FDA reports)
LIPASE INCREASED ( 22 FDA reports)
LIVER INJURY ( 22 FDA reports)
MULTIPLE SCLEROSIS ( 22 FDA reports)
ORAL CANDIDIASIS ( 22 FDA reports)
ORAL INFECTION ( 22 FDA reports)
RENAL CYST ( 22 FDA reports)
ROTATOR CUFF SYNDROME ( 22 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 22 FDA reports)
UNEVALUABLE EVENT ( 22 FDA reports)
VAGINAL HAEMORRHAGE ( 22 FDA reports)
BLOOD AMYLASE INCREASED ( 21 FDA reports)
BLOOD CALCIUM DECREASED ( 21 FDA reports)
BONE MARROW TOXICITY ( 21 FDA reports)
BREAST CANCER FEMALE ( 21 FDA reports)
CLOSTRIDIAL INFECTION ( 21 FDA reports)
DISEASE RECURRENCE ( 21 FDA reports)
ENCEPHALOPATHY ( 21 FDA reports)
EYE PAIN ( 21 FDA reports)
EYE SWELLING ( 21 FDA reports)
FLATULENCE ( 21 FDA reports)
ILL-DEFINED DISORDER ( 21 FDA reports)
MOVEMENT DISORDER ( 21 FDA reports)
ROAD TRAFFIC ACCIDENT ( 21 FDA reports)
SINUS CONGESTION ( 21 FDA reports)
TOOTH DISORDER ( 21 FDA reports)
TOOTH FRACTURE ( 21 FDA reports)
TOOTH LOSS ( 21 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 20 FDA reports)
BRAIN OEDEMA ( 20 FDA reports)
CACHEXIA ( 20 FDA reports)
DEMYELINATION ( 20 FDA reports)
EPILEPSY ( 20 FDA reports)
GOITRE ( 20 FDA reports)
HEPATORENAL SYNDROME ( 20 FDA reports)
HYPOVOLAEMIA ( 20 FDA reports)
KIDNEY INFECTION ( 20 FDA reports)
METABOLIC ACIDOSIS ( 20 FDA reports)
MUCOSAL INFLAMMATION ( 20 FDA reports)
ORAL DISORDER ( 20 FDA reports)
PERONEAL NERVE PALSY ( 20 FDA reports)
SENSATION OF HEAVINESS ( 20 FDA reports)
TOOTH ABSCESS ( 20 FDA reports)
TOOTH INFECTION ( 20 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 20 FDA reports)
WOUND DEHISCENCE ( 20 FDA reports)
ANAPHYLACTIC REACTION ( 19 FDA reports)
ANEURYSM ( 19 FDA reports)
ANGIOPATHY ( 19 FDA reports)
BACTERIAL INFECTION ( 19 FDA reports)
BRONCHIECTASIS ( 19 FDA reports)
CARDIAC VALVE DISEASE ( 19 FDA reports)
CEREBRAL HAEMORRHAGE ( 19 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 19 FDA reports)
DECUBITUS ULCER ( 19 FDA reports)
DEPRESSED MOOD ( 19 FDA reports)
DERMATITIS ALLERGIC ( 19 FDA reports)
DERMATITIS PSORIASIFORM ( 19 FDA reports)
DIVERTICULAR PERFORATION ( 19 FDA reports)
DRUG INTOLERANCE ( 19 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 19 FDA reports)
DYSSTASIA ( 19 FDA reports)
FEBRILE NEUTROPENIA ( 19 FDA reports)
FISTULA ( 19 FDA reports)
GALLBLADDER DISORDER ( 19 FDA reports)
HAEMOLYTIC ANAEMIA ( 19 FDA reports)
HAEMOPTYSIS ( 19 FDA reports)
HEARING IMPAIRED ( 19 FDA reports)
HEPATITIS FULMINANT ( 19 FDA reports)
HOSPITALISATION ( 19 FDA reports)
ISCHAEMIC STROKE ( 19 FDA reports)
NO ADVERSE EVENT ( 19 FDA reports)
PERIPHERAL ISCHAEMIA ( 19 FDA reports)
PROTHROMBIN TIME PROLONGED ( 19 FDA reports)
RIB FRACTURE ( 19 FDA reports)
SINUS DISORDER ( 19 FDA reports)
SKIN INFECTION ( 19 FDA reports)
SPONDYLOLISTHESIS ( 19 FDA reports)
STOMACH DISCOMFORT ( 19 FDA reports)
VENTRICULAR FIBRILLATION ( 19 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 18 FDA reports)
AUTOIMMUNE HEPATITIS ( 18 FDA reports)
BACK DISORDER ( 18 FDA reports)
CARDIAC FAILURE ACUTE ( 18 FDA reports)
COLITIS COLLAGENOUS ( 18 FDA reports)
DERMATITIS EXFOLIATIVE ( 18 FDA reports)
DIFFICULTY IN WALKING ( 18 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 18 FDA reports)
HELICOBACTER INFECTION ( 18 FDA reports)
HEPATIC NECROSIS ( 18 FDA reports)
HERPES SIMPLEX ( 18 FDA reports)
HYPERBILIRUBINAEMIA ( 18 FDA reports)
KERATITIS ( 18 FDA reports)
LEUKOENCEPHALOPATHY ( 18 FDA reports)
MENORRHAGIA ( 18 FDA reports)
MENTAL DISORDER ( 18 FDA reports)
PURULENT DISCHARGE ( 18 FDA reports)
SPINAL COMPRESSION FRACTURE ( 18 FDA reports)
AGEUSIA ( 17 FDA reports)
AMYLOIDOSIS ( 17 FDA reports)
ANGINA UNSTABLE ( 17 FDA reports)
BACTERAEMIA ( 17 FDA reports)
BRONCHOSPASM ( 17 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 17 FDA reports)
DEVICE FAILURE ( 17 FDA reports)
DYSAESTHESIA ( 17 FDA reports)
ECONOMIC PROBLEM ( 17 FDA reports)
ENDOCARDITIS ( 17 FDA reports)
FOOT DEFORMITY ( 17 FDA reports)
GASTRITIS EROSIVE ( 17 FDA reports)
GUILLAIN-BARRE SYNDROME ( 17 FDA reports)
HEART RATE DECREASED ( 17 FDA reports)
HERPES VIRUS INFECTION ( 17 FDA reports)
HYPERLIPIDAEMIA ( 17 FDA reports)
INJECTION SITE DISCOLOURATION ( 17 FDA reports)
INJECTION SITE NODULE ( 17 FDA reports)
NECROTISING FASCIITIS ( 17 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 17 FDA reports)
ORAL PAIN ( 17 FDA reports)
SENSORY LOSS ( 17 FDA reports)
SKIN CANCER ( 17 FDA reports)
SNEEZING ( 17 FDA reports)
SUBCUTANEOUS ABSCESS ( 17 FDA reports)
SUBCUTANEOUS NODULE ( 17 FDA reports)
TACHYPNOEA ( 17 FDA reports)
UROSEPSIS ( 17 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 17 FDA reports)
ACNE ( 16 FDA reports)
ACUTE PULMONARY OEDEMA ( 16 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 16 FDA reports)
BLOOD TEST ABNORMAL ( 16 FDA reports)
COGNITIVE DISORDER ( 16 FDA reports)
COLD SWEAT ( 16 FDA reports)
DEVICE RELATED INFECTION ( 16 FDA reports)
EAR PAIN ( 16 FDA reports)
EOSINOPHIL COUNT INCREASED ( 16 FDA reports)
EXTRASYSTOLES ( 16 FDA reports)
HEPATIC TRAUMA ( 16 FDA reports)
HEPATOCELLULAR INJURY ( 16 FDA reports)
HYPERTHYROIDISM ( 16 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 16 FDA reports)
IMMUNOSUPPRESSION ( 16 FDA reports)
LIP SWELLING ( 16 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 16 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 16 FDA reports)
METRORRHAGIA ( 16 FDA reports)
ODYNOPHAGIA ( 16 FDA reports)
POLYARTHRITIS ( 16 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 16 FDA reports)
POSTOPERATIVE INFECTION ( 16 FDA reports)
PULMONARY GRANULOMA ( 16 FDA reports)
SCLERITIS ( 16 FDA reports)
SJOGREN'S SYNDROME ( 16 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 16 FDA reports)
TONSILLITIS ( 16 FDA reports)
AGITATION ( 15 FDA reports)
ARTHRODESIS ( 15 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 15 FDA reports)
COLLAPSE OF LUNG ( 15 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 15 FDA reports)
DYSKINESIA ( 15 FDA reports)
EAR INFECTION ( 15 FDA reports)
ENTEROCOLITIS BACTERIAL ( 15 FDA reports)
EYE IRRITATION ( 15 FDA reports)
FACIAL PALSY ( 15 FDA reports)
FOETAL DISTRESS SYNDROME ( 15 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 15 FDA reports)
HEART RATE IRREGULAR ( 15 FDA reports)
HYPERTENSIVE HEART DISEASE ( 15 FDA reports)
HYPOACUSIS ( 15 FDA reports)
INTESTINAL ISCHAEMIA ( 15 FDA reports)
IRRITABILITY ( 15 FDA reports)
IRRITABLE BOWEL SYNDROME ( 15 FDA reports)
KLEBSIELLA INFECTION ( 15 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 15 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 15 FDA reports)
MYOCLONUS ( 15 FDA reports)
NEUTROPHIL COUNT INCREASED ( 15 FDA reports)
OPEN WOUND ( 15 FDA reports)
OSTEONECROSIS OF JAW ( 15 FDA reports)
PULMONARY CONGESTION ( 15 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 15 FDA reports)
RESPIRATORY ARREST ( 15 FDA reports)
RETINAL HAEMORRHAGE ( 15 FDA reports)
SKIN NODULE ( 15 FDA reports)
SPINAL OPERATION ( 15 FDA reports)
SUICIDE ATTEMPT ( 15 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 15 FDA reports)
THYROID DISORDER ( 15 FDA reports)
TRISMUS ( 15 FDA reports)
URINE OUTPUT DECREASED ( 15 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 15 FDA reports)
ABDOMINAL RIGIDITY ( 14 FDA reports)
ABORTION ( 14 FDA reports)
ACUTE SINUSITIS ( 14 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 14 FDA reports)
BUNION ( 14 FDA reports)
CONJUNCTIVITIS ( 14 FDA reports)
DEFORMITY ( 14 FDA reports)
DEVICE MALFUNCTION ( 14 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 14 FDA reports)
EATING DISORDER ( 14 FDA reports)
ELECTROLYTE IMBALANCE ( 14 FDA reports)
EMOTIONAL DISTRESS ( 14 FDA reports)
ERYTHEMA MULTIFORME ( 14 FDA reports)
ERYTHEMA NODOSUM ( 14 FDA reports)
EYELID OEDEMA ( 14 FDA reports)
FEAR ( 14 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 14 FDA reports)
HAEMORRHAGIC STROKE ( 14 FDA reports)
HEMIPLEGIA ( 14 FDA reports)
HODGKIN'S DISEASE ( 14 FDA reports)
IMMUNE SYSTEM DISORDER ( 14 FDA reports)
IMPAIRED WORK ABILITY ( 14 FDA reports)
INCREASED TENDENCY TO BRUISE ( 14 FDA reports)
INJECTION SITE MASS ( 14 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 14 FDA reports)
JOINT DISLOCATION ( 14 FDA reports)
LIMB DISCOMFORT ( 14 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 14 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 14 FDA reports)
MYOPATHY ( 14 FDA reports)
NEUTROPHIL COUNT DECREASED ( 14 FDA reports)
NIGHTMARE ( 14 FDA reports)
ORTHOSTATIC HYPOTENSION ( 14 FDA reports)
PANIC ATTACK ( 14 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 14 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 14 FDA reports)
PLEURAL FIBROSIS ( 14 FDA reports)
PROCEDURAL PAIN ( 14 FDA reports)
REFLUX OESOPHAGITIS ( 14 FDA reports)
RESPIRATORY TRACT CONGESTION ( 14 FDA reports)
SARCOIDOSIS ( 14 FDA reports)
STRESS FRACTURE ( 14 FDA reports)
THROAT TIGHTNESS ( 14 FDA reports)
THYROID NEOPLASM ( 14 FDA reports)
TROPONIN INCREASED ( 14 FDA reports)
UTERINE DISORDER ( 14 FDA reports)
UVEITIS ( 14 FDA reports)
WOUND COMPLICATION ( 14 FDA reports)
ACCIDENTAL OVERDOSE ( 13 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 13 FDA reports)
ANOSMIA ( 13 FDA reports)
APPENDICITIS PERFORATED ( 13 FDA reports)
ATRIAL FLUTTER ( 13 FDA reports)
B-CELL LYMPHOMA ( 13 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 13 FDA reports)
BODY HEIGHT DECREASED ( 13 FDA reports)
BONE EROSION ( 13 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 13 FDA reports)
COLITIS MICROSCOPIC ( 13 FDA reports)
DISCOMFORT ( 13 FDA reports)
DISEASE PROGRESSION ( 13 FDA reports)
ENCEPHALITIS ( 13 FDA reports)
EXOSTOSIS ( 13 FDA reports)
FACE OEDEMA ( 13 FDA reports)
FAECAL INCONTINENCE ( 13 FDA reports)
GANGRENE ( 13 FDA reports)
GASTRODUODENAL ULCER ( 13 FDA reports)
GENERALISED ERYTHEMA ( 13 FDA reports)
GINGIVITIS ( 13 FDA reports)
GLOSSODYNIA ( 13 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 13 FDA reports)
HALLUCINATION, AUDITORY ( 13 FDA reports)
HEPATIC NEOPLASM ( 13 FDA reports)
HYPERVENTILATION ( 13 FDA reports)
LARGE INTESTINE PERFORATION ( 13 FDA reports)
LIGAMENT SPRAIN ( 13 FDA reports)
LOW TURNOVER OSTEOPATHY ( 13 FDA reports)
LYMPH NODE TUBERCULOSIS ( 13 FDA reports)
MENINGIOMA ( 13 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 13 FDA reports)
MOTOR DYSFUNCTION ( 13 FDA reports)
NEOPLASM MALIGNANT ( 13 FDA reports)
NEPHRITIS INTERSTITIAL ( 13 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 13 FDA reports)
ORAL HERPES ( 13 FDA reports)
OSTEITIS ( 13 FDA reports)
PAPILLOEDEMA ( 13 FDA reports)
PARKINSON'S DISEASE ( 13 FDA reports)
PAROTID GLAND ENLARGEMENT ( 13 FDA reports)
PELVIC PAIN ( 13 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 13 FDA reports)
PETECHIAE ( 13 FDA reports)
PROCEDURAL COMPLICATION ( 13 FDA reports)
PROTHROMBIN TIME SHORTENED ( 13 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 13 FDA reports)
RALES ( 13 FDA reports)
RETINAL DETACHMENT ( 13 FDA reports)
SENSORY DISTURBANCE ( 13 FDA reports)
SKIN HYPERPIGMENTATION ( 13 FDA reports)
SKIN REACTION ( 13 FDA reports)
SKIN WARM ( 13 FDA reports)
SPLENOMEGALY ( 13 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 13 FDA reports)
T-CELL LYMPHOMA ( 13 FDA reports)
TENOSYNOVITIS ( 13 FDA reports)
UPPER LIMB FRACTURE ( 13 FDA reports)
WRIST FRACTURE ( 13 FDA reports)
ABSCESS JAW ( 12 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 12 FDA reports)
ARTERIOSCLEROSIS ( 12 FDA reports)
BLOOD URIC ACID INCREASED ( 12 FDA reports)
BRONCHIAL CARCINOMA ( 12 FDA reports)
BRONCHITIS CHRONIC ( 12 FDA reports)
CHEILITIS ( 12 FDA reports)
CHOKING ( 12 FDA reports)
DELUSION ( 12 FDA reports)
DIVERTICULUM ( 12 FDA reports)
EMPYEMA ( 12 FDA reports)
FLUID RETENTION ( 12 FDA reports)
GINGIVAL DISORDER ( 12 FDA reports)
HEAD INJURY ( 12 FDA reports)
HEPATIC FIBROSIS ( 12 FDA reports)
HEPATITIS ACUTE ( 12 FDA reports)
HUNGER ( 12 FDA reports)
HYPERKALAEMIA ( 12 FDA reports)
HYPOCALCAEMIA ( 12 FDA reports)
JAUNDICE CHOLESTATIC ( 12 FDA reports)
JOINT FLUID DRAINAGE ( 12 FDA reports)
LARYNGITIS ( 12 FDA reports)
LOBAR PNEUMONIA ( 12 FDA reports)
LOCAL SWELLING ( 12 FDA reports)
LYMPHOEDEMA ( 12 FDA reports)
MACULAR DEGENERATION ( 12 FDA reports)
MENISCUS LESION ( 12 FDA reports)
METASTASES TO LIVER ( 12 FDA reports)
MUSCLE STRAIN ( 12 FDA reports)
MUSCLE TIGHTNESS ( 12 FDA reports)
MUSCULOSKELETAL DISORDER ( 12 FDA reports)
MYOCARDITIS ( 12 FDA reports)
NAIL DISORDER ( 12 FDA reports)
OCULAR ICTERUS ( 12 FDA reports)
ORTHOPNOEA ( 12 FDA reports)
PERIPHERAL COLDNESS ( 12 FDA reports)
PHARYNGEAL ULCERATION ( 12 FDA reports)
PHLEBITIS ( 12 FDA reports)
PLEURAL DISORDER ( 12 FDA reports)
PNEUMONIA LEGIONELLA ( 12 FDA reports)
PO2 DECREASED ( 12 FDA reports)
RESTLESS LEGS SYNDROME ( 12 FDA reports)
STREPTOCOCCAL INFECTION ( 12 FDA reports)
STRESS SYMPTOMS ( 12 FDA reports)
SUBDURAL HAEMATOMA ( 12 FDA reports)
SUICIDAL IDEATION ( 12 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 12 FDA reports)
TOXIC SKIN ERUPTION ( 12 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 12 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
UTERINE LEIOMYOMA ( 12 FDA reports)
VENTRICULAR HYPERTROPHY ( 12 FDA reports)
ABDOMINAL HERNIA ( 11 FDA reports)
ANURIA ( 11 FDA reports)
AORTIC VALVE STENOSIS ( 11 FDA reports)
AUTOIMMUNE DISORDER ( 11 FDA reports)
BEDRIDDEN ( 11 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 11 FDA reports)
BLOOD GLUCOSE DECREASED ( 11 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 11 FDA reports)
BLOOD IRON DECREASED ( 11 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 11 FDA reports)
COLITIS ISCHAEMIC ( 11 FDA reports)
DERMATITIS BULLOUS ( 11 FDA reports)
DEVICE BREAKAGE ( 11 FDA reports)
DRUG ADMINISTRATION ERROR ( 11 FDA reports)
DRUG DEPENDENCE ( 11 FDA reports)
DRY THROAT ( 11 FDA reports)
DYSPNOEA AT REST ( 11 FDA reports)
EJECTION FRACTION DECREASED ( 11 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 11 FDA reports)
EOSINOPHILIC PNEUMONIA ( 11 FDA reports)
ESCHERICHIA INFECTION ( 11 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 11 FDA reports)
FIBROSIS ( 11 FDA reports)
FIBULA FRACTURE ( 11 FDA reports)
FUNGAL SKIN INFECTION ( 11 FDA reports)
GASTRIC HAEMORRHAGE ( 11 FDA reports)
GLAUCOMA ( 11 FDA reports)
HAEMODYNAMIC INSTABILITY ( 11 FDA reports)
HAEMORRHAGIC DIATHESIS ( 11 FDA reports)
HALLUCINATION, VISUAL ( 11 FDA reports)
HEPATITIS B ( 11 FDA reports)
HEPATOSPLENOMEGALY ( 11 FDA reports)
HYDRONEPHROSIS ( 11 FDA reports)
HYPOKINESIA ( 11 FDA reports)
ILEUS ( 11 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 11 FDA reports)
INTENTIONAL OVERDOSE ( 11 FDA reports)
INTRACRANIAL ANEURYSM ( 11 FDA reports)
IRON DEFICIENCY ANAEMIA ( 11 FDA reports)
JOINT ARTHROPLASTY ( 11 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 11 FDA reports)
LIVEDO RETICULARIS ( 11 FDA reports)
LOCALISED OEDEMA ( 11 FDA reports)
MULTIPLE INJURIES ( 11 FDA reports)
MUSCLE ATROPHY ( 11 FDA reports)
NERVE INJURY ( 11 FDA reports)
NEURALGIA ( 11 FDA reports)
NEUROPATHY ( 11 FDA reports)
NODULE ON EXTREMITY ( 11 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 11 FDA reports)
PHARYNGEAL OEDEMA ( 11 FDA reports)
PHOTOPHOBIA ( 11 FDA reports)
PLANTAR FASCIITIS ( 11 FDA reports)
PSYCHOTIC DISORDER ( 11 FDA reports)
RETROPERITONEAL ABSCESS ( 11 FDA reports)
SINUS HEADACHE ( 11 FDA reports)
SKELETAL INJURY ( 11 FDA reports)
THERAPY NON-RESPONDER ( 11 FDA reports)
TIBIA FRACTURE ( 11 FDA reports)
TOE AMPUTATION ( 11 FDA reports)
TRACHEITIS ( 11 FDA reports)
URINE ANALYSIS ABNORMAL ( 11 FDA reports)
VENTRICULAR DYSFUNCTION ( 11 FDA reports)
VISUAL DISTURBANCE ( 11 FDA reports)
ABDOMINAL ABSCESS ( 10 FDA reports)
ACIDOSIS ( 10 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 10 FDA reports)
ANAEMIA MEGALOBLASTIC ( 10 FDA reports)
ANGIOPLASTY ( 10 FDA reports)
AORTIC STENOSIS ( 10 FDA reports)
BLOOD CHLORIDE DECREASED ( 10 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 10 FDA reports)
BLOOD PRESSURE ABNORMAL ( 10 FDA reports)
BRAIN NEOPLASM ( 10 FDA reports)
CHONDROPATHY ( 10 FDA reports)
COMPUTERISED TOMOGRAM NORMAL ( 10 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 10 FDA reports)
DEMENTIA ( 10 FDA reports)
DERMAL CYST ( 10 FDA reports)
DERMATITIS CONTACT ( 10 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 10 FDA reports)
DILATATION VENTRICULAR ( 10 FDA reports)
DIZZINESS POSTURAL ( 10 FDA reports)
DRUG TOLERANCE DECREASED ( 10 FDA reports)
DYSLIPIDAEMIA ( 10 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 10 FDA reports)
EXCORIATION ( 10 FDA reports)
EYE PRURITUS ( 10 FDA reports)
FEELING COLD ( 10 FDA reports)
FINGER DEFORMITY ( 10 FDA reports)
FOLLICULITIS ( 10 FDA reports)
FOOT OPERATION ( 10 FDA reports)
FRACTURE DELAYED UNION ( 10 FDA reports)
HYPERSOMNIA ( 10 FDA reports)
HYPOTHERMIA ( 10 FDA reports)
IMPAIRED SELF-CARE ( 10 FDA reports)
INTESTINAL OBSTRUCTION ( 10 FDA reports)
ISCHAEMIA ( 10 FDA reports)
ISCHAEMIC HEPATITIS ( 10 FDA reports)
LEFT VENTRICULAR FAILURE ( 10 FDA reports)
LEG AMPUTATION ( 10 FDA reports)
MENINGITIS ( 10 FDA reports)
MONOPARESIS ( 10 FDA reports)
MUCOUS MEMBRANE DISORDER ( 10 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 10 FDA reports)
MYCOBACTERIAL INFECTION ( 10 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 10 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 10 FDA reports)
ORGANISING PNEUMONIA ( 10 FDA reports)
PANNICULITIS ( 10 FDA reports)
PARAPARESIS ( 10 FDA reports)
PEPTIC ULCER ( 10 FDA reports)
PNEUMOMEDIASTINUM ( 10 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 10 FDA reports)
PYOTHORAX ( 10 FDA reports)
RENAL TUBULAR NECROSIS ( 10 FDA reports)
RESTLESSNESS ( 10 FDA reports)
RETCHING ( 10 FDA reports)
RHEUMATOID FACTOR INCREASED ( 10 FDA reports)
RHINITIS ( 10 FDA reports)
SERUM FERRITIN INCREASED ( 10 FDA reports)
SKIN DEPIGMENTATION ( 10 FDA reports)
SPUTUM DISCOLOURED ( 10 FDA reports)
SUDDEN DEATH ( 10 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 10 FDA reports)
TACHYARRHYTHMIA ( 10 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 10 FDA reports)
THROAT CANCER ( 10 FDA reports)
THYROID CYST ( 10 FDA reports)
TOOTH EXTRACTION ( 10 FDA reports)
ABSCESS INTESTINAL ( 9 FDA reports)
ACTINIC KERATOSIS ( 9 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 9 FDA reports)
AGGRESSION ( 9 FDA reports)
APLASIA PURE RED CELL ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK ( 9 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 9 FDA reports)
BACTERIAL SEPSIS ( 9 FDA reports)
BODY TEMPERATURE DECREASED ( 9 FDA reports)
CHOLECYSTECTOMY ( 9 FDA reports)
CHOLURIA ( 9 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 9 FDA reports)
COORDINATION ABNORMAL ( 9 FDA reports)
CREPITATIONS ( 9 FDA reports)
DIVERTICULUM INTESTINAL ( 9 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 9 FDA reports)
ECCHYMOSIS ( 9 FDA reports)
ENTEROCOCCAL INFECTION ( 9 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 9 FDA reports)
ERB'S PALSY ( 9 FDA reports)
EXTREMITY CONTRACTURE ( 9 FDA reports)
FEMORAL NECK FRACTURE ( 9 FDA reports)
FIBRIN D DIMER INCREASED ( 9 FDA reports)
FRACTURE NONUNION ( 9 FDA reports)
GASTRIC POLYPS ( 9 FDA reports)
GINGIVAL ABSCESS ( 9 FDA reports)
GOUT ( 9 FDA reports)
GROIN PAIN ( 9 FDA reports)
HAEMANGIOMA ( 9 FDA reports)
HYPERCALCAEMIA ( 9 FDA reports)
HYPOAESTHESIA FACIAL ( 9 FDA reports)
HYPOPHAGIA ( 9 FDA reports)
ILEUS PARALYTIC ( 9 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 9 FDA reports)
INCREASED APPETITE ( 9 FDA reports)
INGUINAL HERNIA ( 9 FDA reports)
INJECTION SITE INFLAMMATION ( 9 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 9 FDA reports)
JAW CYST ( 9 FDA reports)
LACERATION ( 9 FDA reports)
LACUNAR INFARCTION ( 9 FDA reports)
LARGE INTESTINAL ULCER ( 9 FDA reports)
LARYNGEAL OEDEMA ( 9 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 9 FDA reports)
LUNG ADENOCARCINOMA ( 9 FDA reports)
LYMPHOCYTOSIS ( 9 FDA reports)
MENINGITIS TUBERCULOUS ( 9 FDA reports)
MICROCYTIC ANAEMIA ( 9 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 9 FDA reports)
NO ADVERSE EFFECT ( 9 FDA reports)
OBESITY ( 9 FDA reports)
OESOPHAGEAL ULCER ( 9 FDA reports)
OPTIC ATROPHY ( 9 FDA reports)
OVARIAN CYST ( 9 FDA reports)
PARALYSIS ( 9 FDA reports)
PATHOLOGICAL FRACTURE ( 9 FDA reports)
PELVIC FRACTURE ( 9 FDA reports)
PERIODONTITIS ( 9 FDA reports)
PRESYNCOPE ( 9 FDA reports)
PYELONEPHRITIS ( 9 FDA reports)
SHOULDER DYSTOCIA ( 9 FDA reports)
SKIN TIGHTNESS ( 9 FDA reports)
SPINAL FRACTURE ( 9 FDA reports)
TONGUE DISORDER ( 9 FDA reports)
TRANSITIONAL CELL CANCER OF THE RENAL PELVIS AND URETER ( 9 FDA reports)
TUBERCULIN TEST POSITIVE ( 9 FDA reports)
VARICOSE VEIN ( 9 FDA reports)
VENTRICULAR HYPOKINESIA ( 9 FDA reports)
WALKING AID USER ( 9 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 9 FDA reports)
WOUND DRAINAGE ( 9 FDA reports)
ABDOMINAL WALL ABSCESS ( 8 FDA reports)
ACCIDENTAL EXPOSURE ( 8 FDA reports)
ADRENAL INSUFFICIENCY ( 8 FDA reports)
ALLERGIC BRONCHITIS ( 8 FDA reports)
ANAPHYLACTIC SHOCK ( 8 FDA reports)
ANKYLOSING SPONDYLITIS ( 8 FDA reports)
AORTIC VALVE INCOMPETENCE ( 8 FDA reports)
APNOEA ( 8 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 8 FDA reports)
ARTHROPOD BITE ( 8 FDA reports)
ASPIRATION ( 8 FDA reports)
ASTERIXIS ( 8 FDA reports)
ATROPHY ( 8 FDA reports)
BENIGN NEOPLASM OF SKIN ( 8 FDA reports)
BIOPSY LIVER ABNORMAL ( 8 FDA reports)
BLOOD CREATINE INCREASED ( 8 FDA reports)
BLOOD CREATININE DECREASED ( 8 FDA reports)
BLOOD CULTURE POSITIVE ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 8 FDA reports)
BLOOD UREA DECREASED ( 8 FDA reports)
CATARACT OPERATION ( 8 FDA reports)
CERVIX CARCINOMA ( 8 FDA reports)
CHRONIC SINUSITIS ( 8 FDA reports)
COMMINUTED FRACTURE ( 8 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 8 FDA reports)
CRYPTOCOCCOSIS ( 8 FDA reports)
DEAFNESS NEUROSENSORY ( 8 FDA reports)
DERMATOMYOSITIS ( 8 FDA reports)
DIASTOLIC DYSFUNCTION ( 8 FDA reports)
DILATATION ATRIAL ( 8 FDA reports)
DISTURBANCE IN ATTENTION ( 8 FDA reports)
DRUG LEVEL INCREASED ( 8 FDA reports)
DYSPHORIA ( 8 FDA reports)
EPIDURITIS ( 8 FDA reports)
FEELING JITTERY ( 8 FDA reports)
FOETAL GROWTH RETARDATION ( 8 FDA reports)
FORMICATION ( 8 FDA reports)
FRACTURE ( 8 FDA reports)
GASTROINTESTINAL INFECTION ( 8 FDA reports)
GLOSSITIS ( 8 FDA reports)
HAEMOLYSIS ( 8 FDA reports)
HEPATIC CYST ( 8 FDA reports)
HEPATIC ENZYME ABNORMAL ( 8 FDA reports)
HEPATIC INFARCTION ( 8 FDA reports)
HEPATIC ISCHAEMIA ( 8 FDA reports)
HORMONE LEVEL ABNORMAL ( 8 FDA reports)
HYPERAEMIA ( 8 FDA reports)
HYPERCOAGULATION ( 8 FDA reports)
HYPERURICAEMIA ( 8 FDA reports)
HYPOMAGNESAEMIA ( 8 FDA reports)
INCISION SITE INFECTION ( 8 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 8 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 8 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 8 FDA reports)
JAW DISORDER ( 8 FDA reports)
JOINT WARMTH ( 8 FDA reports)
LIMB DEFORMITY ( 8 FDA reports)
LUNG CONSOLIDATION ( 8 FDA reports)
MASS ( 8 FDA reports)
MEGACOLON ( 8 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 8 FDA reports)
NEOPLASM ( 8 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 8 FDA reports)
OCCULT BLOOD POSITIVE ( 8 FDA reports)
ONYCHOCLASIS ( 8 FDA reports)
ONYCHOMYCOSIS ( 8 FDA reports)
PARAESTHESIA ORAL ( 8 FDA reports)
PERIORBITAL OEDEMA ( 8 FDA reports)
PHLEBITIS SUPERFICIAL ( 8 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 8 FDA reports)
POST PROCEDURAL INFECTION ( 8 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 8 FDA reports)
PROTEIN TOTAL INCREASED ( 8 FDA reports)
RENAL CANCER ( 8 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 8 FDA reports)
RENAL MASS ( 8 FDA reports)
RENAL PAIN ( 8 FDA reports)
RETINAL VASCULITIS ( 8 FDA reports)
RHEUMATOID VASCULITIS ( 8 FDA reports)
RHINITIS ALLERGIC ( 8 FDA reports)
SINUS BRADYCARDIA ( 8 FDA reports)
SKIN BURNING SENSATION ( 8 FDA reports)
SKIN CANDIDA ( 8 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 8 FDA reports)
SPUTUM CULTURE POSITIVE ( 8 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 8 FDA reports)
SUFFOCATION FEELING ( 8 FDA reports)
T-CELL LYMPHOMA STAGE IV ( 8 FDA reports)
TENDERNESS ( 8 FDA reports)
VASCULITIS NECROTISING ( 8 FDA reports)
VENTRICULAR HYPOPLASIA ( 8 FDA reports)
WEGENER'S GRANULOMATOSIS ( 8 FDA reports)
WOUND SECRETION ( 8 FDA reports)
ABNORMAL SENSATION IN EYE ( 7 FDA reports)
ACCIDENT ( 7 FDA reports)
ACUTE CORONARY SYNDROME ( 7 FDA reports)
AMENORRHOEA ( 7 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 7 FDA reports)
ANGER ( 7 FDA reports)
AORTIC VALVE DISEASE ( 7 FDA reports)
APPENDICITIS ( 7 FDA reports)
ATHEROSCLEROSIS ( 7 FDA reports)
BLOOD ALBUMIN INCREASED ( 7 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 7 FDA reports)
BLOOD MAGNESIUM DECREASED ( 7 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 7 FDA reports)
BRUXISM ( 7 FDA reports)
CAROTID ARTERY STENOSIS ( 7 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 7 FDA reports)
CEREBRAL HAEMATOMA ( 7 FDA reports)
CHOLECYSTITIS INFECTIVE ( 7 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 7 FDA reports)
COLON ADENOMA ( 7 FDA reports)
COLON CANCER RECURRENT ( 7 FDA reports)
CORONARY ARTERY BYPASS ( 7 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 7 FDA reports)
CUTANEOUS VASCULITIS ( 7 FDA reports)
DERMATITIS ATOPIC ( 7 FDA reports)
DEVICE COMPONENT ISSUE ( 7 FDA reports)
DEVICE DISLOCATION ( 7 FDA reports)
DIABETIC NEUROPATHY ( 7 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 7 FDA reports)
DUODENITIS ( 7 FDA reports)
DYSPNOEA EXACERBATED ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 7 FDA reports)
ENCEPHALITIS VIRAL ( 7 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 7 FDA reports)
ERECTILE DYSFUNCTION ( 7 FDA reports)
ESCHERICHIA SEPSIS ( 7 FDA reports)
EXFOLIATIVE RASH ( 7 FDA reports)
EXPOSURE VIA FATHER ( 7 FDA reports)
EYE INFECTION ( 7 FDA reports)
FLANK PAIN ( 7 FDA reports)
FLUID OVERLOAD ( 7 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 7 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 7 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 7 FDA reports)
GLOMERULONEPHRITIS ( 7 FDA reports)
GLOMERULOSCLEROSIS ( 7 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 7 FDA reports)
HAND DEFORMITY ( 7 FDA reports)
HEAD DISCOMFORT ( 7 FDA reports)
HEPATIC ENCEPHALOPATHY ( 7 FDA reports)
HEPATIC LESION ( 7 FDA reports)
HEPATITIS C ( 7 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 7 FDA reports)
HUMERUS FRACTURE ( 7 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 7 FDA reports)
HYPOVOLAEMIC SHOCK ( 7 FDA reports)
INFARCTION ( 7 FDA reports)
INTRACARDIAC THROMBUS ( 7 FDA reports)
JOINT DESTRUCTION ( 7 FDA reports)
JOINT PROSTHESIS USER ( 7 FDA reports)
LACRIMATION INCREASED ( 7 FDA reports)
LENTIGO MALIGNA STAGE I ( 7 FDA reports)
LEUKAEMIA ( 7 FDA reports)
LIGAMENT LAXITY ( 7 FDA reports)
LOOSE STOOLS ( 7 FDA reports)
LYMPHATIC OBSTRUCTION ( 7 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 7 FDA reports)
LYMPHOPENIA ( 7 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 7 FDA reports)
MENINGITIS ASEPTIC ( 7 FDA reports)
MENOPAUSAL DISORDER ( 7 FDA reports)
MENSTRUATION IRREGULAR ( 7 FDA reports)
MENTAL IMPAIRMENT ( 7 FDA reports)
METABOLIC DISORDER ( 7 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 7 FDA reports)
METASTASES TO LYMPH NODES ( 7 FDA reports)
MULTIPLE MYELOMA ( 7 FDA reports)
MUSCLE CRAMP ( 7 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 7 FDA reports)
NERVE ROOT COMPRESSION ( 7 FDA reports)
NIPPLE PAIN ( 7 FDA reports)
NO THERAPEUTIC RESPONSE ( 7 FDA reports)
NOCTURIA ( 7 FDA reports)
NON-CARDIAC CHEST PAIN ( 7 FDA reports)
OLIGURIA ( 7 FDA reports)
ORAL MUCOSAL DISORDER ( 7 FDA reports)
OROPHARYNGEAL BLISTERING ( 7 FDA reports)
PANCREATITIS NECROTISING ( 7 FDA reports)
PARANOIA ( 7 FDA reports)
PCO2 DECREASED ( 7 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 7 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 7 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 7 FDA reports)
POLYURIA ( 7 FDA reports)
PRE-ECLAMPSIA ( 7 FDA reports)
PREGNANCY OF PARTNER ( 7 FDA reports)
PREMATURE LABOUR ( 7 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 7 FDA reports)
RASH VESICULAR ( 7 FDA reports)
SARCOMA ( 7 FDA reports)
SCAB ( 7 FDA reports)
SKIN ODOUR ABNORMAL ( 7 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 7 FDA reports)
SUPERINFECTION ( 7 FDA reports)
TENDON DISORDER ( 7 FDA reports)
TOOTHACHE ( 7 FDA reports)
TRANSFUSION ( 7 FDA reports)
TUBERCULOSIS OF CENTRAL NERVOUS SYSTEM ( 7 FDA reports)
ULCERATIVE KERATITIS ( 7 FDA reports)
VARICOSE ULCERATION ( 7 FDA reports)
VENOUS INSUFFICIENCY ( 7 FDA reports)
VIITH NERVE PARALYSIS ( 7 FDA reports)
VISUAL FIELD DEFECT ( 7 FDA reports)
WRIST SURGERY ( 7 FDA reports)
ABDOMINAL PAIN LOWER ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 6 FDA reports)
ABNORMAL FAECES ( 6 FDA reports)
ABSCESS NECK ( 6 FDA reports)
AKINESIA ( 6 FDA reports)
ALVEOLAR PROTEINOSIS ( 6 FDA reports)
ALVEOLITIS ( 6 FDA reports)
ANAPHYLACTOID SHOCK ( 6 FDA reports)
ANEURYSM RUPTURED ( 6 FDA reports)
ANKLE OPERATION ( 6 FDA reports)
AORTIC THROMBOSIS ( 6 FDA reports)
APLASTIC ANAEMIA ( 6 FDA reports)
APPLICATION SITE PAIN ( 6 FDA reports)
ATAXIA ( 6 FDA reports)
BK VIRUS INFECTION ( 6 FDA reports)
BLEPHARITIS ( 6 FDA reports)
BLOOD COUNT ABNORMAL ( 6 FDA reports)
BLOOD DISORDER ( 6 FDA reports)
BLOOD OESTROGEN DECREASED ( 6 FDA reports)
BLOOD PH INCREASED ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 6 FDA reports)
BRAIN ABSCESS ( 6 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 6 FDA reports)
CARDIAC ANEURYSM ( 6 FDA reports)
CARDIAC TAMPONADE ( 6 FDA reports)
CAROTID ARTERY OCCLUSION ( 6 FDA reports)
CEREBROVASCULAR DISORDER ( 6 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 6 FDA reports)
COLONIC POLYP ( 6 FDA reports)
COMPRESSION FRACTURE ( 6 FDA reports)
CONGENITAL ANOMALY ( 6 FDA reports)
CYSTITIS KLEBSIELLA ( 6 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 6 FDA reports)
DIABETIC KETOACIDOSIS ( 6 FDA reports)
DRUG ABUSER ( 6 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 6 FDA reports)
EMBOLISM ( 6 FDA reports)
EMOTIONAL DISORDER ( 6 FDA reports)
EPIGASTRIC DISCOMFORT ( 6 FDA reports)
EXTRADURAL ABSCESS ( 6 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 6 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 6 FDA reports)
FOETAL DISORDER ( 6 FDA reports)
GASTRIC CANCER RECURRENT ( 6 FDA reports)
GASTRIC PERFORATION ( 6 FDA reports)
GASTRIC ULCER PERFORATION ( 6 FDA reports)
GASTRITIS HAEMORRHAGIC ( 6 FDA reports)
GASTROINTESTINAL PAIN ( 6 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 6 FDA reports)
GINGIVITIS ULCERATIVE ( 6 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 6 FDA reports)
HEPATITIS CHOLESTATIC ( 6 FDA reports)
HIP SURGERY ( 6 FDA reports)
HYPOPHOSPHATAEMIA ( 6 FDA reports)
HYPOREFLEXIA ( 6 FDA reports)
HYSTERECTOMY ( 6 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
INCONTINENCE ( 6 FDA reports)
INJECTION SITE INFECTION ( 6 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 6 FDA reports)
INTERVERTEBRAL DISCITIS ( 6 FDA reports)
LEIOMYOMA ( 6 FDA reports)
LEIOMYOSARCOMA ( 6 FDA reports)
LEUKOPLAKIA ORAL ( 6 FDA reports)
LIMB ASYMMETRY ( 6 FDA reports)
LYMPHADENITIS ( 6 FDA reports)
LYMPHOCYTIC LYMPHOMA ( 6 FDA reports)
MEDICAL DEVICE COMPLICATION ( 6 FDA reports)
MELANOCYTIC NAEVUS ( 6 FDA reports)
METASTASES TO LUNG ( 6 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 6 FDA reports)
MITRAL VALVE PROLAPSE ( 6 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 6 FDA reports)
MONONEUROPATHY MULTIPLEX ( 6 FDA reports)
MOUTH INJURY ( 6 FDA reports)
MUSCLE ENZYME INCREASED ( 6 FDA reports)
MUSCLE RIGIDITY ( 6 FDA reports)
MYDRIASIS ( 6 FDA reports)
NECK MASS ( 6 FDA reports)
NEOPLASM SKIN ( 6 FDA reports)
OEDEMATOUS PANCREATITIS ( 6 FDA reports)
ORAL INTAKE REDUCED ( 6 FDA reports)
ORGAN FAILURE ( 6 FDA reports)
OVARIAN NEOPLASM ( 6 FDA reports)
PANCREATITIS RELAPSING ( 6 FDA reports)
PARATHYROID DISORDER ( 6 FDA reports)
PERIODONTAL DISEASE ( 6 FDA reports)
PERITONEAL EFFUSION ( 6 FDA reports)
PERSONALITY CHANGE ( 6 FDA reports)
PHARYNGEAL ERYTHEMA ( 6 FDA reports)
PITTING OEDEMA ( 6 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 6 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 6 FDA reports)
PORTAL HYPERTENSION ( 6 FDA reports)
PRODUCT QUALITY ISSUE ( 6 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 6 FDA reports)
PSEUDOMONAL SEPSIS ( 6 FDA reports)
PULMONARY CAVITATION ( 6 FDA reports)
PURULENCE ( 6 FDA reports)
PURULENT PERICARDITIS ( 6 FDA reports)
PYODERMA GANGRENOSUM ( 6 FDA reports)
RADICULOPATHY ( 6 FDA reports)
RAYNAUD'S PHENOMENON ( 6 FDA reports)
RECTAL CANCER ( 6 FDA reports)
RENAL INJURY ( 6 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 6 FDA reports)
SENSATION OF FOREIGN BODY ( 6 FDA reports)
SPONDYLOARTHROPATHY ( 6 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 6 FDA reports)
STRIDOR ( 6 FDA reports)
TARDIVE DYSKINESIA ( 6 FDA reports)
TARSAL TUNNEL SYNDROME ( 6 FDA reports)
TENDONITIS ( 6 FDA reports)
THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
THYROID CANCER ( 6 FDA reports)
TINEA PEDIS ( 6 FDA reports)
TONGUE ULCERATION ( 6 FDA reports)
UNRESPONSIVE TO STIMULI ( 6 FDA reports)
URINARY OCCULT BLOOD POSITIVE ( 6 FDA reports)
URINARY TRACT DISORDER ( 6 FDA reports)
URINE COLOUR ABNORMAL ( 6 FDA reports)
VITREOUS FLOATERS ( 6 FDA reports)
VOCAL CORD DISORDER ( 6 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 6 FDA reports)
ABDOMINAL TENDERNESS ( 5 FDA reports)
ACINETOBACTER INFECTION ( 5 FDA reports)
ADENOMA BENIGN ( 5 FDA reports)
ADRENAL MASS ( 5 FDA reports)
ANAEMIA MACROCYTIC ( 5 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ( 5 FDA reports)
ANHEDONIA ( 5 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 5 FDA reports)
AORTIC ANEURYSM RUPTURE ( 5 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 5 FDA reports)
AORTIC BYPASS ( 5 FDA reports)
APPLICATION SITE REACTION ( 5 FDA reports)
AREFLEXIA ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 5 FDA reports)
AZOTAEMIA ( 5 FDA reports)
BACK INJURY ( 5 FDA reports)
BENIGN LUNG NEOPLASM ( 5 FDA reports)
BILE DUCT CANCER ( 5 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 5 FDA reports)
BILIARY COLIC ( 5 FDA reports)
BILIARY DILATATION ( 5 FDA reports)
BIOPSY LUNG ABNORMAL ( 5 FDA reports)
BLINDNESS UNILATERAL ( 5 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 5 FDA reports)
BLOOD BICARBONATE DECREASED ( 5 FDA reports)
BLOOD CHLORIDE INCREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 5 FDA reports)
BLOOD PH DECREASED ( 5 FDA reports)
BLOOD URIC ACID DECREASED ( 5 FDA reports)
BONE CYST ( 5 FDA reports)
BONE DENSITY DECREASED ( 5 FDA reports)
BONE FISTULA ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
BREAST CALCIFICATIONS ( 5 FDA reports)
BREAST DISCHARGE ( 5 FDA reports)
BRONCHOPLEURAL FISTULA ( 5 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 5 FDA reports)
CALCULUS URINARY ( 5 FDA reports)
CARDIOPULMONARY FAILURE ( 5 FDA reports)
CEREBELLAR INFARCTION ( 5 FDA reports)
CERUMEN IMPACTION ( 5 FDA reports)
CERVICAL ROOT PAIN ( 5 FDA reports)
CHEST WALL PAIN ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 5 FDA reports)
COCCIDIOIDOMYCOSIS ( 5 FDA reports)
COLLAGEN DISORDER ( 5 FDA reports)
COMPLETED SUICIDE ( 5 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 5 FDA reports)
CORONARY ARTERY STENOSIS ( 5 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 5 FDA reports)
DENTAL OPERATION ( 5 FDA reports)
DEPENDENCE ( 5 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 5 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 5 FDA reports)
DIABETIC GASTROPARESIS ( 5 FDA reports)
DRUG LEVEL DECREASED ( 5 FDA reports)
DUODENAL FISTULA ( 5 FDA reports)
DUODENAL ULCER PERFORATION ( 5 FDA reports)
DYSHIDROSIS ( 5 FDA reports)
EAR NEOPLASM ( 5 FDA reports)
EMBOLIC STROKE ( 5 FDA reports)
ENTERITIS ( 5 FDA reports)
ENTEROCOLITIS ( 5 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 5 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 5 FDA reports)
EYE INFLAMMATION ( 5 FDA reports)
EYELID PTOSIS ( 5 FDA reports)
FAECALOMA ( 5 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 5 FDA reports)
FINGER AMPUTATION ( 5 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 5 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
FUNGAL SEPSIS ( 5 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 5 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 5 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 5 FDA reports)
HAEMOTHORAX ( 5 FDA reports)
HAIR DISORDER ( 5 FDA reports)
HEMIANOPIA ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
HERNIA ( 5 FDA reports)
HISTIOCYTOSIS ( 5 FDA reports)
HISTOPLASMOSIS ( 5 FDA reports)
HOARSENESS ( 5 FDA reports)
HYDROCEPHALUS ( 5 FDA reports)
HYPERAESTHESIA ( 5 FDA reports)
HYPERAMMONAEMIA ( 5 FDA reports)
HYPERAMYLASAEMIA ( 5 FDA reports)
HYPOTONIA ( 5 FDA reports)
INADEQUATE ANALGESIA ( 5 FDA reports)
INCISION SITE COMPLICATION ( 5 FDA reports)
INCOHERENT ( 5 FDA reports)
INCORRECT STORAGE OF DRUG ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 5 FDA reports)
INTESTINAL ULCER ( 5 FDA reports)
INTRAOCULAR LENS IMPLANT ( 5 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 5 FDA reports)
INVESTIGATION ABNORMAL ( 5 FDA reports)
IRIDOCYCLITIS ( 5 FDA reports)
IRON DEFICIENCY ( 5 FDA reports)
LICHEN PLANUS ( 5 FDA reports)
LIPIDS INCREASED ( 5 FDA reports)
LIVER TRANSPLANT ( 5 FDA reports)
LOOSE TOOTH ( 5 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 5 FDA reports)
MACROCYTOSIS ( 5 FDA reports)
MACULAR HOLE ( 5 FDA reports)
MAJOR DEPRESSION ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 5 FDA reports)
MICTURITION DISORDER ( 5 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 5 FDA reports)
MONOCYTE COUNT INCREASED ( 5 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 5 FDA reports)
MONOPLEGIA ( 5 FDA reports)
MOUTH HAEMORRHAGE ( 5 FDA reports)
MUCOSAL EROSION ( 5 FDA reports)
MYELITIS TRANSVERSE ( 5 FDA reports)
NASAL SEPTUM DEVIATION ( 5 FDA reports)
NECROTISING OESOPHAGITIS ( 5 FDA reports)
NERVE ROOT LESION ( 5 FDA reports)
NITRITE URINE ( 5 FDA reports)
NO ADVERSE DRUG EFFECT ( 5 FDA reports)
NOSOCOMIAL INFECTION ( 5 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 5 FDA reports)
NYSTAGMUS ( 5 FDA reports)
OPTIC NEURITIS ( 5 FDA reports)
OROPHARYNGITIS FUNGAL ( 5 FDA reports)
OSTEOMYELITIS CHRONIC ( 5 FDA reports)
PAINFUL RESPIRATION ( 5 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 5 FDA reports)
PARAPSORIASIS ( 5 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 5 FDA reports)
PENIS DISORDER ( 5 FDA reports)
PERITONEAL TUBERCULOSIS ( 5 FDA reports)
PETIT MAL EPILEPSY ( 5 FDA reports)
PHOTOPSIA ( 5 FDA reports)
PLATELET COUNT ABNORMAL ( 5 FDA reports)
POOR QUALITY SLEEP ( 5 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 5 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 5 FDA reports)
PRODUCT COUNTERFEIT ( 5 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 5 FDA reports)
PSEUDARTHROSIS ( 5 FDA reports)
PSOAS ABSCESS ( 5 FDA reports)
PULSE ABSENT ( 5 FDA reports)
QRS AXIS ABNORMAL ( 5 FDA reports)
QUADRIPARESIS ( 5 FDA reports)
RENAL ABSCESS ( 5 FDA reports)
RENAL CELL CARCINOMA ( 5 FDA reports)
RENAL NEOPLASM ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 5 FDA reports)
RHONCHI ( 5 FDA reports)
SALIVARY HYPERSECRETION ( 5 FDA reports)
SALPINGITIS ( 5 FDA reports)
SENSE OF OPPRESSION ( 5 FDA reports)
SEPSIS SYNDROME ( 5 FDA reports)
SHOCK HAEMORRHAGIC ( 5 FDA reports)
SINUSITIS ASPERGILLUS ( 5 FDA reports)
SKIN HYPERTROPHY ( 5 FDA reports)
SMALL FOR DATES BABY ( 5 FDA reports)
SPINAL FUSION SURGERY ( 5 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 5 FDA reports)
STENOTROPHOMONAS INFECTION ( 5 FDA reports)
STREPTOCOCCAL SEPSIS ( 5 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 5 FDA reports)
SURGICAL FAILURE ( 5 FDA reports)
TEETH BRITTLE ( 5 FDA reports)
TENSION HEADACHE ( 5 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 5 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 5 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 5 FDA reports)
TONSIL CANCER ( 5 FDA reports)
TONSILLAR DISORDER ( 5 FDA reports)
ULCER HAEMORRHAGE ( 5 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 5 FDA reports)
VASCULITIC RASH ( 5 FDA reports)
VENOUS THROMBOSIS ( 5 FDA reports)
VENTRICULAR ARRHYTHMIA ( 5 FDA reports)
VITH NERVE PARALYSIS ( 5 FDA reports)
VULVOVAGINAL DRYNESS ( 5 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 5 FDA reports)
ABDOMINAL MASS ( 4 FDA reports)
ABSCESS ORAL ( 4 FDA reports)
ACROCHORDON ( 4 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 4 FDA reports)
ACUTE LEUKAEMIA ( 4 FDA reports)
ADENOIDAL DISORDER ( 4 FDA reports)
ADENOMYOSIS ( 4 FDA reports)
AFFECT LABILITY ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANAEMIA POSTOPERATIVE ( 4 FDA reports)
ANAL ABSCESS ( 4 FDA reports)
ANAL SPHINCTER ATONY ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 4 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 4 FDA reports)
AORTIC ANEURYSM ( 4 FDA reports)
APPENDIX DISORDER ( 4 FDA reports)
APPLICATION SITE ERYTHEMA ( 4 FDA reports)
APRAXIA ( 4 FDA reports)
ARTHROSCOPY ( 4 FDA reports)
ASEPTIC NECROSIS BONE ( 4 FDA reports)
ATRIAL TACHYCARDIA ( 4 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 4 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 4 FDA reports)
BACTERIA URINE IDENTIFIED ( 4 FDA reports)
BACTERIAL DNA TEST POSITIVE ( 4 FDA reports)
BARRETT'S OESOPHAGUS ( 4 FDA reports)
BENIGN BREAST NEOPLASM ( 4 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 4 FDA reports)
BIOPSY SKIN ABNORMAL ( 4 FDA reports)
BLADDER CANCER RECURRENT ( 4 FDA reports)
BLADDER NEOPLASM ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
BREAKTHROUGH PAIN ( 4 FDA reports)
BREAST CANCER IN SITU ( 4 FDA reports)
BREAST CANCER METASTATIC ( 4 FDA reports)
BREATH SOUNDS ABNORMAL ( 4 FDA reports)
BRONCHITIS ACUTE ( 4 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 4 FDA reports)
BURSITIS INFECTIVE ( 4 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 4 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 4 FDA reports)
CARDIAC FAILURE CHRONIC ( 4 FDA reports)
CARDIAC OUTPUT DECREASED ( 4 FDA reports)
CARDIAC VALVE VEGETATION ( 4 FDA reports)
CARTILAGE INJURY ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CEREBRAL DISORDER ( 4 FDA reports)
CEREBRAL VASOCONSTRICTION ( 4 FDA reports)
CERVICAL DYSPLASIA ( 4 FDA reports)
CERVICAL MYELOPATHY ( 4 FDA reports)
CERVICAL SPINAL STENOSIS ( 4 FDA reports)
CERVICOBRACHIAL SYNDROME ( 4 FDA reports)
CHOLECYSTITIS CHRONIC ( 4 FDA reports)
CHOROIDITIS ( 4 FDA reports)
CLEFT PALATE ( 4 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 4 FDA reports)
CONGENITAL CORNEAL ANOMALY ( 4 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 4 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 4 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 4 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 4 FDA reports)
CSF PROTEIN INCREASED ( 4 FDA reports)
DECREASED ACTIVITY ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 4 FDA reports)
DESMOID TUMOUR ( 4 FDA reports)
DRUG-INDUCED LIVER INJURY ( 4 FDA reports)
DYSPLASIA ( 4 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
EAR DISCOMFORT ( 4 FDA reports)
ECHINOCOCCIASIS ( 4 FDA reports)
ESSENTIAL HYPERTENSION ( 4 FDA reports)
EXERCISE TOLERANCE DECREASED ( 4 FDA reports)
EXTREMITY NECROSIS ( 4 FDA reports)
EYELID FUNCTION DISORDER ( 4 FDA reports)
FAECES PALE ( 4 FDA reports)
FAILURE TO THRIVE ( 4 FDA reports)
FAT NECROSIS ( 4 FDA reports)
FELTY'S SYNDROME ( 4 FDA reports)
FOOD INTOLERANCE ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
FOREARM FRACTURE ( 4 FDA reports)
FULL BLOOD COUNT DECREASED ( 4 FDA reports)
GALLBLADDER OPERATION ( 4 FDA reports)
GASTROINTESTINAL NECROSIS ( 4 FDA reports)
GASTROINTESTINAL ULCER ( 4 FDA reports)
GINGIVAL BLEEDING ( 4 FDA reports)
GLIOBLASTOMA ( 4 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 4 FDA reports)
GRANULOMA ANNULARE ( 4 FDA reports)
HAIR TEXTURE ABNORMAL ( 4 FDA reports)
HAPTOGLOBIN DECREASED ( 4 FDA reports)
HEART DISEASE CONGENITAL ( 4 FDA reports)
HEART SOUNDS ABNORMAL ( 4 FDA reports)
HEPATIC ECHINOCOCCIASIS ( 4 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 4 FDA reports)
HEPATITIS VIRAL ( 4 FDA reports)
HERPES OESOPHAGITIS ( 4 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 4 FDA reports)
HIRSUTISM ( 4 FDA reports)
HODGKIN'S DISEASE STAGE III ( 4 FDA reports)
HYPOPHARYNGEAL CANCER ( 4 FDA reports)
HYPOTRICHOSIS ( 4 FDA reports)
IATROGENIC INJURY ( 4 FDA reports)
ICTERUS INDEX INCREASED ( 4 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 4 FDA reports)
INCISION SITE HAEMORRHAGE ( 4 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 4 FDA reports)
INFECTED CYST ( 4 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 4 FDA reports)
INFLAMMATORY MARKER INCREASED ( 4 FDA reports)
INJECTION SITE DISCOMFORT ( 4 FDA reports)
INJECTION SITE VESICLES ( 4 FDA reports)
INJURY ASPHYXIATION ( 4 FDA reports)
INTERMEDIATE UVEITIS ( 4 FDA reports)
INTESTINAL HAEMORRHAGE ( 4 FDA reports)
INTRA-UTERINE DEATH ( 4 FDA reports)
INTRACRANIAL HYPOTENSION ( 4 FDA reports)
JUGULAR VEIN DISTENSION ( 4 FDA reports)
KERATITIS HERPETIC ( 4 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
LEGIONELLA SEROLOGY POSITIVE ( 4 FDA reports)
LIGAMENT RUPTURE ( 4 FDA reports)
LIMB OPERATION ( 4 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 4 FDA reports)
LISTERIOSIS ( 4 FDA reports)
LUMBAR RADICULOPATHY ( 4 FDA reports)
LUNG INJURY ( 4 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
LUPUS HEPATITIS ( 4 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 4 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MACULAR FIBROSIS ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
MALIGNANT ASCITES ( 4 FDA reports)
MALIGNANT RESPIRATORY TRACT NEOPLASM ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 4 FDA reports)
MEAN CELL VOLUME DECREASED ( 4 FDA reports)
MELANOSIS ( 4 FDA reports)
MENSTRUAL DISORDER ( 4 FDA reports)
MESOTHELIOMA ( 4 FDA reports)
METASTATIC NEOPLASM ( 4 FDA reports)
MIDDLE INSOMNIA ( 4 FDA reports)
MITRAL VALVE CALCIFICATION ( 4 FDA reports)
MITRAL VALVE DISEASE ( 4 FDA reports)
MORTON'S NEUROMA ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MUSCLE INJURY ( 4 FDA reports)
MUSCLE RUPTURE ( 4 FDA reports)
MYASTHENIA GRAVIS ( 4 FDA reports)
MYCOPLASMA INFECTION ( 4 FDA reports)
MYCOSIS FUNGOIDES ( 4 FDA reports)
MYELITIS ( 4 FDA reports)
MYELOFIBROSIS ( 4 FDA reports)
MYOPATHY STEROID ( 4 FDA reports)
NAIL PSORIASIS ( 4 FDA reports)
NASAL ULCER ( 4 FDA reports)
NECK INJURY ( 4 FDA reports)
NEURITIS ( 4 FDA reports)
NEURODERMATITIS ( 4 FDA reports)
NO ADVERSE REACTION ( 4 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 4 FDA reports)
OESOPHAGEAL STENOSIS ( 4 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 4 FDA reports)
ORAL CAVITY FISTULA ( 4 FDA reports)
OROPHARYNGEAL SWELLING ( 4 FDA reports)
OVARIAN EPITHELIAL CANCER ( 4 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 4 FDA reports)
PANCREATIC CARCINOMA RESECTABLE ( 4 FDA reports)
PANCREATITIS CHRONIC ( 4 FDA reports)
PATHOGEN RESISTANCE ( 4 FDA reports)
PEMPHIGUS ( 4 FDA reports)
PENILE PAIN ( 4 FDA reports)
PERFORMANCE STATUS DECREASED ( 4 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 4 FDA reports)
PERITONEAL HAEMORRHAGE ( 4 FDA reports)
PHARYNGEAL DISORDER ( 4 FDA reports)
PLEURAL DECORTICATION ( 4 FDA reports)
PLEURITIC PAIN ( 4 FDA reports)
PNEUMOCOCCAL INFECTION ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
PNEUMONIA HAEMOPHILUS ( 4 FDA reports)
PNEUMONIA MYCOPLASMAL ( 4 FDA reports)
PNEUMONIA NECROTISING ( 4 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 4 FDA reports)
POLYP ( 4 FDA reports)
POOR PERIPHERAL CIRCULATION ( 4 FDA reports)
PORTAL VEIN THROMBOSIS ( 4 FDA reports)
PRECANCEROUS SKIN LESION ( 4 FDA reports)
PROLONGED LABOUR ( 4 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 4 FDA reports)
PULMONARY THROMBOSIS ( 4 FDA reports)
PULMONARY VALVE STENOSIS ( 4 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 4 FDA reports)
RENAL COLIC ( 4 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 4 FDA reports)
RENAL ISCHAEMIA ( 4 FDA reports)
RENAL TUBULAR ACIDOSIS ( 4 FDA reports)
RESPIRATORY ACIDOSIS ( 4 FDA reports)
RESPIRATORY RATE INCREASED ( 4 FDA reports)
RETINAL DISORDER ( 4 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 4 FDA reports)
ROSACEA ( 4 FDA reports)
SACROILIITIS ( 4 FDA reports)
SALIVA ALTERED ( 4 FDA reports)
SCIATIC NERVE INJURY ( 4 FDA reports)
SECRETION DISCHARGE ( 4 FDA reports)
SEDATION ( 4 FDA reports)
SELF-MEDICATION ( 4 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 4 FDA reports)
SHIFT TO THE LEFT ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SKIN MASS ( 4 FDA reports)
SKIN PAPILLOMA ( 4 FDA reports)
SKIN TEST POSITIVE ( 4 FDA reports)
SPONDYLITIS ( 4 FDA reports)
STENT PLACEMENT ( 4 FDA reports)
STRESS CARDIOMYOPATHY ( 4 FDA reports)
SUBACUTE ENDOCARDITIS ( 4 FDA reports)
SUTURE RELATED COMPLICATION ( 4 FDA reports)
SYNCOPE VASOVAGAL ( 4 FDA reports)
TENDON INJURY ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 4 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 4 FDA reports)
TONGUE DISCOLOURATION ( 4 FDA reports)
TRACHEAL HAEMORRHAGE ( 4 FDA reports)
TRACHEAL INJURY ( 4 FDA reports)
TRIGEMINAL NEURALGIA ( 4 FDA reports)
TUBERCULOUS PLEURISY ( 4 FDA reports)
TWIN PREGNANCY ( 4 FDA reports)
TYPE I HYPERSENSITIVITY ( 4 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 4 FDA reports)
UMBILICAL HERNIA ( 4 FDA reports)
URETERAL DISORDER ( 4 FDA reports)
URINE ABNORMALITY ( 4 FDA reports)
URINE OUTPUT INCREASED ( 4 FDA reports)
VASOSPASM ( 4 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 4 FDA reports)
VITAL CAPACITY DECREASED ( 4 FDA reports)
VITAMIN D DECREASED ( 4 FDA reports)
VITREOUS DETACHMENT ( 4 FDA reports)
VITREOUS HAEMORRHAGE ( 4 FDA reports)
VOCAL CORD PARALYSIS ( 4 FDA reports)
VOMITING PROJECTILE ( 4 FDA reports)
WOUND HAEMORRHAGE ( 4 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ABORTION MISSED ( 3 FDA reports)
ACCIDENTAL DEATH ( 3 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 3 FDA reports)
ACCIDENTAL NEEDLE STICK ( 3 FDA reports)
ACQUIRED CLAW TOE ( 3 FDA reports)
ADRENAL NEOPLASM ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 3 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
ALVEOLAR OSTEITIS ( 3 FDA reports)
ALVEOLITIS ALLERGIC ( 3 FDA reports)
AMAUROSIS ( 3 FDA reports)
AMAUROSIS FUGAX ( 3 FDA reports)
AMYLASE INCREASED ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANAL FISSURE ( 3 FDA reports)
ANDROGEN DEFICIENCY ( 3 FDA reports)
ANDROGENS DECREASED ( 3 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 3 FDA reports)
ANIMAL BITE ( 3 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 3 FDA reports)
ANTI FACTOR XII ANTIBODY POSITIVE ( 3 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 3 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
AORTIC DILATATION ( 3 FDA reports)
AORTIC VALVE SCLEROSIS ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
ARTERIAL THROMBOSIS ( 3 FDA reports)
ARTERIOSPASM CORONARY ( 3 FDA reports)
ARTERITIS ( 3 FDA reports)
ASBESTOSIS ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
AXILLARY PAIN ( 3 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
BASOPHIL COUNT INCREASED ( 3 FDA reports)
BILE DUCT STENOSIS ( 3 FDA reports)
BILE DUCT STONE ( 3 FDA reports)
BIOPSY CHORIONIC VILLOUS ABNORMAL ( 3 FDA reports)
BLEEDING TIME PROLONGED ( 3 FDA reports)
BLEPHAROPLASTY ( 3 FDA reports)
BLOOD BICARBONATE INCREASED ( 3 FDA reports)
BLOOD BLISTER ( 3 FDA reports)
BLOOD URINE ( 3 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 3 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BREAST CANCER RECURRENT ( 3 FDA reports)
BREAST CYST ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
BRONCHIAL IRRITATION ( 3 FDA reports)
BRONCHITIS BACTERIAL ( 3 FDA reports)
BRONCHOPNEUMOPATHY ( 3 FDA reports)
CARDIAC INFECTION ( 3 FDA reports)
CARDIAC OPERATION ( 3 FDA reports)
CARDIAC SEPTAL DEFECT ( 3 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 3 FDA reports)
CARDIOTOXICITY ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 3 FDA reports)
CEREBELLAR ATAXIA ( 3 FDA reports)
CERVICITIS ( 3 FDA reports)
CERVIX NEOPLASM ( 3 FDA reports)
CHANGE OF BOWEL HABIT ( 3 FDA reports)
CHLAMYDIA SEROLOGY POSITIVE ( 3 FDA reports)
CHOLANGITIS ( 3 FDA reports)
CHONDROCALCINOSIS ( 3 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 3 FDA reports)
CLAVICLE FRACTURE ( 3 FDA reports)
CLONUS ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
COLORECTAL CANCER METASTATIC ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 3 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 3 FDA reports)
CONNECTIVE TISSUE DISORDER ( 3 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
CORNEAL EPITHELIUM DISORDER ( 3 FDA reports)
CORNEAL EROSION ( 3 FDA reports)
CORNEAL ULCER ( 3 FDA reports)
CORONARY ARTERY SURGERY ( 3 FDA reports)
COXSACKIE VIRAL INFECTION ( 3 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 3 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 3 FDA reports)
CSF PROTEIN ABNORMAL ( 3 FDA reports)
CULTURE URINE POSITIVE ( 3 FDA reports)
CUSHINGOID ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DERMATOSIS ( 3 FDA reports)
DNA ANTIBODY POSITIVE ( 3 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
DYSGLOBULINAEMIA ( 3 FDA reports)
DYSMENORRHOEA ( 3 FDA reports)
ECZEMA ASTEATOTIC ( 3 FDA reports)
EJECTION FRACTION ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
ENCEPHALOMYELITIS ( 3 FDA reports)
ENDARTERECTOMY ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
EROSIVE DUODENITIS ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
EUPHORIC MOOD ( 3 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 3 FDA reports)
EYE OEDEMA ( 3 FDA reports)
EYE REDNESS ( 3 FDA reports)
FAILURE OF IMPLANT ( 3 FDA reports)
FAT REDISTRIBUTION ( 3 FDA reports)
FAT TISSUE INCREASED ( 3 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 3 FDA reports)
FOOD AVERSION ( 3 FDA reports)
FRACTURED SACRUM ( 3 FDA reports)
FUNGAL RASH ( 3 FDA reports)
GASTROENTERITIS SALMONELLA ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
GINGIVAL INFECTION ( 3 FDA reports)
GINGIVAL PAIN ( 3 FDA reports)
GINGIVAL SWELLING ( 3 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 3 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 3 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 3 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
HAEMOCHROMATOSIS ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 3 FDA reports)
HAEMORRHAGIC CYST ( 3 FDA reports)
HEART INJURY ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 3 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 3 FDA reports)
HYPERPARATHYROIDISM ( 3 FDA reports)
HYPERPLASIA ( 3 FDA reports)
HYPERTRICHOSIS ( 3 FDA reports)
HYPOCAPNIA ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOURICAEMIA ( 3 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 3 FDA reports)
ICHTHYOSIS ( 3 FDA reports)
ILEITIS ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
IMPLANT SITE INFECTION ( 3 FDA reports)
INCISIONAL DRAINAGE ( 3 FDA reports)
INCISIONAL HERNIA ( 3 FDA reports)
INDURATION ( 3 FDA reports)
INFECTED SKIN ULCER ( 3 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 3 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 3 FDA reports)
INJECTION SITE ANAESTHESIA ( 3 FDA reports)
INJECTION SITE CELLULITIS ( 3 FDA reports)
INJECTION SITE MACULE ( 3 FDA reports)
INJECTION SITE NECROSIS ( 3 FDA reports)
INJECTION SITE PAPULE ( 3 FDA reports)
INTESTINAL FISTULA ( 3 FDA reports)
INTESTINAL MASS ( 3 FDA reports)
JAW OPERATION ( 3 FDA reports)
JOINT ABSCESS ( 3 FDA reports)
JOINT INSTABILITY ( 3 FDA reports)
JUVENILE ARTHRITIS ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
KYPHOSIS ( 3 FDA reports)
LABORATORY TEST INTERFERENCE ( 3 FDA reports)
LABYRINTHITIS ( 3 FDA reports)
LIMB MALFORMATION ( 3 FDA reports)
LIP BLISTER ( 3 FDA reports)
LISTLESS ( 3 FDA reports)
LIVER ABSCESS ( 3 FDA reports)
LOWER EXTREMITY MASS ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 3 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 3 FDA reports)
LUNG CREPITATION ( 3 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 3 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
MEAN CELL VOLUME INCREASED ( 3 FDA reports)
MEASLES ( 3 FDA reports)
MEDICAL DEVICE CHANGE ( 3 FDA reports)
MENINGISM ( 3 FDA reports)
MENINGITIS LISTERIA ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
METASTASES TO PERITONEUM ( 3 FDA reports)
METASTASIS ( 3 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
MICROALBUMINURIA ( 3 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 3 FDA reports)
MILIA ( 3 FDA reports)
MONARTHRITIS ( 3 FDA reports)
MULTI-ORGAN DISORDER ( 3 FDA reports)
MUSCLE FATIGUE ( 3 FDA reports)
MUSCLE HYPERTROPHY ( 3 FDA reports)
MUSCLE MASS ( 3 FDA reports)
MYASTHENIC SYNDROME ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
NECROTISING COLITIS ( 3 FDA reports)
NEPHRITIS ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
NEPHROSCLEROSIS ( 3 FDA reports)
NEURAL TUBE DEFECT ( 3 FDA reports)
NEUROLOGIC NEGLECT SYNDROME ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NO ADVERSE DRUG REACTION ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
OESOPHAGEAL DISORDER ( 3 FDA reports)
OESTRIOL ABNORMAL ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
OSTEOPOROTIC FRACTURE ( 3 FDA reports)
OTITIS MEDIA ( 3 FDA reports)
OVARIAN CANCER METASTATIC ( 3 FDA reports)
PANCREATIC DISORDER ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PAROSMIA ( 3 FDA reports)
PATELLA FRACTURE ( 3 FDA reports)
PERIODONTAL DESTRUCTION ( 3 FDA reports)
PERITONITIS BACTERIAL ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
POSTOPERATIVE ILEUS ( 3 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 3 FDA reports)
PREMATURE MENOPAUSE ( 3 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA RECURRENT ( 3 FDA reports)
PROCEDURAL HYPOTENSION ( 3 FDA reports)
PROTEIN URINE ( 3 FDA reports)
PROTEUS INFECTION ( 3 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 3 FDA reports)
PULMONARY HYPERTENSIVE CRISIS ( 3 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 3 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 3 FDA reports)
RENAL ATROPHY ( 3 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 3 FDA reports)
RESUSCITATION ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
RETINAL VASCULAR OCCLUSION ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
SALIVARY GLAND NEOPLASM ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SCOLIOSIS ( 3 FDA reports)
SCRATCH ( 3 FDA reports)
SEASONAL ALLERGY ( 3 FDA reports)
SEBORRHOEIC DERMATITIS ( 3 FDA reports)
SEBORRHOEIC KERATOSIS ( 3 FDA reports)
SEROMA ( 3 FDA reports)
SIALOADENITIS ( 3 FDA reports)
SIGMOIDITIS ( 3 FDA reports)
SKIN ATROPHY ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN INDURATION ( 3 FDA reports)
SKIN INFLAMMATION ( 3 FDA reports)
SKIN PLAQUE ( 3 FDA reports)
SLUGGISHNESS ( 3 FDA reports)
SMEAR CERVIX ABNORMAL ( 3 FDA reports)
SOMATOFORM DISORDER CARDIOVASCULAR ( 3 FDA reports)
SPINAL COLUMN INJURY ( 3 FDA reports)
SPINAL CORD COMPRESSION ( 3 FDA reports)
SPINAL CORD HERNIATION ( 3 FDA reports)
SPINAL MENINGIOMA BENIGN ( 3 FDA reports)
SPINAL VASCULAR DISORDER ( 3 FDA reports)
SPUTUM PURULENT ( 3 FDA reports)
SPUTUM RETENTION ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
STASIS DERMATITIS ( 3 FDA reports)
SUDDEN HEARING LOSS ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 3 FDA reports)
THERAPY REGIMEN CHANGED ( 3 FDA reports)
THYROXINE INCREASED ( 3 FDA reports)
TINEA BLANCA ( 3 FDA reports)
TOE OPERATION ( 3 FDA reports)
TONGUE BLISTERING ( 3 FDA reports)
TONSILLECTOMY ( 3 FDA reports)
TRACHEOBRONCHITIS ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
TUBERCULOSIS LIVER ( 3 FDA reports)
TYPHOID FEVER ( 3 FDA reports)
UMBILICAL CORD AROUND NECK ( 3 FDA reports)
UNDERDOSE ( 3 FDA reports)
URGE INCONTINENCE ( 3 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 3 FDA reports)
URINARY CASTS ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 3 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
UTERINE DILATION AND CURETTAGE ( 3 FDA reports)
VAGINAL INFECTION ( 3 FDA reports)
VAGINAL ULCERATION ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
VENOUS OCCLUSION ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
VESSEL PERFORATION ( 3 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 3 FDA reports)
VITAMIN B12 DEFICIENCY ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
VITILIGO ( 3 FDA reports)
VULVAL DISORDER ( 3 FDA reports)
VULVAR DYSPLASIA ( 3 FDA reports)
VULVOVAGINAL PRURITUS ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
WEIGHT BEARING DIFFICULTY ( 3 FDA reports)
WHOLE BLOOD TRANSFUSION ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
WRIST DEFORMITY ( 3 FDA reports)
ABNORMAL WEIGHT GAIN ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ACANTHOMA ( 2 FDA reports)
ACCIDENT AT WORK ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ADENOIDECTOMY ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ALLERGIC PHARYNGITIS ( 2 FDA reports)
ALLERGY TO CHEMICALS ( 2 FDA reports)
ALOPECIA TOTALIS ( 2 FDA reports)
ALPHA 1 GLOBULIN ABNORMAL ( 2 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 2 FDA reports)
ALPHA 2 GLOBULIN ABNORMAL ( 2 FDA reports)
ALPHA 2 GLOBULIN DECREASED ( 2 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 2 FDA reports)
AMNIOCENTESIS ABNORMAL ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANASTOMOTIC FISTULA ( 2 FDA reports)
ANGIOMYOLIPOMA ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANKLE ARTHROPLASTY ( 2 FDA reports)
ANKLE DEFORMITY ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 2 FDA reports)
ANTINUCLEAR ANTIBODY ( 2 FDA reports)
ANTITHROMBIN III DECREASED ( 2 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 2 FDA reports)
AORTIC ATHEROSCLEROSIS ( 2 FDA reports)
AORTIC CALCIFICATION ( 2 FDA reports)
AORTIC VALVE CALCIFICATION ( 2 FDA reports)
APALLIC SYNDROME ( 2 FDA reports)
APHONIA ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
ARACHNOIDITIS ( 2 FDA reports)
ARRESTED LABOUR ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ARTHROSCOPIC SURGERY ( 2 FDA reports)
ASTHMATIC CRISIS ( 2 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
AXILLARY MASS ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BARTHOLIN'S ABSCESS ( 2 FDA reports)
BASILAR MIGRAINE ( 2 FDA reports)
BEHCET'S SYNDROME ( 2 FDA reports)
BENIGN HYDATIDIFORM MOLE ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BENIGN NEOPLASM ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BENIGN RESPIRATORY TRACT NEOPLASM ( 2 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLADDER NECK SCLEROSIS ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
BLINDNESS CONGENITAL ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 2 FDA reports)
BODY FAT DISORDER ( 2 FDA reports)
BODY HEIGHT ABNORMAL ( 2 FDA reports)
BODY TINEA ( 2 FDA reports)
BONE DENSITY INCREASED ( 2 FDA reports)
BONE FISSURE ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BONE MARROW OEDEMA ( 2 FDA reports)
BONE SARCOMA ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BOWEN'S DISEASE ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BREAST ATROPHY ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
BREAST DISCOMFORT ( 2 FDA reports)
BREAST DISORDER ( 2 FDA reports)
BREAST INFECTION ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BREECH PRESENTATION ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
BULLOUS LUNG DISEASE ( 2 FDA reports)
BURSA INJURY ( 2 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 2 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CALCIUM METABOLISM DISORDER ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 2 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CATARACT CORTICAL ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 2 FDA reports)
CELLULITIS STREPTOCOCCAL ( 2 FDA reports)
CEREBELLAR ISCHAEMIA ( 2 FDA reports)
CEREBRAL ARTERITIS ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CERVIX DYSTOCIA ( 2 FDA reports)
CHLAMYDIAL INFECTION ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHONDRODYSTROPHY ( 2 FDA reports)
CILIARY HYPERAEMIA ( 2 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COCCYDYNIA ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
COLOSTOMY CLOSURE ( 2 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 2 FDA reports)
COMPLEMENT FACTOR DECREASED ( 2 FDA reports)
COMPLICATED FRACTURE ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CONGENITAL TONGUE ANOMALY ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
COPROPORPHYRINOGEN INCREASED ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORNEAL ABSCESS ( 2 FDA reports)
CORNEAL DYSTROPHY ( 2 FDA reports)
CORNEAL PERFORATION ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CRACKLES LUNG ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 2 FDA reports)
CRYING ( 2 FDA reports)
CSF PRESSURE INCREASED ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CYST RUPTURE ( 2 FDA reports)
CYSTITIS GLANDULARIS ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DECREASED INTEREST ( 2 FDA reports)
DEFORMITY THORAX ( 2 FDA reports)
DENTAL FISTULA ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIABETIC MICROANGIOPATHY ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE II ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 2 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 2 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 2 FDA reports)
DRUG EFFECT DELAYED ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DUODENAL NEOPLASM ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DYSENTERY ( 2 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 2 FDA reports)
DYSPHEMIA ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
ELECTIVE SURGERY ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
ENTEROVESICAL FISTULA ( 2 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 2 FDA reports)
EPHELIDES ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ERYTHEMA ANNULARE ( 2 FDA reports)
ERYTHEMA INDURATUM ( 2 FDA reports)
ERYTHRODERMIC PSORIASIS ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 2 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 2 FDA reports)
EYE ALLERGY ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYE INFECTION BACTERIAL ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
EYELID CYST ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FAECAL VOLUME INCREASED ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FEMALE STERILISATION ( 2 FDA reports)
FIBROMA ( 2 FDA reports)
FIBROMATOSIS ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FOETAL DEATH ( 2 FDA reports)
FOETAL HEART RATE ABNORMAL ( 2 FDA reports)
FOETAL MALFORMATION ( 2 FDA reports)
FONTANELLE DEPRESSED ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FRACTURE DISPLACEMENT ( 2 FDA reports)
FREEZING PHENOMENON ( 2 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 2 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
GASTRIC HYPOMOTILITY ( 2 FDA reports)
GASTRIC MUCOSAL LESION ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
GASTROENTERITIS BACTERIAL ( 2 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 2 FDA reports)
GINGIVAL RECESSION ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
GLAUCOMA SURGERY ( 2 FDA reports)
GLIOMA ( 2 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
GRIEF REACTION ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
GYNAECOLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
HAEMODILUTION ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAEMORRHAGIC INFARCTION ( 2 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HEART BLOCK CONGENITAL ( 2 FDA reports)
HEART VALVE CALCIFICATION ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC CANCER METASTATIC ( 2 FDA reports)
HEPATIC MASS ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HIDRADENITIS ( 2 FDA reports)
HISTAMINE INTOLERANCE ( 2 FDA reports)
HISTAMINE LEVEL INCREASED ( 2 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY STAGE III ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYDROPNEUMOTHORAX ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERCHLORAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTONIC BLADDER ( 2 FDA reports)
HYPERTRANSAMINASAEMIA ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
ILEAL ULCER ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 2 FDA reports)
IMPLANT SITE PAIN ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INCISION SITE ERYTHEMA ( 2 FDA reports)
INCISION SITE OEDEMA ( 2 FDA reports)
INCISION SITE PAIN ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INFUSION SITE INFECTION ( 2 FDA reports)
INFUSION SITE SWELLING ( 2 FDA reports)
INGROWN HAIR ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE PARAESTHESIA ( 2 FDA reports)
INJECTION SITE PUSTULE ( 2 FDA reports)
INJECTION SITE STREAKING ( 2 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTESTINAL POLYP ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
IRITIS ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 2 FDA reports)
ISCHAEMIC ULCER ( 2 FDA reports)
JC VIRUS INFECTION ( 2 FDA reports)
JOINT CONTRACTURE ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
KAPOSI'S SARCOMA ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LARYNGEAL NEOPLASM ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LENS IMPLANT ( 2 FDA reports)
LESION EXCISION ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LICHEN SCLEROSUS ( 2 FDA reports)
LINEAR IGA DISEASE ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LISTERIA SEPSIS ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LUNG OPERATION ( 2 FDA reports)
LUNG TRANSPLANT ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE ( 2 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
MACULE ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MASTITIS ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MEDICAL DEVICE REMOVAL ( 2 FDA reports)
MENINGITIS CHEMICAL ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 2 FDA reports)
MILK ALLERGY ( 2 FDA reports)
MITRAL VALVE SCLEROSIS ( 2 FDA reports)
MIXED LIVER INJURY ( 2 FDA reports)
MONOCLONAL GAMMOPATHY ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MONOCYTOPENIA ( 2 FDA reports)
MONOCYTOSIS ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MUCORMYCOSIS ( 2 FDA reports)
MUCOSAL ULCERATION ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MULTIPLE FRACTURES ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 2 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 2 FDA reports)
MYELOID LEUKAEMIA ( 2 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 2 FDA reports)
MYOCARDIAL RUPTURE ( 2 FDA reports)
MYOCARDITIS RHEUMATIC ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NEUROBORRELIOSIS ( 2 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
NIPPLE DISORDER ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NODAL ARRHYTHMIA ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 2 FDA reports)
OBESITY SURGERY ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OCULAR NEOPLASM ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL TORUS ( 2 FDA reports)
OROPHARYNGEAL NEOPLASM ( 2 FDA reports)
ORTHOPEDIC PROCEDURE ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
OSTEOMYELITIS ACUTE ( 2 FDA reports)
OVARIAN FAILURE ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PANCREAS TRANSPLANT ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PARTIAL LIPODYSTROPHY ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERITONEAL ABSCESS ( 2 FDA reports)
PERITONEAL CARCINOMA ( 2 FDA reports)
PERONEAL NERVE INJURY ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PHARYNGEAL NEOPLASM ( 2 FDA reports)
PHYSICAL DISABILITY ( 2 FDA reports)
PIERRE ROBIN SYNDROME ( 2 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 2 FDA reports)
PLACENTA PRAEVIA ( 2 FDA reports)
PLASTIC SURGERY TO THE FACE ( 2 FDA reports)
PLATELET AGGREGATION INCREASED ( 2 FDA reports)
PLEOCYTOSIS ( 2 FDA reports)
PLEUROPERICARDITIS ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
PORPHYRIA ( 2 FDA reports)
PORPHYRIA NON-ACUTE ( 2 FDA reports)
PORPHYRINS URINE INCREASED ( 2 FDA reports)
POST PROCEDURAL FISTULA ( 2 FDA reports)
POST PROCEDURAL OEDEMA ( 2 FDA reports)
POST THROMBOTIC SYNDROME ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PREALBUMIN DECREASED ( 2 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROCTOCOLITIS ( 2 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 2 FDA reports)
PROSTATIC ADENOMA ( 2 FDA reports)
PROSTATISM ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROSTATOMEGALY ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PROTEUS TEST POSITIVE ( 2 FDA reports)
PSEUDOMONAS BRONCHITIS ( 2 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 2 FDA reports)
PULMONARY EOSINOPHILIA ( 2 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RADIATION INJURY ( 2 FDA reports)
RADICULAR PAIN ( 2 FDA reports)
RADICULITIS BRACHIAL ( 2 FDA reports)
RASH SCALY ( 2 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 2 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 2 FDA reports)
RENAL NECROSIS ( 2 FDA reports)
RENAL OSTEODYSTROPHY ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
RETINITIS PIGMENTOSA ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 2 FDA reports)
SECONDARY AMYLOIDOSIS ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SENSORIMOTOR DISORDER ( 2 FDA reports)
SHOULDER ARTHROPLASTY ( 2 FDA reports)
SHOULDER OPERATION ( 2 FDA reports)
SINUS POLYP ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SKIN TOXICITY ( 2 FDA reports)
SKIN ULCER HAEMORRHAGE ( 2 FDA reports)
SKULL MALFORMATION ( 2 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SPINA BIFIDA OCCULTA ( 2 FDA reports)
SPINAL CLAUDICATION ( 2 FDA reports)
SPINAL LAMINECTOMY ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
STITCH ABSCESS ( 2 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE UNSPECIFIED ( 2 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TEMPORAL ARTERITIS ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
TESTICULAR SWELLING ( 2 FDA reports)
THEFT ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOANGIITIS OBLITERANS ( 2 FDA reports)
THROMBOLYSIS ( 2 FDA reports)
THYROID GLAND CANCER ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
THYROIDITIS ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
THYROXINE FREE INCREASED ( 2 FDA reports)
TINEA INFECTION ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 2 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 2 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
ULTRASOUND ANTENATAL SCREEN ( 2 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
UNWANTED PREGNANCY ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
URINARY SEDIMENT PRESENT ( 2 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VARICOPHLEBITIS ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VEIN PAIN ( 2 FDA reports)
VENOUS OPERATION ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VIRAL PERICARDITIS ( 2 FDA reports)
VITAMIN B12 INCREASED ( 2 FDA reports)
VITH NERVE DISORDER ( 2 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 2 FDA reports)
VULVOVAGINAL ERYTHEMA ( 2 FDA reports)
VULVOVAGINAL SWELLING ( 2 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL EXPLORATION ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABNORMAL PRODUCT OF CONCEPTION ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABORTION EARLY ( 1 FDA reports)
ABORTION INCOMPLETE ( 1 FDA reports)
ABORTION THREATENED ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACNE CONGLOBATA ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 1 FDA reports)
ACUTE ENDOCARDITIS ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADENOID CYSTIC CARCINOMA ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE IV ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALOPECIA UNIVERSALIS ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN ABNORMAL ( 1 FDA reports)
ALPHA-1 ACID GLYCOPROTEIN INCREASED ( 1 FDA reports)
ALTERNARIA INFECTION ( 1 FDA reports)
AMNIORRHEXIS ( 1 FDA reports)
AMNIOTIC INFECTION SYNDROME OF BLANE ( 1 FDA reports)
AMPUTATION REVISION ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL NEOPLASM ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANDROGENS INCREASED ( 1 FDA reports)
ANGIOGRAM PERIPHERAL ABNORMAL ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APATHY ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APLASIA CUTIS CONGENITA ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE INDURATION ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL FIBROSIS ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATYPICAL MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTERIAL PERICARDITIS ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BASOPHIL PERCENTAGE ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF EYELID ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BETA GLOBULIN ABNORMAL ( 1 FDA reports)
BILATERAL HYDRONEPHROSIS ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLADDER PERFORATION ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD BETA-D-GLUCAN ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CALCITONIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GASTRIN INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD PH ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
BONE DECALCIFICATION ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BRAIN STEM THROMBOSIS ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BREAST NECROSIS ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIAL ULCERATION ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BURSAL OPERATION ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL VENOUS PRESSURE ABNORMAL ( 1 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBROSPINAL FLUID RETENTION ( 1 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVICAL SPINE FLATTENING ( 1 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST TUBE INSERTION ( 1 FDA reports)
CHLORACNE ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHOROID MELANOMA ( 1 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 1 FDA reports)
COMPLEMENT FACTOR C4 INCREASED ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 1 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COR PULMONALE ACUTE ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CRYPTORCHISM ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CUTANEOUS TUBERCULOSIS ( 1 FDA reports)
CUTIS LAXA ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DELAYED PUBERTY ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DENTAL CARE ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DENTAL IMPLANTATION ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIFFUSE AXONAL INJURY ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE III ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DOUGLAS' POUCH EFFUSION ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DYSCALCULIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSKINESIA OESOPHAGEAL ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR CANAL ERYTHEMA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR LOBE INFECTION ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ECCRINE CARCINOMA ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ELBOW OPERATION ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
EOSINOPHIL PERCENTAGE ABNORMAL ( 1 FDA reports)
EOSINOPHILIC PUSTULOSIS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPITHELIOMA ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EVAN'S SYNDROME ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXPIRATORY RESERVE VOLUME DECREASED ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRACORPOREAL MEMBRANE OXYGENATION ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTRAVASATION BLOOD ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE INFECTION TOXOPLASMAL ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR XII DEFICIENCY ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FALSE POSITIVE TUBERCULOSIS TEST ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FIBRIN D DIMER DECREASED ( 1 FDA reports)
FIBRINOLYSIS INCREASED ( 1 FDA reports)
FIBROUS HISTIOCYTOMA ( 1 FDA reports)
FINGER REPAIR OPERATION ( 1 FDA reports)
FISTULA DISCHARGE ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE I ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE PAIN ( 1 FDA reports)
FUNGAL DNA TEST POSITIVE ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
FUSOBACTERIUM INFECTION ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 1 FDA reports)
GASTROENTERITIS PSEUDOMONAS ( 1 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GINGIVAL EROSION ( 1 FDA reports)
GINGIVAL INJURY ( 1 FDA reports)
GINGIVAL OEDEMA ( 1 FDA reports)
GINGIVAL OPERATION ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HBV DNA INCREASED ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEART VALVE STENOSIS ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B E ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS E ( 1 FDA reports)
HEPATITIS E ANTIBODY ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HERPES SIMPLEX DNA TEST POSITIVE ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HIP DISARTICULATION ( 1 FDA reports)
HISTOLOGY ABNORMAL ( 1 FDA reports)
HODGKIN'S DISEASE LYMPHOCYTE DEPLETION TYPE STAGE III ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HORSESHOE KIDNEY ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERKINETIC HEART SYNDROME ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPOCOMPLEMENTAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYSTEROSALPINGO-OOPHORECTOMY ( 1 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFECTIVE TENOSYNOVITIS ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INFLAMMATORY PAIN ( 1 FDA reports)
INFLAMMATORY PSEUDOTUMOUR ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INFUSION SITE PARAESTHESIA ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION RELATED REACTION ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE HYPERTROPHY ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 1 FDA reports)
INTESTINAL ADENOCARCINOMA ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL VILLI ATROPHY ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT TUBERCULOSIS ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KERATORHEXIS ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LABIA ENLARGED ( 1 FDA reports)
LAPAROSCOPY ( 1 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 1 FDA reports)
LEPTOSPIROSIS ( 1 FDA reports)
LEUKAEMIA CUTIS ( 1 FDA reports)
LEUKAEMIA GRANULOCYTIC ( 1 FDA reports)
LEUKAEMIA MONOCYTIC ( 1 FDA reports)
LEUKAEMOID REACTION ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIGAMENT INJURY ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIMB SALVAGE THERAPY ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER STAGE III ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LISTERIA TEST POSITIVE ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOSS OF ANATOMICAL ALIGNMENT AFTER FRACTURE REDUCTION ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LUDWIG ANGINA ( 1 FDA reports)
LUMBAR HERNIA ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALFORMATION VENOUS ( 1 FDA reports)
MALIGNANT MELANOMA STAGE III ( 1 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 1 FDA reports)
MALIGNANT URINARY TRACT NEOPLASM ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS HAEMOPHILUS ( 1 FDA reports)
MENINGITIS LEPTOSPIRAL ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MISSED LABOUR ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MYCOBACTERIA SPUTUM TEST POSITIVE ( 1 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 1 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
MYELOBLASTOMA ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOPERICARDITIS ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL POLYPECTOMY ( 1 FDA reports)
NECROBIOSIS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEONATAL APNOEIC ATTACK ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEOPLASM OF APPENDIX ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEURILEMMOMA BENIGN ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OEDEMA DUE TO RENAL DISEASE ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL PUSTULE ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
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OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OSTEOSYNTHESIS ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
OXYGEN CONSUMPTION ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALATITIS ( 1 FDA reports)
PANCOAST'S SYNDROME ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
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PANNICULITIS LOBULAR ( 1 FDA reports)
PANOPHTHALMITIS ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
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PARAPROTEINAEMIA ( 1 FDA reports)
PARASITE URINE TEST POSITIVE ( 1 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 1 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 1 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 1 FDA reports)
PERFORATION BILE DUCT ( 1 FDA reports)
PERIANAL ERYTHEMA ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERIPORTAL SINUS DILATATION ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBOSCLEROSIS ( 1 FDA reports)
PHOBIA OF DRIVING ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOTODYNAMIC THERAPY ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITYRIASIS LICHENOIDES ET VARIOLIFORMIS ACUTA ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLACENTAL INSUFFICIENCY ( 1 FDA reports)
PLACENTAL TRANSFUSION SYNDROME ( 1 FDA reports)
PLASMA CELLS PRESENT ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET DISTRIBUTION WIDTH ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PLEURAL INFECTION BACTERIAL ( 1 FDA reports)
PLEURAL NEOPLASM ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
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POLYMERASE CHAIN REACTION ( 1 FDA reports)
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POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POOR DENTAL CONDITION ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PORPHYRIA ACUTE ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRIMARY SEQUESTRUM ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROLONGED PREGNANCY ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
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PROSTATIC DISORDER ( 1 FDA reports)
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PROTEIN C DECREASED ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PSEUDOMYXOMA PERITONEI ( 1 FDA reports)
PSEUDOPOLYPOSIS ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY ATRESIA ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY COCCIDIOIDES ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULPITIS DENTAL ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PUNCTURE SITE PAIN ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
PYELONEPHRITIS CHRONIC ( 1 FDA reports)
PYURIA ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
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RADIOTHERAPY TO BRAIN ( 1 FDA reports)
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RECTAL ADENOMA ( 1 FDA reports)
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RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
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REFLEXES ABNORMAL ( 1 FDA reports)
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REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
REMOVAL OF INTERNAL FIXATION ( 1 FDA reports)
RENAL AMYLOIDOSIS ( 1 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
RENAL CORTICAL NECROSIS ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
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RENAL SURGERY ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
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RETAINED PRODUCTS OF CONCEPTION ( 1 FDA reports)
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RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
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RIGHT ATRIAL DILATATION ( 1 FDA reports)
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SALIVARY GLAND FISTULA ( 1 FDA reports)
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SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
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SKIN CHAPPED ( 1 FDA reports)
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