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

NAUSEA ( 1093 FDA reports)
DRUG INEFFECTIVE ( 891 FDA reports)
DIZZINESS ( 616 FDA reports)
FATIGUE ( 566 FDA reports)
WEIGHT INCREASED ( 546 FDA reports)
PAIN ( 525 FDA reports)
DEPRESSION ( 516 FDA reports)
DYSPNOEA ( 516 FDA reports)
HEADACHE ( 516 FDA reports)
INSOMNIA ( 499 FDA reports)
MALAISE ( 498 FDA reports)
VOMITING ( 460 FDA reports)
FEELING ABNORMAL ( 455 FDA reports)
SOMNOLENCE ( 451 FDA reports)
ANXIETY ( 448 FDA reports)
DIARRHOEA ( 410 FDA reports)
WEIGHT DECREASED ( 395 FDA reports)
OEDEMA PERIPHERAL ( 365 FDA reports)
DRUG INTERACTION ( 348 FDA reports)
FALL ( 347 FDA reports)
ABNORMAL DREAMS ( 329 FDA reports)
BLOOD GLUCOSE INCREASED ( 329 FDA reports)
CONVULSION ( 321 FDA reports)
ASTHENIA ( 311 FDA reports)
CONSTIPATION ( 311 FDA reports)
CHEST PAIN ( 285 FDA reports)
VISION BLURRED ( 284 FDA reports)
GAIT DISTURBANCE ( 280 FDA reports)
PAIN IN EXTREMITY ( 271 FDA reports)
TREMOR ( 270 FDA reports)
ABDOMINAL PAIN UPPER ( 268 FDA reports)
HYPERTENSION ( 251 FDA reports)
PYREXIA ( 245 FDA reports)
BACK PAIN ( 243 FDA reports)
HYPERSENSITIVITY ( 239 FDA reports)
HALLUCINATION ( 231 FDA reports)
LOSS OF CONSCIOUSNESS ( 231 FDA reports)
MYALGIA ( 228 FDA reports)
BLOOD PRESSURE INCREASED ( 227 FDA reports)
RASH ( 221 FDA reports)
CONFUSIONAL STATE ( 218 FDA reports)
DRY MOUTH ( 218 FDA reports)
PNEUMONIA ( 216 FDA reports)
MYOCARDIAL INFARCTION ( 207 FDA reports)
NERVOUSNESS ( 205 FDA reports)
ARTHRALGIA ( 200 FDA reports)
DEATH ( 198 FDA reports)
CONDITION AGGRAVATED ( 193 FDA reports)
FLATULENCE ( 193 FDA reports)
SLEEP DISORDER ( 193 FDA reports)
AMNESIA ( 191 FDA reports)
CEREBROVASCULAR ACCIDENT ( 189 FDA reports)
MEMORY IMPAIRMENT ( 185 FDA reports)
PRURITUS ( 180 FDA reports)
SUICIDAL IDEATION ( 178 FDA reports)
RENAL FAILURE ( 175 FDA reports)
ABDOMINAL PAIN ( 173 FDA reports)
IRRITABILITY ( 172 FDA reports)
MUSCLE SPASMS ( 171 FDA reports)
AGITATION ( 170 FDA reports)
DECREASED APPETITE ( 163 FDA reports)
PANIC ATTACK ( 160 FDA reports)
SUICIDE ATTEMPT ( 160 FDA reports)
HEART RATE INCREASED ( 157 FDA reports)
PARAESTHESIA ( 156 FDA reports)
HYPERHIDROSIS ( 155 FDA reports)
HYPOAESTHESIA ( 155 FDA reports)
DISTURBANCE IN ATTENTION ( 151 FDA reports)
DYSGEUSIA ( 150 FDA reports)
ABDOMINAL DISTENSION ( 149 FDA reports)
ARTHRITIS ( 149 FDA reports)
COUGH ( 148 FDA reports)
URINARY TRACT INFECTION ( 148 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 143 FDA reports)
ILL-DEFINED DISORDER ( 142 FDA reports)
ABNORMAL BEHAVIOUR ( 140 FDA reports)
ATRIAL FIBRILLATION ( 140 FDA reports)
STRESS ( 140 FDA reports)
OVERDOSE ( 139 FDA reports)
RENAL FAILURE ACUTE ( 137 FDA reports)
HYPOTENSION ( 135 FDA reports)
NIGHTMARE ( 135 FDA reports)
ANGER ( 132 FDA reports)
VISUAL IMPAIRMENT ( 132 FDA reports)
ANAEMIA ( 129 FDA reports)
BALANCE DISORDER ( 129 FDA reports)
ABASIA ( 124 FDA reports)
ALOPECIA ( 124 FDA reports)
UNEVALUABLE EVENT ( 123 FDA reports)
HYPERGLYCAEMIA ( 122 FDA reports)
DEHYDRATION ( 121 FDA reports)
ABDOMINAL DISCOMFORT ( 119 FDA reports)
VISUAL ACUITY REDUCED ( 119 FDA reports)
ANOREXIA ( 118 FDA reports)
CARDIAC DISORDER ( 118 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 118 FDA reports)
MEDICATION ERROR ( 116 FDA reports)
MUSCULAR WEAKNESS ( 116 FDA reports)
BLOOD CREATININE INCREASED ( 114 FDA reports)
CHEST DISCOMFORT ( 113 FDA reports)
DYSPEPSIA ( 113 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 112 FDA reports)
BLOOD PRESSURE DECREASED ( 111 FDA reports)
INFLUENZA LIKE ILLNESS ( 111 FDA reports)
HYPERSOMNIA ( 110 FDA reports)
BLOOD GLUCOSE DECREASED ( 109 FDA reports)
BRONCHITIS ( 109 FDA reports)
MOOD ALTERED ( 109 FDA reports)
DYSARTHRIA ( 108 FDA reports)
OEDEMA ( 108 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 107 FDA reports)
HYPOGLYCAEMIA ( 106 FDA reports)
SWELLING ( 106 FDA reports)
THROMBOSIS ( 106 FDA reports)
COMPLETED SUICIDE ( 105 FDA reports)
MENTAL IMPAIRMENT ( 105 FDA reports)
PALPITATIONS ( 105 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 101 FDA reports)
SPEECH DISORDER ( 100 FDA reports)
CRYING ( 99 FDA reports)
INCREASED APPETITE ( 99 FDA reports)
TACHYCARDIA ( 99 FDA reports)
AGGRESSION ( 98 FDA reports)
CATARACT ( 98 FDA reports)
SEPSIS ( 98 FDA reports)
COMA ( 97 FDA reports)
TOBACCO USER ( 97 FDA reports)
URTICARIA ( 97 FDA reports)
WITHDRAWAL SYNDROME ( 95 FDA reports)
CARDIAC FAILURE ( 94 FDA reports)
BLINDNESS ( 93 FDA reports)
ERYTHEMA ( 92 FDA reports)
FEELING COLD ( 92 FDA reports)
PLATELET COUNT DECREASED ( 92 FDA reports)
SYNCOPE ( 92 FDA reports)
DIABETES MELLITUS ( 91 FDA reports)
DYSPHAGIA ( 89 FDA reports)
CARDIAC ARREST ( 87 FDA reports)
RHABDOMYOLYSIS ( 87 FDA reports)
MENTAL DISORDER ( 85 FDA reports)
CONTUSION ( 82 FDA reports)
SOMNAMBULISM ( 82 FDA reports)
HALLUCINATION, AUDITORY ( 81 FDA reports)
VERTIGO ( 81 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 80 FDA reports)
HAEMORRHAGE ( 80 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 80 FDA reports)
VIRAL INFECTION ( 80 FDA reports)
NEUROPATHY PERIPHERAL ( 79 FDA reports)
ASTHMA ( 78 FDA reports)
FIBROMYALGIA ( 78 FDA reports)
FRUSTRATION ( 78 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 76 FDA reports)
BURNING SENSATION ( 76 FDA reports)
DISORIENTATION ( 76 FDA reports)
DRUG HYPERSENSITIVITY ( 76 FDA reports)
ARTHROPATHY ( 75 FDA reports)
JOINT SWELLING ( 75 FDA reports)
MUSCULOSKELETAL PAIN ( 75 FDA reports)
RENAL IMPAIRMENT ( 74 FDA reports)
SLEEP TALKING ( 74 FDA reports)
THROMBOCYTOPENIA ( 74 FDA reports)
FLUID RETENTION ( 73 FDA reports)
INTERSTITIAL LUNG DISEASE ( 73 FDA reports)
SWELLING FACE ( 73 FDA reports)
SEPTIC SHOCK ( 71 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 70 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 70 FDA reports)
HOMICIDAL IDEATION ( 70 FDA reports)
PRODUCT QUALITY ISSUE ( 70 FDA reports)
SURGERY ( 70 FDA reports)
ABORTION SPONTANEOUS ( 69 FDA reports)
CHILLS ( 69 FDA reports)
EMOTIONAL DISORDER ( 69 FDA reports)
EUPHORIC MOOD ( 69 FDA reports)
BLISTER ( 68 FDA reports)
TENSION ( 68 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 67 FDA reports)
DRUG EFFECT DECREASED ( 67 FDA reports)
LIVER DISORDER ( 67 FDA reports)
MENSTRUAL DISORDER ( 67 FDA reports)
SINUSITIS ( 67 FDA reports)
INCORRECT DOSE ADMINISTERED ( 65 FDA reports)
INTENTIONAL DRUG MISUSE ( 65 FDA reports)
LETHARGY ( 65 FDA reports)
DYSKINESIA ( 64 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 64 FDA reports)
HYPOKALAEMIA ( 64 FDA reports)
ROAD TRAFFIC ACCIDENT ( 64 FDA reports)
ARRHYTHMIA ( 63 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 63 FDA reports)
INTENTIONAL OVERDOSE ( 63 FDA reports)
POLYDIPSIA ( 63 FDA reports)
ADVERSE EVENT ( 62 FDA reports)
BIPOLAR DISORDER ( 62 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 62 FDA reports)
HAEMOGLOBIN DECREASED ( 62 FDA reports)
NECK PAIN ( 62 FDA reports)
THINKING ABNORMAL ( 62 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 62 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 62 FDA reports)
MIGRAINE ( 61 FDA reports)
TINNITUS ( 61 FDA reports)
CORONARY ARTERY OCCLUSION ( 60 FDA reports)
MENOPAUSE ( 60 FDA reports)
VISUAL DISTURBANCE ( 59 FDA reports)
NASOPHARYNGITIS ( 58 FDA reports)
RENAL DISORDER ( 58 FDA reports)
BED REST ( 57 FDA reports)
DIPLOPIA ( 57 FDA reports)
DYSSTASIA ( 57 FDA reports)
ENURESIS ( 57 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 57 FDA reports)
EYE PAIN ( 56 FDA reports)
GASTROINTESTINAL DISORDER ( 56 FDA reports)
PAROSMIA ( 56 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 55 FDA reports)
BLOOD UREA INCREASED ( 54 FDA reports)
HOT FLUSH ( 53 FDA reports)
LUNG DISORDER ( 53 FDA reports)
MANIA ( 53 FDA reports)
HEPATIC ENZYME INCREASED ( 52 FDA reports)
HYPONATRAEMIA ( 52 FDA reports)
MULTI-ORGAN FAILURE ( 52 FDA reports)
MUSCLE TIGHTNESS ( 52 FDA reports)
POLLAKIURIA ( 52 FDA reports)
RESPIRATORY TRACT INFECTION ( 52 FDA reports)
RESTLESSNESS ( 52 FDA reports)
BODY HEIGHT DECREASED ( 51 FDA reports)
DEPRESSED MOOD ( 51 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 51 FDA reports)
HYPOTHYROIDISM ( 51 FDA reports)
RESPIRATORY FAILURE ( 51 FDA reports)
DRUG TOXICITY ( 50 FDA reports)
DRY EYE ( 50 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 50 FDA reports)
MOBILITY DECREASED ( 50 FDA reports)
PARALYSIS ( 50 FDA reports)
SEDATION ( 50 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 49 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 49 FDA reports)
SKIN LESION ( 49 FDA reports)
ADVERSE REACTION ( 48 FDA reports)
INFLUENZA ( 48 FDA reports)
STEVENS-JOHNSON SYNDROME ( 48 FDA reports)
TREATMENT NONCOMPLIANCE ( 48 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 48 FDA reports)
DRUG INTOLERANCE ( 47 FDA reports)
DRY THROAT ( 47 FDA reports)
OFF LABEL USE ( 47 FDA reports)
BLOOD POTASSIUM DECREASED ( 46 FDA reports)
CELLULITIS ( 46 FDA reports)
DRUG DOSE OMISSION ( 46 FDA reports)
EMPHYSEMA ( 46 FDA reports)
GASTRIC DISORDER ( 46 FDA reports)
GASTRITIS ( 46 FDA reports)
HEPATIC FAILURE ( 46 FDA reports)
INFECTION ( 46 FDA reports)
NEUTROPENIA ( 46 FDA reports)
PSYCHOTIC DISORDER ( 46 FDA reports)
JAUNDICE ( 45 FDA reports)
MOOD SWINGS ( 45 FDA reports)
PULMONARY EMBOLISM ( 45 FDA reports)
URINARY INCONTINENCE ( 45 FDA reports)
ANGINA PECTORIS ( 44 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 44 FDA reports)
EPISTAXIS ( 44 FDA reports)
EYE DISORDER ( 44 FDA reports)
MENORRHAGIA ( 44 FDA reports)
PANCYTOPENIA ( 44 FDA reports)
PARANOIA ( 44 FDA reports)
DEMENTIA ( 43 FDA reports)
DRUG DEPENDENCE ( 43 FDA reports)
DYSURIA ( 43 FDA reports)
POOR QUALITY SLEEP ( 43 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 43 FDA reports)
BRADYCARDIA ( 42 FDA reports)
HORMONE LEVEL ABNORMAL ( 42 FDA reports)
MACULAR DEGENERATION ( 42 FDA reports)
SKIN DISORDER ( 41 FDA reports)
COGNITIVE DISORDER ( 40 FDA reports)
CORONARY ARTERY DISEASE ( 40 FDA reports)
EYE HAEMORRHAGE ( 40 FDA reports)
FEELING HOT ( 40 FDA reports)
OCULAR HYPERAEMIA ( 40 FDA reports)
ORAL PAIN ( 40 FDA reports)
SHOCK ( 40 FDA reports)
SKIN DISCOLOURATION ( 40 FDA reports)
STAPHYLOCOCCAL INFECTION ( 40 FDA reports)
FLUSHING ( 39 FDA reports)
IMPAIRED DRIVING ABILITY ( 39 FDA reports)
SWOLLEN TONGUE ( 39 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 39 FDA reports)
ANAPHYLACTIC SHOCK ( 38 FDA reports)
FEELING DRUNK ( 38 FDA reports)
INJECTION SITE PAIN ( 38 FDA reports)
INJURY ( 38 FDA reports)
LOCALISED INFECTION ( 38 FDA reports)
OSTEOPOROSIS ( 38 FDA reports)
THIRST ( 38 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 37 FDA reports)
FEAR ( 37 FDA reports)
HAEMOPTYSIS ( 37 FDA reports)
LEUKOPENIA ( 37 FDA reports)
LICE INFESTATION ( 37 FDA reports)
OSTEOARTHRITIS ( 37 FDA reports)
SMOKER ( 37 FDA reports)
CYSTITIS ( 36 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 36 FDA reports)
DRY SKIN ( 36 FDA reports)
DYSPHONIA ( 36 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 36 FDA reports)
MENTAL STATUS CHANGES ( 36 FDA reports)
MUSCLE TWITCHING ( 36 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 36 FDA reports)
SLEEP APNOEA SYNDROME ( 36 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 35 FDA reports)
BREAST CANCER ( 35 FDA reports)
DEAFNESS ( 35 FDA reports)
DELIRIUM ( 35 FDA reports)
GLAUCOMA ( 35 FDA reports)
GRAND MAL CONVULSION ( 35 FDA reports)
MALNUTRITION ( 35 FDA reports)
NEURALGIA ( 35 FDA reports)
RETCHING ( 35 FDA reports)
APHASIA ( 34 FDA reports)
EATING DISORDER ( 34 FDA reports)
INFLAMMATION ( 34 FDA reports)
PANCREATITIS ( 34 FDA reports)
URINARY RETENTION ( 34 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 33 FDA reports)
BONE PAIN ( 33 FDA reports)
GINGIVAL BLEEDING ( 33 FDA reports)
HEPATITIS ( 33 FDA reports)
IMPAIRED HEALING ( 33 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 33 FDA reports)
RESPIRATORY DISORDER ( 33 FDA reports)
ACUTE RESPIRATORY FAILURE ( 32 FDA reports)
BLOOD BILIRUBIN INCREASED ( 32 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 32 FDA reports)
DELUSION ( 32 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 32 FDA reports)
HEAD INJURY ( 32 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 32 FDA reports)
LUNG NEOPLASM MALIGNANT ( 32 FDA reports)
RHINORRHOEA ( 32 FDA reports)
SKIN EXFOLIATION ( 32 FDA reports)
STOMACH DISCOMFORT ( 32 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 31 FDA reports)
BEDRIDDEN ( 31 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 31 FDA reports)
MUSCLE DISORDER ( 31 FDA reports)
PLEURAL EFFUSION ( 31 FDA reports)
ADVERSE DRUG REACTION ( 30 FDA reports)
DISEASE PROGRESSION ( 30 FDA reports)
EYE IRRITATION ( 30 FDA reports)
JOINT INJURY ( 30 FDA reports)
MIDDLE INSOMNIA ( 30 FDA reports)
MOVEMENT DISORDER ( 30 FDA reports)
OSTEONECROSIS ( 30 FDA reports)
RENAL PAIN ( 30 FDA reports)
TRANSAMINASES INCREASED ( 30 FDA reports)
VENTRICULAR FIBRILLATION ( 30 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 29 FDA reports)
BLOOD POTASSIUM INCREASED ( 29 FDA reports)
CEREBRAL HAEMORRHAGE ( 29 FDA reports)
ERECTILE DYSFUNCTION ( 29 FDA reports)
FEELING JITTERY ( 29 FDA reports)
HERPES ZOSTER ( 29 FDA reports)
HYPOXIA ( 29 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 29 FDA reports)
INFUSION RELATED REACTION ( 29 FDA reports)
OROPHARYNGEAL PAIN ( 29 FDA reports)
PULMONARY OEDEMA ( 29 FDA reports)
STENT PLACEMENT ( 29 FDA reports)
STOMATITIS ( 29 FDA reports)
WHEEZING ( 29 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 28 FDA reports)
HIP FRACTURE ( 28 FDA reports)
HUNGER ( 28 FDA reports)
LIP SWELLING ( 28 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 28 FDA reports)
NERVOUS SYSTEM DISORDER ( 28 FDA reports)
NICOTINE DEPENDENCE ( 28 FDA reports)
POST PROCEDURAL COMPLICATION ( 28 FDA reports)
APATHY ( 27 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 27 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 27 FDA reports)
ELECTROLYTE IMBALANCE ( 27 FDA reports)
EYELID PTOSIS ( 27 FDA reports)
HEART RATE IRREGULAR ( 27 FDA reports)
INTESTINAL OBSTRUCTION ( 27 FDA reports)
KNEE ARTHROPLASTY ( 27 FDA reports)
NIGHT SWEATS ( 27 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 27 FDA reports)
RASH ERYTHEMATOUS ( 27 FDA reports)
BLOOD SODIUM DECREASED ( 26 FDA reports)
CHOLELITHIASIS ( 26 FDA reports)
COLD SWEAT ( 26 FDA reports)
ENCEPHALOPATHY ( 26 FDA reports)
EXPIRED DRUG ADMINISTERED ( 26 FDA reports)
GASTROENTERITIS ( 26 FDA reports)
GENERALISED OEDEMA ( 26 FDA reports)
HEART RATE DECREASED ( 26 FDA reports)
IMPAIRED WORK ABILITY ( 26 FDA reports)
NASAL CONGESTION ( 26 FDA reports)
PULMONARY HYPERTENSION ( 26 FDA reports)
RASH GENERALISED ( 26 FDA reports)
RECTAL HAEMORRHAGE ( 26 FDA reports)
RESPIRATORY ARREST ( 26 FDA reports)
SPINAL DISORDER ( 26 FDA reports)
SUICIDAL BEHAVIOUR ( 26 FDA reports)
FORMICATION ( 25 FDA reports)
HEPATIC STEATOSIS ( 25 FDA reports)
INJECTION SITE HAEMATOMA ( 25 FDA reports)
ISCHAEMIC STROKE ( 25 FDA reports)
LIMB INJURY ( 25 FDA reports)
MELAENA ( 25 FDA reports)
MULTIPLE SCLEROSIS ( 25 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 25 FDA reports)
PROTEINURIA ( 25 FDA reports)
RHEUMATOID ARTHRITIS ( 25 FDA reports)
TYPE 2 DIABETES MELLITUS ( 25 FDA reports)
VENTRICULAR TACHYCARDIA ( 25 FDA reports)
ANAPHYLACTIC REACTION ( 24 FDA reports)
BLINDNESS UNILATERAL ( 24 FDA reports)
CARDIO-RESPIRATORY ARREST ( 24 FDA reports)
EYE SWELLING ( 24 FDA reports)
FUNGAL INFECTION ( 24 FDA reports)
GANGRENE ( 24 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 24 FDA reports)
LACRIMATION INCREASED ( 24 FDA reports)
OXYGEN SATURATION DECREASED ( 24 FDA reports)
PRESYNCOPE ( 24 FDA reports)
RASH MACULAR ( 24 FDA reports)
RESPIRATORY DISTRESS ( 24 FDA reports)
SCIATICA ( 24 FDA reports)
TOOTH EXTRACTION ( 24 FDA reports)
UNRESPONSIVE TO STIMULI ( 24 FDA reports)
BACK DISORDER ( 23 FDA reports)
DIFFICULTY IN WALKING ( 23 FDA reports)
DISSOCIATION ( 23 FDA reports)
EXERCISE LACK OF ( 23 FDA reports)
EYELID OEDEMA ( 23 FDA reports)
HALLUCINATION, VISUAL ( 23 FDA reports)
LYMPHOMA ( 23 FDA reports)
POISONING ( 23 FDA reports)
PROSTATE CANCER ( 23 FDA reports)
SNEEZING ( 23 FDA reports)
TENDONITIS ( 23 FDA reports)
THROAT TIGHTNESS ( 23 FDA reports)
TONGUE DISORDER ( 23 FDA reports)
UPPER LIMB FRACTURE ( 23 FDA reports)
VISUAL FIELD DEFECT ( 23 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 22 FDA reports)
AGEUSIA ( 22 FDA reports)
ANGINA UNSTABLE ( 22 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 22 FDA reports)
COORDINATION ABNORMAL ( 22 FDA reports)
DEVICE MALFUNCTION ( 22 FDA reports)
DIVERTICULITIS ( 22 FDA reports)
DRUG ADMINISTRATION ERROR ( 22 FDA reports)
FACE OEDEMA ( 22 FDA reports)
FEMUR FRACTURE ( 22 FDA reports)
HAEMATEMESIS ( 22 FDA reports)
HUMERUS FRACTURE ( 22 FDA reports)
MICTURITION URGENCY ( 22 FDA reports)
MUSCLE ATROPHY ( 22 FDA reports)
NAIL DISORDER ( 22 FDA reports)
NEOPLASM MALIGNANT ( 22 FDA reports)
NEUROPATHY ( 22 FDA reports)
NOCTURIA ( 22 FDA reports)
ORAL DISCOMFORT ( 22 FDA reports)
RIB FRACTURE ( 22 FDA reports)
SCAB ( 22 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 22 FDA reports)
BONE MARROW FAILURE ( 21 FDA reports)
CORONARY ARTERY STENOSIS ( 21 FDA reports)
DEEP VEIN THROMBOSIS ( 21 FDA reports)
FACIAL PAIN ( 21 FDA reports)
GINGIVITIS ( 21 FDA reports)
INCONTINENCE ( 21 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 21 FDA reports)
PERICARDIAL EFFUSION ( 21 FDA reports)
BLOOD URINE PRESENT ( 20 FDA reports)
CATARACT OPERATION ( 20 FDA reports)
CHOLESTASIS ( 20 FDA reports)
CROHN'S DISEASE ( 20 FDA reports)
EPILEPSY ( 20 FDA reports)
GASTRIC HAEMORRHAGE ( 20 FDA reports)
HYPOAESTHESIA ORAL ( 20 FDA reports)
HYPOKINESIA ( 20 FDA reports)
LYMPHADENOPATHY ( 20 FDA reports)
MUSCLE RIGIDITY ( 20 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 20 FDA reports)
PHARYNGEAL OEDEMA ( 20 FDA reports)
RETINAL DETACHMENT ( 20 FDA reports)
SEROTONIN SYNDROME ( 20 FDA reports)
THERAPY REGIMEN CHANGED ( 20 FDA reports)
ACUTE HEPATIC FAILURE ( 19 FDA reports)
ANGIOEDEMA ( 19 FDA reports)
BLOOD TEST ABNORMAL ( 19 FDA reports)
CIRCULATORY COLLAPSE ( 19 FDA reports)
COLITIS ( 19 FDA reports)
CONCUSSION ( 19 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 19 FDA reports)
ECCHYMOSIS ( 19 FDA reports)
GLOSSODYNIA ( 19 FDA reports)
HAEMATOCHEZIA ( 19 FDA reports)
HERNIA ( 19 FDA reports)
LABORATORY TEST ABNORMAL ( 19 FDA reports)
MYDRIASIS ( 19 FDA reports)
NERVE INJURY ( 19 FDA reports)
PRURITUS GENERALISED ( 19 FDA reports)
RENAL FAILURE CHRONIC ( 19 FDA reports)
RESPIRATORY DEPRESSION ( 19 FDA reports)
SENSORY DISTURBANCE ( 19 FDA reports)
SKIN ULCER ( 19 FDA reports)
AFFECTIVE DISORDER ( 18 FDA reports)
AGRANULOCYTOSIS ( 18 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 18 FDA reports)
ASCITES ( 18 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 18 FDA reports)
BONE DENSITY DECREASED ( 18 FDA reports)
CEREBRAL INFARCTION ( 18 FDA reports)
DIABETIC RETINOPATHY ( 18 FDA reports)
DISABILITY ( 18 FDA reports)
DISCOMFORT ( 18 FDA reports)
DISEASE RECURRENCE ( 18 FDA reports)
FISTULA ( 18 FDA reports)
HAEMATURIA ( 18 FDA reports)
HYPERKALAEMIA ( 18 FDA reports)
INJECTION SITE REACTION ( 18 FDA reports)
IRRITABLE BOWEL SYNDROME ( 18 FDA reports)
LOWER LIMB FRACTURE ( 18 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 18 FDA reports)
ORAL INTAKE REDUCED ( 18 FDA reports)
PERSONALITY CHANGE ( 18 FDA reports)
PETIT MAL EPILEPSY ( 18 FDA reports)
PULMONARY CONGESTION ( 18 FDA reports)
RASH PRURITIC ( 18 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 18 FDA reports)
SUDDEN DEATH ( 18 FDA reports)
THERAPY NON-RESPONDER ( 18 FDA reports)
THYROID DISORDER ( 18 FDA reports)
ACCIDENTAL OVERDOSE ( 17 FDA reports)
ALCOHOLISM ( 17 FDA reports)
BLADDER DISORDER ( 17 FDA reports)
BRONCHOSPASM ( 17 FDA reports)
CARDIOMEGALY ( 17 FDA reports)
CARDIOVASCULAR DISORDER ( 17 FDA reports)
CHOKING ( 17 FDA reports)
DIABETIC NEUROPATHY ( 17 FDA reports)
ECZEMA ( 17 FDA reports)
ERUCTATION ( 17 FDA reports)
EXTRASYSTOLES ( 17 FDA reports)
EYE PRURITUS ( 17 FDA reports)
GALACTORRHOEA ( 17 FDA reports)
HAEMORRHOIDS ( 17 FDA reports)
HEARING IMPAIRED ( 17 FDA reports)
HYPOPHAGIA ( 17 FDA reports)
MULTIPLE DRUG OVERDOSE ( 17 FDA reports)
MYOCLONUS ( 17 FDA reports)
PSORIASIS ( 17 FDA reports)
ROTATOR CUFF SYNDROME ( 17 FDA reports)
SEBORRHOEIC DERMATITIS ( 17 FDA reports)
VAGINAL HAEMORRHAGE ( 17 FDA reports)
ALCOHOL USE ( 16 FDA reports)
BREAST PAIN ( 16 FDA reports)
CARDIAC OPERATION ( 16 FDA reports)
DERMATITIS ( 16 FDA reports)
DRUG LEVEL INCREASED ( 16 FDA reports)
EYE MOVEMENT DISORDER ( 16 FDA reports)
GASTRIC ULCER ( 16 FDA reports)
GINGIVAL INFECTION ( 16 FDA reports)
GLOSSITIS ( 16 FDA reports)
HIP ARTHROPLASTY ( 16 FDA reports)
HYPERVENTILATION ( 16 FDA reports)
HYSTERECTOMY ( 16 FDA reports)
JOINT DISLOCATION ( 16 FDA reports)
NEPHROLITHIASIS ( 16 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 16 FDA reports)
OSTEOMYELITIS ( 16 FDA reports)
PALLOR ( 16 FDA reports)
PHOTOSENSITIVITY REACTION ( 16 FDA reports)
RESTLESS LEGS SYNDROME ( 16 FDA reports)
SCREAMING ( 16 FDA reports)
SEXUAL DYSFUNCTION ( 16 FDA reports)
SKIN BURNING SENSATION ( 16 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 16 FDA reports)
THROAT IRRITATION ( 16 FDA reports)
TOOTH LOSS ( 16 FDA reports)
ULCER ( 16 FDA reports)
VAGINAL INFECTION ( 16 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 16 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 16 FDA reports)
AMENORRHOEA ( 15 FDA reports)
ATAXIA ( 15 FDA reports)
CAROTID ARTERY OCCLUSION ( 15 FDA reports)
CHOLECYSTECTOMY ( 15 FDA reports)
COAGULOPATHY ( 15 FDA reports)
COLITIS ULCERATIVE ( 15 FDA reports)
CYTOLYTIC HEPATITIS ( 15 FDA reports)
DIALYSIS ( 15 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 15 FDA reports)
FEEDING DISORDER ( 15 FDA reports)
GASTROENTERITIS VIRAL ( 15 FDA reports)
GINGIVAL SWELLING ( 15 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 15 FDA reports)
GOUT ( 15 FDA reports)
HAEMATOMA ( 15 FDA reports)
HEPATOMEGALY ( 15 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 15 FDA reports)
HYPERTENSIVE CRISIS ( 15 FDA reports)
MUCOSAL INFLAMMATION ( 15 FDA reports)
MUSCLE INJURY ( 15 FDA reports)
MUTISM ( 15 FDA reports)
ORTHOSTATIC HYPOTENSION ( 15 FDA reports)
OSTEOPENIA ( 15 FDA reports)
PERIPHERAL COLDNESS ( 15 FDA reports)
PETECHIAE ( 15 FDA reports)
PHOTOPHOBIA ( 15 FDA reports)
PNEUMONIA ASPIRATION ( 15 FDA reports)
PRODUCTIVE COUGH ( 15 FDA reports)
SENSATION OF HEAVINESS ( 15 FDA reports)
SPINAL OSTEOARTHRITIS ( 15 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 15 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 15 FDA reports)
URINE OUTPUT DECREASED ( 15 FDA reports)
VASCULAR OCCLUSION ( 15 FDA reports)
ANEURYSM ( 14 FDA reports)
AORTIC DISSECTION ( 14 FDA reports)
BODY TEMPERATURE INCREASED ( 14 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 14 FDA reports)
CARDIAC PACEMAKER INSERTION ( 14 FDA reports)
DRUG ERUPTION ( 14 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 14 FDA reports)
DYSTONIA ( 14 FDA reports)
EMOTIONAL DISTRESS ( 14 FDA reports)
EYE INFECTION ( 14 FDA reports)
FEBRILE NEUTROPENIA ( 14 FDA reports)
FURUNCLE ( 14 FDA reports)
GRIP STRENGTH DECREASED ( 14 FDA reports)
HEAD DISCOMFORT ( 14 FDA reports)
HYPERAESTHESIA ( 14 FDA reports)
HYPERCALCAEMIA ( 14 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 14 FDA reports)
LIBIDO DECREASED ( 14 FDA reports)
MOUTH HAEMORRHAGE ( 14 FDA reports)
MOUTH ULCERATION ( 14 FDA reports)
NECK INJURY ( 14 FDA reports)
NERVE COMPRESSION ( 14 FDA reports)
OESOPHAGITIS ( 14 FDA reports)
PANCREATIC CARCINOMA ( 14 FDA reports)
PNEUMONIA BACTERIAL ( 14 FDA reports)
POLYURIA ( 14 FDA reports)
POOR PERIPHERAL CIRCULATION ( 14 FDA reports)
PULSE ABSENT ( 14 FDA reports)
RASH PAPULAR ( 14 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 14 FDA reports)
SCAR ( 14 FDA reports)
SENSORY LOSS ( 14 FDA reports)
SINUS TACHYCARDIA ( 14 FDA reports)
ABORTION ( 13 FDA reports)
APHONIA ( 13 FDA reports)
BLUE TOE SYNDROME ( 13 FDA reports)
COLLAPSE OF LUNG ( 13 FDA reports)
DERMATITIS ALLERGIC ( 13 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 13 FDA reports)
EAR INFECTION ( 13 FDA reports)
EJECTION FRACTION DECREASED ( 13 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 13 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 13 FDA reports)
FOOT FRACTURE ( 13 FDA reports)
HAEMATOCRIT DECREASED ( 13 FDA reports)
HAEMOLYTIC ANAEMIA ( 13 FDA reports)
HAIR TEXTURE ABNORMAL ( 13 FDA reports)
HEMIPARESIS ( 13 FDA reports)
HEPATOCELLULAR DAMAGE ( 13 FDA reports)
HYPERLIPIDAEMIA ( 13 FDA reports)
INCOHERENT ( 13 FDA reports)
KNEE OPERATION ( 13 FDA reports)
LIMB DISCOMFORT ( 13 FDA reports)
LUNG INFECTION ( 13 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 13 FDA reports)
MITRAL VALVE INCOMPETENCE ( 13 FDA reports)
MYOPATHY ( 13 FDA reports)
ORAL CANDIDIASIS ( 13 FDA reports)
PANIC REACTION ( 13 FDA reports)
PARAESTHESIA ORAL ( 13 FDA reports)
RASH MACULO-PAPULAR ( 13 FDA reports)
RHINITIS ( 13 FDA reports)
SHOULDER OPERATION ( 13 FDA reports)
SINUS DISORDER ( 13 FDA reports)
TOXIC SKIN ERUPTION ( 13 FDA reports)
WRIST FRACTURE ( 13 FDA reports)
ANKLE FRACTURE ( 12 FDA reports)
ARTERIOSCLEROSIS ( 12 FDA reports)
ATELECTASIS ( 12 FDA reports)
BACK INJURY ( 12 FDA reports)
BLOOD CALCIUM INCREASED ( 12 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 12 FDA reports)
BLOOD PROLACTIN INCREASED ( 12 FDA reports)
BRAIN OEDEMA ( 12 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 12 FDA reports)
CARPAL TUNNEL SYNDROME ( 12 FDA reports)
DRUG ABUSER ( 12 FDA reports)
EAR PAIN ( 12 FDA reports)
ERYSIPELAS ( 12 FDA reports)
FAECAL INCONTINENCE ( 12 FDA reports)
GALLBLADDER DISORDER ( 12 FDA reports)
HEPATIC CIRRHOSIS ( 12 FDA reports)
HEPATITIS ACUTE ( 12 FDA reports)
HEPATITIS C ( 12 FDA reports)
HEPATITIS FULMINANT ( 12 FDA reports)
HOSPITALISATION ( 12 FDA reports)
HYPOAESTHESIA FACIAL ( 12 FDA reports)
INJECTION SITE HAEMORRHAGE ( 12 FDA reports)
LIVER INJURY ( 12 FDA reports)
LOSS OF CONTROL OF LEGS ( 12 FDA reports)
MAJOR DEPRESSION ( 12 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 12 FDA reports)
MEDICATION RESIDUE ( 12 FDA reports)
MOTION SICKNESS ( 12 FDA reports)
MYOSITIS ( 12 FDA reports)
NEPHROTIC SYNDROME ( 12 FDA reports)
NO ADVERSE EVENT ( 12 FDA reports)
OLIGURIA ( 12 FDA reports)
ONYCHOCLASIS ( 12 FDA reports)
OPTIC NERVE DISORDER ( 12 FDA reports)
PARKINSON'S DISEASE ( 12 FDA reports)
SLUGGISHNESS ( 12 FDA reports)
SPINAL OPERATION ( 12 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 12 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 12 FDA reports)
TORSADE DE POINTES ( 12 FDA reports)
UNDERDOSE ( 12 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
VASCULAR GRAFT ( 12 FDA reports)
ANURIA ( 11 FDA reports)
BLINDNESS TRANSIENT ( 11 FDA reports)
CARDIAC VALVE DISEASE ( 11 FDA reports)
CERVICOBRACHIAL SYNDROME ( 11 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 11 FDA reports)
CLOSTRIDIAL INFECTION ( 11 FDA reports)
COELIAC DISEASE ( 11 FDA reports)
COLITIS ISCHAEMIC ( 11 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 11 FDA reports)
DEAFNESS UNILATERAL ( 11 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 11 FDA reports)
EOSINOPHILIA ( 11 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 11 FDA reports)
HEPATORENAL SYNDROME ( 11 FDA reports)
HYPERTHERMIA ( 11 FDA reports)
IMMUNE SYSTEM DISORDER ( 11 FDA reports)
IRON DEFICIENCY ANAEMIA ( 11 FDA reports)
JOINT STIFFNESS ( 11 FDA reports)
LACERATION ( 11 FDA reports)
LOCAL SWELLING ( 11 FDA reports)
LUNG NEOPLASM ( 11 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 11 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 11 FDA reports)
OBESITY ( 11 FDA reports)
OPTIC NERVE INJURY ( 11 FDA reports)
PAIN IN JAW ( 11 FDA reports)
PNEUMONIA VIRAL ( 11 FDA reports)
PROCEDURAL PAIN ( 11 FDA reports)
ROTATOR CUFF REPAIR ( 11 FDA reports)
SELF-INJURIOUS IDEATION ( 11 FDA reports)
SPINAL FRACTURE ( 11 FDA reports)
STATUS EPILEPTICUS ( 11 FDA reports)
STRESS FRACTURE ( 11 FDA reports)
THERAPEUTIC PROCEDURE ( 11 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 11 FDA reports)
TOOTH FRACTURE ( 11 FDA reports)
VITAMIN D DECREASED ( 11 FDA reports)
WRONG DRUG ADMINISTERED ( 11 FDA reports)
YELLOW SKIN ( 11 FDA reports)
ABSCESS ( 10 FDA reports)
ACCIDENTAL EXPOSURE ( 10 FDA reports)
ADRENAL INSUFFICIENCY ( 10 FDA reports)
ANOSMIA ( 10 FDA reports)
AURA ( 10 FDA reports)
BLOOD CALCIUM DECREASED ( 10 FDA reports)
BREAST MASS ( 10 FDA reports)
CARDIOGENIC SHOCK ( 10 FDA reports)
CEREBRAL ISCHAEMIA ( 10 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 10 FDA reports)
CORONARY ARTERY BYPASS ( 10 FDA reports)
DENTAL CARIES ( 10 FDA reports)
DRUG SCREEN POSITIVE ( 10 FDA reports)
EAR DISORDER ( 10 FDA reports)
EYE OPERATION ( 10 FDA reports)
FEELING OF DESPAIR ( 10 FDA reports)
GENITAL DISCHARGE ( 10 FDA reports)
GINGIVAL PAIN ( 10 FDA reports)
HAEMODIALYSIS ( 10 FDA reports)
HEPATOCELLULAR INJURY ( 10 FDA reports)
HICCUPS ( 10 FDA reports)
HOSTILITY ( 10 FDA reports)
HYPOACUSIS ( 10 FDA reports)
HYPOVOLAEMIA ( 10 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 10 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 10 FDA reports)
INITIAL INSOMNIA ( 10 FDA reports)
INTENTIONAL SELF-INJURY ( 10 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 10 FDA reports)
KIDNEY INFECTION ( 10 FDA reports)
LYMPHOEDEMA ( 10 FDA reports)
METABOLIC ENCEPHALOPATHY ( 10 FDA reports)
MULTIPLE MYELOMA ( 10 FDA reports)
NECROTISING FASCIITIS ( 10 FDA reports)
NEPHROPATHY ( 10 FDA reports)
NEUROSIS ( 10 FDA reports)
PAIN OF SKIN ( 10 FDA reports)
PHOBIA ( 10 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 10 FDA reports)
PSYCHIATRIC SYMPTOM ( 10 FDA reports)
PULMONARY FIBROSIS ( 10 FDA reports)
RETINAL VASCULAR DISORDER ( 10 FDA reports)
SCHIZOPHRENIA ( 10 FDA reports)
SINUS BRADYCARDIA ( 10 FDA reports)
SINUS CONGESTION ( 10 FDA reports)
SKIN HAEMORRHAGE ( 10 FDA reports)
SKIN INJURY ( 10 FDA reports)
THERMAL BURN ( 10 FDA reports)
VITREOUS HAEMORRHAGE ( 10 FDA reports)
ACCIDENT ( 9 FDA reports)
ANGIOPLASTY ( 9 FDA reports)
ANORGASMIA ( 9 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 9 FDA reports)
ARTERIAL DISORDER ( 9 FDA reports)
ATRIAL FLUTTER ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK ( 9 FDA reports)
BLOOD PRESSURE ABNORMAL ( 9 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 9 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 9 FDA reports)
BRAIN NEOPLASM ( 9 FDA reports)
BREAST CANCER FEMALE ( 9 FDA reports)
BURSITIS ( 9 FDA reports)
CYANOSIS ( 9 FDA reports)
DECREASED ACTIVITY ( 9 FDA reports)
DECUBITUS ULCER ( 9 FDA reports)
DEPENDENCE ( 9 FDA reports)
DIABETIC COMA ( 9 FDA reports)
DIABETIC KETOACIDOSIS ( 9 FDA reports)
DYSPHEMIA ( 9 FDA reports)
EAR DISCOMFORT ( 9 FDA reports)
ECONOMIC PROBLEM ( 9 FDA reports)
FAECES DISCOLOURED ( 9 FDA reports)
FOOD CRAVING ( 9 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 9 FDA reports)
HALLUCINATIONS, MIXED ( 9 FDA reports)
HIATUS HERNIA ( 9 FDA reports)
HYPERPHAGIA ( 9 FDA reports)
HYPERTONIC BLADDER ( 9 FDA reports)
HYPOCALCAEMIA ( 9 FDA reports)
IMMOBILE ( 9 FDA reports)
INCORRECT STORAGE OF DRUG ( 9 FDA reports)
INFARCTION ( 9 FDA reports)
LARYNGEAL OEDEMA ( 9 FDA reports)
LIPOMA ( 9 FDA reports)
NODULE ( 9 FDA reports)
NON-SMALL CELL LUNG CANCER ( 9 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 9 FDA reports)
ORGANISING PNEUMONIA ( 9 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 9 FDA reports)
PLEURISY ( 9 FDA reports)
POLYNEUROPATHY ( 9 FDA reports)
PROCEDURAL COMPLICATION ( 9 FDA reports)
RENAL INJURY ( 9 FDA reports)
RENAL TUBULAR NECROSIS ( 9 FDA reports)
RETINAL DISORDER ( 9 FDA reports)
RETINAL HAEMORRHAGE ( 9 FDA reports)
SELF ESTEEM DECREASED ( 9 FDA reports)
SKIN IRRITATION ( 9 FDA reports)
SPINAL COLUMN STENOSIS ( 9 FDA reports)
SUBCUTANEOUS NODULE ( 9 FDA reports)
TENDON RUPTURE ( 9 FDA reports)
TOOTH ABSCESS ( 9 FDA reports)
TOOTH DISORDER ( 9 FDA reports)
UROSEPSIS ( 9 FDA reports)
WALKING AID USER ( 9 FDA reports)
ABDOMINAL PAIN LOWER ( 8 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 8 FDA reports)
ALCOHOL POISONING ( 8 FDA reports)
AORTIC VALVE INCOMPETENCE ( 8 FDA reports)
APNOEA ( 8 FDA reports)
BLOOD CHLORIDE INCREASED ( 8 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 8 FDA reports)
BODY TEMPERATURE DECREASED ( 8 FDA reports)
CANDIDIASIS ( 8 FDA reports)
CARDIAC DEATH ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 8 FDA reports)
CHOLECYSTITIS ( 8 FDA reports)
CLUSTER HEADACHE ( 8 FDA reports)
COLON CANCER ( 8 FDA reports)
CONJUNCTIVITIS ( 8 FDA reports)
DEPERSONALISATION ( 8 FDA reports)
DYSPNOEA EXERTIONAL ( 8 FDA reports)
ERECTION INCREASED ( 8 FDA reports)
EXTRADURAL ABSCESS ( 8 FDA reports)
EYE OEDEMA ( 8 FDA reports)
FOOD ALLERGY ( 8 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 8 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 8 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 8 FDA reports)
HEPATITIS A ( 8 FDA reports)
HERNIA REPAIR ( 8 FDA reports)
HYPOPROTEINAEMIA ( 8 FDA reports)
ILEUS ( 8 FDA reports)
IMPATIENCE ( 8 FDA reports)
INJECTION SITE SWELLING ( 8 FDA reports)
LEUKOCYTOSIS ( 8 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 8 FDA reports)
MEDICAL DEVICE COMPLICATION ( 8 FDA reports)
METASTASES TO LUNG ( 8 FDA reports)
MUSCULOSKELETAL DISORDER ( 8 FDA reports)
MYOCARDIAL ISCHAEMIA ( 8 FDA reports)
NAIL GROWTH ABNORMAL ( 8 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 8 FDA reports)
NEUTROPHIL COUNT DECREASED ( 8 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 8 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 8 FDA reports)
OEDEMA MOUTH ( 8 FDA reports)
OESOPHAGEAL ULCER ( 8 FDA reports)
PHYSICAL ASSAULT ( 8 FDA reports)
PIGMENTATION DISORDER ( 8 FDA reports)
PNEUMOTHORAX ( 8 FDA reports)
PROSTATE CANCER METASTATIC ( 8 FDA reports)
PROTHROMBIN TIME PROLONGED ( 8 FDA reports)
PSEUDOMONAS INFECTION ( 8 FDA reports)
REFLUX OESOPHAGITIS ( 8 FDA reports)
RENAL CYST ( 8 FDA reports)
SCRATCH ( 8 FDA reports)
SPINAL LAMINECTOMY ( 8 FDA reports)
TRIGEMINAL NEURALGIA ( 8 FDA reports)
VENOUS STASIS ( 8 FDA reports)
VENTRICULAR HYPERTROPHY ( 8 FDA reports)
VITREOUS FLOATERS ( 8 FDA reports)
AFFECT LABILITY ( 7 FDA reports)
ANGIOLIPOMA ( 7 FDA reports)
ANGIOPATHY ( 7 FDA reports)
APALLIC SYNDROME ( 7 FDA reports)
AREFLEXIA ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 7 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 7 FDA reports)
BIPOLAR I DISORDER ( 7 FDA reports)
BLOOD ALBUMIN DECREASED ( 7 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 7 FDA reports)
BLOOD UREA DECREASED ( 7 FDA reports)
BONE SARCOMA ( 7 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 7 FDA reports)
BREAST DISCHARGE ( 7 FDA reports)
CAESAREAN SECTION ( 7 FDA reports)
CARDIAC MURMUR ( 7 FDA reports)
CEREBRAL THROMBOSIS ( 7 FDA reports)
CHANGE OF BOWEL HABIT ( 7 FDA reports)
CHROMATURIA ( 7 FDA reports)
COLONIC POLYP ( 7 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 7 FDA reports)
DEVICE FAILURE ( 7 FDA reports)
DRUG ABUSE ( 7 FDA reports)
DRUG LEVEL DECREASED ( 7 FDA reports)
EROSIVE OESOPHAGITIS ( 7 FDA reports)
FAILURE OF IMPLANT ( 7 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 7 FDA reports)
FRACTURE ( 7 FDA reports)
GINGIVAL BLISTER ( 7 FDA reports)
GINGIVAL HYPERTROPHY ( 7 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 7 FDA reports)
HAIR GROWTH ABNORMAL ( 7 FDA reports)
HEPATITIS CHOLESTATIC ( 7 FDA reports)
HEPATITIS TOXIC ( 7 FDA reports)
HYPERAMMONAEMIA ( 7 FDA reports)
HYPOTONIA ( 7 FDA reports)
ILEUS PARALYTIC ( 7 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 7 FDA reports)
INCREASED TENDENCY TO BRUISE ( 7 FDA reports)
INTESTINAL PERFORATION ( 7 FDA reports)
LACTIC ACIDOSIS ( 7 FDA reports)
LOGORRHOEA ( 7 FDA reports)
LUMBAR RADICULOPATHY ( 7 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 7 FDA reports)
MALIGNANT MELANOMA ( 7 FDA reports)
METABOLIC ACIDOSIS ( 7 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 7 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 7 FDA reports)
MUSCLE CONTRACTURE ( 7 FDA reports)
NEPHROSCLEROSIS ( 7 FDA reports)
OBSTRUCTION GASTRIC ( 7 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 7 FDA reports)
PANCREATITIS ACUTE ( 7 FDA reports)
PERIPHERAL ISCHAEMIA ( 7 FDA reports)
PHARYNGITIS ( 7 FDA reports)
PHOTOPSIA ( 7 FDA reports)
POLYMYALGIA RHEUMATICA ( 7 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 7 FDA reports)
PSOAS ABSCESS ( 7 FDA reports)
SALIVARY HYPERSECRETION ( 7 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 7 FDA reports)
SINUS HEADACHE ( 7 FDA reports)
SKIN FISSURES ( 7 FDA reports)
SKIN ODOUR ABNORMAL ( 7 FDA reports)
SKIN SWELLING ( 7 FDA reports)
STRESS SYMPTOMS ( 7 FDA reports)
SYNCOPE VASOVAGAL ( 7 FDA reports)
SYNOVIAL RUPTURE ( 7 FDA reports)
TENDERNESS ( 7 FDA reports)
TETANY ( 7 FDA reports)
TOOTH INFECTION ( 7 FDA reports)
TOOTHACHE ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 7 FDA reports)
URINE ODOUR ABNORMAL ( 7 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 7 FDA reports)
VENOUS INSUFFICIENCY ( 7 FDA reports)
VENTRICULAR ARRHYTHMIA ( 7 FDA reports)
VULVOVAGINAL PRURITUS ( 7 FDA reports)
WEIGHT FLUCTUATION ( 7 FDA reports)
WOUND INFECTION ( 7 FDA reports)
ABDOMINAL ADHESIONS ( 6 FDA reports)
ABDOMINAL TENDERNESS ( 6 FDA reports)
ABNORMAL FAECES ( 6 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 6 FDA reports)
AORTIC ANEURYSM ( 6 FDA reports)
APPLICATION SITE BURN ( 6 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 6 FDA reports)
ASPIRATION ( 6 FDA reports)
BASAL CELL CARCINOMA ( 6 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 6 FDA reports)
BLADDER NEOPLASM ( 6 FDA reports)
BLADDER PAIN ( 6 FDA reports)
BLEPHARITIS ( 6 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 6 FDA reports)
BLOOD MAGNESIUM DECREASED ( 6 FDA reports)
BONE DISORDER ( 6 FDA reports)
BREATH ODOUR ( 6 FDA reports)
BRUXISM ( 6 FDA reports)
CARDIAC FAILURE ACUTE ( 6 FDA reports)
CATHETERISATION CARDIAC ( 6 FDA reports)
CHOLELITHOTOMY ( 6 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 6 FDA reports)
COAGULATION TEST ABNORMAL ( 6 FDA reports)
COMPRESSION FRACTURE ( 6 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 6 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 6 FDA reports)
DEAFNESS NEUROSENSORY ( 6 FDA reports)
DERMATITIS EXFOLIATIVE ( 6 FDA reports)
DIASTOLIC DYSFUNCTION ( 6 FDA reports)
DUODENAL ULCER ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
ERYTHEMA OF EYELID ( 6 FDA reports)
EXOSTOSIS ( 6 FDA reports)
FACIAL PALSY ( 6 FDA reports)
FEAR OF DEATH ( 6 FDA reports)
FOETAL DISTRESS SYNDROME ( 6 FDA reports)
FOOT DEFORMITY ( 6 FDA reports)
GALLBLADDER OPERATION ( 6 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 6 FDA reports)
GINGIVAL DISORDER ( 6 FDA reports)
GRAFT VERSUS HOST DISEASE ( 6 FDA reports)
HEPATIC ENCEPHALOPATHY ( 6 FDA reports)
HYDROCEPHALUS ( 6 FDA reports)
HYDRONEPHROSIS ( 6 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 6 FDA reports)
ILLUSION ( 6 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 6 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 6 FDA reports)
INTESTINAL ISCHAEMIA ( 6 FDA reports)
INTRACRANIAL ANEURYSM ( 6 FDA reports)
JAW DISORDER ( 6 FDA reports)
JOINT SPRAIN ( 6 FDA reports)
LARYNGOSPASM ( 6 FDA reports)
LEUKAEMIA ( 6 FDA reports)
MALABSORPTION ( 6 FDA reports)
METASTASES TO BONE ( 6 FDA reports)
MUSCLE STRAIN ( 6 FDA reports)
MYASTHENIA GRAVIS ( 6 FDA reports)
MYOPIA ( 6 FDA reports)
NEGATIVE THOUGHTS ( 6 FDA reports)
NEOPLASM PROGRESSION ( 6 FDA reports)
NEUTROPHIL COUNT ( 6 FDA reports)
NYSTAGMUS ( 6 FDA reports)
OPTIC NEURITIS ( 6 FDA reports)
OVERWEIGHT ( 6 FDA reports)
PANIC DISORDER ( 6 FDA reports)
PARTIAL SEIZURES ( 6 FDA reports)
PERFORMANCE STATUS DECREASED ( 6 FDA reports)
PERIARTHRITIS ( 6 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 6 FDA reports)
PERITONITIS ( 6 FDA reports)
PNEUMONITIS ( 6 FDA reports)
PREMATURE BABY ( 6 FDA reports)
PRURIGO ( 6 FDA reports)
PURPURA ( 6 FDA reports)
RASH PUSTULAR ( 6 FDA reports)
RETINOPATHY ( 6 FDA reports)
SENSATION OF FOREIGN BODY ( 6 FDA reports)
SKIN INDURATION ( 6 FDA reports)
SKIN LACERATION ( 6 FDA reports)
SKIN WARM ( 6 FDA reports)
SPINAL FUSION SURGERY ( 6 FDA reports)
SUBDURAL HAEMATOMA ( 6 FDA reports)
SUFFOCATION FEELING ( 6 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 6 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
TONGUE INJURY ( 6 FDA reports)
TONGUE OEDEMA ( 6 FDA reports)
TOOTH DISCOLOURATION ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
URINE COLOUR ABNORMAL ( 6 FDA reports)
VAGINAL POLYP ( 6 FDA reports)
VASCULAR BYPASS GRAFT ( 6 FDA reports)
VIITH NERVE PARALYSIS ( 6 FDA reports)
VITAMIN D DEFICIENCY ( 6 FDA reports)
VOMITING PROJECTILE ( 6 FDA reports)
WEGENER'S GRANULOMATOSIS ( 6 FDA reports)
ABNORMAL SENSATION IN EYE ( 5 FDA reports)
ABSCESS LIMB ( 5 FDA reports)
ACCIDENT AT WORK ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ACUTE PULMONARY OEDEMA ( 5 FDA reports)
ALCOHOL INTERACTION ( 5 FDA reports)
ANGIONEUROTIC OEDEMA ( 5 FDA reports)
ANHEDONIA ( 5 FDA reports)
ANXIETY DISORDER ( 5 FDA reports)
AORTIC ANEURYSM RUPTURE ( 5 FDA reports)
APTYALISM ( 5 FDA reports)
ASPHYXIA ( 5 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 5 FDA reports)
BACTERIA URINE ( 5 FDA reports)
BLADDER CANCER ( 5 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 5 FDA reports)
BLOOD IRON DECREASED ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 5 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 5 FDA reports)
BRADYPHRENIA ( 5 FDA reports)
BRAIN INJURY ( 5 FDA reports)
BRONCHIAL DISORDER ( 5 FDA reports)
BRONCHIOLITIS ( 5 FDA reports)
CAPILLARY LEAK SYNDROME ( 5 FDA reports)
CARBON DIOXIDE INCREASED ( 5 FDA reports)
CARDIAC FLUTTER ( 5 FDA reports)
CARDIAC TAMPONADE ( 5 FDA reports)
CARDIOPULMONARY FAILURE ( 5 FDA reports)
CAROTID ARTERY DISEASE ( 5 FDA reports)
CEREBRAL DISORDER ( 5 FDA reports)
CEREBROVASCULAR DISORDER ( 5 FDA reports)
CHROMATOPSIA ( 5 FDA reports)
CHRONIC SINUSITIS ( 5 FDA reports)
COGWHEEL RIGIDITY ( 5 FDA reports)
COSTOCHONDRITIS ( 5 FDA reports)
CYST ( 5 FDA reports)
DECREASED INTEREST ( 5 FDA reports)
DERMATITIS ACNEIFORM ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DETOXIFICATION ( 5 FDA reports)
DEVICE OCCLUSION ( 5 FDA reports)
DEVICE RELATED INFECTION ( 5 FDA reports)
DIVERTICULUM ( 5 FDA reports)
DRUG CLEARANCE DECREASED ( 5 FDA reports)
DRUG DISPENSING ERROR ( 5 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
DRUG LEVEL FLUCTUATING ( 5 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
EJACULATION FAILURE ( 5 FDA reports)
ENDOMETRIOSIS ( 5 FDA reports)
ENERGY INCREASED ( 5 FDA reports)
EOSINOPHILIC PNEUMONIA ( 5 FDA reports)
EXCORIATION ( 5 FDA reports)
EXERCISE TOLERANCE DECREASED ( 5 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 5 FDA reports)
EYE ALLERGY ( 5 FDA reports)
EYE DISCHARGE ( 5 FDA reports)
FLIGHT OF IDEAS ( 5 FDA reports)
FOLLICULITIS ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
GINGIVAL ULCERATION ( 5 FDA reports)
GLUCOSE URINE PRESENT ( 5 FDA reports)
HAEMODYNAMIC INSTABILITY ( 5 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 5 FDA reports)
HAEMORRHAGE URINARY TRACT ( 5 FDA reports)
HAEMORRHAGIC DIATHESIS ( 5 FDA reports)
HAIR COLOUR CHANGES ( 5 FDA reports)
HELICOBACTER INFECTION ( 5 FDA reports)
HEMIPLEGIA ( 5 FDA reports)
HEPATIC NEOPLASM ( 5 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
HIGH FREQUENCY ABLATION ( 5 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 5 FDA reports)
HYPERCHOLESTEROLAEMIA ( 5 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 5 FDA reports)
HYPOGLYCAEMIC COMA ( 5 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 5 FDA reports)
HYPOMAGNESAEMIA ( 5 FDA reports)
HYPOREFLEXIA ( 5 FDA reports)
HYPOTHERMIA ( 5 FDA reports)
HYPOVOLAEMIC SHOCK ( 5 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 5 FDA reports)
INAPPROPRIATE AFFECT ( 5 FDA reports)
INGUINAL HERNIA ( 5 FDA reports)
INJECTION SITE EXTRAVASATION ( 5 FDA reports)
INJECTION SITE INDURATION ( 5 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 5 FDA reports)
INTESTINAL STOMA ( 5 FDA reports)
KLEBSIELLA INFECTION ( 5 FDA reports)
LARGE INTESTINE PERFORATION ( 5 FDA reports)
LEFT ATRIAL DILATATION ( 5 FDA reports)
LIBIDO INCREASED ( 5 FDA reports)
LIGAMENT RUPTURE ( 5 FDA reports)
LIMB OPERATION ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
LOCALISED OEDEMA ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
LUPUS-LIKE SYNDROME ( 5 FDA reports)
MALIGNANT TUMOUR EXCISION ( 5 FDA reports)
MENIERE'S DISEASE ( 5 FDA reports)
MENSTRUATION IRREGULAR ( 5 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 5 FDA reports)
MICTURITION DISORDER ( 5 FDA reports)
MIOSIS ( 5 FDA reports)
MOTOR DYSFUNCTION ( 5 FDA reports)
MULTIPLE ALLERGIES ( 5 FDA reports)
MULTIPLE FRACTURES ( 5 FDA reports)
MUSCLE HAEMORRHAGE ( 5 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 5 FDA reports)
OBSTRUCTION ( 5 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 5 FDA reports)
OCULAR VASCULAR DISORDER ( 5 FDA reports)
OESOPHAGEAL DISORDER ( 5 FDA reports)
OESOPHAGEAL SPASM ( 5 FDA reports)
ORAL MUCOSAL BLISTERING ( 5 FDA reports)
OROPHARYNGEAL BLISTERING ( 5 FDA reports)
PARAPLEGIA ( 5 FDA reports)
PELVIC FRACTURE ( 5 FDA reports)
PENILE PAIN ( 5 FDA reports)
PERIORBITAL HAEMATOMA ( 5 FDA reports)
PHLEBITIS ( 5 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 5 FDA reports)
POLYP ( 5 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 5 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 5 FDA reports)
PREMENSTRUAL SYNDROME ( 5 FDA reports)
PROSTATIC DISORDER ( 5 FDA reports)
PROTEIN TOTAL DECREASED ( 5 FDA reports)
PULMONARY HAEMORRHAGE ( 5 FDA reports)
PYODERMA GANGRENOSUM ( 5 FDA reports)
RESORPTION BONE INCREASED ( 5 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 5 FDA reports)
RHINALGIA ( 5 FDA reports)
ROSACEA ( 5 FDA reports)
SELF-MEDICATION ( 5 FDA reports)
SEXUAL ABUSE ( 5 FDA reports)
SHOCK HAEMORRHAGIC ( 5 FDA reports)
SICK SINUS SYNDROME ( 5 FDA reports)
SKIN NODULE ( 5 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 5 FDA reports)
STILLBIRTH ( 5 FDA reports)
STRONGYLOIDIASIS ( 5 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
TARDIVE DYSKINESIA ( 5 FDA reports)
TEMPERATURE INTOLERANCE ( 5 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 5 FDA reports)
THYROID NEOPLASM ( 5 FDA reports)
TONGUE DISCOLOURATION ( 5 FDA reports)
TUBERCULOSIS ( 5 FDA reports)
URINARY TRACT DISORDER ( 5 FDA reports)
URINARY TRACT OBSTRUCTION ( 5 FDA reports)
URINE FLOW DECREASED ( 5 FDA reports)
UTERINE DILATION AND CURETTAGE ( 5 FDA reports)
VEIN DISORDER ( 5 FDA reports)
VENOUS OCCLUSION ( 5 FDA reports)
VICTIM OF SEXUAL ABUSE ( 5 FDA reports)
WEIGHT BEARING DIFFICULTY ( 5 FDA reports)
WOUND ( 5 FDA reports)
WOUND SECRETION ( 5 FDA reports)
ACNE ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
ACUTE SINUSITIS ( 4 FDA reports)
ADRENAL MASS ( 4 FDA reports)
ALLERGY TO CHEMICALS ( 4 FDA reports)
ALVEOLITIS ALLERGIC ( 4 FDA reports)
AMPUTATION ( 4 FDA reports)
ANAESTHETIC COMPLICATION ( 4 FDA reports)
ANAL HAEMORRHAGE ( 4 FDA reports)
ANDROPAUSE ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 4 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
APPLICATION SITE PAIN ( 4 FDA reports)
ARTERIOSPASM CORONARY ( 4 FDA reports)
ARTHRITIS BACTERIAL ( 4 FDA reports)
ATYPICAL FEMUR FRACTURE ( 4 FDA reports)
BLADDER OPERATION ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD COUNT ABNORMAL ( 4 FDA reports)
BLOOD DISORDER ( 4 FDA reports)
BLOOD IRON INCREASED ( 4 FDA reports)
BLOOD URINE ( 4 FDA reports)
BRADYARRHYTHMIA ( 4 FDA reports)
BREAST SWELLING ( 4 FDA reports)
BULIMIA NERVOSA ( 4 FDA reports)
CARDIAC ENZYMES INCREASED ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CAROTID ARTERY THROMBOSIS ( 4 FDA reports)
CATATONIA ( 4 FDA reports)
CERVICAL SPINAL STENOSIS ( 4 FDA reports)
CHEST X-RAY ABNORMAL ( 4 FDA reports)
CHOKING SENSATION ( 4 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
CLAVICLE FRACTURE ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
COLONOSCOPY ( 4 FDA reports)
CONVERSION DISORDER ( 4 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 4 FDA reports)
CORONARY ARTERY SURGERY ( 4 FDA reports)
CORONARY ARTERY THROMBOSIS ( 4 FDA reports)
CYANOPSIA ( 4 FDA reports)
DEAFNESS TRAUMATIC ( 4 FDA reports)
DEFORMITY ( 4 FDA reports)
DENGUE FEVER ( 4 FDA reports)
DERMATITIS CONTACT ( 4 FDA reports)
DERMATITIS PSORIASIFORM ( 4 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 4 FDA reports)
DILATATION ATRIAL ( 4 FDA reports)
DIZZINESS POSTURAL ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
DRUG TOLERANCE ( 4 FDA reports)
DRUG-INDUCED LIVER INJURY ( 4 FDA reports)
EAR HAEMORRHAGE ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
ENANTHEMA ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
EPILEPTIC AURA ( 4 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
FACIAL NEURALGIA ( 4 FDA reports)
FAECES HARD ( 4 FDA reports)
FIBRINOLYSIS INCREASED ( 4 FDA reports)
FOOD AVERSION ( 4 FDA reports)
FOOT OPERATION ( 4 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 4 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 4 FDA reports)
FRACTURED SACRUM ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
GASTRODUODENAL ULCER ( 4 FDA reports)
GASTROINTESTINAL PAIN ( 4 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GENITAL INJURY ( 4 FDA reports)
GINGIVAL RECESSION ( 4 FDA reports)
GUN SHOT WOUND ( 4 FDA reports)
GYNAECOMASTIA ( 4 FDA reports)
H1N1 INFLUENZA ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HANGOVER ( 4 FDA reports)
HEART RATE ABNORMAL ( 4 FDA reports)
HEART VALVE OPERATION ( 4 FDA reports)
HEAT EXHAUSTION ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HEPATIC ENZYME ABNORMAL ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 4 FDA reports)
HEPATIC PAIN ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
HEPATOSPLENOMEGALY ( 4 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
HYPERTHYROIDISM ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
HYPOVENTILATION ( 4 FDA reports)
ILEECTOMY ( 4 FDA reports)
INCREASED BRONCHIAL SECRETION ( 4 FDA reports)
INHIBITORY DRUG INTERACTION ( 4 FDA reports)
INJECTION SITE DISCOLOURATION ( 4 FDA reports)
INJECTION SITE INFLAMMATION ( 4 FDA reports)
INJECTION SITE NODULE ( 4 FDA reports)
INJECTION SITE ULCER ( 4 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 4 FDA reports)
JUDGEMENT IMPAIRED ( 4 FDA reports)
LABILE BLOOD PRESSURE ( 4 FDA reports)
LABYRINTHITIS ( 4 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 4 FDA reports)
LEUKOENCEPHALOPATHY ( 4 FDA reports)
LIPIDS INCREASED ( 4 FDA reports)
LOBAR PNEUMONIA ( 4 FDA reports)
LOCALISED OSTEOARTHRITIS ( 4 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 4 FDA reports)
LYMPHOCYTOSIS ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
MIGRAINE WITH AURA ( 4 FDA reports)
MONOCYTOSIS ( 4 FDA reports)
MONOPLEGIA ( 4 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME ( 4 FDA reports)
MYOCLONIC EPILEPSY ( 4 FDA reports)
NASAL MUCOSAL DISORDER ( 4 FDA reports)
NEOPLASM ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEUROGENIC BLADDER ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
NOCTURNAL DYSPNOEA ( 4 FDA reports)
NOSOCOMIAL INFECTION ( 4 FDA reports)
OBSESSIVE THOUGHTS ( 4 FDA reports)
OPEN WOUND ( 4 FDA reports)
ORTHOPEDIC PROCEDURE ( 4 FDA reports)
PAIN EXACERBATED ( 4 FDA reports)
PALATAL OEDEMA ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
PARESIS ( 4 FDA reports)
PARKINSONISM ( 4 FDA reports)
PELVIC HAEMATOMA ( 4 FDA reports)
PELVIC PAIN ( 4 FDA reports)
PERIORBITAL OEDEMA ( 4 FDA reports)
PERIPHERAL EMBOLISM ( 4 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 4 FDA reports)
PERSONALITY DISORDER ( 4 FDA reports)
PHARYNGEAL DISORDER ( 4 FDA reports)
PITTING OEDEMA ( 4 FDA reports)
PLEURITIC PAIN ( 4 FDA reports)
PNEUMOPERITONEUM ( 4 FDA reports)
POST PROCEDURAL PAIN ( 4 FDA reports)
POUCHITIS ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PREMATURE DELIVERY ( 4 FDA reports)
PRIAPISM ( 4 FDA reports)
PROCTITIS ( 4 FDA reports)
PRODUCT TASTE ABNORMAL ( 4 FDA reports)
PROTEIN URINE PRESENT ( 4 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
RALES ( 4 FDA reports)
RECTAL PROLAPSE ( 4 FDA reports)
RECTAL ULCER ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 4 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 4 FDA reports)
RENAL CELL CARCINOMA ( 4 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
RETINAL TEAR ( 4 FDA reports)
SINOATRIAL BLOCK ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
SKIN TIGHTNESS ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
SPINAL ANAESTHESIA ( 4 FDA reports)
SPINAL CORD INJURY ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
SPONDYLITIS ( 4 FDA reports)
STRESS URINARY INCONTINENCE ( 4 FDA reports)
STUPOR ( 4 FDA reports)
SUBDURAL HYGROMA ( 4 FDA reports)
SUBILEUS ( 4 FDA reports)
SUDDEN ONSET OF SLEEP ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
TENDON DISORDER ( 4 FDA reports)
TERMINAL INSOMNIA ( 4 FDA reports)
THROMBOPHLEBITIS ( 4 FDA reports)
THROMBOSIS IN DEVICE ( 4 FDA reports)
TIBIA FRACTURE ( 4 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 4 FDA reports)
TONGUE BLACK HAIRY ( 4 FDA reports)
TONGUE BLISTERING ( 4 FDA reports)
TOOTH DECALCIFICATION ( 4 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 4 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 4 FDA reports)
TUNNEL VISION ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
VENTRICULAR DYSFUNCTION ( 4 FDA reports)
VISUAL BRIGHTNESS ( 4 FDA reports)
VULVOVAGINAL PAIN ( 4 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
ABDOMINAL OPERATION ( 3 FDA reports)
ABNORMAL WEIGHT GAIN ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
ACUTE PSYCHOSIS ( 3 FDA reports)
ALCOHOL ABUSE ( 3 FDA reports)
ALCOHOLIC LIVER DISEASE ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 3 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 3 FDA reports)
ANORECTAL DISORDER ( 3 FDA reports)
AORTIC OCCLUSION ( 3 FDA reports)
AORTIC VALVE REPLACEMENT ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
APPLICATION SITE DISCOLOURATION ( 3 FDA reports)
ARTHROPOD BITE ( 3 FDA reports)
ARTHROPOD STING ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
AUTOTRANSFUSION ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BIOPSY LIVER ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD KETONE BODY ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD OSMOLARITY INCREASED ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BRAIN DAMAGE ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BRAIN STEM SYNDROME ( 3 FDA reports)
BREAST CANCER METASTATIC ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
BURNING SENSATION MUCOSAL ( 3 FDA reports)
BUTTOCK PAIN ( 3 FDA reports)
CALCINOSIS ( 3 FDA reports)
CARCINOID TUMOUR ( 3 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 3 FDA reports)
CARDIAC STRESS TEST ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CAROTID ARTERY STENT INSERTION ( 3 FDA reports)
CELL DEATH ( 3 FDA reports)
CHEMOTHERAPY ( 3 FDA reports)
CHOLANGITIS ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CHRONIC FATIGUE SYNDROME ( 3 FDA reports)
CLAUSTROPHOBIA ( 3 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 3 FDA reports)
COLOSTOMY ( 3 FDA reports)
COLOUR BLINDNESS ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CONGENITAL NEUROLOGICAL DISORDER ( 3 FDA reports)
CORNEAL OPACITY ( 3 FDA reports)
CORONARY OSTIAL STENOSIS ( 3 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 3 FDA reports)
DAYDREAMING ( 3 FDA reports)
DEJA VU ( 3 FDA reports)
DELIRIUM TREMENS ( 3 FDA reports)
DELUSIONAL PERCEPTION ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DENTAL PROSTHESIS USER ( 3 FDA reports)
DEPRESSIVE SYMPTOM ( 3 FDA reports)
DERMATOMYOSITIS ( 3 FDA reports)
DEVELOPMENTAL DELAY ( 3 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DILATATION VENTRICULAR ( 3 FDA reports)
DREAMY STATE ( 3 FDA reports)
DROOLING ( 3 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 3 FDA reports)
DYSGRAPHIA ( 3 FDA reports)
DYSHIDROSIS ( 3 FDA reports)
DYSLALIA ( 3 FDA reports)
DYSLEXIA ( 3 FDA reports)
DYSPAREUNIA ( 3 FDA reports)
DYSPHASIA ( 3 FDA reports)
DYSPHORIA ( 3 FDA reports)
DYSTHYMIC DISORDER ( 3 FDA reports)
EAR CONGESTION ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 3 FDA reports)
EMPYEMA ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
ENZYME ABNORMALITY ( 3 FDA reports)
ERYTHEMA NODOSUM ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
EXOPHTHALMOS ( 3 FDA reports)
EYELID FUNCTION DISORDER ( 3 FDA reports)
EYELIDS PRURITUS ( 3 FDA reports)
FACE INJURY ( 3 FDA reports)
FACIAL NERVE DISORDER ( 3 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
FOOD INTOLERANCE ( 3 FDA reports)
FOOT AMPUTATION ( 3 FDA reports)
GASTROINTESTINAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GENERALISED ANXIETY DISORDER ( 3 FDA reports)
GINGIVAL HYPERPLASIA ( 3 FDA reports)
GOITRE ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
GRUNTING ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HEAD BANGING ( 3 FDA reports)
HEART DISEASE CONGENITAL ( 3 FDA reports)
HEPATIC CONGESTION ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HIP SURGERY ( 3 FDA reports)
HODGKIN'S DISEASE ( 3 FDA reports)
HOMICIDE ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPERTRICHOSIS ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOCHLORAEMIA ( 3 FDA reports)
IATROGENIC INJURY ( 3 FDA reports)
IMMUNODEFICIENCY ( 3 FDA reports)
IMPULSE-CONTROL DISORDER ( 3 FDA reports)
IMPULSIVE BEHAVIOUR ( 3 FDA reports)
INDURATION ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
INTERVERTEBRAL DISC INJURY ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
IRITIS ( 3 FDA reports)
IRON DEFICIENCY ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
JOINT EFFUSION ( 3 FDA reports)
KNEE DEFORMITY ( 3 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 3 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LARGE INTESTINE CARCINOMA ( 3 FDA reports)
LARYNGITIS ( 3 FDA reports)
LAZINESS ( 3 FDA reports)
LIGAMENT SPRAIN ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LIPIDS ABNORMAL ( 3 FDA reports)
LIVEDO RETICULARIS ( 3 FDA reports)
LIVER TRANSPLANT ( 3 FDA reports)
LOWER EXTREMITY MASS ( 3 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 3 FDA reports)
MACROCYTOSIS ( 3 FDA reports)
MASS ( 3 FDA reports)
MENINGITIS HERPES ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
METASTASIS ( 3 FDA reports)
METASTATIC NEOPLASM ( 3 FDA reports)
MICROCYTIC ANAEMIA ( 3 FDA reports)
MITRAL VALVE DISEASE ( 3 FDA reports)
MORBID THOUGHTS ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MUCOSAL DRYNESS ( 3 FDA reports)
MUSCLE CRAMP ( 3 FDA reports)
MUSCLE SPASTICITY ( 3 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 3 FDA reports)
MYOGLOBIN URINE PRESENT ( 3 FDA reports)
NAIL OPERATION ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 3 FDA reports)
NECK MASS ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NIPPLE PAIN ( 3 FDA reports)
NO ADVERSE DRUG EFFECT ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
OCULAR ICTERUS ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 3 FDA reports)
OESOPHAGEAL PAIN ( 3 FDA reports)
ONYCHOMYCOSIS ( 3 FDA reports)
ORAL DISORDER ( 3 FDA reports)
ORAL HERPES ( 3 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
ORAL SURGERY ( 3 FDA reports)
OTITIS MEDIA ( 3 FDA reports)
PANCREATIC DISORDER ( 3 FDA reports)
PANCREATIC INSUFFICIENCY ( 3 FDA reports)
PANCREATIC NECROSIS ( 3 FDA reports)
PAPULE ( 3 FDA reports)
PARASPINAL ABSCESS ( 3 FDA reports)
PARATHYROID DISORDER ( 3 FDA reports)
PARATHYROID TUMOUR BENIGN ( 3 FDA reports)
PATELLA FRACTURE ( 3 FDA reports)
PERIODONTAL DESTRUCTION ( 3 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 3 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 3 FDA reports)
PERITONEAL DIALYSIS ( 3 FDA reports)
PERNICIOUS ANAEMIA ( 3 FDA reports)
PERONEAL NERVE PALSY ( 3 FDA reports)
PERSECUTORY DELUSION ( 3 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 3 FDA reports)
PHARYNGEAL MASS ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
POLYCYSTIC OVARIES ( 3 FDA reports)
POLYTRAUMATISM ( 3 FDA reports)
POST HERPETIC NEURALGIA ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 3 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 3 FDA reports)
PROSTATIC OPERATION ( 3 FDA reports)
PROTEIN TOTAL INCREASED ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
PSYCHOTIC BEHAVIOUR ( 3 FDA reports)
PULMONARY MYCOSIS ( 3 FDA reports)
PULSE ABNORMAL ( 3 FDA reports)
QUALITY OF LIFE DECREASED ( 3 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 3 FDA reports)
READING DISORDER ( 3 FDA reports)
RECTAL OBSTRUCTION ( 3 FDA reports)
RENAL ABSCESS ( 3 FDA reports)
RENAL ATROPHY ( 3 FDA reports)
RENAL NECROSIS ( 3 FDA reports)
RESIDUAL URINE ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RETINAL OEDEMA ( 3 FDA reports)
RHINITIS ALLERGIC ( 3 FDA reports)
RHONCHI ( 3 FDA reports)
SALIVA ALTERED ( 3 FDA reports)
SARCOIDOSIS ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 3 FDA reports)
SCLERAL DISORDER ( 3 FDA reports)
SCLERITIS ( 3 FDA reports)
SKIN HYPERTROPHY ( 3 FDA reports)
SKIN PLAQUE ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SPERMATOZOA ABNORMAL ( 3 FDA reports)
SPUTUM RETENTION ( 3 FDA reports)
STARING ( 3 FDA reports)
STRABISMUS ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SUBSTANCE ABUSE ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
SUPERINFECTION ( 3 FDA reports)
SURGICAL PROCEDURE REPEATED ( 3 FDA reports)
SYMPATHECTOMY ( 3 FDA reports)
SYSTEMIC CANDIDA ( 3 FDA reports)
T-CELL LYMPHOMA ( 3 FDA reports)
TEMPORAL LOBE EPILEPSY ( 3 FDA reports)
TENDON INJURY ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
THROAT CANCER ( 3 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 3 FDA reports)
TIC ( 3 FDA reports)
TOE AMPUTATION ( 3 FDA reports)
TONGUE COATED ( 3 FDA reports)
TONGUE DRY ( 3 FDA reports)
TONSILLAR DISORDER ( 3 FDA reports)
TOOTH EROSION ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
TRAUMATIC BRAIN INJURY ( 3 FDA reports)
TRAUMATIC HAEMATOMA ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
TUMOUR HAEMORRHAGE ( 3 FDA reports)
TUMOUR NECROSIS ( 3 FDA reports)
ULNAR NERVE PALSY ( 3 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
URINE OUTPUT INCREASED ( 3 FDA reports)
VASCULAR OPERATION ( 3 FDA reports)
VASCULAR RUPTURE ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VASODILATATION ( 3 FDA reports)
VENTRICLE RUPTURE ( 3 FDA reports)
VENTRICULAR HYPOKINESIA ( 3 FDA reports)
VESTIBULAR DISORDER ( 3 FDA reports)
VOCAL CORD PARALYSIS ( 3 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
WATER INTOXICATION ( 3 FDA reports)
WEIGHT GAIN POOR ( 3 FDA reports)
WOUND DEHISCENCE ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL NEOPLASM ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ABSTAINS FROM ALCOHOL ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACQUIRED HAEMOPHILIA ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ACUTE TONSILLITIS ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
ALCOHOL INTOLERANCE ( 2 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 2 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 2 FDA reports)
AMYLOIDOSIS ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANALGESIC ASTHMA SYNDROME ( 2 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 2 FDA reports)
ANENCEPHALY ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
ANHIDROSIS ( 2 FDA reports)
ANORECTAL OPERATION ( 2 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ARTERIAL STENOSIS LIMB ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ASPERMIA ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
BENIGN HEPATIC NEOPLASM ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLADDER DYSFUNCTION ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
BLADDER PROLAPSE ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 2 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 2 FDA reports)
BLOOD URIC ACID ABNORMAL ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
BREAST ENGORGEMENT ( 2 FDA reports)
BREAST OEDEMA ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BRONCHIAL CARCINOMA ( 2 FDA reports)
BRONCHIAL ULCERATION ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARBON MONOXIDE POISONING ( 2 FDA reports)
CARDIAC DISCOMFORT ( 2 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 2 FDA reports)
CARDIOSPASM ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 2 FDA reports)
CATHETER SITE CELLULITIS ( 2 FDA reports)
CATHETER THROMBOSIS ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL CYST ( 2 FDA reports)
CEREBRAL LOBOTOMY ( 2 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 2 FDA reports)
CERVICAL ROOT PAIN ( 2 FDA reports)
CHEST WALL MASS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONJUNCTIVAL SCAR ( 2 FDA reports)
CORNEAL DEPOSITS ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 2 FDA reports)
CSF GLUCOSE DECREASED ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
CUTIS LAXA ( 2 FDA reports)
CYSTITIS NONINFECTIVE ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DEATH OF RELATIVE ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DEVICE DEPLOYMENT ISSUE ( 2 FDA reports)
DIAPHRAGMATIC INJURY ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DRESSLER'S SYNDROME ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DRUG INTERACTION POTENTIATION ( 2 FDA reports)
DRUG LEVEL ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSPLASIA ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENDODONTIC PROCEDURE ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
EPHELIDES ( 2 FDA reports)
EPIDURAL ANAESTHESIA ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EWING'S SARCOMA ( 2 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FASCIITIS ( 2 FDA reports)
FEELING GUILTY ( 2 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FLAIL CHEST ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FLASHBACK ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOETAL GROWTH RESTRICTION ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTRITIS BACTERIAL ( 2 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GENERAL SYMPTOM ( 2 FDA reports)
GENITAL LESION ( 2 FDA reports)
GLAUCOMA SURGERY ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GOUTY ARTHRITIS ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
GROWTH RETARDATION ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HAEMORRHAGIC INFARCTION ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEART VALVE REPLACEMENT ( 2 FDA reports)
HEPATIC MASS ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEREDITARY HAEMOCHROMATOSIS ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HIGH RISK PREGNANCY ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HUNGRY BONE SYNDROME ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERKINESIA ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
HYPOTONIA NEONATAL ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
IMPRISONMENT ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INCISION SITE CELLULITIS ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INCISIONAL DRAINAGE ( 2 FDA reports)
INCORRECT PRODUCT STORAGE ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFECTION PARASITIC ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INFUSION SITE INFECTION ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJECTION SITE MASS ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 2 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 2 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
JOB DISSATISFACTION ( 2 FDA reports)
JOINT ARTHROPLASTY ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
KAPOSI'S SARCOMA ( 2 FDA reports)
KAWASAKI'S DISEASE ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LACRIMAL DISORDER ( 2 FDA reports)
LACTOSE INTOLERANCE ( 2 FDA reports)
LASER THERAPY ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LIGAMENT INJURY ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LUPUS NEPHRITIS ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
MALARIA ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 2 FDA reports)
MARFAN'S SYNDROME ( 2 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MICROVASCULAR ANGINA ( 2 FDA reports)
MICTURITION FREQUENCY DECREASED ( 2 FDA reports)
MILK ALLERGY ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MIXED INCONTINENCE ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MYASTHENIC SYNDROME ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NASAL CYST ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEGATIVISM ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEPHROGENIC ANAEMIA ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NERVE ROOT INJURY CERVICAL ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NEUROSURGERY ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NODAL ARRHYTHMIA ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
NUCHAL RIGIDITY ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OBESITY SURGERY ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL DILATATION ( 2 FDA reports)
OESOPHAGEAL PERFORATION ( 2 FDA reports)
OPEN ANGLE GLAUCOMA ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL CAVITY FISTULA ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
ORAL MUCOSAL DISORDER ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OSTEONECROSIS OF JAW ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PALATAL DISORDER ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PARKINSONIAN GAIT ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PELVIC HAEMORRHAGE ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PENILE SIZE REDUCED ( 2 FDA reports)
PERFORATED ULCER ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERINEAL ERYTHEMA ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 2 FDA reports)
PILONIDAL CYST ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
PLASMAPHERESIS ( 2 FDA reports)
PNEUMONIA HERPES VIRAL ( 2 FDA reports)
PNEUMONIA INFLUENZAL ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
POOR SUCKING REFLEX ( 2 FDA reports)
PORPHYRIA NON-ACUTE ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POST PROCEDURAL SEPSIS ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 2 FDA reports)
PRECANCEROUS CELLS PRESENT ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PROCEDURAL VOMITING ( 2 FDA reports)
PRODUCT ODOUR ABNORMAL ( 2 FDA reports)
PROSTATE CANCER RECURRENT ( 2 FDA reports)
PROSTATE INFECTION ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTEUS INFECTION ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
PYELOCALIECTASIS ( 2 FDA reports)
PYLORIC STENOSIS ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
RADICULAR PAIN ( 2 FDA reports)
RADICULOPATHY ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RECTAL LESION ( 2 FDA reports)
RECTAL STENOSIS ( 2 FDA reports)
RECURRENT CANCER ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
RED MAN SYNDROME ( 2 FDA reports)
REFRACTION DISORDER ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETINAL INJURY ( 2 FDA reports)
SCAN BRAIN ( 2 FDA reports)
SCIATIC NERVE INJURY ( 2 FDA reports)
SCLERODERMA ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SCROTAL ERYTHEMA ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SINOBRONCHITIS ( 2 FDA reports)
SINUS OPERATION ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SKIN DISCOMFORT ( 2 FDA reports)
SKIN FIBROSIS ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SKIN SENSITISATION ( 2 FDA reports)
SKIN WRINKLING ( 2 FDA reports)
SKULL FRACTURED BASE ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
SMALL FOR DATES BABY ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SNORING ( 2 FDA reports)
SOCIAL FEAR ( 2 FDA reports)
SOMATISATION DISORDER ( 2 FDA reports)
SOMNOLENCE NEONATAL ( 2 FDA reports)
SOPOR ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
SPINAL CORPECTOMY ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SPONTANEOUS HAEMATOMA ( 2 FDA reports)
SPONTANEOUS PENILE ERECTION ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 2 FDA reports)
STENT-GRAFT MALFUNCTION ( 2 FDA reports)
STRANGURY ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SYMPATHICOTONIA ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TEETH BRITTLE ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
TESTICULAR OEDEMA ( 2 FDA reports)
TESTICULAR SWELLING ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THYROIDITIS ( 2 FDA reports)
THYROXINE INCREASED ( 2 FDA reports)
TOBACCO ABUSE ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TREMOR NEONATAL ( 2 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
TYPE II HYPERSENSITIVITY ( 2 FDA reports)
UNIVENTRICULAR HEART ( 2 FDA reports)
UPPER EXTREMITY MASS ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URINARY HESITATION ( 2 FDA reports)
UROBILIN URINE ( 2 FDA reports)
URTICARIA GENERALISED ( 2 FDA reports)
UTERINE ENLARGEMENT ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VASOMOTOR RHINITIS ( 2 FDA reports)
VENOUS HAEMORRHAGE ( 2 FDA reports)
VESTIBULAR NEURONITIS ( 2 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VIROLOGIC FAILURE ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
VITAMIN D ABNORMAL ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VITREOUS DISORDER ( 2 FDA reports)
WEIGHT LOSS DIET ( 2 FDA reports)
WEIGHT LOSS POOR ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
WHITE CLOT SYNDROME ( 2 FDA reports)
WOUND DRAINAGE ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
5'NUCLEOTIDASE INCREASED ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABDOMINAL WALL MASS ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACROCHORDON ( 1 FDA reports)
ACROMEGALY ( 1 FDA reports)
ACUTE LUNG INJURY ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADMINISTRATION SITE REACTION ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAEMIA OF PREGNANCY ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANAL ATRESIA ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANTI FACTOR VII ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APHERESIS ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARM AMPUTATION ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACK CRUSHING ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY BRAIN ABNORMAL ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLADDER STENOSIS ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD HOMOCYSTEINE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD OESTROGEN DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BONE OPERATION ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BORRELIA INFECTION ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRAIN TUMOUR OPERATION ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST ADENOMA ( 1 FDA reports)
BREAST CANCER MALE ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIAC VALVE ABSCESS ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CENTRAL PAIN SYNDROME ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL ASPERGILLOSIS ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHILLBLAINS ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHONDROLYSIS ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL DEFORMITY OF CLAVICLE ( 1 FDA reports)
CONGENITAL GREAT VESSEL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONTACT LENS INTOLERANCE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORNEAL IMPLANT ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
COXSACKIE VIRAL INFECTION ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
DACTYLITIS ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DEATH OF SPOUSE ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELAYED SLEEP PHASE ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DISSOCIATIVE FUGUE ( 1 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG WITHDRAWAL MAINTENANCE THERAPY ( 1 FDA reports)
DURAL TEAR ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELBOW DEFORMITY ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENDARTERECTOMY ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENGRAFT FAILURE ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR DECREASED ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIGLOTTIS ULCER ( 1 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EVANS SYNDROME ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXPLORATORY OPERATION ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTRUSION OF DEVICE ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FUNGAL ENDOCARDITIS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
GALLBLADDER NECROSIS ( 1 FDA reports)
GALLBLADDER OBSTRUCTION ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC CANCER STAGE IV ( 1 FDA reports)
GASTRIC HYPOMOTILITY ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRIN SECRETION DISORDER ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL GANGRENE ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GINGIVAL CYST ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL INJURY ( 1 FDA reports)
GLARE ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
GLOSSOPHARYNGEAL NERVE PARALYSIS ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
GRAFT HAEMORRHAGE ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
GROWTH OF EYELASHES ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 1 FDA reports)
HAEMATURIA TRAUMATIC ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 1 FDA reports)
HAEMORRHAGE IN PREGNANCY ( 1 FDA reports)
HAIR METAL TEST ABNORMAL ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HAND AMPUTATION ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HAND DERMATITIS ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HETEROPHORIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HOMEOPATHY ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HYDROCELE ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERKINETIC HEART SYNDROME ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERTENSIVE ANGIOPATHY ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPOPARATHYROIDISM ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTONIC-HYPORESPONSIVE EPISODE ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED INSULIN SECRETION ( 1 FDA reports)
IMPAIRED REASONING ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
INCISION SITE BLISTER ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE JOINT REDNESS ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INSTILLATION SITE REACTION ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTESTINAL CONGESTION ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
IRON METABOLISM DISORDER ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
JEALOUS DELUSION ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KIDNEY MALFORMATION ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACK OF SATIETY ( 1 FDA reports)
LACRIMAL CYST ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LANGERHANS' CELL HISTIOCYTOSIS ( 1 FDA reports)
LAPAROSCOPY ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNGOPHARYNGITIS ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEGIONELLA SEROLOGY ( 1 FDA reports)
LEGIONELLA SEROLOGY POSITIVE ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKODERMA ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPIDS DECREASED ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUMBAR PUNCTURE ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MASTOPTOSIS ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MECONIUM STAIN ( 1 FDA reports)
MEDICAL DEVICE REMOVAL ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MEIBOMIANITIS ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESENTERIC PANNICULITIS ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTASES TO STOMACH ( 1 FDA reports)
METASTASES TO THORAX ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
METASTATIC UTERINE CANCER ( 1 FDA reports)
MIDDLE EAR DISORDER ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE GATED ACQUISITION SCAN ABNORMAL ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE OPERATION ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYCOTIC ALLERGY ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOMECTOMY ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECK EXPLORATION ( 1 FDA reports)
NECROBIOSIS ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OESTRADIOL INCREASED ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
OPTIC DISC DRUSEN ( 1 FDA reports)
OPTIC NERVE HYPOPLASIA ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
ORAL DYSAESTHESIA ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
OROANTRAL FISTULA ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OTOSALPINGITIS ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCREATIC OPERATION ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARENT-CHILD PROBLEM ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERINEURIAL CYST ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERSISTENT GENERALISED LYMPHADENOPATHY ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 1 FDA reports)
PHOBIA OF DRIVING ( 1 FDA reports)
PHOTOKERATITIS ( 1 FDA reports)
PHYSICAL ABUSE ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PILONIDAL CYST CONGENITAL ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLACENTAL INSUFFICIENCY ( 1 FDA reports)
PLASMA CELLS INCREASED ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PLEUROTHOTONUS ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POSTPARTUM DEPRESSION ( 1 FDA reports)
POSTPARTUM UTERINE SUBINVOLUTION ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREMATURE AGEING ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCTITIS ULCERATIVE ( 1 FDA reports)
PRODUCT CLOSURE REMOVAL DIFFICULT ( 1 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PROGESTERONE DECREASED ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PSEUDOALDOSTERONISM ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PURPURA SENILE ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYROGLUTAMATE INCREASED ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RECTAL PERFORATION ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REDUCED DEXTERITY ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RELATIONSHIP BREAKDOWN ( 1 FDA reports)
RENAL APLASIA ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 1 FDA reports)
RETAINED PRODUCTS OF CONCEPTION ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL DEPIGMENTATION ( 1 FDA reports)
RETINAL DYSTROPHY ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOMA ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROSEOLA ( 1 FDA reports)
SALIVA ANALYSIS ABNORMAL ( 1 FDA reports)
SALIVA DISCOLOURATION ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SEMEN DISCOLOURATION ( 1 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 1 FDA reports)
SEPTIC NECROSIS ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SIGHT DISABILITY ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOLAR URTICARIA ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPERMATOGENESIS ABNORMAL ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL CORD HERNIATION ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)
SPINAL LIGAMENT OSSIFICATION ( 1 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPONDYLOSIS ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STIFF-MAN SYNDROME ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SURGICAL STAPLING ( 1 FDA reports)
SYMBLEPHARON ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TACITURNITY ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TESTICULAR CYST ( 1 FDA reports)
TESTICULAR MASS ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THERAPEUTIC AGENT URINE POSITIVE ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THREAT OF REDUNDANCY ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROIDITIS SUBACUTE ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH IMPACTED ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TOOTH MALFORMATION ( 1 FDA reports)
TOXIC OPTIC NEUROPATHY ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRAUMATIC SHOCK ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
TYPHOID FEVER ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
UREAPLASMA INFECTION ( 1 FDA reports)
URETERIC DIVERSION OPERATION ( 1 FDA reports)
URETHRAL MEATUS STENOSIS ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINARY TRACT MALFORMATION ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
UVULOPALATOPHARYNGOPLASTY ( 1 FDA reports)
VAGINAL CANCER ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL EROSION ( 1 FDA reports)
VAGINAL NEOPLASM ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VICTIM OF SPOUSAL ABUSE ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VISUAL ACUITY TESTS ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WISDOM TEETH REMOVAL ( 1 FDA reports)
WOUND INFECTION FUNGAL ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
XITH NERVE PARALYSIS ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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