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

WEIGHT INCREASED ( 2004 FDA reports)
DIABETES MELLITUS ( 1950 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1533 FDA reports)
TARDIVE DYSKINESIA ( 1124 FDA reports)
INSOMNIA ( 1109 FDA reports)
TREMOR ( 1063 FDA reports)
ANXIETY ( 935 FDA reports)
DEPRESSION ( 920 FDA reports)
NAUSEA ( 897 FDA reports)
DRUG INEFFECTIVE ( 848 FDA reports)
DIZZINESS ( 809 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 755 FDA reports)
FATIGUE ( 751 FDA reports)
SUICIDAL IDEATION ( 746 FDA reports)
VOMITING ( 728 FDA reports)
PREGNANCY ( 725 FDA reports)
HEADACHE ( 708 FDA reports)
SOMNOLENCE ( 698 FDA reports)
DYSKINESIA ( 694 FDA reports)
CONVULSION ( 658 FDA reports)
OBESITY ( 643 FDA reports)
PSYCHOTIC DISORDER ( 635 FDA reports)
PANCREATITIS ( 623 FDA reports)
AKATHISIA ( 619 FDA reports)
AGITATION ( 568 FDA reports)
DRUG INTERACTION ( 562 FDA reports)
SUICIDE ATTEMPT ( 556 FDA reports)
HYPERTENSION ( 535 FDA reports)
DYSPNOEA ( 533 FDA reports)
BLOOD GLUCOSE INCREASED ( 526 FDA reports)
RESTLESSNESS ( 504 FDA reports)
VISION BLURRED ( 490 FDA reports)
FALL ( 489 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 485 FDA reports)
DYSTONIA ( 466 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 465 FDA reports)
DEATH ( 464 FDA reports)
AGGRESSION ( 463 FDA reports)
PAIN ( 461 FDA reports)
CHEST PAIN ( 459 FDA reports)
CONFUSIONAL STATE ( 459 FDA reports)
WEIGHT DECREASED ( 458 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 453 FDA reports)
FEELING ABNORMAL ( 452 FDA reports)
HALLUCINATION ( 438 FDA reports)
PYREXIA ( 437 FDA reports)
HYPERGLYCAEMIA ( 419 FDA reports)
MANIA ( 414 FDA reports)
RASH ( 413 FDA reports)
OEDEMA PERIPHERAL ( 398 FDA reports)
OVERDOSE ( 391 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 388 FDA reports)
DIABETIC KETOACIDOSIS ( 383 FDA reports)
ASTHENIA ( 369 FDA reports)
DIARRHOEA ( 364 FDA reports)
HYPERLIPIDAEMIA ( 363 FDA reports)
NEUROPATHY PERIPHERAL ( 358 FDA reports)
PAIN IN EXTREMITY ( 357 FDA reports)
BACK PAIN ( 346 FDA reports)
CONSTIPATION ( 342 FDA reports)
DELUSION ( 341 FDA reports)
LOSS OF CONSCIOUSNESS ( 340 FDA reports)
GAIT DISTURBANCE ( 330 FDA reports)
ABNORMAL BEHAVIOUR ( 321 FDA reports)
MALAISE ( 320 FDA reports)
MUSCLE SPASMS ( 319 FDA reports)
ARTHRALGIA ( 312 FDA reports)
SCHIZOPHRENIA ( 307 FDA reports)
DIABETIC NEUROPATHY ( 305 FDA reports)
PULMONARY EMBOLISM ( 302 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 297 FDA reports)
DYSPHAGIA ( 293 FDA reports)
HYPERHIDROSIS ( 292 FDA reports)
IRRITABILITY ( 291 FDA reports)
HALLUCINATION, AUDITORY ( 288 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 283 FDA reports)
TYPE 1 DIABETES MELLITUS ( 279 FDA reports)
TACHYCARDIA ( 278 FDA reports)
COMPLETED SUICIDE ( 275 FDA reports)
PNEUMONIA ( 274 FDA reports)
URINARY TRACT INFECTION ( 268 FDA reports)
BIPOLAR DISORDER ( 267 FDA reports)
CONDITION AGGRAVATED ( 264 FDA reports)
SEDATION ( 251 FDA reports)
DYSARTHRIA ( 250 FDA reports)
AMNESIA ( 246 FDA reports)
MENTAL DISORDER ( 245 FDA reports)
ABDOMINAL PAIN ( 242 FDA reports)
MYOCARDIAL INFARCTION ( 240 FDA reports)
HYPOTENSION ( 239 FDA reports)
ABDOMINAL PAIN UPPER ( 233 FDA reports)
PARANOIA ( 233 FDA reports)
HYPOAESTHESIA ( 232 FDA reports)
MEMORY IMPAIRMENT ( 226 FDA reports)
PALPITATIONS ( 224 FDA reports)
SYNCOPE ( 223 FDA reports)
MYALGIA ( 221 FDA reports)
PARKINSONISM ( 215 FDA reports)
DIABETIC COMA ( 213 FDA reports)
DISTURBANCE IN ATTENTION ( 213 FDA reports)
COMA ( 212 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 208 FDA reports)
DECREASED APPETITE ( 206 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 204 FDA reports)
ANGER ( 202 FDA reports)
CEREBROVASCULAR ACCIDENT ( 200 FDA reports)
DEEP VEIN THROMBOSIS ( 198 FDA reports)
SPEECH DISORDER ( 196 FDA reports)
BLOOD PRESSURE INCREASED ( 191 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 189 FDA reports)
ANAEMIA ( 183 FDA reports)
DEHYDRATION ( 183 FDA reports)
MUSCLE TWITCHING ( 183 FDA reports)
ALOPECIA ( 182 FDA reports)
RENAL FAILURE ( 181 FDA reports)
CARDIAC DISORDER ( 179 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 178 FDA reports)
RHABDOMYOLYSIS ( 176 FDA reports)
SLEEP DISORDER ( 176 FDA reports)
DRY MOUTH ( 170 FDA reports)
URINARY INCONTINENCE ( 170 FDA reports)
INTENTIONAL OVERDOSE ( 169 FDA reports)
HYPOGLYCAEMIA ( 168 FDA reports)
THINKING ABNORMAL ( 168 FDA reports)
PANIC ATTACK ( 167 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 167 FDA reports)
DROOLING ( 166 FDA reports)
INCREASED APPETITE ( 165 FDA reports)
LETHARGY ( 165 FDA reports)
COUGH ( 163 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 163 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 162 FDA reports)
RENAL FAILURE ACUTE ( 162 FDA reports)
DISORIENTATION ( 160 FDA reports)
PARAESTHESIA ( 160 FDA reports)
TREATMENT NONCOMPLIANCE ( 160 FDA reports)
NERVOUSNESS ( 159 FDA reports)
PRURITUS ( 158 FDA reports)
HYPOTHYROIDISM ( 156 FDA reports)
URINARY RETENTION ( 156 FDA reports)
BALANCE DISORDER ( 154 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 153 FDA reports)
CONTUSION ( 152 FDA reports)
HEART RATE INCREASED ( 152 FDA reports)
MIGRAINE ( 152 FDA reports)
MUSCLE RIGIDITY ( 151 FDA reports)
SLEEP APNOEA SYNDROME ( 148 FDA reports)
DIABETIC COMPLICATION ( 146 FDA reports)
MUSCULAR WEAKNESS ( 144 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 140 FDA reports)
INJURY ( 140 FDA reports)
HEPATIC ENZYME INCREASED ( 138 FDA reports)
LEUKOPENIA ( 137 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 137 FDA reports)
ABORTION SPONTANEOUS ( 128 FDA reports)
MOOD SWINGS ( 128 FDA reports)
BRONCHITIS ( 127 FDA reports)
LIVER DISORDER ( 127 FDA reports)
OEDEMA ( 127 FDA reports)
POLLAKIURIA ( 127 FDA reports)
SWOLLEN TONGUE ( 127 FDA reports)
CHILLS ( 126 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 126 FDA reports)
MOVEMENT DISORDER ( 126 FDA reports)
PANCREATITIS ACUTE ( 126 FDA reports)
MEDICATION ERROR ( 125 FDA reports)
NIGHTMARE ( 123 FDA reports)
ROAD TRAFFIC ACCIDENT ( 122 FDA reports)
ERYTHEMA ( 121 FDA reports)
OFF LABEL USE ( 119 FDA reports)
PSYCHIATRIC SYMPTOM ( 116 FDA reports)
ERECTILE DYSFUNCTION ( 115 FDA reports)
HYPONATRAEMIA ( 115 FDA reports)
STRESS ( 115 FDA reports)
CELLULITIS ( 114 FDA reports)
RESTLESS LEGS SYNDROME ( 114 FDA reports)
THIRST ( 114 FDA reports)
CHOLELITHIASIS ( 113 FDA reports)
COGNITIVE DISORDER ( 113 FDA reports)
EMOTIONAL DISTRESS ( 113 FDA reports)
GRAND MAL CONVULSION ( 112 FDA reports)
SALIVARY HYPERSECRETION ( 111 FDA reports)
ADVERSE EVENT ( 110 FDA reports)
FEAR ( 109 FDA reports)
VERTIGO ( 109 FDA reports)
DELIRIUM ( 108 FDA reports)
HEPATIC STEATOSIS ( 108 FDA reports)
DRUG DOSE OMISSION ( 107 FDA reports)
HYPERSENSITIVITY ( 107 FDA reports)
ARTHRITIS ( 106 FDA reports)
DYSURIA ( 106 FDA reports)
TIC ( 105 FDA reports)
EPISTAXIS ( 103 FDA reports)
ASTHMA ( 102 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 102 FDA reports)
CRYING ( 100 FDA reports)
METABOLIC SYNDROME ( 100 FDA reports)
VISUAL IMPAIRMENT ( 100 FDA reports)
CARDIAC ARREST ( 99 FDA reports)
DEPRESSED MOOD ( 99 FDA reports)
PRESCRIBED OVERDOSE ( 99 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 98 FDA reports)
ABORTION INDUCED ( 97 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 96 FDA reports)
MENTAL IMPAIRMENT ( 96 FDA reports)
MUSCULOSKELETAL PAIN ( 96 FDA reports)
ARRHYTHMIA ( 95 FDA reports)
GALLBLADDER DISORDER ( 95 FDA reports)
NORMAL NEWBORN ( 95 FDA reports)
SUDDEN DEATH ( 95 FDA reports)
ATRIAL FIBRILLATION ( 93 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 93 FDA reports)
HYPOKALAEMIA ( 93 FDA reports)
KETOACIDOSIS ( 93 FDA reports)
PRODUCT QUALITY ISSUE ( 93 FDA reports)
THROMBOSIS ( 93 FDA reports)
ABNORMAL DREAMS ( 92 FDA reports)
DEMENTIA ( 92 FDA reports)
HIATUS HERNIA ( 92 FDA reports)
ABDOMINAL DISCOMFORT ( 91 FDA reports)
DYSPEPSIA ( 91 FDA reports)
ABDOMINAL DISTENSION ( 90 FDA reports)
ILL-DEFINED DISORDER ( 90 FDA reports)
OROPHARYNGEAL PAIN ( 90 FDA reports)
ANOREXIA ( 89 FDA reports)
CAESAREAN SECTION ( 89 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 89 FDA reports)
NECK PAIN ( 89 FDA reports)
MENTAL STATUS CHANGES ( 87 FDA reports)
BRADYCARDIA ( 86 FDA reports)
GALACTORRHOEA ( 86 FDA reports)
TONGUE DISORDER ( 86 FDA reports)
HALLUCINATION, VISUAL ( 85 FDA reports)
PREMATURE BABY ( 84 FDA reports)
ACCIDENTAL OVERDOSE ( 83 FDA reports)
HYPERSOMNIA ( 83 FDA reports)
HYPOMANIA ( 83 FDA reports)
MAJOR DEPRESSION ( 83 FDA reports)
CORONARY ARTERY DISEASE ( 81 FDA reports)
EMOTIONAL DISORDER ( 81 FDA reports)
SEXUAL DYSFUNCTION ( 81 FDA reports)
BIPOLAR I DISORDER ( 80 FDA reports)
BLOOD PRESSURE DECREASED ( 80 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 80 FDA reports)
DRUG ABUSE ( 80 FDA reports)
DRUG EFFECT DECREASED ( 80 FDA reports)
SPINAL OSTEOARTHRITIS ( 80 FDA reports)
NEUTROPENIA ( 79 FDA reports)
JOINT SWELLING ( 78 FDA reports)
RESPIRATORY FAILURE ( 78 FDA reports)
HOSPITALISATION ( 77 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 77 FDA reports)
EYE DISORDER ( 76 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 76 FDA reports)
OSTEOARTHRITIS ( 76 FDA reports)
SEROTONIN SYNDROME ( 76 FDA reports)
SWELLING FACE ( 76 FDA reports)
DIABETIC RETINOPATHY ( 75 FDA reports)
SINUS TACHYCARDIA ( 75 FDA reports)
APHASIA ( 74 FDA reports)
CHEST DISCOMFORT ( 74 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 74 FDA reports)
HOT FLUSH ( 74 FDA reports)
HAEMORRHAGE ( 73 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 73 FDA reports)
BODY TEMPERATURE INCREASED ( 72 FDA reports)
INFECTION ( 72 FDA reports)
SINUSITIS ( 72 FDA reports)
SWELLING ( 72 FDA reports)
CARDIAC FAILURE ( 71 FDA reports)
CATATONIA ( 71 FDA reports)
LYMPHADENOPATHY ( 71 FDA reports)
MUSCLE TIGHTNESS ( 71 FDA reports)
ADVERSE DRUG REACTION ( 70 FDA reports)
COORDINATION ABNORMAL ( 70 FDA reports)
MOOD ALTERED ( 70 FDA reports)
THROMBOCYTOPENIA ( 70 FDA reports)
DIABETIC NEPHROPATHY ( 69 FDA reports)
HAEMOGLOBIN DECREASED ( 69 FDA reports)
WITHDRAWAL SYNDROME ( 69 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 68 FDA reports)
DIPLOPIA ( 68 FDA reports)
OSTEONECROSIS OF JAW ( 68 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 67 FDA reports)
APATHY ( 67 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 67 FDA reports)
BLOOD CREATININE INCREASED ( 67 FDA reports)
CARDIAC MURMUR ( 67 FDA reports)
ILEUS ( 67 FDA reports)
NEPHROLITHIASIS ( 67 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 67 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 67 FDA reports)
CARDIOMEGALY ( 66 FDA reports)
INTESTINAL OBSTRUCTION ( 66 FDA reports)
RECTAL HAEMORRHAGE ( 65 FDA reports)
STEVENS-JOHNSON SYNDROME ( 65 FDA reports)
URTICARIA ( 65 FDA reports)
NEOPLASM MALIGNANT ( 64 FDA reports)
HEAD INJURY ( 63 FDA reports)
INFLUENZA LIKE ILLNESS ( 63 FDA reports)
MOBILITY DECREASED ( 63 FDA reports)
SUICIDAL BEHAVIOUR ( 63 FDA reports)
CARDIOMYOPATHY ( 62 FDA reports)
FEELING HOT ( 62 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 62 FDA reports)
PRIAPISM ( 62 FDA reports)
EPILEPSY ( 61 FDA reports)
FLUSHING ( 61 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 61 FDA reports)
INJECTION SITE PAIN ( 61 FDA reports)
CARDIO-RESPIRATORY ARREST ( 60 FDA reports)
PLATELET COUNT DECREASED ( 60 FDA reports)
PNEUMONIA ASPIRATION ( 60 FDA reports)
ANGINA PECTORIS ( 59 FDA reports)
DRUG TOXICITY ( 59 FDA reports)
HYPERCHOLESTEROLAEMIA ( 59 FDA reports)
HYPERPROLACTINAEMIA ( 59 FDA reports)
IRON DEFICIENCY ANAEMIA ( 59 FDA reports)
ABASIA ( 58 FDA reports)
INCONTINENCE ( 58 FDA reports)
NO ADVERSE EVENT ( 58 FDA reports)
STAPHYLOCOCCAL INFECTION ( 58 FDA reports)
TACHYPHRENIA ( 58 FDA reports)
GASTROINTESTINAL DISORDER ( 57 FDA reports)
INCORRECT DOSE ADMINISTERED ( 57 FDA reports)
LEUKOCYTOSIS ( 57 FDA reports)
METABOLIC DISORDER ( 57 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 57 FDA reports)
SEPSIS ( 57 FDA reports)
VISUAL ACUITY REDUCED ( 57 FDA reports)
BLOOD PROLACTIN INCREASED ( 56 FDA reports)
BRUXISM ( 56 FDA reports)
DRUG HYPERSENSITIVITY ( 56 FDA reports)
DYSGEUSIA ( 56 FDA reports)
HOMICIDAL IDEATION ( 56 FDA reports)
INTENTIONAL SELF-INJURY ( 56 FDA reports)
NASOPHARYNGITIS ( 56 FDA reports)
PERSECUTORY DELUSION ( 56 FDA reports)
CHOLECYSTECTOMY ( 55 FDA reports)
FLATULENCE ( 55 FDA reports)
HICCUPS ( 55 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 55 FDA reports)
PARKINSON'S DISEASE ( 55 FDA reports)
AGRANULOCYTOSIS ( 54 FDA reports)
BLOOD GLUCOSE DECREASED ( 54 FDA reports)
COGWHEEL RIGIDITY ( 54 FDA reports)
DRUG LEVEL INCREASED ( 54 FDA reports)
LIVE BIRTH ( 54 FDA reports)
NEUTROPHIL COUNT INCREASED ( 54 FDA reports)
RESPIRATORY ARREST ( 54 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 53 FDA reports)
LUNG DISORDER ( 53 FDA reports)
MULTIPLE SCLEROSIS ( 53 FDA reports)
PHYSICAL ASSAULT ( 53 FDA reports)
RENAL DISORDER ( 53 FDA reports)
BACK INJURY ( 52 FDA reports)
EYE MOVEMENT DISORDER ( 52 FDA reports)
FAECAL INCONTINENCE ( 52 FDA reports)
FEELING JITTERY ( 52 FDA reports)
GLYCOSURIA ( 52 FDA reports)
MULTIPLE DRUG OVERDOSE ( 52 FDA reports)
MYDRIASIS ( 52 FDA reports)
ORTHOSTATIC HYPOTENSION ( 52 FDA reports)
STOMATITIS ( 52 FDA reports)
CIRCULATORY COLLAPSE ( 51 FDA reports)
PREMATURE LABOUR ( 51 FDA reports)
BLINDNESS ( 50 FDA reports)
FLUID RETENTION ( 50 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 50 FDA reports)
HEPATITIS ( 50 FDA reports)
PALLOR ( 50 FDA reports)
UNEVALUABLE EVENT ( 50 FDA reports)
VISUAL DISTURBANCE ( 50 FDA reports)
DYSPHONIA ( 49 FDA reports)
EATING DISORDER ( 49 FDA reports)
IMPULSIVE BEHAVIOUR ( 49 FDA reports)
CHOLECYSTITIS CHRONIC ( 48 FDA reports)
EYE ROLLING ( 48 FDA reports)
HEPATITIS C ( 48 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 48 FDA reports)
RASH GENERALISED ( 48 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 48 FDA reports)
BLISTER ( 47 FDA reports)
DYSLIPIDAEMIA ( 47 FDA reports)
HAEMORRHOIDS ( 47 FDA reports)
HEPATIC CIRRHOSIS ( 47 FDA reports)
PANCREATITIS CHRONIC ( 47 FDA reports)
POLYDIPSIA ( 47 FDA reports)
THYROID DISORDER ( 47 FDA reports)
UNRESPONSIVE TO STIMULI ( 47 FDA reports)
ANHEDONIA ( 46 FDA reports)
NIGHT SWEATS ( 46 FDA reports)
ARTHROPATHY ( 45 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 45 FDA reports)
DRUG DEPENDENCE ( 45 FDA reports)
EUPHORIC MOOD ( 45 FDA reports)
GASTRITIS ( 45 FDA reports)
HUNGER ( 45 FDA reports)
HYPOTHERMIA ( 45 FDA reports)
ILEUS PARALYTIC ( 45 FDA reports)
NERVOUS SYSTEM DISORDER ( 45 FDA reports)
STUPOR ( 45 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 45 FDA reports)
CATARACT ( 44 FDA reports)
HYPERPHAGIA ( 44 FDA reports)
JOINT STIFFNESS ( 44 FDA reports)
MYOCARDIAL ISCHAEMIA ( 44 FDA reports)
BLOOD POTASSIUM DECREASED ( 43 FDA reports)
BLOOD SODIUM DECREASED ( 43 FDA reports)
BREAST CANCER ( 43 FDA reports)
ENURESIS ( 43 FDA reports)
FACIAL PALSY ( 43 FDA reports)
GRANULOCYTOPENIA ( 43 FDA reports)
HAEMATURIA ( 43 FDA reports)
HALLUCINATIONS, MIXED ( 43 FDA reports)
TOOTH LOSS ( 43 FDA reports)
AFFECTIVE DISORDER ( 42 FDA reports)
DRUG ADMINISTRATION ERROR ( 42 FDA reports)
GASTROENTERITIS ( 42 FDA reports)
HAEMATOCHEZIA ( 42 FDA reports)
ORAL PAIN ( 42 FDA reports)
PARALYSIS ( 42 FDA reports)
SKIN DISORDER ( 42 FDA reports)
TORTICOLLIS ( 42 FDA reports)
ACNE ( 41 FDA reports)
ANAPHYLACTIC REACTION ( 41 FDA reports)
DRUG SCREEN POSITIVE ( 41 FDA reports)
FIBROMYALGIA ( 41 FDA reports)
FOOD CRAVING ( 41 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 41 FDA reports)
MULTI-ORGAN FAILURE ( 41 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 41 FDA reports)
PATHOLOGICAL GAMBLING ( 41 FDA reports)
THROAT TIGHTNESS ( 41 FDA reports)
ABORTION ( 40 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 40 FDA reports)
BURNING SENSATION ( 40 FDA reports)
DENTAL CARIES ( 40 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 40 FDA reports)
EYE SWELLING ( 40 FDA reports)
LIBIDO DECREASED ( 40 FDA reports)
NASAL CONGESTION ( 40 FDA reports)
PANCYTOPENIA ( 40 FDA reports)
RENAL IMPAIRMENT ( 40 FDA reports)
FACE OEDEMA ( 39 FDA reports)
HEART RATE IRREGULAR ( 39 FDA reports)
HEPATOMEGALY ( 39 FDA reports)
HYPOAESTHESIA ORAL ( 39 FDA reports)
IMPAIRED DRIVING ABILITY ( 39 FDA reports)
INCOHERENT ( 39 FDA reports)
LOGORRHOEA ( 39 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 39 FDA reports)
OSTEOPOROSIS ( 39 FDA reports)
POLYURIA ( 39 FDA reports)
TINNITUS ( 39 FDA reports)
TRISMUS ( 39 FDA reports)
ACUTE CORONARY SYNDROME ( 38 FDA reports)
BONE PAIN ( 38 FDA reports)
BRADYPHRENIA ( 38 FDA reports)
GASTRIC DISORDER ( 38 FDA reports)
GENERALISED OEDEMA ( 38 FDA reports)
GYNAECOMASTIA ( 38 FDA reports)
HEPATIC FAILURE ( 38 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 38 FDA reports)
METASTASES TO BONE ( 38 FDA reports)
MICTURITION URGENCY ( 38 FDA reports)
MUSCLE STRAIN ( 38 FDA reports)
PHARYNGEAL OEDEMA ( 38 FDA reports)
PLEURAL EFFUSION ( 38 FDA reports)
RHINORRHOEA ( 38 FDA reports)
ARTERIOSCLEROSIS ( 37 FDA reports)
ATELECTASIS ( 37 FDA reports)
ATRIAL FLUTTER ( 37 FDA reports)
COMPULSIONS ( 37 FDA reports)
CYSTITIS ( 37 FDA reports)
DRUG DISPENSING ERROR ( 37 FDA reports)
EAR PAIN ( 37 FDA reports)
ENCEPHALOPATHY ( 37 FDA reports)
FLAT AFFECT ( 37 FDA reports)
RASH PRURITIC ( 37 FDA reports)
SELF-INJURIOUS IDEATION ( 37 FDA reports)
ACUTE RESPIRATORY FAILURE ( 36 FDA reports)
DIZZINESS POSTURAL ( 36 FDA reports)
GESTATIONAL DIABETES ( 36 FDA reports)
HOSTILITY ( 36 FDA reports)
HYSTERECTOMY ( 36 FDA reports)
IMPAIRED WORK ABILITY ( 36 FDA reports)
JOINT INJURY ( 36 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 36 FDA reports)
OCULOGYRIC CRISIS ( 36 FDA reports)
SKIN DISCOLOURATION ( 36 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 36 FDA reports)
ACCIDENTAL EXPOSURE ( 35 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 35 FDA reports)
AFFECT LABILITY ( 35 FDA reports)
AMENORRHOEA ( 35 FDA reports)
IRRITABLE BOWEL SYNDROME ( 35 FDA reports)
LIBIDO INCREASED ( 35 FDA reports)
MENISCUS LESION ( 35 FDA reports)
PULMONARY CONGESTION ( 35 FDA reports)
RESPIRATORY DISTRESS ( 35 FDA reports)
RHEUMATOID ARTHRITIS ( 35 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 35 FDA reports)
CHOLECYSTITIS ( 34 FDA reports)
DRUG INTOLERANCE ( 34 FDA reports)
DYSSTASIA ( 34 FDA reports)
EYE PAIN ( 34 FDA reports)
FUNGAL INFECTION ( 34 FDA reports)
HAEMATOCRIT DECREASED ( 34 FDA reports)
MENSTRUATION IRREGULAR ( 34 FDA reports)
PHOTOPHOBIA ( 34 FDA reports)
BLOOD BILIRUBIN INCREASED ( 33 FDA reports)
BONE DISORDER ( 33 FDA reports)
FOOT FRACTURE ( 33 FDA reports)
FORMICATION ( 33 FDA reports)
MIDDLE INSOMNIA ( 33 FDA reports)
OXYGEN SATURATION DECREASED ( 33 FDA reports)
RENAL FAILURE CHRONIC ( 33 FDA reports)
ABDOMINAL TENDERNESS ( 32 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 32 FDA reports)
DRY EYE ( 32 FDA reports)
HEPATIC CYST ( 32 FDA reports)
INTENTIONAL DRUG MISUSE ( 32 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 32 FDA reports)
JAUNDICE ( 32 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 32 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 32 FDA reports)
RESPIRATORY DISORDER ( 32 FDA reports)
TRANSAMINASES INCREASED ( 32 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 32 FDA reports)
VIRAL INFECTION ( 32 FDA reports)
ACUTE PSYCHOSIS ( 31 FDA reports)
BLEPHAROSPASM ( 31 FDA reports)
BREAST PAIN ( 31 FDA reports)
CHROMATURIA ( 31 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 31 FDA reports)
HEMIPARESIS ( 31 FDA reports)
INFLUENZA ( 31 FDA reports)
MENORRHAGIA ( 31 FDA reports)
MOTOR DYSFUNCTION ( 31 FDA reports)
PHARYNGITIS ( 31 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 31 FDA reports)
TOOTH INFECTION ( 31 FDA reports)
CHOLECYSTITIS ACUTE ( 30 FDA reports)
CROHN'S DISEASE ( 30 FDA reports)
CYST ( 30 FDA reports)
ECONOMIC PROBLEM ( 30 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 30 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 30 FDA reports)
LACRIMATION INCREASED ( 30 FDA reports)
MOUTH ULCERATION ( 30 FDA reports)
PHOTOSENSITIVITY REACTION ( 30 FDA reports)
WATER INTOXICATION ( 30 FDA reports)
BACK DISORDER ( 29 FDA reports)
BITE ( 29 FDA reports)
CYANOSIS ( 29 FDA reports)
GASTRIC ULCER ( 29 FDA reports)
HAEMATEMESIS ( 29 FDA reports)
HYPOXIA ( 29 FDA reports)
LOWER LIMB FRACTURE ( 29 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 29 FDA reports)
MUSCLE DISORDER ( 29 FDA reports)
SUBDURAL HAEMATOMA ( 29 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 28 FDA reports)
CARPAL TUNNEL SYNDROME ( 28 FDA reports)
EOSINOPHIL COUNT INCREASED ( 28 FDA reports)
HYPERKALAEMIA ( 28 FDA reports)
IMPAIRED HEALING ( 28 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 28 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 28 FDA reports)
MONOCYTE COUNT INCREASED ( 28 FDA reports)
PULMONARY OEDEMA ( 28 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 28 FDA reports)
THROMBOCYTOSIS ( 28 FDA reports)
TOOTHACHE ( 28 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 28 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 27 FDA reports)
DISSOCIATION ( 27 FDA reports)
GLAUCOMA ( 27 FDA reports)
HAEMOPTYSIS ( 27 FDA reports)
HEART RATE DECREASED ( 27 FDA reports)
HYPERTHERMIA ( 27 FDA reports)
HYPOKINESIA ( 27 FDA reports)
METASTASES TO SPINE ( 27 FDA reports)
OVARIAN CYST ( 27 FDA reports)
PERSONALITY CHANGE ( 27 FDA reports)
SKIN LESION ( 27 FDA reports)
ULCER ( 27 FDA reports)
URINE OUTPUT INCREASED ( 27 FDA reports)
VASCULITIS ( 27 FDA reports)
ASPIRATION ( 26 FDA reports)
BLOOD UREA INCREASED ( 26 FDA reports)
DEPRESSIVE SYMPTOM ( 26 FDA reports)
DYSPHASIA ( 26 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 26 FDA reports)
HUMERUS FRACTURE ( 26 FDA reports)
HYPOPHAGIA ( 26 FDA reports)
INSULIN RESISTANCE ( 26 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 26 FDA reports)
NEUTROPHIL COUNT DECREASED ( 26 FDA reports)
OVERWEIGHT ( 26 FDA reports)
POOR QUALITY SLEEP ( 26 FDA reports)
PRESYNCOPE ( 26 FDA reports)
PSYCHOMOTOR RETARDATION ( 26 FDA reports)
PYELONEPHRITIS ( 26 FDA reports)
RETCHING ( 26 FDA reports)
SKIN EXFOLIATION ( 26 FDA reports)
SUDDEN CARDIAC DEATH ( 26 FDA reports)
ATAXIA ( 25 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 25 FDA reports)
BODY MASS INDEX DECREASED ( 25 FDA reports)
CEREBRAL INFARCTION ( 25 FDA reports)
EXPOSED BONE IN JAW ( 25 FDA reports)
HAEMATOMA ( 25 FDA reports)
HYPOTONIA ( 25 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 25 FDA reports)
JAW DISORDER ( 25 FDA reports)
LUNG NEOPLASM ( 25 FDA reports)
MEAN CELL VOLUME DECREASED ( 25 FDA reports)
MENSTRUAL DISORDER ( 25 FDA reports)
METRORRHAGIA ( 25 FDA reports)
NOCTURIA ( 25 FDA reports)
OSTEONECROSIS ( 25 FDA reports)
POSTURE ABNORMAL ( 25 FDA reports)
PSORIASIS ( 25 FDA reports)
PULMONARY HYPERTENSION ( 25 FDA reports)
BRADYKINESIA ( 24 FDA reports)
CARDIOVASCULAR DISORDER ( 24 FDA reports)
DIABETIC FOOT ( 24 FDA reports)
DISEASE RECURRENCE ( 24 FDA reports)
DRY SKIN ( 24 FDA reports)
EAR CONGESTION ( 24 FDA reports)
EXCORIATION ( 24 FDA reports)
EYELID PTOSIS ( 24 FDA reports)
FLANK PAIN ( 24 FDA reports)
FRACTURE ( 24 FDA reports)
HOMICIDE ( 24 FDA reports)
HYPERTHYROIDISM ( 24 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 24 FDA reports)
NERVE INJURY ( 24 FDA reports)
ORAL CANDIDIASIS ( 24 FDA reports)
SOMNAMBULISM ( 24 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 24 FDA reports)
TWIN PREGNANCY ( 24 FDA reports)
VAGINAL HAEMORRHAGE ( 24 FDA reports)
AMMONIA INCREASED ( 23 FDA reports)
BLADDER DISORDER ( 23 FDA reports)
CYTOLYTIC HEPATITIS ( 23 FDA reports)
DECREASED ACTIVITY ( 23 FDA reports)
DISCOMFORT ( 23 FDA reports)
DRUG ABUSER ( 23 FDA reports)
DRUG PRESCRIBING ERROR ( 23 FDA reports)
DYSPHEMIA ( 23 FDA reports)
FEELING COLD ( 23 FDA reports)
HAEMATOCRIT INCREASED ( 23 FDA reports)
OCULAR HYPERAEMIA ( 23 FDA reports)
PANIC DISORDER ( 23 FDA reports)
PEPTIC ULCER ( 23 FDA reports)
PERSONALITY DISORDER ( 23 FDA reports)
PLATELET COUNT INCREASED ( 23 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 23 FDA reports)
PSYCHOTIC BEHAVIOUR ( 23 FDA reports)
SCAR ( 23 FDA reports)
STOMACH DISCOMFORT ( 23 FDA reports)
WHEEZING ( 23 FDA reports)
WOUND ( 23 FDA reports)
ABDOMINAL PAIN LOWER ( 22 FDA reports)
ANGIOEDEMA ( 22 FDA reports)
ANKLE FRACTURE ( 22 FDA reports)
ASPHYXIA ( 22 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 22 FDA reports)
BLOOD URINE PRESENT ( 22 FDA reports)
CANDIDIASIS ( 22 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 22 FDA reports)
DYSPHORIA ( 22 FDA reports)
EXOSTOSIS ( 22 FDA reports)
FRUSTRATION ( 22 FDA reports)
FURUNCLE ( 22 FDA reports)
GASTRIC BYPASS ( 22 FDA reports)
LACERATION ( 22 FDA reports)
LUMBAR SPINAL STENOSIS ( 22 FDA reports)
MALNUTRITION ( 22 FDA reports)
PAIN IN JAW ( 22 FDA reports)
PANCREATITIS RELAPSING ( 22 FDA reports)
PNEUMOTHORAX ( 22 FDA reports)
RASH ERYTHEMATOUS ( 22 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 22 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 22 FDA reports)
WHITE BLOOD CELL DISORDER ( 22 FDA reports)
AGORAPHOBIA ( 21 FDA reports)
ALCOHOL USE ( 21 FDA reports)
BRONCHOSPASM ( 21 FDA reports)
COAGULOPATHY ( 21 FDA reports)
COLD SWEAT ( 21 FDA reports)
DEAFNESS ( 21 FDA reports)
DRUG ERUPTION ( 21 FDA reports)
DYSPNOEA EXERTIONAL ( 21 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 21 FDA reports)
INJECTION SITE HAEMATOMA ( 21 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 21 FDA reports)
JUDGEMENT IMPAIRED ( 21 FDA reports)
LIMB INJURY ( 21 FDA reports)
METASTASES TO LIVER ( 21 FDA reports)
MUTISM ( 21 FDA reports)
MYOCLONUS ( 21 FDA reports)
OBSESSIVE THOUGHTS ( 21 FDA reports)
ONYCHOMYCOSIS ( 21 FDA reports)
OSTEOMYELITIS ( 21 FDA reports)
PRURITUS GENERALISED ( 21 FDA reports)
RESPIRATORY DEPRESSION ( 21 FDA reports)
SEPTIC SHOCK ( 21 FDA reports)
SPLENOMEGALY ( 21 FDA reports)
TENSION ( 21 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 21 FDA reports)
THREATENED LABOUR ( 21 FDA reports)
TOOTH FRACTURE ( 21 FDA reports)
VENTRICULAR TACHYCARDIA ( 21 FDA reports)
ALCOHOL ABUSE ( 20 FDA reports)
ANXIETY DISORDER ( 20 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 20 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 20 FDA reports)
BLOOD PRESSURE ABNORMAL ( 20 FDA reports)
BONE LESION ( 20 FDA reports)
CONJUNCTIVITIS ( 20 FDA reports)
DERMATITIS EXFOLIATIVE ( 20 FDA reports)
DYSGRAPHIA ( 20 FDA reports)
ELECTROLYTE IMBALANCE ( 20 FDA reports)
EYE PRURITUS ( 20 FDA reports)
HERPES ZOSTER ( 20 FDA reports)
INAPPROPRIATE AFFECT ( 20 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 20 FDA reports)
INFLAMMATION ( 20 FDA reports)
INFUSION RELATED REACTION ( 20 FDA reports)
INJECTION SITE ERYTHEMA ( 20 FDA reports)
KIDNEY INFECTION ( 20 FDA reports)
KNEE OPERATION ( 20 FDA reports)
METASTASES TO THORAX ( 20 FDA reports)
PELVIC FRACTURE ( 20 FDA reports)
RASH PUSTULAR ( 20 FDA reports)
RESPIRATORY RATE INCREASED ( 20 FDA reports)
RHINITIS ( 20 FDA reports)
RIB FRACTURE ( 20 FDA reports)
SKIN ULCER ( 20 FDA reports)
SMALL FOR DATES BABY ( 20 FDA reports)
STARING ( 20 FDA reports)
THERMAL BURN ( 20 FDA reports)
TOOTH ABSCESS ( 20 FDA reports)
VASCULAR ANOMALY ( 20 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 19 FDA reports)
CHOKING ( 19 FDA reports)
DECREASED INTEREST ( 19 FDA reports)
DIALYSIS ( 19 FDA reports)
FAECES DISCOLOURED ( 19 FDA reports)
HERNIA ( 19 FDA reports)
HYPOAESTHESIA FACIAL ( 19 FDA reports)
HYPOPNOEA ( 19 FDA reports)
KNEE ARTHROPLASTY ( 19 FDA reports)
LIVER INJURY ( 19 FDA reports)
MASKED FACIES ( 19 FDA reports)
NEURALGIA ( 19 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 19 FDA reports)
RASH PAPULAR ( 19 FDA reports)
SPINAL COLUMN STENOSIS ( 19 FDA reports)
SPLENIC INJURY ( 19 FDA reports)
SUBCUTANEOUS ABSCESS ( 19 FDA reports)
TOURETTE'S DISORDER ( 19 FDA reports)
UTERINE LEIOMYOMA ( 19 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 18 FDA reports)
BACTERIAL INFECTION ( 18 FDA reports)
BASAL CELL CARCINOMA ( 18 FDA reports)
BLOOD CALCIUM DECREASED ( 18 FDA reports)
BLOOD CALCIUM INCREASED ( 18 FDA reports)
CEREBRAL HAEMORRHAGE ( 18 FDA reports)
COMMUNICATION DISORDER ( 18 FDA reports)
DIABETES INSIPIDUS ( 18 FDA reports)
DIABETIC EYE DISEASE ( 18 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 18 FDA reports)
DIFFICULTY IN WALKING ( 18 FDA reports)
EAR INFECTION ( 18 FDA reports)
EJACULATION DISORDER ( 18 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 18 FDA reports)
EMPHYSEMA ( 18 FDA reports)
ERYTHEMA MULTIFORME ( 18 FDA reports)
FLUID INTAKE REDUCED ( 18 FDA reports)
GAZE PALSY ( 18 FDA reports)
GLOSSODYNIA ( 18 FDA reports)
HYPERACUSIS ( 18 FDA reports)
HYPERSEXUALITY ( 18 FDA reports)
HYPERTENSIVE CRISIS ( 18 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 18 FDA reports)
LIP SWELLING ( 18 FDA reports)
PARKINSONIAN REST TREMOR ( 18 FDA reports)
PERIODONTITIS ( 18 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 18 FDA reports)
PROTHROMBIN TIME PROLONGED ( 18 FDA reports)
PULMONARY THROMBOSIS ( 18 FDA reports)
SENSORY DISTURBANCE ( 18 FDA reports)
SLUGGISHNESS ( 18 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 18 FDA reports)
TOOTH DISORDER ( 18 FDA reports)
UROSEPSIS ( 18 FDA reports)
ACUTE SINUSITIS ( 17 FDA reports)
ATRIAL SEPTAL DEFECT ( 17 FDA reports)
BLOOD CHLORIDE DECREASED ( 17 FDA reports)
BLOOD POTASSIUM INCREASED ( 17 FDA reports)
BRAIN INJURY ( 17 FDA reports)
BREAST MASS ( 17 FDA reports)
CARDIOPULMONARY FAILURE ( 17 FDA reports)
CONGENITAL ANOMALY ( 17 FDA reports)
DEPRESSION SUICIDAL ( 17 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 17 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 17 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 17 FDA reports)
DYSTHYMIC DISORDER ( 17 FDA reports)
FEEDING DISORDER NEONATAL ( 17 FDA reports)
GALLBLADDER OPERATION ( 17 FDA reports)
HEAD BANGING ( 17 FDA reports)
INITIAL INSOMNIA ( 17 FDA reports)
INTENTIONAL MISUSE ( 17 FDA reports)
LOCALISED INFECTION ( 17 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 17 FDA reports)
MITRAL VALVE INCOMPETENCE ( 17 FDA reports)
MULTIPLE INJURIES ( 17 FDA reports)
NECK INJURY ( 17 FDA reports)
NEGATIVISM ( 17 FDA reports)
NO THERAPEUTIC RESPONSE ( 17 FDA reports)
OPEN ANGLE GLAUCOMA ( 17 FDA reports)
PANCREATIC DISORDER ( 17 FDA reports)
PELVIC PAIN ( 17 FDA reports)
PHOTOPSIA ( 17 FDA reports)
RENAL PAIN ( 17 FDA reports)
ROSACEA ( 17 FDA reports)
SENSATION OF HEAVINESS ( 17 FDA reports)
SKIN LACERATION ( 17 FDA reports)
SNORING ( 17 FDA reports)
STATUS EPILEPTICUS ( 17 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 17 FDA reports)
TACHYPNOEA ( 17 FDA reports)
TEARFULNESS ( 17 FDA reports)
TENDERNESS ( 17 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 17 FDA reports)
TOBACCO USER ( 17 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 16 FDA reports)
BINGE EATING ( 16 FDA reports)
BODY TEMPERATURE DECREASED ( 16 FDA reports)
BREECH PRESENTATION ( 16 FDA reports)
CHEILITIS ( 16 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 16 FDA reports)
DECUBITUS ULCER ( 16 FDA reports)
DISINHIBITION ( 16 FDA reports)
DIVERTICULITIS ( 16 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 16 FDA reports)
EYE IRRITATION ( 16 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 16 FDA reports)
GALLBLADDER OEDEMA ( 16 FDA reports)
INTERSTITIAL LUNG DISEASE ( 16 FDA reports)
JOINT SPRAIN ( 16 FDA reports)
LIGAMENT RUPTURE ( 16 FDA reports)
LIP ULCERATION ( 16 FDA reports)
LIPIDS INCREASED ( 16 FDA reports)
LUNG INFILTRATION ( 16 FDA reports)
METABOLIC ACIDOSIS ( 16 FDA reports)
NEGATIVE THOUGHTS ( 16 FDA reports)
ORAL DISORDER ( 16 FDA reports)
OTITIS MEDIA ( 16 FDA reports)
PETIT MAL EPILEPSY ( 16 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 16 FDA reports)
PHLEBITIS ( 16 FDA reports)
PROTRUSION TONGUE ( 16 FDA reports)
RHINITIS ALLERGIC ( 16 FDA reports)
SARCOIDOSIS ( 16 FDA reports)
SCREAMING ( 16 FDA reports)
SHOCK ( 16 FDA reports)
SKIN CANDIDA ( 16 FDA reports)
SPINA BIFIDA ( 16 FDA reports)
SURGERY ( 16 FDA reports)
TENDONITIS ( 16 FDA reports)
TORSADE DE POINTES ( 16 FDA reports)
VISUAL FIELD DEFECT ( 16 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 16 FDA reports)
ANTISOCIAL BEHAVIOUR ( 15 FDA reports)
APNOEA ( 15 FDA reports)
APPLICATION SITE ERYTHEMA ( 15 FDA reports)
ATRIOVENTRICULAR BLOCK ( 15 FDA reports)
BILIARY COLIC ( 15 FDA reports)
BILIARY DYSKINESIA ( 15 FDA reports)
BLOOD CORTISOL ABNORMAL ( 15 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 15 FDA reports)
BONE MARROW FAILURE ( 15 FDA reports)
CARDIAC FAILURE ACUTE ( 15 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 15 FDA reports)
DERMATITIS ( 15 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 15 FDA reports)
DIABETIC GASTROPARESIS ( 15 FDA reports)
DYSMENORRHOEA ( 15 FDA reports)
EOSINOPHILIA ( 15 FDA reports)
EXCESSIVE EYE BLINKING ( 15 FDA reports)
EXCITABILITY ( 15 FDA reports)
EYELID FUNCTION DISORDER ( 15 FDA reports)
GASTROINTESTINAL CARCINOMA ( 15 FDA reports)
GINGIVAL DISORDER ( 15 FDA reports)
HAEMODIALYSIS ( 15 FDA reports)
HEPATITIS ACUTE ( 15 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 15 FDA reports)
HYDRONEPHROSIS ( 15 FDA reports)
HYPOVOLAEMIA ( 15 FDA reports)
INFECTED SEBACEOUS CYST ( 15 FDA reports)
INTRA-UTERINE DEATH ( 15 FDA reports)
JOINT DISLOCATION ( 15 FDA reports)
LIMB DISCOMFORT ( 15 FDA reports)
LOSS OF LIBIDO ( 15 FDA reports)
MELAENA ( 15 FDA reports)
OESOPHAGITIS ( 15 FDA reports)
ORAL INTAKE REDUCED ( 15 FDA reports)
PERIPHERAL COLDNESS ( 15 FDA reports)
PNEUMONITIS ( 15 FDA reports)
POLYNEUROPATHY ( 15 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 15 FDA reports)
PROCTALGIA ( 15 FDA reports)
PULMONARY FIBROSIS ( 15 FDA reports)
RASH MACULAR ( 15 FDA reports)
RASH MACULO-PAPULAR ( 15 FDA reports)
RESPIRATORY TRACT INFECTION ( 15 FDA reports)
SOPOR ( 15 FDA reports)
STRESS URINARY INCONTINENCE ( 15 FDA reports)
UPPER LIMB FRACTURE ( 15 FDA reports)
VULVOVAGINAL DRYNESS ( 15 FDA reports)
ACIDOSIS ( 14 FDA reports)
ADJUSTMENT DISORDER ( 14 FDA reports)
APHONIA ( 14 FDA reports)
BLOOD DISORDER ( 14 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 14 FDA reports)
BRAIN OEDEMA ( 14 FDA reports)
CARDIAC VALVE DISEASE ( 14 FDA reports)
COELIAC DISEASE ( 14 FDA reports)
CONCUSSION ( 14 FDA reports)
DRUG LEVEL DECREASED ( 14 FDA reports)
ENERGY INCREASED ( 14 FDA reports)
EXTRASYSTOLES ( 14 FDA reports)
FOETAL MALFORMATION ( 14 FDA reports)
GINGIVAL BLEEDING ( 14 FDA reports)
INJECTION SITE HAEMORRHAGE ( 14 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 14 FDA reports)
LOSS OF EMPLOYMENT ( 14 FDA reports)
LYMPHOEDEMA ( 14 FDA reports)
MEDICATION RESIDUE ( 14 FDA reports)
MERYCISM ( 14 FDA reports)
MIOSIS ( 14 FDA reports)
MYOCARDITIS ( 14 FDA reports)
MYOPIA ( 14 FDA reports)
ODYNOPHAGIA ( 14 FDA reports)
POLYCYTHAEMIA ( 14 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 14 FDA reports)
PRODUCTIVE COUGH ( 14 FDA reports)
SINUS BRADYCARDIA ( 14 FDA reports)
SOLILOQUY ( 14 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 14 FDA reports)
THROAT IRRITATION ( 14 FDA reports)
URINE ODOUR ABNORMAL ( 14 FDA reports)
UTERINE CANCER ( 14 FDA reports)
ABNORMAL SENSATION IN EYE ( 13 FDA reports)
APHAGIA ( 13 FDA reports)
BLUNTED AFFECT ( 13 FDA reports)
BRONCHOPNEUMONIA ( 13 FDA reports)
CEREBRAL ATROPHY ( 13 FDA reports)
DISABILITY ( 13 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 13 FDA reports)
ECZEMA ( 13 FDA reports)
ESSENTIAL HYPERTENSION ( 13 FDA reports)
EYELID OEDEMA ( 13 FDA reports)
GRIMACING ( 13 FDA reports)
HIP FRACTURE ( 13 FDA reports)
HYPERREFLEXIA ( 13 FDA reports)
HYPERTENSIVE HEART DISEASE ( 13 FDA reports)
IMPAIRED SELF-CARE ( 13 FDA reports)
INDIFFERENCE ( 13 FDA reports)
ISCHAEMIC STROKE ( 13 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 13 FDA reports)
LYMPHADENITIS ( 13 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 13 FDA reports)
MACROCYTOSIS ( 13 FDA reports)
MENINGOMYELOCELE ( 13 FDA reports)
MUSCLE ATROPHY ( 13 FDA reports)
MUSCLE CONTRACTURE ( 13 FDA reports)
OCULOGYRATION ( 13 FDA reports)
OEDEMA MOUTH ( 13 FDA reports)
READING DISORDER ( 13 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 13 FDA reports)
ROTATOR CUFF SYNDROME ( 13 FDA reports)
SCIATICA ( 13 FDA reports)
SELF-MEDICATION ( 13 FDA reports)
SENSORY LOSS ( 13 FDA reports)
SPINAL FRACTURE ( 13 FDA reports)
TOOTH EXTRACTION ( 13 FDA reports)
URINARY HESITATION ( 13 FDA reports)
UTERINE DISORDER ( 13 FDA reports)
VENTRICULAR HYPERTROPHY ( 13 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 13 FDA reports)
WEIGHT LOSS POOR ( 13 FDA reports)
ACCIDENT ( 12 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 12 FDA reports)
ANGINA UNSTABLE ( 12 FDA reports)
ANGIOPATHY ( 12 FDA reports)
APPENDICITIS ( 12 FDA reports)
BLOOD ALBUMIN DECREASED ( 12 FDA reports)
BONE FRAGMENTATION ( 12 FDA reports)
BREAST DISCHARGE ( 12 FDA reports)
CATARACT OPERATION ( 12 FDA reports)
CLUSTER HEADACHE ( 12 FDA reports)
COLITIS ( 12 FDA reports)
CONVERSION DISORDER ( 12 FDA reports)
DILATATION VENTRICULAR ( 12 FDA reports)
ECCHYMOSIS ( 12 FDA reports)
EJECTION FRACTION DECREASED ( 12 FDA reports)
EXPIRED DRUG ADMINISTERED ( 12 FDA reports)
FACIAL PAIN ( 12 FDA reports)
FEELING DRUNK ( 12 FDA reports)
GOUT ( 12 FDA reports)
HEARING IMPAIRED ( 12 FDA reports)
HERPES SIMPLEX ( 12 FDA reports)
HYPERKINESIA ( 12 FDA reports)
HYPOACUSIS ( 12 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 12 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 12 FDA reports)
MASTICATION DISORDER ( 12 FDA reports)
MENIERE'S DISEASE ( 12 FDA reports)
MYOSITIS ( 12 FDA reports)
NEOPLASM ( 12 FDA reports)
NEUROPATHY ( 12 FDA reports)
OCULAR ICTERUS ( 12 FDA reports)
PANCREATIC PSEUDOCYST ( 12 FDA reports)
PANIC REACTION ( 12 FDA reports)
PERICARDIAL EFFUSION ( 12 FDA reports)
PETECHIAE ( 12 FDA reports)
RETINOPATHY ( 12 FDA reports)
TENSION HEADACHE ( 12 FDA reports)
THYROID NEOPLASM ( 12 FDA reports)
YELLOW SKIN ( 12 FDA reports)
AKINESIA ( 11 FDA reports)
ANAPHYLACTIC SHOCK ( 11 FDA reports)
ANURIA ( 11 FDA reports)
AORTIC ANEURYSM ( 11 FDA reports)
BLINDNESS TRANSIENT ( 11 FDA reports)
BLOOD LACTIC ACID INCREASED ( 11 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 11 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 11 FDA reports)
BREAST ENLARGEMENT ( 11 FDA reports)
BREAST TENDERNESS ( 11 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 11 FDA reports)
BURSITIS ( 11 FDA reports)
CHRONIC SINUSITIS ( 11 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 11 FDA reports)
DENTAL PLAQUE ( 11 FDA reports)
DERMAL CYST ( 11 FDA reports)
DIABETIC ULCER ( 11 FDA reports)
DIVERTICULUM INTESTINAL ( 11 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 11 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 11 FDA reports)
DYSKINESIA OESOPHAGEAL ( 11 FDA reports)
EJACULATION FAILURE ( 11 FDA reports)
EOSINOPHIL COUNT DECREASED ( 11 FDA reports)
ERECTION INCREASED ( 11 FDA reports)
FACIAL BONES FRACTURE ( 11 FDA reports)
FEBRILE NEUTROPENIA ( 11 FDA reports)
GASTROENTERITIS VIRAL ( 11 FDA reports)
GENERALISED ERYTHEMA ( 11 FDA reports)
GROIN PAIN ( 11 FDA reports)
HAEMANGIOMA ( 11 FDA reports)
HAEMOLYTIC ANAEMIA ( 11 FDA reports)
HAIR GROWTH ABNORMAL ( 11 FDA reports)
HILAR LYMPHADENOPATHY ( 11 FDA reports)
HIP ARTHROPLASTY ( 11 FDA reports)
HYPERVENTILATION ( 11 FDA reports)
ILLUSION ( 11 FDA reports)
INCISIONAL HERNIA ( 11 FDA reports)
JAW OPERATION ( 11 FDA reports)
JOINT EFFUSION ( 11 FDA reports)
LIPASE INCREASED ( 11 FDA reports)
MENISCUS REMOVAL ( 11 FDA reports)
METASTASES TO LYMPH NODES ( 11 FDA reports)
MOANING ( 11 FDA reports)
MONOCLONAL GAMMOPATHY ( 11 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 11 FDA reports)
MUSCLE CRAMP ( 11 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 11 FDA reports)
NEONATAL DISORDER ( 11 FDA reports)
NEPHROPATHY ( 11 FDA reports)
NERVE COMPRESSION ( 11 FDA reports)
NO ADVERSE EFFECT ( 11 FDA reports)
NON-CARDIAC CHEST PAIN ( 11 FDA reports)
ORAL CAVITY FISTULA ( 11 FDA reports)
OROPHARYNGEAL SPASM ( 11 FDA reports)
ORTHOPNOEA ( 11 FDA reports)
PAINFUL ERECTION ( 11 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 11 FDA reports)
PORIOMANIA ( 11 FDA reports)
PRIMARY SEQUESTRUM ( 11 FDA reports)
PROTEINURIA ( 11 FDA reports)
RADIOTHERAPY TO BRAIN ( 11 FDA reports)
RESPIRATORY RATE DECREASED ( 11 FDA reports)
SCOLIOSIS ( 11 FDA reports)
SOMATISATION DISORDER ( 11 FDA reports)
STILLBIRTH ( 11 FDA reports)
STRABISMUS ( 11 FDA reports)
SUBSTANCE ABUSE ( 11 FDA reports)
TESTICULAR PAIN ( 11 FDA reports)
TONGUE ULCERATION ( 11 FDA reports)
TRAUMATIC BRAIN INJURY ( 11 FDA reports)
UMBILICAL HERNIA ( 11 FDA reports)
URINARY TRACT DISORDER ( 11 FDA reports)
URINE KETONE BODY PRESENT ( 11 FDA reports)
VIITH NERVE PARALYSIS ( 11 FDA reports)
VITAMIN D DECREASED ( 11 FDA reports)
ABSCESS ( 10 FDA reports)
ALCOHOLISM ( 10 FDA reports)
ANORGASMIA ( 10 FDA reports)
ANOSMIA ( 10 FDA reports)
BILE DUCT CANCER ( 10 FDA reports)
BLOOD SODIUM INCREASED ( 10 FDA reports)
BODY MASS INDEX INCREASED ( 10 FDA reports)
CACHEXIA ( 10 FDA reports)
CARDIAC FLUTTER ( 10 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 10 FDA reports)
CLUMSINESS ( 10 FDA reports)
COLITIS ISCHAEMIC ( 10 FDA reports)
COLONIC POLYP ( 10 FDA reports)
CONGENITAL ECTOPIC BLADDER ( 10 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 10 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 10 FDA reports)
EOSINOPHILIC PNEUMONIA ( 10 FDA reports)
FEEDING DISORDER ( 10 FDA reports)
FEELING GUILTY ( 10 FDA reports)
FOOD INTOLERANCE ( 10 FDA reports)
GALLBLADDER INJURY ( 10 FDA reports)
GRUNTING ( 10 FDA reports)
HEAT STROKE ( 10 FDA reports)
HEPATITIS B ( 10 FDA reports)
HYPERAMMONAEMIA ( 10 FDA reports)
HYPERCALCAEMIA ( 10 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 10 FDA reports)
IMPULSE-CONTROL DISORDER ( 10 FDA reports)
LACTATION DISORDER ( 10 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 10 FDA reports)
MACULAR DEGENERATION ( 10 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 10 FDA reports)
MICROCEPHALY ( 10 FDA reports)
MONONEURITIS ( 10 FDA reports)
NYSTAGMUS ( 10 FDA reports)
OESOPHAGEAL DISORDER ( 10 FDA reports)
ORAL DISCOMFORT ( 10 FDA reports)
OTITIS EXTERNA ( 10 FDA reports)
PERFORMANCE STATUS DECREASED ( 10 FDA reports)
PERICARDITIS ( 10 FDA reports)
PITUITARY TUMOUR ( 10 FDA reports)
POLYCYSTIC OVARIES ( 10 FDA reports)
PRESSURE OF SPEECH ( 10 FDA reports)
RAYNAUD'S PHENOMENON ( 10 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 10 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 10 FDA reports)
SKIN REACTION ( 10 FDA reports)
THYROID CANCER ( 10 FDA reports)
UNDERDOSE ( 10 FDA reports)
URINE OUTPUT DECREASED ( 10 FDA reports)
VENOUS THROMBOSIS ( 10 FDA reports)
VITAMIN D DEFICIENCY ( 10 FDA reports)
ABNORMAL WEIGHT GAIN ( 9 FDA reports)
ACCOMMODATION DISORDER ( 9 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 9 FDA reports)
ALPHA 1 FOETOPROTEIN AMNIOTIC FLUID INCREASED ( 9 FDA reports)
APHTHOUS STOMATITIS ( 9 FDA reports)
AZOTAEMIA ( 9 FDA reports)
BLOOD MAGNESIUM DECREASED ( 9 FDA reports)
BRAIN DEATH ( 9 FDA reports)
BREAST ABSCESS ( 9 FDA reports)
BREAST DISORDER ( 9 FDA reports)
CALCULUS URETERIC ( 9 FDA reports)
CEREBRAL ISCHAEMIA ( 9 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 9 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 9 FDA reports)
COMPLEX PARTIAL SEIZURES ( 9 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 9 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 9 FDA reports)
DIET REFUSAL ( 9 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 9 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 9 FDA reports)
EYELID DISORDER ( 9 FDA reports)
FAECALOMA ( 9 FDA reports)
FEELING OF DESPAIR ( 9 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 9 FDA reports)
GINGIVAL PAIN ( 9 FDA reports)
GLOSSITIS ( 9 FDA reports)
GLUCOSE TOLERANCE INCREASED ( 9 FDA reports)
GOITRE ( 9 FDA reports)
GRANDIOSITY ( 9 FDA reports)
HAEMOGLOBIN INCREASED ( 9 FDA reports)
HEART VALVE REPLACEMENT ( 9 FDA reports)
HEPATITIS CHOLESTATIC ( 9 FDA reports)
HEPATOCELLULAR INJURY ( 9 FDA reports)
HEPATOTOXICITY ( 9 FDA reports)
HYPERTONIA ( 9 FDA reports)
INJECTION SITE PRURITUS ( 9 FDA reports)
INJECTION SITE REACTION ( 9 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 9 FDA reports)
LABORATORY TEST ABNORMAL ( 9 FDA reports)
MENINGITIS ( 9 FDA reports)
METABOLIC ENCEPHALOPATHY ( 9 FDA reports)
MULTIPLE ALLERGIES ( 9 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 9 FDA reports)
MUSCLE FATIGUE ( 9 FDA reports)
MUSCULOSKELETAL DISORDER ( 9 FDA reports)
NUCHAL RIGIDITY ( 9 FDA reports)
OVARIAN CANCER ( 9 FDA reports)
PAIN OF SKIN ( 9 FDA reports)
PANCREATITIS NECROTISING ( 9 FDA reports)
PARKINSONIAN GAIT ( 9 FDA reports)
POLYP ( 9 FDA reports)
POTENTIATING DRUG INTERACTION ( 9 FDA reports)
PRESBYOPIA ( 9 FDA reports)
PROSTATE CANCER ( 9 FDA reports)
PROTEIN URINE PRESENT ( 9 FDA reports)
PULMONARY INFARCTION ( 9 FDA reports)
PULMONARY VENOUS THROMBOSIS ( 9 FDA reports)
QUALITY OF LIFE DECREASED ( 9 FDA reports)
RADICULITIS LUMBOSACRAL ( 9 FDA reports)
RETINAL HAEMORRHAGE ( 9 FDA reports)
SIALOADENITIS ( 9 FDA reports)
SINUS DISORDER ( 9 FDA reports)
SKIN BURNING SENSATION ( 9 FDA reports)
SPINAL DISORDER ( 9 FDA reports)
SYNOVITIS ( 9 FDA reports)
TEMPERATURE INTOLERANCE ( 9 FDA reports)
TERATOMA ( 9 FDA reports)
TREATMENT FAILURE ( 9 FDA reports)
UMBILICAL CORD AROUND NECK ( 9 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
VAGINAL INFECTION ( 9 FDA reports)
VITAMIN B12 DEFICIENCY ( 9 FDA reports)
WRIST FRACTURE ( 9 FDA reports)
YAWNING ( 9 FDA reports)
ABSCESS LIMB ( 8 FDA reports)
ALCOHOL POISONING ( 8 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 8 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 8 FDA reports)
AORTIC VALVE INCOMPETENCE ( 8 FDA reports)
APPLICATION SITE PRURITUS ( 8 FDA reports)
AUTISM ( 8 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 8 FDA reports)
BONE DENSITY DECREASED ( 8 FDA reports)
BULIMIA NERVOSA ( 8 FDA reports)
CARTILAGE ATROPHY ( 8 FDA reports)
CEREBROVASCULAR DISORDER ( 8 FDA reports)
CHOLESTASIS ( 8 FDA reports)
COLITIS ULCERATIVE ( 8 FDA reports)
CORONARY ARTERY BYPASS ( 8 FDA reports)
DEVICE BREAKAGE ( 8 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 8 FDA reports)
DRY THROAT ( 8 FDA reports)
DUODENAL ULCER ( 8 FDA reports)
DUODENITIS ( 8 FDA reports)
DYSMORPHISM ( 8 FDA reports)
ERUCTATION ( 8 FDA reports)
EXERCISE TOLERANCE DECREASED ( 8 FDA reports)
FLIGHT OF IDEAS ( 8 FDA reports)
FOOT OPERATION ( 8 FDA reports)
GAMBLING ( 8 FDA reports)
GANGRENE ( 8 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 8 FDA reports)
GASTROINTESTINAL PAIN ( 8 FDA reports)
GINGIVITIS ( 8 FDA reports)
HAEMOLYSIS ( 8 FDA reports)
HALLUCINATION, OLFACTORY ( 8 FDA reports)
HEPATIC PAIN ( 8 FDA reports)
HYPERCHLORHYDRIA ( 8 FDA reports)
IMPAIRED FASTING GLUCOSE ( 8 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 8 FDA reports)
KIDNEY MALFORMATION ( 8 FDA reports)
LEG AMPUTATION ( 8 FDA reports)
LIPIDS ABNORMAL ( 8 FDA reports)
LIPOMA ( 8 FDA reports)
LOCAL SWELLING ( 8 FDA reports)
LONG QT SYNDROME ( 8 FDA reports)
LOOSE TOOTH ( 8 FDA reports)
LOSS OF CONTROL OF LEGS ( 8 FDA reports)
LUNG NEOPLASM MALIGNANT ( 8 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 8 FDA reports)
MASS ( 8 FDA reports)
MEAN CELL HAEMOGLOBIN ( 8 FDA reports)
MICROGRAPHIA ( 8 FDA reports)
MICTURITION DISORDER ( 8 FDA reports)
MONOCYTE COUNT DECREASED ( 8 FDA reports)
MOUTH INJURY ( 8 FDA reports)
MULTIPLE FRACTURES ( 8 FDA reports)
MUSCLE SPASTICITY ( 8 FDA reports)
ORAL INFECTION ( 8 FDA reports)
ORGAN FAILURE ( 8 FDA reports)
PHARYNGEAL DISORDER ( 8 FDA reports)
PLEURISY ( 8 FDA reports)
POLYMEDICATION ( 8 FDA reports)
POOR PERIPHERAL CIRCULATION ( 8 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 8 FDA reports)
PSORIATIC ARTHROPATHY ( 8 FDA reports)
RADICULOPATHY ( 8 FDA reports)
RENAL CANCER ( 8 FDA reports)
RENAL CYST ( 8 FDA reports)
RENAL INJURY ( 8 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 8 FDA reports)
RESPIRATORY TRACT CONGESTION ( 8 FDA reports)
SERUM FERRITIN INCREASED ( 8 FDA reports)
SPONDYLITIS ( 8 FDA reports)
SUSPICIOUSNESS ( 8 FDA reports)
TEETH BRITTLE ( 8 FDA reports)
TONGUE BLISTERING ( 8 FDA reports)
TONGUE OEDEMA ( 8 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 8 FDA reports)
UTERINE HAEMORRHAGE ( 8 FDA reports)
UVEITIS ( 8 FDA reports)
VENTRICULAR FIBRILLATION ( 8 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 8 FDA reports)
VIRAL LOAD INCREASED ( 8 FDA reports)
WRONG DRUG ADMINISTERED ( 8 FDA reports)
X-RAY ABNORMAL ( 8 FDA reports)
ACUTE HEPATIC FAILURE ( 7 FDA reports)
ADVERSE REACTION ( 7 FDA reports)
AGEUSIA ( 7 FDA reports)
ALCOHOLIC PANCREATITIS ( 7 FDA reports)
ANHIDROSIS ( 7 FDA reports)
ANORECTAL DISCOMFORT ( 7 FDA reports)
AORTIC VALVE DISEASE ( 7 FDA reports)
APLASTIC ANAEMIA ( 7 FDA reports)
BLADDER DILATATION ( 7 FDA reports)
BLADDER PROLAPSE ( 7 FDA reports)
BLOOD PROLACTIN DECREASED ( 7 FDA reports)
BOWEL SOUNDS ABNORMAL ( 7 FDA reports)
BRAIN STEM HAEMORRHAGE ( 7 FDA reports)
BREAST FEEDING ( 7 FDA reports)
BURNING MOUTH SYNDROME ( 7 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 7 FDA reports)
CERVICOBRACHIAL SYNDROME ( 7 FDA reports)
CHLAMYDIAL INFECTION ( 7 FDA reports)
CLAVICLE FRACTURE ( 7 FDA reports)
COMPRESSION FRACTURE ( 7 FDA reports)
CONGENITAL URETERIC ANOMALY ( 7 FDA reports)
DEFORMITY ( 7 FDA reports)
DEPERSONALISATION ( 7 FDA reports)
DERMATITIS CONTACT ( 7 FDA reports)
DEVICE RELATED INFECTION ( 7 FDA reports)
DROWNING ( 7 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 7 FDA reports)
ELECTROCONVULSIVE THERAPY ( 7 FDA reports)
ELEVATED MOOD ( 7 FDA reports)
EROSIVE OESOPHAGITIS ( 7 FDA reports)
FAILURE TO THRIVE ( 7 FDA reports)
FIBULA FRACTURE ( 7 FDA reports)
FUNGAL SKIN INFECTION ( 7 FDA reports)
GASTRIC HAEMORRHAGE ( 7 FDA reports)
GASTRIC POLYPS ( 7 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 7 FDA reports)
GRANULOCYTE COUNT DECREASED ( 7 FDA reports)
GRAVITATIONAL OEDEMA ( 7 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 7 FDA reports)
HAIR TEXTURE ABNORMAL ( 7 FDA reports)
HEAD DEFORMITY ( 7 FDA reports)
HEART DISEASE CONGENITAL ( 7 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 7 FDA reports)
HERPES VIRUS INFECTION ( 7 FDA reports)
HYPERNATRAEMIA ( 7 FDA reports)
IMPATIENCE ( 7 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 7 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 7 FDA reports)
KETONURIA ( 7 FDA reports)
LEGAL PROBLEM ( 7 FDA reports)
LIMB MALFORMATION ( 7 FDA reports)
MICROCYTIC ANAEMIA ( 7 FDA reports)
NEOPLASM PROGRESSION ( 7 FDA reports)
NEUROGENIC BLADDER ( 7 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 7 FDA reports)
ORAL SURGERY ( 7 FDA reports)
PERITONITIS ( 7 FDA reports)
PILONIDAL CYST ( 7 FDA reports)
PORTAL HYPERTENSION ( 7 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 7 FDA reports)
PROSTATE CANCER RECURRENT ( 7 FDA reports)
PROSTATIC DISORDER ( 7 FDA reports)
PROSTATIC OBSTRUCTION ( 7 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 7 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 7 FDA reports)
PULMONARY HAEMORRHAGE ( 7 FDA reports)
PULSE ABSENT ( 7 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 7 FDA reports)
RADICULITIS ( 7 FDA reports)
RASH VESICULAR ( 7 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 7 FDA reports)
REFLUX OESOPHAGITIS ( 7 FDA reports)
RHONCHI ( 7 FDA reports)
SCAB ( 7 FDA reports)
SCRATCH ( 7 FDA reports)
SEASONAL ALLERGY ( 7 FDA reports)
SELF MUTILATION ( 7 FDA reports)
SHOULDER OPERATION ( 7 FDA reports)
SKIN PAPILLOMA ( 7 FDA reports)
SLEEP WALKING ( 7 FDA reports)
SLEEP-RELATED EATING DISORDER ( 7 FDA reports)
SNEEZING ( 7 FDA reports)
SOCIAL PROBLEM ( 7 FDA reports)
SPINAL COMPRESSION FRACTURE ( 7 FDA reports)
STRESS FRACTURE ( 7 FDA reports)
SUNBURN ( 7 FDA reports)
SUPPRESSED LACTATION ( 7 FDA reports)
TENDON DISORDER ( 7 FDA reports)
THERAPY NON-RESPONDER ( 7 FDA reports)
THROMBOPHLEBITIS ( 7 FDA reports)
TINEA PEDIS ( 7 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 7 FDA reports)
TRICHOTILLOMANIA ( 7 FDA reports)
TRIGEMINAL NEURALGIA ( 7 FDA reports)
UMBILICAL CORD ABNORMALITY ( 7 FDA reports)
WEIGHT BEARING DIFFICULTY ( 7 FDA reports)
ABDOMINAL HERNIA ( 6 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 6 FDA reports)
ABORTION THREATENED ( 6 FDA reports)
ABSCESS NECK ( 6 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 6 FDA reports)
ADRENAL ADENOMA ( 6 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 6 FDA reports)
APPLICATION SITE RASH ( 6 FDA reports)
BACTERAEMIA ( 6 FDA reports)
BENCE JONES PROTEINURIA ( 6 FDA reports)
BIPOLAR II DISORDER ( 6 FDA reports)
BLOOD COUNT ABNORMAL ( 6 FDA reports)
BLOOD URINE ( 6 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 6 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 6 FDA reports)
BREAST CANCER METASTATIC ( 6 FDA reports)
BRONCHITIS CHRONIC ( 6 FDA reports)
BUNDLE BRANCH BLOCK ( 6 FDA reports)
CARDIAC OPERATION ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 6 FDA reports)
CHOKING SENSATION ( 6 FDA reports)
CHORIOAMNIONITIS ( 6 FDA reports)
CLOSTRIDIAL INFECTION ( 6 FDA reports)
COMPARTMENT SYNDROME ( 6 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 6 FDA reports)
CORONARY ARTERY STENOSIS ( 6 FDA reports)
COSTOCHONDRITIS ( 6 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 6 FDA reports)
CRYPTORCHISM ( 6 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 6 FDA reports)
DERMATITIS ACNEIFORM ( 6 FDA reports)
DEVICE MALFUNCTION ( 6 FDA reports)
DISSOCIATIVE DISORDER ( 6 FDA reports)
DISSOCIATIVE FUGUE ( 6 FDA reports)
ECTOPIC PREGNANCY ( 6 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 6 FDA reports)
EMBOLIC STROKE ( 6 FDA reports)
ENDOTRACHEAL INTUBATION ( 6 FDA reports)
ESCHERICHIA INFECTION ( 6 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 6 FDA reports)
EYES SUNKEN ( 6 FDA reports)
FACIAL PARESIS ( 6 FDA reports)
FAT TISSUE INCREASED ( 6 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 6 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 6 FDA reports)
FOETAL GROWTH RETARDATION ( 6 FDA reports)
FOLLICULITIS ( 6 FDA reports)
FOOT DEFORMITY ( 6 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 6 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 6 FDA reports)
GINGIVAL EROSION ( 6 FDA reports)
GRANULOCYTES ABNORMAL ( 6 FDA reports)
GUN SHOT WOUND ( 6 FDA reports)
HEAD DISCOMFORT ( 6 FDA reports)
HEPATIC NECROSIS ( 6 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 6 FDA reports)
HYDROCEPHALUS ( 6 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 6 FDA reports)
HYPERKERATOSIS ( 6 FDA reports)
HYPERPYREXIA ( 6 FDA reports)
HYPERTONIC BLADDER ( 6 FDA reports)
HYPERTROPHY BREAST ( 6 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 6 FDA reports)
HYPOTONIA NEONATAL ( 6 FDA reports)
INCORRECT STORAGE OF DRUG ( 6 FDA reports)
INCREASED TENDENCY TO BRUISE ( 6 FDA reports)
INJECTION SITE MASS ( 6 FDA reports)
INTERMITTENT CLAUDICATION ( 6 FDA reports)
ISCHAEMIA ( 6 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 6 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 6 FDA reports)
LACRIMAL DISORDER ( 6 FDA reports)
LEFT VENTRICULAR FAILURE ( 6 FDA reports)
LYMPHOMA ( 6 FDA reports)
MALABSORPTION ( 6 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 6 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 6 FDA reports)
MITRAL VALVE PROLAPSE ( 6 FDA reports)
MIXED HYPERLIPIDAEMIA ( 6 FDA reports)
MORBID THOUGHTS ( 6 FDA reports)
MUSCLE HYPERTROPHY ( 6 FDA reports)
NASAL DRYNESS ( 6 FDA reports)
NEOPLASM PROSTATE ( 6 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 6 FDA reports)
NICOTINE DEPENDENCE ( 6 FDA reports)
OEDEMA MUCOSAL ( 6 FDA reports)
OPTIC NEURITIS ( 6 FDA reports)
OVARIAN LOW MALIGNANT POTENTIAL TUMOUR ( 6 FDA reports)
PANCREATIC CYST ( 6 FDA reports)
PAPILLOEDEMA ( 6 FDA reports)
PAPILLOMA VIRAL INFECTION ( 6 FDA reports)
PATELLA FRACTURE ( 6 FDA reports)
PERIARTHRITIS ( 6 FDA reports)
PERIPHERAL ISCHAEMIA ( 6 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 6 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 6 FDA reports)
POLYP COLORECTAL ( 6 FDA reports)
POOR PERSONAL HYGIENE ( 6 FDA reports)
PSEUDOMONAS INFECTION ( 6 FDA reports)
PULMONARY SARCOIDOSIS ( 6 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 6 FDA reports)
RETROGRADE EJACULATION ( 6 FDA reports)
SCHIZOTYPAL PERSONALITY DISORDER ( 6 FDA reports)
SEBORRHOEIC DERMATITIS ( 6 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 6 FDA reports)
SINUS CONGESTION ( 6 FDA reports)
SKELETAL INJURY ( 6 FDA reports)
SKIN HYPERPIGMENTATION ( 6 FDA reports)
SKIN IRRITATION ( 6 FDA reports)
SKIN ODOUR ABNORMAL ( 6 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 6 FDA reports)
STASIS DERMATITIS ( 6 FDA reports)
STENT PLACEMENT ( 6 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 6 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 6 FDA reports)
THROMBOSIS IN DEVICE ( 6 FDA reports)
TINEA INFECTION ( 6 FDA reports)
TONGUE DISCOLOURATION ( 6 FDA reports)
TOOTH INJURY ( 6 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 6 FDA reports)
TROPONIN INCREASED ( 6 FDA reports)
URINE ABNORMALITY ( 6 FDA reports)
URINE ANALYSIS ABNORMAL ( 6 FDA reports)
VAGINAL DISCHARGE ( 6 FDA reports)
VAGINITIS BACTERIAL ( 6 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 6 FDA reports)
WEIGHT FLUCTUATION ( 6 FDA reports)
ABORTION MISSED ( 5 FDA reports)
ACARODERMATITIS ( 5 FDA reports)
ACUTE PRERENAL FAILURE ( 5 FDA reports)
ADRENAL MASS ( 5 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 5 FDA reports)
ALVEOLAR OSTEITIS ( 5 FDA reports)
AMPUTATION ( 5 FDA reports)
ANAL FISSURE ( 5 FDA reports)
ANGIONEUROTIC OEDEMA ( 5 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 5 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 5 FDA reports)
AUTONOMIC NEUROPATHY ( 5 FDA reports)
BEDRIDDEN ( 5 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 5 FDA reports)
BILE DUCT STONE ( 5 FDA reports)
BLADDER OBSTRUCTION ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BLOOD BLISTER ( 5 FDA reports)
BLOOD CHLORIDE INCREASED ( 5 FDA reports)
BLOOD CREATINE INCREASED ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 5 FDA reports)
BLOOD TEST ABNORMAL ( 5 FDA reports)
BLOOD URIC ACID INCREASED ( 5 FDA reports)
BONE SWELLING ( 5 FDA reports)
BRAIN NEOPLASM ( 5 FDA reports)
BRAIN STEM INFARCTION ( 5 FDA reports)
BREAST ENGORGEMENT ( 5 FDA reports)
BREAST NEOPLASM ( 5 FDA reports)
CARDIOTOXICITY ( 5 FDA reports)
CATHETERISATION CARDIAC ( 5 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 5 FDA reports)
CEREBRAL HAEMATOMA ( 5 FDA reports)
CERVIX DISORDER ( 5 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 5 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 5 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 5 FDA reports)
CONJUNCTIVAL ABRASION ( 5 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 5 FDA reports)
CONSTRICTED AFFECT ( 5 FDA reports)
CORONARY ARTERY OCCLUSION ( 5 FDA reports)
CRANIAL NERVE DISORDER ( 5 FDA reports)
CUSHING'S SYNDROME ( 5 FDA reports)
CYST REMOVAL ( 5 FDA reports)
DEJA VU ( 5 FDA reports)
DELAYED PUBERTY ( 5 FDA reports)
DIAPHRAGMATIC HERNIA ( 5 FDA reports)
DILATATION ATRIAL ( 5 FDA reports)
DYSAESTHESIA ( 5 FDA reports)
EAR DISCOMFORT ( 5 FDA reports)
EAR MALFORMATION ( 5 FDA reports)
EARLY MENARCHE ( 5 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 5 FDA reports)
EDUCATIONAL PROBLEM ( 5 FDA reports)
EJACULATION DELAYED ( 5 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 5 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 5 FDA reports)
EMBOLISM ( 5 FDA reports)
ENCOPRESIS ( 5 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 5 FDA reports)
EYE DISCHARGE ( 5 FDA reports)
FACIAL SPASM ( 5 FDA reports)
FAMILY STRESS ( 5 FDA reports)
FIBRIN D DIMER INCREASED ( 5 FDA reports)
FIBROMA ( 5 FDA reports)
FOETAL MOVEMENTS DECREASED ( 5 FDA reports)
GASTROSTOMY TUBE INSERTION ( 5 FDA reports)
GENERALISED ANXIETY DISORDER ( 5 FDA reports)
GLUCOSE URINE PRESENT ( 5 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 5 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 5 FDA reports)
HALLUCINATION, TACTILE ( 5 FDA reports)
HEAD TITUBATION ( 5 FDA reports)
HEART RATE ABNORMAL ( 5 FDA reports)
HEART VALVE OPERATION ( 5 FDA reports)
HEPATIC ENCEPHALOPATHY ( 5 FDA reports)
HEPATIC ENZYME ABNORMAL ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
HEPATITIS VIRAL ( 5 FDA reports)
HEPATOCELLULAR DAMAGE ( 5 FDA reports)
HYPERBILIRUBINAEMIA ( 5 FDA reports)
HYPERCOAGULATION ( 5 FDA reports)
HYPERINSULINAEMIA ( 5 FDA reports)
HYPERINSULINISM ( 5 FDA reports)
HYPOCALCAEMIA ( 5 FDA reports)
HYPOCHLORAEMIA ( 5 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 5 FDA reports)
HYPOREFLEXIA ( 5 FDA reports)
HYPOVENTILATION ( 5 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
IMMUNE SYSTEM DISORDER ( 5 FDA reports)
INFECTED DERMAL CYST ( 5 FDA reports)
INJECTION SITE INFECTION ( 5 FDA reports)
INJECTION SITE NODULE ( 5 FDA reports)
INJECTION SITE SWELLING ( 5 FDA reports)
INJECTION SITE URTICARIA ( 5 FDA reports)
INJURY ASPHYXIATION ( 5 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 5 FDA reports)
KYPHOSCOLIOSIS ( 5 FDA reports)
LARGE INTESTINAL ULCER ( 5 FDA reports)
LARYNGITIS ( 5 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 5 FDA reports)
LIP DRY ( 5 FDA reports)
LOW BIRTH WEIGHT BABY ( 5 FDA reports)
LUMBAR RADICULOPATHY ( 5 FDA reports)
LUPUS-LIKE SYNDROME ( 5 FDA reports)
MENOMETRORRHAGIA ( 5 FDA reports)
MENOPAUSAL SYMPTOMS ( 5 FDA reports)
MITRAL VALVE DISEASE ( 5 FDA reports)
MONOPLEGIA ( 5 FDA reports)
MOUTH HAEMORRHAGE ( 5 FDA reports)
MYASTHENIA GRAVIS ( 5 FDA reports)
MYOGLOBIN URINE PRESENT ( 5 FDA reports)
NASAL DISORDER ( 5 FDA reports)
NECK MASS ( 5 FDA reports)
NEPHROTIC SYNDROME ( 5 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 5 FDA reports)
NEUROLOGICAL SYMPTOM ( 5 FDA reports)
NIPPLE PAIN ( 5 FDA reports)
OEDEMA GENITAL ( 5 FDA reports)
OLIGOMENORRHOEA ( 5 FDA reports)
OPEN REDUCTION OF FRACTURE ( 5 FDA reports)
ORAL HERPES ( 5 FDA reports)
OSTEOPENIA ( 5 FDA reports)
OSTEOTOMY ( 5 FDA reports)
OTITIS MEDIA ACUTE ( 5 FDA reports)
PALATAL DISORDER ( 5 FDA reports)
PANCREATIC INSUFFICIENCY ( 5 FDA reports)
PARAPHILIA ( 5 FDA reports)
PENILE PAIN ( 5 FDA reports)
PHARYNGEAL ULCERATION ( 5 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 5 FDA reports)
POISONING ( 5 FDA reports)
POLYHYDRAMNIOS ( 5 FDA reports)
POLYNEUROPATHY ALCOHOLIC ( 5 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
PROCEDURAL PAIN ( 5 FDA reports)
PRODUCT ADHESION ISSUE ( 5 FDA reports)
PROTEIN TOTAL DECREASED ( 5 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 5 FDA reports)
PULMONARY MASS ( 5 FDA reports)
RADIOTHERAPY ( 5 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 5 FDA reports)
RENAL COLIC ( 5 FDA reports)
SALIVARY GLAND CALCULUS ( 5 FDA reports)
SCROTAL ULCER ( 5 FDA reports)
SEQUESTRECTOMY ( 5 FDA reports)
SEXUAL ASSAULT VICTIM ( 5 FDA reports)
SHOULDER ARTHROPLASTY ( 5 FDA reports)
SINUS ARRHYTHMIA ( 5 FDA reports)
SKIN INFECTION ( 5 FDA reports)
SKIN STRIAE ( 5 FDA reports)
SKULL FRACTURE ( 5 FDA reports)
SLEEP TERROR ( 5 FDA reports)
SMOKER ( 5 FDA reports)
SOCIAL PHOBIA ( 5 FDA reports)
SOMATOFORM DISORDER ( 5 FDA reports)
SPONTANEOUS PENILE ERECTION ( 5 FDA reports)
STREPTOCOCCAL INFECTION ( 5 FDA reports)
TEMPERATURE REGULATION DISORDER ( 5 FDA reports)
TENDON RUPTURE ( 5 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 5 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 5 FDA reports)
THYROID MASS ( 5 FDA reports)
TONGUE BITING ( 5 FDA reports)
TONGUE PARALYSIS ( 5 FDA reports)
TOOTH DISCOLOURATION ( 5 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 5 FDA reports)
TUBERCULOSIS ( 5 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 5 FDA reports)
TUNNEL VISION ( 5 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 5 FDA reports)
URINE AMPHETAMINE POSITIVE ( 5 FDA reports)
URINE COLOUR ABNORMAL ( 5 FDA reports)
VAGINAL CANCER ( 5 FDA reports)
VARICES OESOPHAGEAL ( 5 FDA reports)
VEIN DISORDER ( 5 FDA reports)
VERBIGERATION ( 5 FDA reports)
VERTEBROPLASTY ( 5 FDA reports)
VULVOVAGINAL PRURITUS ( 5 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 5 FDA reports)
WOUND INFECTION ( 5 FDA reports)
ABORTION EARLY ( 4 FDA reports)
ACETONAEMIA ( 4 FDA reports)
ADHESION ( 4 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 4 FDA reports)
ALCOHOLIC ( 4 FDA reports)
ALOPECIA AREATA ( 4 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
AORTIC VALVE STENOSIS ( 4 FDA reports)
APPETITE DISORDER ( 4 FDA reports)
APPLICATION SITE IRRITATION ( 4 FDA reports)
APPLICATION SITE PAIN ( 4 FDA reports)
APTYALISM ( 4 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 4 FDA reports)
ASPIRATION BRONCHIAL ( 4 FDA reports)
ASTHENOPIA ( 4 FDA reports)
ASTIGMATISM ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 4 FDA reports)
AZOOSPERMIA ( 4 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 4 FDA reports)
BELLIGERENCE ( 4 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 4 FDA reports)
BILIARY TRACT DISORDER ( 4 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 4 FDA reports)
BLADDER SPASM ( 4 FDA reports)
BLOOD CREATINE ABNORMAL ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 4 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 4 FDA reports)
BLOOD OSMOLARITY DECREASED ( 4 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
BLOOD PH INCREASED ( 4 FDA reports)
BLOOD UREA DECREASED ( 4 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 4 FDA reports)
BREAST CANCER RECURRENT ( 4 FDA reports)
BREAST OPERATION ( 4 FDA reports)
CAPILLARY LEAK SYNDROME ( 4 FDA reports)
CARCINOID TUMOUR ( 4 FDA reports)
CARDIAC FIBRILLATION ( 4 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CATARACT NUCLEAR ( 4 FDA reports)
CEREBELLAR INFARCTION ( 4 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 4 FDA reports)
CHOLECYSTITIS INFECTIVE ( 4 FDA reports)
CHONDROPATHY ( 4 FDA reports)
CHOREA ( 4 FDA reports)
CLONUS ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 4 FDA reports)
COLONIC OBSTRUCTION ( 4 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 4 FDA reports)
CONDUCTION DISORDER ( 4 FDA reports)
CYCLOTHYMIC DISORDER ( 4 FDA reports)
DELIVERY ( 4 FDA reports)
DELUSION OF GRANDEUR ( 4 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 4 FDA reports)
DEVICE MISUSE ( 4 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 4 FDA reports)
DIABETIC GASTROPATHY ( 4 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 4 FDA reports)
DIVERTICULUM ( 4 FDA reports)
DRUG EFFECT DELAYED ( 4 FDA reports)
DRUG EFFECT INCREASED ( 4 FDA reports)
DRUG TOLERANCE ( 4 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 4 FDA reports)
ENDOCARDITIS BACTERIAL ( 4 FDA reports)
ENTEROCOCCAL INFECTION ( 4 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 4 FDA reports)
ESSENTIAL TREMOR ( 4 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 4 FDA reports)
EXOPHTHALMOS ( 4 FDA reports)
EXPOSURE VIA FATHER ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
FATTY LIVER ALCOHOLIC ( 4 FDA reports)
FISTULA ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
FOETAL CHROMOSOME ABNORMALITY ( 4 FDA reports)
FOETAL DISTRESS SYNDROME ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
FOREIGN BODY ASPIRATION ( 4 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 4 FDA reports)
GASTRIC CANCER ( 4 FDA reports)
GENITAL HAEMORRHAGE ( 4 FDA reports)
GINGIVAL SWELLING ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HAEMORRHAGIC STROKE ( 4 FDA reports)
HEART INJURY ( 4 FDA reports)
HEPATOSPLENOMEGALY ( 4 FDA reports)
HIRSUTISM ( 4 FDA reports)
HORDEOLUM ( 4 FDA reports)
HORMONE LEVEL ABNORMAL ( 4 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 4 FDA reports)
HYPERAEMIA ( 4 FDA reports)
HYPEROSMOLAR STATE ( 4 FDA reports)
HYPERTHERMIA MALIGNANT ( 4 FDA reports)
HYPOCHROMIC ANAEMIA ( 4 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 4 FDA reports)
HYPOGONADISM ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 4 FDA reports)
IMMUNODEFICIENCY ( 4 FDA reports)
IMPRISONMENT ( 4 FDA reports)
INFANTILE APNOEIC ATTACK ( 4 FDA reports)
INFARCTION ( 4 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 4 FDA reports)
INJECTION SITE RASH ( 4 FDA reports)
INSULIN RESISTANT DIABETES ( 4 FDA reports)
JOINT CONTRACTURE ( 4 FDA reports)
KETOSIS ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LABILE BLOOD PRESSURE ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
LARYNGOSPASM ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LIBIDO DISORDER ( 4 FDA reports)
LIGAMENT INJURY ( 4 FDA reports)
LIGAMENT SPRAIN ( 4 FDA reports)
LIP EROSION ( 4 FDA reports)
LOCALISED OEDEMA ( 4 FDA reports)
LOOSE ASSOCIATIONS ( 4 FDA reports)
LUPUS NEPHRITIS ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
MELANOCYTIC NAEVUS ( 4 FDA reports)
MENSTRUATION DELAYED ( 4 FDA reports)
MIGRAINE WITH AURA ( 4 FDA reports)
MYOGLOBINURIA ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
MYOPERICARDITIS ( 4 FDA reports)
NASAL SEPTUM DEVIATION ( 4 FDA reports)
NECROTISING FASCIITIS ( 4 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 4 FDA reports)
NEUROSIS ( 4 FDA reports)
NIGHT BLINDNESS ( 4 FDA reports)
NIPPLE DISORDER ( 4 FDA reports)
NODULE ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 4 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 4 FDA reports)
OBSTRUCTION GASTRIC ( 4 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 4 FDA reports)
OESOPHAGEAL SPASM ( 4 FDA reports)
OLIGOHYDRAMNIOS ( 4 FDA reports)
OLIGURIA ( 4 FDA reports)
ONYCHOCLASIS ( 4 FDA reports)
OPIATES POSITIVE ( 4 FDA reports)
OTORRHOEA ( 4 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 4 FDA reports)
PARADOXICAL DRUG REACTION ( 4 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 4 FDA reports)
PARANOID PERSONALITY DISORDER ( 4 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 4 FDA reports)
PATHOLOGICAL FRACTURE ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
PERIUMBILICAL ABSCESS ( 4 FDA reports)
PERONEAL NERVE PALSY ( 4 FDA reports)
PIGMENTATION DISORDER ( 4 FDA reports)
PLACENTA PRAEVIA ( 4 FDA reports)
PLAGIOCEPHALY ( 4 FDA reports)
PLANTAR FASCIITIS ( 4 FDA reports)
PLEUROTHOTONUS ( 4 FDA reports)
PNEUMOBILIA ( 4 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 4 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 4 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 4 FDA reports)
PORPHYRIA ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
POST-TRAUMATIC PAIN ( 4 FDA reports)
POSTICTAL STATE ( 4 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 4 FDA reports)
PREMATURE EJACULATION ( 4 FDA reports)
PREMENSTRUAL SYNDROME ( 4 FDA reports)
PROSTATE CANCER METASTATIC ( 4 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 4 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 4 FDA reports)
PULMONARY MALFORMATION ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
RALES ( 4 FDA reports)
REGURGITATION ( 4 FDA reports)
RESPIRATORY ACIDOSIS ( 4 FDA reports)
RETINAL DETACHMENT ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
ROTATOR CUFF REPAIR ( 4 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 4 FDA reports)
SCLERODERMA ( 4 FDA reports)
SCOTOMA ( 4 FDA reports)
SELF ESTEEM DECREASED ( 4 FDA reports)
SEMEN VISCOSITY ABNORMAL ( 4 FDA reports)
SEMEN VOLUME DECREASED ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SLOW SPEECH ( 4 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 4 FDA reports)
SOCIAL FEAR ( 4 FDA reports)
SPINAL CORD COMPRESSION ( 4 FDA reports)
SPINAL CORD DISORDER ( 4 FDA reports)
SPINAL DEFORMITY ( 4 FDA reports)
SPLEEN DISORDER ( 4 FDA reports)
SPUTUM DISCOLOURED ( 4 FDA reports)
STARVATION ( 4 FDA reports)
SUPERIOR MESENTERIC ARTERY SYNDROME ( 4 FDA reports)
THEFT ( 4 FDA reports)
THERAPY CESSATION ( 4 FDA reports)
THOUGHT BLOCKING ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
THYROID ADENOMA ( 4 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 4 FDA reports)
TONGUE SPASM ( 4 FDA reports)
TOOTH EROSION ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
TRANSFUSION ( 4 FDA reports)
TRISOMY 21 ( 4 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
URETHRAL STENOSIS ( 4 FDA reports)
UTERINE ENLARGEMENT ( 4 FDA reports)
UTERINE INFECTION ( 4 FDA reports)
UTERINE PROLAPSE ( 4 FDA reports)
VASCULAR OCCLUSION ( 4 FDA reports)
VERBAL ABUSE ( 4 FDA reports)
VIRAL DIARRHOEA ( 4 FDA reports)
VOMITING PROJECTILE ( 4 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 4 FDA reports)
WEIGHT GAIN POOR ( 4 FDA reports)
WOUND COMPLICATION ( 4 FDA reports)
ABDOMINAL SEPSIS ( 3 FDA reports)
ABDOMINAL SYMPTOM ( 3 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 3 FDA reports)
ABORTION INFECTED ( 3 FDA reports)
ABSCESS ORAL ( 3 FDA reports)
ACCIDENTAL DEATH ( 3 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 3 FDA reports)
ACTIVATED PROTEIN C RESISTANCE ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
ALCOHOL INTERACTION ( 3 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 3 FDA reports)
ANAL ATRESIA ( 3 FDA reports)
ANEURYSM ( 3 FDA reports)
ANIMAL BITE ( 3 FDA reports)
ANION GAP DECREASED ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 3 FDA reports)
AORTIC CALCIFICATION ( 3 FDA reports)
APPARENT LIFE THREATENING EVENT ( 3 FDA reports)
APPENDICECTOMY ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
ARTHROPOD BITE ( 3 FDA reports)
ASPERGER'S DISORDER ( 3 FDA reports)
ASTROCYTOMA ( 3 FDA reports)
AURICULAR SWELLING ( 3 FDA reports)
AXILLARY MASS ( 3 FDA reports)
BALLISMUS ( 3 FDA reports)
BASOPHIL COUNT INCREASED ( 3 FDA reports)
BENIGN EAR NEOPLASM ( 3 FDA reports)
BLADDER DISCOMFORT ( 3 FDA reports)
BLOOD ALCOHOL INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 3 FDA reports)
BLOOD INSULIN INCREASED ( 3 FDA reports)
BLOOD IRON DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 3 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES ( 3 FDA reports)
BLOODY DISCHARGE ( 3 FDA reports)
BODY HEIGHT INCREASED ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BRAIN NEOPLASM BENIGN ( 3 FDA reports)
BREATH ODOUR ( 3 FDA reports)
BUNION ( 3 FDA reports)
BUTTERFLY RASH ( 3 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 3 FDA reports)
CALCULUS URETHRAL ( 3 FDA reports)
CARBON DIOXIDE ABNORMAL ( 3 FDA reports)
CARBON DIOXIDE DECREASED ( 3 FDA reports)
CARBON MONOXIDE POISONING ( 3 FDA reports)
CARDIAC DISCOMFORT ( 3 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 3 FDA reports)
CENTRAL OBESITY ( 3 FDA reports)
CEPHALHAEMATOMA ( 3 FDA reports)
CEREBELLAR SYNDROME ( 3 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 3 FDA reports)
CERVICAL DYSPLASIA ( 3 FDA reports)
CERVICITIS ( 3 FDA reports)
CHOLANGITIS ( 3 FDA reports)
CHOLANGITIS ACUTE ( 3 FDA reports)
CHOLINERGIC SYNDROME ( 3 FDA reports)
CHROMATOPSIA ( 3 FDA reports)
CHRONIC HEPATITIS ( 3 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 3 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 3 FDA reports)
COAGULATION TEST ABNORMAL ( 3 FDA reports)
COMPLICATED FRACTURE ( 3 FDA reports)
COMPULSIVE SHOPPING ( 3 FDA reports)
CONGENITAL TONGUE ANOMALY ( 3 FDA reports)
CORNEAL OEDEMA ( 3 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 3 FDA reports)
CYSTITIS INTERSTITIAL ( 3 FDA reports)
CYTOGENETIC ABNORMALITY ( 3 FDA reports)
DAYDREAMING ( 3 FDA reports)
DEAFNESS NEUROSENSORY ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DEATH NEONATAL ( 3 FDA reports)
DELUSIONAL PERCEPTION ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DEPENDENCE ( 3 FDA reports)
DEVICE DAMAGE ( 3 FDA reports)
DEVICE OCCLUSION ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
DYSLEXIA ( 3 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 3 FDA reports)
EAR, NOSE AND THROAT EXAMINATION ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 3 FDA reports)
ENCEPHALOMALACIA ( 3 FDA reports)
ENDOMETRIOSIS ( 3 FDA reports)
ENTHESOPATHY ( 3 FDA reports)
EPICONDYLITIS ( 3 FDA reports)
EPIDERMAL NECROSIS ( 3 FDA reports)
EPIGLOTTIC OEDEMA ( 3 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
EXCESSIVE MASTURBATION ( 3 FDA reports)
EXERCISE LACK OF ( 3 FDA reports)
EXHIBITIONISM ( 3 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 3 FDA reports)
EYE INJURY ( 3 FDA reports)
EYELID MARGIN CRUSTING ( 3 FDA reports)
FACE INJURY ( 3 FDA reports)
FACTITIOUS DISORDER ( 3 FDA reports)
FALLOT'S TETRALOGY ( 3 FDA reports)
FEBRILE CONVULSION ( 3 FDA reports)
FIGHT IN SCHOOL ( 3 FDA reports)
FINGER DEFORMITY ( 3 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 3 FDA reports)
FOOD INTERACTION ( 3 FDA reports)
FUNGAL RASH ( 3 FDA reports)
GAIT SPASTIC ( 3 FDA reports)
GALLBLADDER PAIN ( 3 FDA reports)
GASTRIC OPERATION ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
GASTROENTERITIS SALMONELLA ( 3 FDA reports)
GASTROINTESTINAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL NECROSIS ( 3 FDA reports)
GENITAL RASH ( 3 FDA reports)
GINGIVAL INFECTION ( 3 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 3 FDA reports)
GLOSSOPTOSIS ( 3 FDA reports)
HAEMORRHAGIC CYST ( 3 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HEPATORENAL FAILURE ( 3 FDA reports)
HORNER'S SYNDROME ( 3 FDA reports)
HOUSE DUST ALLERGY ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPERCAPNIA ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOVITAMINOSIS ( 3 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
INJECTION SITE INFLAMMATION ( 3 FDA reports)
INJECTION SITE ULCER ( 3 FDA reports)
INTENTION TREMOR ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
INTESTINAL POLYP ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 3 FDA reports)
IRON DEFICIENCY ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
JAUNDICE NEONATAL ( 3 FDA reports)
JOINT CREPITATION ( 3 FDA reports)
JUVENILE ARTHRITIS ( 3 FDA reports)
KERATOCONUS ( 3 FDA reports)
KIDNEY SMALL ( 3 FDA reports)
KLEBSIELLA BACTERAEMIA ( 3 FDA reports)
LABYRINTHITIS ( 3 FDA reports)
LEARNING DISABILITY ( 3 FDA reports)
LEFT ATRIAL DILATATION ( 3 FDA reports)
LIP DISORDER ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 3 FDA reports)
MACROGLOSSIA ( 3 FDA reports)
MAMMOPLASTY ( 3 FDA reports)
MEAN CELL VOLUME INCREASED ( 3 FDA reports)
MEASLES ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MEDICAL DEVICE REMOVAL ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
MENINGOCELE ( 3 FDA reports)
METAMORPHOPSIA ( 3 FDA reports)
METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY ( 3 FDA reports)
MITRAL VALVE STENOSIS ( 3 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MYELOCYTE COUNT INCREASED ( 3 FDA reports)
MYELOID MATURATION ARREST ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NASAL POLYPS ( 3 FDA reports)
NEONATAL OVERSEDATION ( 3 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NEURITIS ( 3 FDA reports)
NEUROENDOCRINE CARCINOMA ( 3 FDA reports)
NEUROMYOPATHY ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OCULAR HYPERTENSION ( 3 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 3 FDA reports)
ONYCHOMADESIS ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
ORGASM ABNORMAL ( 3 FDA reports)
OROPHARYNGEAL BLISTERING ( 3 FDA reports)
OVARIAN DISORDER ( 3 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 3 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 3 FDA reports)
PANCREATIC MASS ( 3 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
PERIORBITAL HAEMATOMA ( 3 FDA reports)
PHAGOPHOBIA ( 3 FDA reports)
PHYSICAL DISABILITY ( 3 FDA reports)
PITTING OEDEMA ( 3 FDA reports)
PLEURAL FIBROSIS ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
POISONING DELIBERATE ( 3 FDA reports)
POLYARTHRITIS ( 3 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 3 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 3 FDA reports)
POST ABORTION HAEMORRHAGE ( 3 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 3 FDA reports)
PRECOCIOUS PUBERTY ( 3 FDA reports)
PREMATURE DELIVERY ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PROLONGED PREGNANCY ( 3 FDA reports)
PROSTHESIS USER ( 3 FDA reports)
PSEUDODEMENTIA ( 3 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 3 FDA reports)
PULSE ABNORMAL ( 3 FDA reports)
PYELONEPHRITIS ACUTE ( 3 FDA reports)
REGRESSIVE BEHAVIOUR ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
RENAL INFARCT ( 3 FDA reports)
SARCOMA ( 3 FDA reports)
SEBACEOUS GLANDS OVERACTIVITY ( 3 FDA reports)
SELF-INDUCED VOMITING ( 3 FDA reports)
SENSITIVITY OF TEETH ( 3 FDA reports)
SEPTOPLASTY ( 3 FDA reports)
SEROMA ( 3 FDA reports)
SHOULDER DYSTOCIA ( 3 FDA reports)
SICK SINUS SYNDROME ( 3 FDA reports)
SINUS HEADACHE ( 3 FDA reports)
SJOGREN'S SYNDROME ( 3 FDA reports)
SKIN CHAPPED ( 3 FDA reports)
SLEEP TALKING ( 3 FDA reports)
SLOW RESPONSE TO STIMULI ( 3 FDA reports)
SPLENIC LESION ( 3 FDA reports)
SPLENIC RUPTURE ( 3 FDA reports)
STEREOTYPY ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SUBILEUS ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
SWEAT DISCOLOURATION ( 3 FDA reports)
TALIPES ( 3 FDA reports)
TENDON CALCIFICATION ( 3 FDA reports)
TERMINAL INSOMNIA ( 3 FDA reports)
TESTIS CANCER ( 3 FDA reports)
THIRST DECREASED ( 3 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
TIBIA FRACTURE ( 3 FDA reports)
TOE AMPUTATION ( 3 FDA reports)
TONGUE DRY ( 3 FDA reports)
TONSILLITIS ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
TRIGGER FINGER ( 3 FDA reports)
TROPONIN T INCREASED ( 3 FDA reports)
UNDERWEIGHT ( 3 FDA reports)
URGE INCONTINENCE ( 3 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 3 FDA reports)
URINE KETONE BODY ( 3 FDA reports)
UTERINE POLYP ( 3 FDA reports)
VARICOSE VEIN ( 3 FDA reports)
VASCULAR GRAFT ( 3 FDA reports)
VASOSPASM ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VERTIGO POSITIONAL ( 3 FDA reports)
VESICOURETERIC REFLUX ( 3 FDA reports)
VICTIM OF CRIME ( 3 FDA reports)
VIRAL MYOCARDITIS ( 3 FDA reports)
VOCAL CORD PARALYSIS ( 3 FDA reports)
VULVOVAGINAL PAIN ( 3 FDA reports)
WHEELCHAIR USER ( 3 FDA reports)
WOUND DRAINAGE ( 3 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ABSCESS JAW ( 2 FDA reports)
ABULIA ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACCIDENT AT HOME ( 2 FDA reports)
ACCIDENT AT WORK ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACTIVATION SYNDROME ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ACUTE TONSILLITIS ( 2 FDA reports)
ADENOMA BENIGN ( 2 FDA reports)
ADENOTONSILLECTOMY ( 2 FDA reports)
ADHESIOLYSIS ( 2 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 2 FDA reports)
AKINAESTHESIA ( 2 FDA reports)
ALCOHOL INTOLERANCE ( 2 FDA reports)
ALCOHOLIC LIVER DISEASE ( 2 FDA reports)
ALLERGY TO ANIMAL ( 2 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 2 FDA reports)
AMIMIA ( 2 FDA reports)
AMNIORRHEXIS ( 2 FDA reports)
AMPHETAMINES POSITIVE ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANAL PRURITUS ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANGIOTENSIN CONVERTING ENZYME DECREASED ( 2 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 2 FDA reports)
ANOXIC ENCEPHALOPATHY ( 2 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
APPLICATION SITE EROSION ( 2 FDA reports)
APPLICATION SITE EXFOLIATION ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
APPLICATION SITE SCAB ( 2 FDA reports)
APPLICATION SITE WARMTH ( 2 FDA reports)
ARM AMPUTATION ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ARTHROSCOPIC SURGERY ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASOCIAL BEHAVIOUR ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
AUTISM SPECTRUM DISORDER ( 2 FDA reports)
AUTISTIC DISORDER ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BALANITIS ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BEHAVIOURAL AND PSYCHIATRIC SYMPTOMS OF DEMENTIA ( 2 FDA reports)
BEREAVEMENT REACTION ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BIOPSY LUNG ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLADDER SPHINCTER ATONY ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
BLIGHTED OVUM ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD ALCOHOL ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN DECREASED ( 2 FDA reports)
BLOOD CHOLESTEROL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BODY TINEA ( 2 FDA reports)
BONE ATROPHY ( 2 FDA reports)
BONE CYST ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
BRAIN MALFORMATION ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
BREAST DISCOMFORT ( 2 FDA reports)
BRIEF PSYCHOTIC DISORDER WITH MARKED STRESSORS ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
BRONCHITIS VIRAL ( 2 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
CARDIAC ANEURYSM ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIAC OUTPUT DECREASED ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CARDIAC SEPTAL DEFECT ( 2 FDA reports)
CAROTID ARTERY DISEASE ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CATHETER SITE ERYTHEMA ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CERVICAL ROOT PAIN ( 2 FDA reports)
CERVIX CANCER METASTATIC ( 2 FDA reports)
CERVIX CARCINOMA STAGE I ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHOLESTEROSIS ( 2 FDA reports)
CHOREOATHETOSIS ( 2 FDA reports)
CHRONIC TONSILLITIS ( 2 FDA reports)
CIRCUMCISION ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 2 FDA reports)
COCCYDYNIA ( 2 FDA reports)
COGNITIVE DETERIORATION ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COLOBOMA ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMPENSATION NEUROSIS ( 2 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 2 FDA reports)
CONGENITAL LARYNGEAL STRIDOR ( 2 FDA reports)
CONGENITAL MULTIPLEX ARTHROGRYPOSIS ( 2 FDA reports)
CONGENITAL SPINAL CORD ANOMALY ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
COTARD'S SYNDROME ( 2 FDA reports)
CRANIOSYNOSTOSIS ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
CYSTITIS NONINFECTIVE ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DEAFNESS TRANSITORY ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DEFORMITY THORAX ( 2 FDA reports)
DEHYDROEPIANDROSTERONE INCREASED ( 2 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DERMATITIS PAPILLARIS CAPILLITII ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DETOXIFICATION ( 2 FDA reports)
DEVICE LEAKAGE ( 2 FDA reports)
DIABETIC BLINDNESS ( 2 FDA reports)
DIABETIC CARDIOMYOPATHY ( 2 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 2 FDA reports)
DIABETIC NEUROPATHIC ULCER ( 2 FDA reports)
DIABETIC VASCULAR DISORDER ( 2 FDA reports)
DIARRHOEA INFECTIOUS ( 2 FDA reports)
DIASTOLIC HYPOTENSION ( 2 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISTRACTIBILITY ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DRUG INTERACTION POTENTIATION ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSLALIA ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTROCARDIOGRAM ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 2 FDA reports)
ELECTROLYTE DEPLETION ( 2 FDA reports)
EMBOLISM VENOUS ( 2 FDA reports)
EMOTIONAL POVERTY ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENDOCRINE TEST ABNORMAL ( 2 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EPIDERMOLYSIS ( 2 FDA reports)
EPIDIDYMITIS ( 2 FDA reports)
EROTOMANIC DELUSION ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 2 FDA reports)
EYE EXCISION ( 2 FDA reports)
FACET JOINT SYNDROME ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FASCIITIS ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEELINGS OF WORTHLESSNESS ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FIXED ERUPTION ( 2 FDA reports)
FLASHBACK ( 2 FDA reports)
FLOPPY INFANT ( 2 FDA reports)
FOETAL DISORDER ( 2 FDA reports)
FOETAL EXPOSURE TIMING UNSPECIFIED ( 2 FDA reports)
FOETAL GROWTH RESTRICTION ( 2 FDA reports)
FOETAL HEART RATE DECREASED ( 2 FDA reports)
FOETAL HEART RATE DISORDER ( 2 FDA reports)
FORAMINOTOMY ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
GASTROINTESTINAL DISORDER CONGENITAL ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
GESTATIONAL HYPERTENSION ( 2 FDA reports)
GLIONEURONAL TUMOUR ( 2 FDA reports)
GRAFT LOSS ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
HAEMATOSPERMIA ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAIRY CELL LEUKAEMIA ( 2 FDA reports)
HAND AMPUTATION ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HANGOVER ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEART TRANSPLANT ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC MASS ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HEREDITARY PANCREATITIS ( 2 FDA reports)
HIGH-PITCHED CRYING ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 2 FDA reports)
HODGKIN'S DISEASE ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPERVIGILANCE ( 2 FDA reports)
HYPOCOMPLEMENTAEMIA ( 2 FDA reports)
HYPOSPADIAS ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INCREASED INSULIN REQUIREMENT ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 2 FDA reports)
INFERTILITY ( 2 FDA reports)
INFUSION SITE INFECTION ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
INGROWING NAIL ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTERVERTEBRAL DISC INJURY ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE INSERTION ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
IRITIS ( 2 FDA reports)
IRREGULAR SLEEP PHASE ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
JOINT ARTHROPLASTY ( 2 FDA reports)
JOINT HYPEREXTENSION ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
KAWASAKI'S DISEASE ( 2 FDA reports)
KERATITIS HERPETIC ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LARGE FOR DATES BABY ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LICE INFESTATION ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIP NEOPLASM ( 2 FDA reports)
LIPID METABOLISM DISORDER ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LOCKED-IN SYNDROME ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
LUMBAR PUNCTURE ( 2 FDA reports)
LUNG OPERATION ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MARITAL PROBLEM ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 2 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 2 FDA reports)
MEDICAL DIET ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
MENTAL DISABILITY ( 2 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 2 FDA reports)
METASTASES TO SKIN ( 2 FDA reports)
METATARSALGIA ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MOROSE ( 2 FDA reports)
MOTION SICKNESS ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 2 FDA reports)
MYOFASCITIS ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NAIL INJURY ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NASAL SEPTAL OPERATION ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NECK DEFORMITY ( 2 FDA reports)
NECK EXPLORATION ( 2 FDA reports)
NECROBIOSIS LIPOIDICA DIABETICORUM ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NEONATAL ASPHYXIA ( 2 FDA reports)
NEPHRITIS ALLERGIC ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NERVE BLOCK ( 2 FDA reports)
NEURODERMATITIS ( 2 FDA reports)
NEUROFIBROMATOSIS ( 2 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 2 FDA reports)
NORMAL TENSION GLAUCOMA ( 2 FDA reports)
OCCIPITAL NEURALGIA ( 2 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 2 FDA reports)
OESOPHAGEAL ATRESIA ( 2 FDA reports)
OESOPHAGEAL DILATATION ( 2 FDA reports)
OESOPHAGEAL MASS ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 2 FDA reports)
OROMANDIBULAR DYSTONIA ( 2 FDA reports)
ORTHOSTATIC PROTEINURIA ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OSTEOMYELITIS BACTERIAL ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PANCREATIC NECROSIS ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PAROTID GLAND ENLARGEMENT ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 2 FDA reports)
PENILE PROSTHESIS USER ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PERICARDIAL DISEASE ( 2 FDA reports)
PERINEAL ABSCESS ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERNICIOUS ANAEMIA ( 2 FDA reports)
PHOBIA ( 2 FDA reports)
PHOBIA OF DRIVING ( 2 FDA reports)
PHYSICAL ABUSE ( 2 FDA reports)
PICA ( 2 FDA reports)
PLACENTAL INSUFFICIENCY ( 2 FDA reports)
PLATELET AGGREGATION DECREASED ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POLYCYTHAEMIA VERA ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POLYSUBSTANCE ABUSE ( 2 FDA reports)
POLYTRAUMATISM ( 2 FDA reports)
POST PROCEDURAL OEDEMA ( 2 FDA reports)
POST PROCEDURAL SWELLING ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PREGNANCY TEST POSITIVE ( 2 FDA reports)
PREMATURE MENOPAUSE ( 2 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 2 FDA reports)
PROCALCITONIN ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PROCTITIS ULCERATIVE ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 2 FDA reports)
PROMISCUITY ( 2 FDA reports)
PROSTATIC OPERATION ( 2 FDA reports)
PROSTATOMEGALY ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
PSOAS ABSCESS ( 2 FDA reports)
PSYCHIATRIC EVALUATION ( 2 FDA reports)
PSYCHOSEXUAL DISORDER ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 2 FDA reports)
PYROMANIA ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RADIATION PERICARDITIS ( 2 FDA reports)
RADICULOTOMY ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
RECURRING SKIN BOILS ( 2 FDA reports)
REFRACTORY ANAEMIA ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL MASS ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
REPETITIVE SPEECH ( 2 FDA reports)
RESORPTION BONE INCREASED ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINAL INJURY ( 2 FDA reports)
RETROPERITONEAL FIBROSIS ( 2 FDA reports)
SACROILIITIS ( 2 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 2 FDA reports)
SALT CRAVING ( 2 FDA reports)
SCAN BRAIN ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER DEPRESSIVE TYPE ( 2 FDA reports)
SCHIZOPHRENIA, CATATONIC TYPE ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SERRATIA BACTERAEMIA ( 2 FDA reports)
SERUM SEROTONIN DECREASED ( 2 FDA reports)
SIMPLE PARTIAL SEIZURES ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SKIN DEGENERATIVE DISORDER ( 2 FDA reports)
SKIN DISCOMFORT ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SKIN FISSURES ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SKIN LESION EXCISION ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN TOXICITY ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SOMATIC HALLUCINATION ( 2 FDA reports)
SPINAL LAMINECTOMY ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
SPINE MALFORMATION ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
SPLENIC CYST ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
SPLENIC VARICES ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
STRESS ULCER ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SYDENHAM'S CHOREA ( 2 FDA reports)
SYNDACTYLY ( 2 FDA reports)
SYNOSTOSIS ( 2 FDA reports)
SYPHILIS TEST POSITIVE ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
TACHYCARDIA PAROXYSMAL ( 2 FDA reports)
TACHYPHYLAXIS ( 2 FDA reports)
TACITURNITY ( 2 FDA reports)
TANGENTIALITY ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
THYROGLOBULIN INCREASED ( 2 FDA reports)
THYROID OPERATION ( 2 FDA reports)
THYROTOXIC CRISIS ( 2 FDA reports)
THYROXINE FREE INCREASED ( 2 FDA reports)
TONGUE ERUPTION ( 2 FDA reports)
TONGUE EXFOLIATION ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TOOTH IMPACTED ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TRACHEITIS ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TRAUMATIC FRACTURE ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TRISOMY 18 ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
TUBEROUS SCLEROSIS ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS AND UVEITIS SYNDROME ( 2 FDA reports)
TYPE I HYPERSENSITIVITY ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 2 FDA reports)
UTERINE CYST ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
UTEROVAGINAL PROLAPSE ( 2 FDA reports)
VAGAL NERVE STIMULATOR IMPLANTATION ( 2 FDA reports)
VAGINAL CANDIDIASIS ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
VICTIM OF HOMICIDE ( 2 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
WAXY FLEXIBILITY ( 2 FDA reports)
WEANING FAILURE ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
WHITE BLOOD CELLS STOOL ( 2 FDA reports)
WHITE BLOOD CELLS URINE ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABORTION INCOMPLETE ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
ADRENERGIC SYNDROME ( 1 FDA reports)
AGITATED DEPRESSION ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOL DETOXIFICATION ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANAL PAP SMEAR ( 1 FDA reports)
ANAL SPASM ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANGIOSCLEROSIS ( 1 FDA reports)
ANION GAP ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANORECTAL AGENESIS ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANOREXIA NERVOSA ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARACHNOPHOBIA ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTHRITIS ENTEROPATHIC ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE NORMAL ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ASTHMA EXERCISE INDUCED ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOIMMUNE PANCREATITIS ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 1 FDA reports)
AVOIDANT PERSONALITY DISORDER ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BILIARY SPHINCTEROTOMY ( 1 FDA reports)
BILIARY TRACT OPERATION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BILIRUBINURIA ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BLADDER CONSTRICTION ( 1 FDA reports)
BLADDER HYPERTROPHY ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD AMINO ACID LEVEL INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CATECHOLAMINES DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES ( 1 FDA reports)
BLOOD ETHANOL INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GASTRIN INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN DECREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD ISOPROPANOL INCREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD OSMOLARITY ABNORMAL ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD THROMBIN INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BODY DYSMORPHIC DISORDER ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BONE SCAN ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BOWEL PREPARATION ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST DISORDER MALE ( 1 FDA reports)
BREAST DYSPLASIA ( 1 FDA reports)
BREAST FIBROMA ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BRIEF PSYCHOTIC DISORDER, WITH POSTPARTUM ONSET ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BRUGADA SYNDROME ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARCINOID TUMOUR PULMONARY ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC ARREST NEONATAL ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATARACT DIABETIC ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CENTRAL AUDITORY PROCESSING DISORDER ( 1 FDA reports)
CEREBELLAR EMBOLISM ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CERULOPLASMIN DECREASED ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLESTEATOMA ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHONDROMALACIA ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COAGULATION FACTOR IX LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR V LEVEL INCREASED ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONGENITAL ABSENCE OF VERTEBRA ( 1 FDA reports)
CONGENITAL AORTIC VALVE STENOSIS ( 1 FDA reports)
CONGENITAL BLADDER ANOMALY ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL NAEVUS ( 1 FDA reports)
CONGENITAL TORTICOLLIS ( 1 FDA reports)
CONJUNCTIVAL SCAR ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONUS MEDULLARIS SYNDROME ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CUTIS LAXA ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEAFNESS CONGENITAL ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DEMENTIA WITH LEWY BODIES ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMABRASION ( 1 FDA reports)
DERMATILLOMANIA ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSKINESIA NEONATAL ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ECTOPIC PREGNANCY TERMINATION ( 1 FDA reports)
ECZEMA INFECTED ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOMETRIAL ABLATION ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
EOSINOPENIA ( 1 FDA reports)
EOSINOPHIL PERCENTAGE ABNORMAL ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EXERTIONAL HEADACHE ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYELID EROSION ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FAILURE OF CHILD RESISTANT MECHANISM FOR PHARMACEUTICAL PRODUCT ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEAR OF WEIGHT GAIN ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 1 FDA reports)
FEMALE STERILISATION ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FOETAL ALCOHOL SYNDROME ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOETAL TOBACCO EXPOSURE ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GASTRIC BANDING ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTROENTERITIS PARACOLON BACILLUS ( 1 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROSS MOTOR DELAY ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 1 FDA reports)
HANTAVIRAL INFECTION ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATITIS A VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS C RNA POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HUMAN ANTICHIMERIC ANTIBODY POSITIVE ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYPERALBUMINAEMIA ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERPROTEINAEMIA ( 1 FDA reports)
HYPERTELORISM OF ORBIT ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPHAEMA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOPLASTIC ANAEMIA ( 1 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 1 FDA reports)
HYPOPROLACTINAEMIA ( 1 FDA reports)
HYPOTONIC-HYPORESPONSIVE EPISODE ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
ILLITERACY ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFANTILE SPASMS ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFERIORITY COMPLEX ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE OEDEMA ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE NERVE DAMAGE ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE STREAKING ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INSOMNIA RELATED TO ANOTHER MENTAL CONDITION ( 1 FDA reports)
INSULIN RESISTANCE SYNDROME ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTELLIGENCE TEST ABNORMAL ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL HAEMATOMA ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE REMOVAL ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KERATOMILEUSIS ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LACK OF SATIETY ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEUKOCYTE ANTIGEN B-27 POSITIVE ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIMB REDUCTION DEFECT ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACROCEPHALY ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALE ORGASMIC DISORDER ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALFORMATION VENOUS ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MATERNAL USE OF ILLICIT DRUGS ( 1 FDA reports)
MAXILLOFACIAL OPERATION ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MECONIUM STAIN ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 1 FDA reports)
MICROPHTHALMOS ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MILIA ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTI-VITAMIN DEFICIENCY ( 1 FDA reports)
MUNCHAUSEN'S SYNDROME ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCARDITIS INFECTIOUS ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOFASCIAL SPASM ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NECK SURGERY ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEONATAL TACHYPNOEA ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
NEURAL TUBE DEFECT ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 1 FDA reports)
NEUTRALISING ANTIBODIES ( 1 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NEUTROPHIL COUNT ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODDING OF HEAD ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-SECRETORY ADENOMA OF PITUITARY ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSTETRIC PROCEDURE COMPLICATION ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OCCUPATIONAL PHYSICAL PROBLEM ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 1 FDA reports)
ONYCHOPHAGIA ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
PACHYGYRIA ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC ABSCESS ( 1 FDA reports)
PANCREATIC CALCIFICATION ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARKINSONIAN CRISIS ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PATIENT RESTRAINT ( 1 FDA reports)
PCO2 ABNORMAL ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PENILE DISCHARGE ( 1 FDA reports)
PENILE SIZE REDUCED ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERINEAL LACERATION ( 1 FDA reports)
PERIOSTITIS ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL NEOPLASM ( 1 FDA reports)
PHARYNGEAL OPERATION ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHONOLOGICAL DISORDER ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PHYSICAL PRODUCT LABEL ISSUE ( 1 FDA reports)
PINEAL GERMINOMA ( 1 FDA reports)
PINEALOBLASTOMA ( 1 FDA reports)
PINEOCYTOMA ( 1 FDA reports)
PITUITARY CYST ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLACENTAL INFARCTION ( 1 FDA reports)
PLANTAR ERYTHEMA ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLICA SYNDROME ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PO2 ABNORMAL ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 1 FDA reports)
POST PROCEDURAL CONSTIPATION ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 1 FDA reports)
POSTMATURE BABY ( 1 FDA reports)
POSTMENOPAUSE ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
POVERTY OF THOUGHT CONTENT ( 1 FDA reports)
PRADER-WILLI SYNDROME ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PREGNANCY TEST NEGATIVE ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREHYPERTENSION ( 1 FDA reports)
PREMATURE RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PRODUCT CONTAINER SEAL ISSUE ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PROGESTERONE DECREASED ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROSTATIC ABSCESS ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOMOTOR AGITATION ( 1 FDA reports)
PSYCHOTHERAPY ( 1 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULMONARY VEIN STENOSIS ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RABBIT SYNDROME ( 1 FDA reports)
RADICAL MASTECTOMY ( 1 FDA reports)
RADICULAR PAIN ( 1 FDA reports)
RADICULITIS CERVICAL ( 1 FDA reports)
RAPID CORRECTION OF HYPONATRAEMIA ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
REMOVAL OF FOREIGN BODY ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY DEPTH DECREASED ( 1 FDA reports)
RESPIRATORY DYSKINESIA ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINITIS PIGMENTOSA ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RETRACTED NIPPLE ( 1 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SALPINGECTOMY ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SCAR EXCISION ( 1 FDA reports)
SCHIZOID PERSONALITY DISORDER ( 1 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 1 FDA reports)
SCHOOL REFUSAL ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SEBORRHOEA ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SECONDARY HYPERTHYROIDISM ( 1 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
SECONDARY SEQUESTRUM ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELECTIVE ABORTION ( 1 FDA reports)
SELF ESTEEM INFLATED ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEPTUM PELLUCIDUM AGENESIS ( 1 FDA reports)
SEXUAL ABUSE ( 1 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SHORTENED CERVIX ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, HYPERSOMNIA TYPE ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SMOKE SENSITIVITY ( 1 FDA reports)
SMOKING CESSATION THERAPY ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SPASMODIC DYSPHONIA ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPLEEN OPERATION ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPOUSAL ABUSE ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 1 FDA reports)
SUBSTANCE ABUSER ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUPERNUMERARY NIPPLE ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SWEAT GLAND INFECTION ( 1 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
TESTICULAR ATROPHY ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR OPERATION ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
TETHERED CORD SYNDROME ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THORACIC OPERATION ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THOUGHT BROADCASTING ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TOOTH DECALCIFICATION ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC NEUROPATHY ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRAUMATIC AMPUTATION ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TYRAMINE REACTION ( 1 FDA reports)
ULTRASOUND FOETAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UMBILICAL CORD SHORT ( 1 FDA reports)
UNIVENTRICULAR HEART ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
URETHRAL REPAIR ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINE BARBITURATES ( 1 FDA reports)
URINE CANNABINOIDS INCREASED ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VAGINAL LACERATION ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL OEDEMA ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VICTIM OF SEXUAL ABUSE ( 1 FDA reports)
VIIITH NERVE INJURY ( 1 FDA reports)
VIRAL MYOSITIS ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
VITAMIN A DECREASED ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITAMIN C DECREASED ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
VITREOUS DEGENERATION ( 1 FDA reports)
VOCAL CORD ATROPHY ( 1 FDA reports)
VOCAL CORD POLYP ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WITHDRAWAL BLEED ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)

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