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

DRUG INEFFECTIVE ( 866 FDA reports)
DIZZINESS ( 408 FDA reports)
FATIGUE ( 326 FDA reports)
ERECTILE DYSFUNCTION ( 284 FDA reports)
ASTHENIA ( 254 FDA reports)
RASH ( 252 FDA reports)
DYSPNOEA ( 249 FDA reports)
PAIN ( 242 FDA reports)
DIARRHOEA ( 231 FDA reports)
POLLAKIURIA ( 218 FDA reports)
GYNAECOMASTIA ( 217 FDA reports)
DYSURIA ( 212 FDA reports)
NAUSEA ( 206 FDA reports)
HEADACHE ( 203 FDA reports)
BREAST TENDERNESS ( 202 FDA reports)
OEDEMA PERIPHERAL ( 200 FDA reports)
LIBIDO DECREASED ( 191 FDA reports)
ANXIETY ( 190 FDA reports)
PRURITUS ( 185 FDA reports)
WEIGHT DECREASED ( 181 FDA reports)
BREAST ENLARGEMENT ( 180 FDA reports)
CHEST PAIN ( 178 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 173 FDA reports)
PNEUMONIA ( 172 FDA reports)
ARTHRALGIA ( 162 FDA reports)
PYREXIA ( 162 FDA reports)
NOCTURIA ( 159 FDA reports)
PAIN IN EXTREMITY ( 158 FDA reports)
BACK PAIN ( 155 FDA reports)
INSOMNIA ( 152 FDA reports)
ATRIAL FIBRILLATION ( 149 FDA reports)
FALL ( 146 FDA reports)
CONSTIPATION ( 142 FDA reports)
MALAISE ( 137 FDA reports)
DEATH ( 133 FDA reports)
ANAEMIA ( 130 FDA reports)
DRUG INTERACTION ( 129 FDA reports)
BLOOD GLUCOSE INCREASED ( 126 FDA reports)
URINARY RETENTION ( 125 FDA reports)
HYPOTENSION ( 123 FDA reports)
URINE FLOW DECREASED ( 123 FDA reports)
COUGH ( 118 FDA reports)
SEMEN VOLUME DECREASED ( 118 FDA reports)
BLOOD PRESSURE INCREASED ( 115 FDA reports)
PARAESTHESIA ( 115 FDA reports)
GAIT DISTURBANCE ( 114 FDA reports)
DYSPHAGIA ( 113 FDA reports)
OSTEOMYELITIS ( 113 FDA reports)
OSTEONECROSIS OF JAW ( 113 FDA reports)
URINARY TRACT INFECTION ( 113 FDA reports)
MYALGIA ( 112 FDA reports)
BREAST PAIN ( 111 FDA reports)
ABDOMINAL PAIN ( 109 FDA reports)
PAIN IN JAW ( 108 FDA reports)
RENAL FAILURE ACUTE ( 103 FDA reports)
PRODUCT QUALITY ISSUE ( 102 FDA reports)
VISION BLURRED ( 102 FDA reports)
HYPERTENSION ( 101 FDA reports)
MUSCLE SPASMS ( 101 FDA reports)
PROSTATE CANCER ( 97 FDA reports)
ABDOMINAL DISCOMFORT ( 96 FDA reports)
MUSCULAR WEAKNESS ( 96 FDA reports)
DIVERTICULUM ( 95 FDA reports)
LOSS OF CONSCIOUSNESS ( 95 FDA reports)
DEPRESSION ( 94 FDA reports)
INJURY ( 94 FDA reports)
FLUSHING ( 93 FDA reports)
RENAL FAILURE ( 88 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 87 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 87 FDA reports)
VOMITING ( 87 FDA reports)
ALOPECIA ( 85 FDA reports)
BREAST SWELLING ( 84 FDA reports)
IMPAIRED HEALING ( 83 FDA reports)
TOOTH EXTRACTION ( 83 FDA reports)
ABDOMINAL PAIN UPPER ( 82 FDA reports)
BONE DISORDER ( 82 FDA reports)
CEREBROVASCULAR ACCIDENT ( 80 FDA reports)
DYSPEPSIA ( 80 FDA reports)
ERYTHEMA ( 80 FDA reports)
HAEMOGLOBIN DECREASED ( 80 FDA reports)
HAEMORRHAGE ( 80 FDA reports)
HOT FLUSH ( 80 FDA reports)
CATARACT ( 78 FDA reports)
WEIGHT INCREASED ( 78 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 77 FDA reports)
LYMPHADENOPATHY ( 77 FDA reports)
THROMBOCYTOPENIA ( 77 FDA reports)
NIPPLE PAIN ( 75 FDA reports)
HYPERHIDROSIS ( 74 FDA reports)
NEOPLASM MALIGNANT ( 74 FDA reports)
ORAL PAIN ( 73 FDA reports)
DEHYDRATION ( 72 FDA reports)
ILL-DEFINED DISORDER ( 71 FDA reports)
MYOCARDIAL INFARCTION ( 71 FDA reports)
PLEURAL EFFUSION ( 71 FDA reports)
URINARY INCONTINENCE ( 71 FDA reports)
DRY MOUTH ( 69 FDA reports)
OSTEOPENIA ( 69 FDA reports)
CHEST DISCOMFORT ( 68 FDA reports)
DECREASED INTEREST ( 68 FDA reports)
DRUG ADMINISTRATION ERROR ( 68 FDA reports)
CONFUSIONAL STATE ( 66 FDA reports)
DECREASED APPETITE ( 66 FDA reports)
SOMNOLENCE ( 66 FDA reports)
SYNCOPE ( 66 FDA reports)
TOOTHACHE ( 66 FDA reports)
URTICARIA ( 65 FDA reports)
CONTUSION ( 64 FDA reports)
HAEMATURIA ( 64 FDA reports)
INFECTION ( 64 FDA reports)
ARTHRITIS ( 63 FDA reports)
NEUROPATHY PERIPHERAL ( 63 FDA reports)
PLATELET COUNT DECREASED ( 63 FDA reports)
DYSGEUSIA ( 62 FDA reports)
FEELING ABNORMAL ( 62 FDA reports)
PANCYTOPENIA ( 62 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 61 FDA reports)
CARDIOMEGALY ( 61 FDA reports)
BALANCE DISORDER ( 60 FDA reports)
MICTURITION URGENCY ( 60 FDA reports)
HEPATIC ENZYME INCREASED ( 57 FDA reports)
HYPOAESTHESIA ( 57 FDA reports)
AMNESIA ( 56 FDA reports)
DEEP VEIN THROMBOSIS ( 56 FDA reports)
MULTIPLE MYELOMA ( 56 FDA reports)
BLOOD URINE PRESENT ( 55 FDA reports)
OSTEOARTHRITIS ( 55 FDA reports)
PROSTATOMEGALY ( 55 FDA reports)
SEXUAL DYSFUNCTION ( 55 FDA reports)
SINUSITIS ( 55 FDA reports)
ATELECTASIS ( 54 FDA reports)
BLOOD CREATININE INCREASED ( 53 FDA reports)
BLOOD PRESSURE DECREASED ( 53 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 53 FDA reports)
HYPERSENSITIVITY ( 53 FDA reports)
HYPOGLYCAEMIA ( 53 FDA reports)
NEUTROPENIA ( 53 FDA reports)
OFF LABEL USE ( 53 FDA reports)
BONE PAIN ( 52 FDA reports)
HEART RATE INCREASED ( 52 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 52 FDA reports)
BREAST MASS ( 51 FDA reports)
CHILLS ( 51 FDA reports)
CONDITION AGGRAVATED ( 50 FDA reports)
HAEMORRHOIDS ( 50 FDA reports)
PALPITATIONS ( 50 FDA reports)
PULMONARY EMBOLISM ( 50 FDA reports)
RHINORRHOEA ( 50 FDA reports)
TOOTH INFECTION ( 50 FDA reports)
ANHEDONIA ( 49 FDA reports)
EJACULATION DISORDER ( 49 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 48 FDA reports)
OSTEONECROSIS ( 48 FDA reports)
ACCIDENTAL EXPOSURE ( 47 FDA reports)
CARDIAC DISORDER ( 47 FDA reports)
CHOLELITHIASIS ( 47 FDA reports)
SINUS DISORDER ( 47 FDA reports)
RECTAL HAEMORRHAGE ( 46 FDA reports)
TREMOR ( 46 FDA reports)
ABDOMINAL DISTENSION ( 45 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 45 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 45 FDA reports)
SWELLING ( 45 FDA reports)
HIATUS HERNIA ( 44 FDA reports)
SKIN LESION ( 44 FDA reports)
GASTROINTESTINAL DISORDER ( 43 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 43 FDA reports)
JOINT SWELLING ( 43 FDA reports)
METASTASES TO BONE ( 43 FDA reports)
OVERDOSE ( 43 FDA reports)
SEPSIS ( 43 FDA reports)
BURNING SENSATION ( 42 FDA reports)
HYPERKALAEMIA ( 42 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 42 FDA reports)
CORONARY ARTERY DISEASE ( 41 FDA reports)
DYSPHONIA ( 41 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 41 FDA reports)
MUSCULOSKELETAL PAIN ( 41 FDA reports)
RENAL FAILURE CHRONIC ( 41 FDA reports)
SPINAL OSTEOARTHRITIS ( 41 FDA reports)
EJACULATION FAILURE ( 40 FDA reports)
EMOTIONAL DISTRESS ( 40 FDA reports)
OSTEOPOROSIS ( 40 FDA reports)
VENTRICULAR TACHYCARDIA ( 40 FDA reports)
VISUAL IMPAIRMENT ( 40 FDA reports)
BONE LESION ( 39 FDA reports)
DENTAL CARIES ( 39 FDA reports)
MEMORY IMPAIRMENT ( 39 FDA reports)
THROAT IRRITATION ( 39 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 38 FDA reports)
FEELING HOT ( 38 FDA reports)
KYPHOSIS ( 38 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 38 FDA reports)
ADVERSE EVENT ( 37 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 37 FDA reports)
CYSTITIS ( 37 FDA reports)
DEMENTIA ( 37 FDA reports)
LOSS OF LIBIDO ( 37 FDA reports)
OROPHARYNGEAL PAIN ( 37 FDA reports)
ARTHROPATHY ( 36 FDA reports)
CANDIDIASIS ( 36 FDA reports)
CELLULITIS ( 36 FDA reports)
CEREBRAL ATROPHY ( 36 FDA reports)
FEBRILE NEUTROPENIA ( 36 FDA reports)
HERPES ZOSTER ( 36 FDA reports)
LUNG INFILTRATION ( 36 FDA reports)
NEPHROLITHIASIS ( 36 FDA reports)
ORTHOSTATIC HYPOTENSION ( 36 FDA reports)
PANCREATITIS ( 36 FDA reports)
RIB FRACTURE ( 36 FDA reports)
SWELLING FACE ( 36 FDA reports)
BLOOD UREA INCREASED ( 35 FDA reports)
GINGIVAL SWELLING ( 35 FDA reports)
HAEMATOCHEZIA ( 35 FDA reports)
HYPONATRAEMIA ( 35 FDA reports)
PROSTATITIS ( 35 FDA reports)
RASH MACULAR ( 35 FDA reports)
DEBRIDEMENT ( 34 FDA reports)
EJECTION FRACTION DECREASED ( 34 FDA reports)
EYE PAIN ( 34 FDA reports)
FLATULENCE ( 34 FDA reports)
PRIMARY SEQUESTRUM ( 34 FDA reports)
TENDERNESS ( 34 FDA reports)
THROMBOSIS ( 34 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 33 FDA reports)
BONE DENSITY DECREASED ( 33 FDA reports)
BREAST CANCER ( 33 FDA reports)
CONVULSION ( 33 FDA reports)
IMPAIRED WORK ABILITY ( 33 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 33 FDA reports)
NECK PAIN ( 33 FDA reports)
ORAL DISCOMFORT ( 33 FDA reports)
VERTIGO ( 33 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 33 FDA reports)
BRONCHITIS ( 32 FDA reports)
PERIODONTITIS ( 32 FDA reports)
SPINAL COMPRESSION FRACTURE ( 32 FDA reports)
TESTICULAR PAIN ( 32 FDA reports)
TINNITUS ( 32 FDA reports)
VISUAL ACUITY REDUCED ( 32 FDA reports)
BLINDNESS ( 31 FDA reports)
HAEMATOCRIT DECREASED ( 31 FDA reports)
INGUINAL HERNIA ( 31 FDA reports)
MIDDLE INSOMNIA ( 31 FDA reports)
OEDEMA ( 31 FDA reports)
ABASIA ( 30 FDA reports)
DRUG EFFECT DECREASED ( 30 FDA reports)
EOSINOPHILIA ( 30 FDA reports)
MEDICATION RESIDUE ( 30 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 30 FDA reports)
RENAL CYST ( 30 FDA reports)
TACHYCARDIA ( 30 FDA reports)
URINARY HESITATION ( 30 FDA reports)
ABSCESS DRAINAGE ( 29 FDA reports)
AGGRESSION ( 29 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 29 FDA reports)
EYE IRRITATION ( 29 FDA reports)
HEART RATE IRREGULAR ( 29 FDA reports)
HYPOTHYROIDISM ( 29 FDA reports)
LIP SWELLING ( 29 FDA reports)
NASOPHARYNGITIS ( 29 FDA reports)
PANCREATITIS ACUTE ( 29 FDA reports)
PENIS DISORDER ( 29 FDA reports)
TOOTH DISORDER ( 29 FDA reports)
DRY SKIN ( 28 FDA reports)
FLANK PAIN ( 28 FDA reports)
HYDRONEPHROSIS ( 28 FDA reports)
LETHARGY ( 28 FDA reports)
MUCOSAL INFLAMMATION ( 28 FDA reports)
MUSCLE ATROPHY ( 28 FDA reports)
NASAL CONGESTION ( 28 FDA reports)
RENAL DISORDER ( 28 FDA reports)
STRESS ( 28 FDA reports)
HAEMATEMESIS ( 27 FDA reports)
MASTICATION DISORDER ( 27 FDA reports)
RESPIRATORY FAILURE ( 27 FDA reports)
UNRESPONSIVE TO STIMULI ( 27 FDA reports)
CHOLECYSTECTOMY ( 26 FDA reports)
DYSPNOEA EXERTIONAL ( 26 FDA reports)
ECZEMA ( 26 FDA reports)
FLUID RETENTION ( 26 FDA reports)
GLOSSODYNIA ( 26 FDA reports)
HAEMOPTYSIS ( 26 FDA reports)
NIGHT SWEATS ( 26 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 26 FDA reports)
ROTATOR CUFF SYNDROME ( 26 FDA reports)
SKIN ULCER ( 26 FDA reports)
SLEEP DISORDER ( 26 FDA reports)
STOMATITIS ( 26 FDA reports)
TOOTH ABSCESS ( 26 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 26 FDA reports)
ANGINA PECTORIS ( 25 FDA reports)
ARRHYTHMIA ( 25 FDA reports)
CARDIOMYOPATHY ( 25 FDA reports)
COMPRESSION FRACTURE ( 25 FDA reports)
DISABILITY ( 25 FDA reports)
FACE OEDEMA ( 25 FDA reports)
GASTRITIS ( 25 FDA reports)
HALLUCINATION ( 25 FDA reports)
HYPERCHOLESTEROLAEMIA ( 25 FDA reports)
ILIAC ARTERY STENOSIS ( 25 FDA reports)
INFLAMMATION ( 25 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 25 FDA reports)
JAW OPERATION ( 25 FDA reports)
OESOPHAGITIS ( 25 FDA reports)
PERIRECTAL ABSCESS ( 25 FDA reports)
SLEEP APNOEA SYNDROME ( 25 FDA reports)
ANGINA UNSTABLE ( 24 FDA reports)
CHROMATURIA ( 24 FDA reports)
EAR PAIN ( 24 FDA reports)
EPISTAXIS ( 24 FDA reports)
GINGIVAL ERYTHEMA ( 24 FDA reports)
HAIR GROWTH ABNORMAL ( 24 FDA reports)
PELVIC PAIN ( 24 FDA reports)
PENILE SIZE REDUCED ( 24 FDA reports)
RASH PRURITIC ( 24 FDA reports)
RETROGRADE EJACULATION ( 24 FDA reports)
SEMEN DISCOLOURATION ( 24 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 23 FDA reports)
BRADYCARDIA ( 23 FDA reports)
CATARACT OPERATION ( 23 FDA reports)
FEELING JITTERY ( 23 FDA reports)
GINGIVAL PAIN ( 23 FDA reports)
GINGIVAL RECESSION ( 23 FDA reports)
HEAD INJURY ( 23 FDA reports)
LIMB DISCOMFORT ( 23 FDA reports)
MENTAL DISORDER ( 23 FDA reports)
METASTASES TO LYMPH NODES ( 23 FDA reports)
NEOPLASM PROGRESSION ( 23 FDA reports)
ANAL FISTULA ( 22 FDA reports)
CARDIAC ARREST ( 22 FDA reports)
MENTAL STATUS CHANGES ( 22 FDA reports)
MITRAL VALVE INCOMPETENCE ( 22 FDA reports)
OSTEOSCLEROSIS ( 22 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 22 FDA reports)
PROSTATE CANCER METASTATIC ( 22 FDA reports)
SICK SINUS SYNDROME ( 22 FDA reports)
SINUS ARRHYTHMIA ( 22 FDA reports)
TOOTH LOSS ( 22 FDA reports)
URINARY TRACT DISORDER ( 22 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 21 FDA reports)
ATRIAL FLUTTER ( 21 FDA reports)
BLADDER CATHETERISATION ( 21 FDA reports)
BONE OPERATION ( 21 FDA reports)
CARDIAC FAILURE ( 21 FDA reports)
DENTAL OPERATION ( 21 FDA reports)
HYPOAESTHESIA ORAL ( 21 FDA reports)
JAUNDICE ( 21 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 21 FDA reports)
LOCAL SWELLING ( 21 FDA reports)
LOOSE TOOTH ( 21 FDA reports)
MEDICATION ERROR ( 21 FDA reports)
PERINEAL PAIN ( 21 FDA reports)
POOR QUALITY SLEEP ( 21 FDA reports)
PROSTATIC DISORDER ( 21 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 21 FDA reports)
TESTICULAR SWELLING ( 21 FDA reports)
WHEEZING ( 21 FDA reports)
ABSCESS JAW ( 20 FDA reports)
ANGIOEDEMA ( 20 FDA reports)
ARTERIOSCLEROSIS ( 20 FDA reports)
BASAL CELL CARCINOMA ( 20 FDA reports)
BLOOD GLUCOSE DECREASED ( 20 FDA reports)
BONE DEBRIDEMENT ( 20 FDA reports)
DENTAL FISTULA ( 20 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 20 FDA reports)
INTERMITTENT CLAUDICATION ( 20 FDA reports)
INTESTINAL HAEMORRHAGE ( 20 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 20 FDA reports)
LIPOMA ( 20 FDA reports)
MACULAR DEGENERATION ( 20 FDA reports)
MENTAL IMPAIRMENT ( 20 FDA reports)
MULTI-ORGAN FAILURE ( 20 FDA reports)
NERVOUSNESS ( 20 FDA reports)
PRESYNCOPE ( 20 FDA reports)
PULMONARY HYPERTENSION ( 20 FDA reports)
QUALITY OF LIFE DECREASED ( 20 FDA reports)
RHINITIS ( 20 FDA reports)
ROSACEA ( 20 FDA reports)
SEBORRHOEIC KERATOSIS ( 20 FDA reports)
SWOLLEN TONGUE ( 20 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 19 FDA reports)
BLADDER OBSTRUCTION ( 19 FDA reports)
CARDIAC PACEMAKER INSERTION ( 19 FDA reports)
DEAFNESS ( 19 FDA reports)
DISEASE PROGRESSION ( 19 FDA reports)
DYSARTHRIA ( 19 FDA reports)
ENCEPHALOPATHY ( 19 FDA reports)
EXTRASYSTOLES ( 19 FDA reports)
FAECES DISCOLOURED ( 19 FDA reports)
GINGIVAL BLEEDING ( 19 FDA reports)
HAEMATOSPERMIA ( 19 FDA reports)
HYPERTROPHY BREAST ( 19 FDA reports)
IRON DEFICIENCY ANAEMIA ( 19 FDA reports)
LEUKOPENIA ( 19 FDA reports)
MUSCLE STRAIN ( 19 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 19 FDA reports)
NEURALGIA ( 19 FDA reports)
OSTEOLYSIS ( 19 FDA reports)
OSTEORADIONECROSIS ( 19 FDA reports)
PEPTIC ULCER ( 19 FDA reports)
RENAL IMPAIRMENT ( 19 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 19 FDA reports)
SINUS BRADYCARDIA ( 19 FDA reports)
SURGERY ( 19 FDA reports)
TOOTH FRACTURE ( 19 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 19 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 19 FDA reports)
BLISTER ( 18 FDA reports)
BLOOD BILIRUBIN INCREASED ( 18 FDA reports)
BODY TEMPERATURE INCREASED ( 18 FDA reports)
DRY EYE ( 18 FDA reports)
EJECTION FRACTION ABNORMAL ( 18 FDA reports)
GENITAL RASH ( 18 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 18 FDA reports)
INCORRECT DOSE ADMINISTERED ( 18 FDA reports)
LUNG NEOPLASM ( 18 FDA reports)
RASH ERYTHEMATOUS ( 18 FDA reports)
SKIN EXFOLIATION ( 18 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 18 FDA reports)
WALKING AID USER ( 18 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 18 FDA reports)
ANAPHYLACTIC REACTION ( 17 FDA reports)
APHASIA ( 17 FDA reports)
ASTHMA ( 17 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 17 FDA reports)
DERMAL CYST ( 17 FDA reports)
DIPLOPIA ( 17 FDA reports)
DYSSTASIA ( 17 FDA reports)
GASTRITIS EROSIVE ( 17 FDA reports)
HYPERLIPIDAEMIA ( 17 FDA reports)
INTRAOCULAR LENS IMPLANT ( 17 FDA reports)
PHYSICAL DISABILITY ( 17 FDA reports)
RESPIRATORY DISORDER ( 17 FDA reports)
SKIN DISORDER ( 17 FDA reports)
TESTICULAR ATROPHY ( 17 FDA reports)
WOUND DEHISCENCE ( 17 FDA reports)
ASCITES ( 16 FDA reports)
BLADDER DISORDER ( 16 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 16 FDA reports)
BONE SWELLING ( 16 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 16 FDA reports)
CHOLECYSTITIS INFECTIVE ( 16 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 16 FDA reports)
DISCOMFORT ( 16 FDA reports)
DYSKINESIA ( 16 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 16 FDA reports)
EMPHYSEMA ( 16 FDA reports)
FISTULA DISCHARGE ( 16 FDA reports)
GASTRIC DISORDER ( 16 FDA reports)
GINGIVAL OEDEMA ( 16 FDA reports)
HYPOXIA ( 16 FDA reports)
ILEUS ( 16 FDA reports)
JAW FRACTURE ( 16 FDA reports)
LEUKOCYTOSIS ( 16 FDA reports)
MUSCLE TIGHTNESS ( 16 FDA reports)
OESOPHAGEAL PAIN ( 16 FDA reports)
PERICARDIAL EFFUSION ( 16 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 16 FDA reports)
PROCTALGIA ( 16 FDA reports)
RHABDOMYOLYSIS ( 16 FDA reports)
SPINAL DISORDER ( 16 FDA reports)
STASIS DERMATITIS ( 16 FDA reports)
TENDON PAIN ( 16 FDA reports)
URINARY TRACT OBSTRUCTION ( 16 FDA reports)
ADVERSE DRUG REACTION ( 15 FDA reports)
BLADDER DISCOMFORT ( 15 FDA reports)
BLOOD POTASSIUM DECREASED ( 15 FDA reports)
DEVICE BREAKAGE ( 15 FDA reports)
ENDODONTIC PROCEDURE ( 15 FDA reports)
FEAR ( 15 FDA reports)
FISTULA ( 15 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 15 FDA reports)
HICCUPS ( 15 FDA reports)
HYPOKALAEMIA ( 15 FDA reports)
IMPETIGO ( 15 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 15 FDA reports)
INCONTINENCE ( 15 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 15 FDA reports)
LEFT ATRIAL DILATATION ( 15 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 15 FDA reports)
METABOLIC ACIDOSIS ( 15 FDA reports)
NO THERAPEUTIC RESPONSE ( 15 FDA reports)
ONYCHOMYCOSIS ( 15 FDA reports)
PLASMACYTOMA ( 15 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 15 FDA reports)
PROSTATE TENDERNESS ( 15 FDA reports)
PROTHROMBIN TIME PROLONGED ( 15 FDA reports)
PULMONARY FIBROSIS ( 15 FDA reports)
PULPITIS DENTAL ( 15 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 15 FDA reports)
SKIN ATROPHY ( 15 FDA reports)
SKIN DISCOLOURATION ( 15 FDA reports)
SPINAL HAEMANGIOMA ( 15 FDA reports)
STEM CELL TRANSPLANT ( 15 FDA reports)
STENT PLACEMENT ( 15 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 15 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 15 FDA reports)
VENOOCCLUSIVE DISEASE ( 15 FDA reports)
VENOUS THROMBOSIS ( 15 FDA reports)
VISUAL DISTURBANCE ( 15 FDA reports)
WOUND ( 15 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 14 FDA reports)
AORTIC ANEURYSM ( 14 FDA reports)
APNOEA ( 14 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 14 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 14 FDA reports)
BLOOD CREATININE DECREASED ( 14 FDA reports)
BREAKTHROUGH PAIN ( 14 FDA reports)
CLAVICLE FRACTURE ( 14 FDA reports)
COLD SWEAT ( 14 FDA reports)
COMA ( 14 FDA reports)
DECREASED ACTIVITY ( 14 FDA reports)
DEVICE MALFUNCTION ( 14 FDA reports)
DIVERTICULITIS ( 14 FDA reports)
EAR DISCOMFORT ( 14 FDA reports)
EPIDIDYMITIS ( 14 FDA reports)
HALLUCINATION, VISUAL ( 14 FDA reports)
HIDRADENITIS ( 14 FDA reports)
INGUINAL HERNIA REPAIR ( 14 FDA reports)
INJECTION SITE PAIN ( 14 FDA reports)
INTENTIONAL DRUG MISUSE ( 14 FDA reports)
LUNG CONSOLIDATION ( 14 FDA reports)
LUNG HYPERINFLATION ( 14 FDA reports)
LUNG NEOPLASM MALIGNANT ( 14 FDA reports)
METASTASES TO SPINE ( 14 FDA reports)
MICTURITION DISORDER ( 14 FDA reports)
PRODUCTIVE COUGH ( 14 FDA reports)
PROSTATIC OBSTRUCTION ( 14 FDA reports)
PULMONARY CONGESTION ( 14 FDA reports)
RASH GENERALISED ( 14 FDA reports)
RESTLESSNESS ( 14 FDA reports)
SKIN BURNING SENSATION ( 14 FDA reports)
SPUTUM DISCOLOURED ( 14 FDA reports)
SUICIDAL IDEATION ( 14 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 13 FDA reports)
BACTERAEMIA ( 13 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 13 FDA reports)
BREAST CANCER MALE ( 13 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 13 FDA reports)
CARDIAC MURMUR ( 13 FDA reports)
CERVICAL CORD COMPRESSION ( 13 FDA reports)
COGNITIVE DISORDER ( 13 FDA reports)
CORONARY ARTERY OCCLUSION ( 13 FDA reports)
CROHN'S DISEASE ( 13 FDA reports)
DARK CIRCLES UNDER EYES ( 13 FDA reports)
DENTAL PROSTHESIS USER ( 13 FDA reports)
DERMATITIS EXFOLIATIVE ( 13 FDA reports)
DISTURBANCE IN ATTENTION ( 13 FDA reports)
ERUCTATION ( 13 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 13 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 13 FDA reports)
GASTRIC ULCER ( 13 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 13 FDA reports)
INFLUENZA LIKE ILLNESS ( 13 FDA reports)
INTERSTITIAL LUNG DISEASE ( 13 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 13 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 13 FDA reports)
MALNUTRITION ( 13 FDA reports)
METASTASES TO REPRODUCTIVE ORGAN ( 13 FDA reports)
MUCOSAL ULCERATION ( 13 FDA reports)
MYASTHENIA GRAVIS ( 13 FDA reports)
NEUTROPENIC SEPSIS ( 13 FDA reports)
OESOPHAGEAL STENOSIS ( 13 FDA reports)
PANCREATIC CARCINOMA ( 13 FDA reports)
PATELLA FRACTURE ( 13 FDA reports)
PEYRONIE'S DISEASE ( 13 FDA reports)
PURULENCE ( 13 FDA reports)
RADICULOPATHY ( 13 FDA reports)
RESIDUAL URINE ( 13 FDA reports)
SENSITIVITY OF TEETH ( 13 FDA reports)
SEPTIC SHOCK ( 13 FDA reports)
SKIN PAPILLOMA ( 13 FDA reports)
SPINAL FUSION ACQUIRED ( 13 FDA reports)
SUBCUTANEOUS NODULE ( 13 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 13 FDA reports)
UPPER LIMB FRACTURE ( 13 FDA reports)
URINE ODOUR ABNORMAL ( 13 FDA reports)
UROSEPSIS ( 13 FDA reports)
ABDOMINAL MASS ( 12 FDA reports)
ABDOMINAL PAIN LOWER ( 12 FDA reports)
ABNORMAL DREAMS ( 12 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 12 FDA reports)
AGEUSIA ( 12 FDA reports)
ANOREXIA ( 12 FDA reports)
AORTIC CALCIFICATION ( 12 FDA reports)
BALANITIS ( 12 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 12 FDA reports)
BLADDER DIVERTICULUM ( 12 FDA reports)
BONE LOSS ( 12 FDA reports)
BRONCHIAL SECRETION RETENTION ( 12 FDA reports)
CARDIO-RESPIRATORY ARREST ( 12 FDA reports)
CHONDROMALACIA ( 12 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 12 FDA reports)
CONNECTIVE TISSUE DISORDER ( 12 FDA reports)
DENTAL PULP DISORDER ( 12 FDA reports)
DIABETES MELLITUS ( 12 FDA reports)
DRUG DISPENSING ERROR ( 12 FDA reports)
DRUG DOSE OMISSION ( 12 FDA reports)
DRUG HYPERSENSITIVITY ( 12 FDA reports)
EAR INFECTION ( 12 FDA reports)
ECONOMIC PROBLEM ( 12 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 12 FDA reports)
ERYTHEMA NODOSUM ( 12 FDA reports)
EXOSTOSIS ( 12 FDA reports)
FISTULA REPAIR ( 12 FDA reports)
HAEMATOMA ( 12 FDA reports)
IRRITABILITY ( 12 FDA reports)
IRRITABLE BOWEL SYNDROME ( 12 FDA reports)
LUDWIG ANGINA ( 12 FDA reports)
LYMPHOMA ( 12 FDA reports)
MULTI-ORGAN DISORDER ( 12 FDA reports)
MUSCLE DISORDER ( 12 FDA reports)
MUSCLE TWITCHING ( 12 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 12 FDA reports)
ONYCHALGIA ( 12 FDA reports)
PHARYNGITIS ( 12 FDA reports)
PNEUMONIA VIRAL ( 12 FDA reports)
RASH MACULO-PAPULAR ( 12 FDA reports)
REGURGITATION ( 12 FDA reports)
RETCHING ( 12 FDA reports)
SCOLIOSIS ( 12 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 12 FDA reports)
SUDDEN DEATH ( 12 FDA reports)
UNEVALUABLE EVENT ( 12 FDA reports)
ABNORMAL BEHAVIOUR ( 11 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 11 FDA reports)
AGITATION ( 11 FDA reports)
ALVEOLOPLASTY ( 11 FDA reports)
BLOOD CALCIUM DECREASED ( 11 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 11 FDA reports)
BONE MARROW FAILURE ( 11 FDA reports)
BREAST INDURATION ( 11 FDA reports)
BRONCHITIS CHRONIC ( 11 FDA reports)
CIRCULATORY COLLAPSE ( 11 FDA reports)
DELIRIUM ( 11 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 11 FDA reports)
DRUG TOXICITY ( 11 FDA reports)
EPILEPSY ( 11 FDA reports)
EYE DISORDER ( 11 FDA reports)
EYE SWELLING ( 11 FDA reports)
GLAUCOMA ( 11 FDA reports)
HEARING IMPAIRED ( 11 FDA reports)
HYPERKERATOSIS ( 11 FDA reports)
HYPERPLASIA ( 11 FDA reports)
HYPERSOMNIA ( 11 FDA reports)
JAW CYST ( 11 FDA reports)
LACRIMATION INCREASED ( 11 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 11 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 11 FDA reports)
MENISCUS LESION ( 11 FDA reports)
METASTASIS ( 11 FDA reports)
MOOD ALTERED ( 11 FDA reports)
NAIL DISORDER ( 11 FDA reports)
NEUTROPHIL COUNT DECREASED ( 11 FDA reports)
NIGHTMARE ( 11 FDA reports)
OCULAR HYPERAEMIA ( 11 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 11 FDA reports)
PNEUMONIA BACTERIAL ( 11 FDA reports)
PURPURA ( 11 FDA reports)
RESPIRATORY DISTRESS ( 11 FDA reports)
SPONDYLOLYSIS ( 11 FDA reports)
TENDONITIS ( 11 FDA reports)
URETHRAL STENOSIS ( 11 FDA reports)
VITAMIN D DECREASED ( 11 FDA reports)
APHONIA ( 10 FDA reports)
BLOOD POTASSIUM INCREASED ( 10 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 10 FDA reports)
BLOOD SODIUM DECREASED ( 10 FDA reports)
BLOOD TEST ABNORMAL ( 10 FDA reports)
CHOKING ( 10 FDA reports)
CYANOSIS ( 10 FDA reports)
DEFORMITY ( 10 FDA reports)
DISORIENTATION ( 10 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 10 FDA reports)
EXPOSED BONE IN JAW ( 10 FDA reports)
GASTRIC POLYPS ( 10 FDA reports)
GINGIVAL DISORDER ( 10 FDA reports)
HEPATIC CYST ( 10 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 10 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 10 FDA reports)
ILEITIS ( 10 FDA reports)
INJECTION SITE ERYTHEMA ( 10 FDA reports)
KERATOACANTHOMA ( 10 FDA reports)
LIGAMENT RUPTURE ( 10 FDA reports)
LUMBAR SPINAL STENOSIS ( 10 FDA reports)
MACULOPATHY ( 10 FDA reports)
OBESITY ( 10 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 10 FDA reports)
OPEN REDUCTION OF FRACTURE ( 10 FDA reports)
ORCHITIS ( 10 FDA reports)
PARKINSON'S DISEASE ( 10 FDA reports)
PENILE PAIN ( 10 FDA reports)
PERIPHERAL COLDNESS ( 10 FDA reports)
PHLEBITIS ( 10 FDA reports)
PURULENT DISCHARGE ( 10 FDA reports)
SOFT TISSUE INFLAMMATION ( 10 FDA reports)
SPINAL COLUMN STENOSIS ( 10 FDA reports)
SPINAL LAMINECTOMY ( 10 FDA reports)
STOMACH DISCOMFORT ( 10 FDA reports)
THIRST ( 10 FDA reports)
TOOTH IMPACTED ( 10 FDA reports)
URINE OUTPUT DECREASED ( 10 FDA reports)
VENTRICULAR HYPERTROPHY ( 10 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 9 FDA reports)
ABSCESS ( 9 FDA reports)
ASTIGMATISM ( 9 FDA reports)
BONE MARROW TRANSPLANT ( 9 FDA reports)
BUNDLE BRANCH BLOCK ( 9 FDA reports)
CARDIAC ABLATION ( 9 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 9 FDA reports)
CEREBELLAR INFARCTION ( 9 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 9 FDA reports)
DERMATITIS ( 9 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 9 FDA reports)
FAECAL INCONTINENCE ( 9 FDA reports)
GENERALISED ERYTHEMA ( 9 FDA reports)
GINGIVAL ULCERATION ( 9 FDA reports)
GOUT ( 9 FDA reports)
HAEMODYNAMIC INSTABILITY ( 9 FDA reports)
HAEMORRHOID OPERATION ( 9 FDA reports)
HEART RATE DECREASED ( 9 FDA reports)
HEPATIC FAILURE ( 9 FDA reports)
HEPATITIS ( 9 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 9 FDA reports)
HYPOPHAGIA ( 9 FDA reports)
ILEUS PARALYTIC ( 9 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 9 FDA reports)
KIDNEY INFECTION ( 9 FDA reports)
LASER THERAPY ( 9 FDA reports)
MYELOMA RECURRENCE ( 9 FDA reports)
NONSPECIFIC REACTION ( 9 FDA reports)
OXYGEN SUPPLEMENTATION ( 9 FDA reports)
PAIN OF SKIN ( 9 FDA reports)
PENILE HAEMORRHAGE ( 9 FDA reports)
PERIODONTAL INFECTION ( 9 FDA reports)
PHARYNGEAL OEDEMA ( 9 FDA reports)
PLEURAL FIBROSIS ( 9 FDA reports)
POSTERIOR CAPSULOTOMY ( 9 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 9 FDA reports)
PROSTATIC HAEMORRHAGE ( 9 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 9 FDA reports)
RENAL MASS ( 9 FDA reports)
SPERM COUNT DECREASED ( 9 FDA reports)
SPINAL FUSION SURGERY ( 9 FDA reports)
TRANSAMINASES INCREASED ( 9 FDA reports)
VENTRICULAR FIBRILLATION ( 9 FDA reports)
VERTEBROPLASTY ( 9 FDA reports)
VITAMIN B12 DEFICIENCY ( 9 FDA reports)
WOUND DRAINAGE ( 9 FDA reports)
ACCIDENTAL OVERDOSE ( 8 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 8 FDA reports)
ADRENAL INSUFFICIENCY ( 8 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 8 FDA reports)
ANAEMIA MACROCYTIC ( 8 FDA reports)
ANGIONEUROTIC OEDEMA ( 8 FDA reports)
ANGIOPATHY ( 8 FDA reports)
ANORECTAL DISCOMFORT ( 8 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 8 FDA reports)
B-CELL LYMPHOMA ( 8 FDA reports)
BABESIOSIS ( 8 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 8 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 8 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 8 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 8 FDA reports)
BOVINE TUBERCULOSIS ( 8 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 8 FDA reports)
BREAST DISCOMFORT ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 8 FDA reports)
CARDIOVASCULAR DISORDER ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 8 FDA reports)
CEREBRAL INFARCTION ( 8 FDA reports)
COLITIS MICROSCOPIC ( 8 FDA reports)
COLITIS ULCERATIVE ( 8 FDA reports)
CYST ( 8 FDA reports)
EOSINOPHIL COUNT INCREASED ( 8 FDA reports)
GASTRIC HAEMORRHAGE ( 8 FDA reports)
GROIN PAIN ( 8 FDA reports)
HEPATIC STEATOSIS ( 8 FDA reports)
HYPOACUSIS ( 8 FDA reports)
INITIAL INSOMNIA ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 8 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 8 FDA reports)
JAW DISORDER ( 8 FDA reports)
JOINT INJURY ( 8 FDA reports)
LIPOMA EXCISION ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
MONOPLEGIA ( 8 FDA reports)
MOVEMENT DISORDER ( 8 FDA reports)
MYELODYSPLASTIC SYNDROME ( 8 FDA reports)
NEPHRITIS INTERSTITIAL ( 8 FDA reports)
NIPPLE DISORDER ( 8 FDA reports)
ORAL INFECTION ( 8 FDA reports)
OXYGEN SATURATION DECREASED ( 8 FDA reports)
PITTING OEDEMA ( 8 FDA reports)
POLYP ( 8 FDA reports)
PROSTATECTOMY ( 8 FDA reports)
PROSTATIC PAIN ( 8 FDA reports)
PRURITUS GENERALISED ( 8 FDA reports)
PULMONARY OEDEMA ( 8 FDA reports)
RECTAL FISTULA REPAIR ( 8 FDA reports)
ROAD TRAFFIC ACCIDENT ( 8 FDA reports)
SCAR ( 8 FDA reports)
SEDATION ( 8 FDA reports)
SENSORY DISTURBANCE ( 8 FDA reports)
SKIN IRRITATION ( 8 FDA reports)
SKIN NEOPLASM EXCISION ( 8 FDA reports)
SPEECH DISORDER ( 8 FDA reports)
TRISMUS ( 8 FDA reports)
URINE OUTPUT INCREASED ( 8 FDA reports)
ANGER ( 7 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 7 FDA reports)
ANURIA ( 7 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 7 FDA reports)
AORTIC STENOSIS ( 7 FDA reports)
AORTIC VALVE INCOMPETENCE ( 7 FDA reports)
APHTHOUS STOMATITIS ( 7 FDA reports)
BLADDER CANCER ( 7 FDA reports)
BLEPHARITIS ( 7 FDA reports)
BODY DYSMORPHIC DISORDER ( 7 FDA reports)
BRAIN OEDEMA ( 7 FDA reports)
CALCULUS URINARY ( 7 FDA reports)
CEREBRAL HAEMORRHAGE ( 7 FDA reports)
CERUMEN IMPACTION ( 7 FDA reports)
CHRONIC SINUSITIS ( 7 FDA reports)
CORONARY ARTERY BYPASS ( 7 FDA reports)
DENTURE WEARER ( 7 FDA reports)
DIALYSIS ( 7 FDA reports)
DIZZINESS POSTURAL ( 7 FDA reports)
DYSPLASIA ( 7 FDA reports)
ESCHERICHIA INFECTION ( 7 FDA reports)
EYE HAEMORRHAGE ( 7 FDA reports)
EYELID OEDEMA ( 7 FDA reports)
FEELING COLD ( 7 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 7 FDA reports)
FOOT DEFORMITY ( 7 FDA reports)
GINGIVAL INFECTION ( 7 FDA reports)
GINGIVITIS ( 7 FDA reports)
HERNIA REPAIR ( 7 FDA reports)
HYPOCALCAEMIA ( 7 FDA reports)
HYPOGONADISM ( 7 FDA reports)
HYPOTRICHOSIS ( 7 FDA reports)
INFLUENZA ( 7 FDA reports)
ISCHAEMIA ( 7 FDA reports)
LIMB INJURY ( 7 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 7 FDA reports)
MELAENA ( 7 FDA reports)
METAPLASIA ( 7 FDA reports)
MULTIPLE INJURIES ( 7 FDA reports)
MYOPERICARDITIS ( 7 FDA reports)
NO ADVERSE EVENT ( 7 FDA reports)
ODYNOPHAGIA ( 7 FDA reports)
ORAL CANDIDIASIS ( 7 FDA reports)
ORAL CAVITY FISTULA ( 7 FDA reports)
ORAL DISORDER ( 7 FDA reports)
ORGASM ABNORMAL ( 7 FDA reports)
PALLOR ( 7 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 7 FDA reports)
PHOTOPSIA ( 7 FDA reports)
POLYURIA ( 7 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 7 FDA reports)
POST PROCEDURAL INFECTION ( 7 FDA reports)
PYURIA ( 7 FDA reports)
RASH PAPULAR ( 7 FDA reports)
SCROTAL SWELLING ( 7 FDA reports)
SENSATION OF FOREIGN BODY ( 7 FDA reports)
SENSORY LOSS ( 7 FDA reports)
SEQUESTRECTOMY ( 7 FDA reports)
SKIN LACERATION ( 7 FDA reports)
SKIN REACTION ( 7 FDA reports)
STEVENS-JOHNSON SYNDROME ( 7 FDA reports)
SUBDURAL HAEMATOMA ( 7 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 7 FDA reports)
TONGUE HAEMORRHAGE ( 7 FDA reports)
TOOTH DEPOSIT ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
WOUND DEBRIDEMENT ( 7 FDA reports)
ABNORMAL FAECES ( 6 FDA reports)
ABSCESS MANAGEMENT ( 6 FDA reports)
ACIDOSIS ( 6 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
ADENOCARCINOMA ( 6 FDA reports)
ANORGASMIA ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 6 FDA reports)
BACTERIAL INFECTION ( 6 FDA reports)
CATARACT NUCLEAR ( 6 FDA reports)
CATHETER PLACEMENT ( 6 FDA reports)
COMPLETED SUICIDE ( 6 FDA reports)
CONJUNCTIVAL ABRASION ( 6 FDA reports)
DEFAECATION URGENCY ( 6 FDA reports)
DEPRESSED MOOD ( 6 FDA reports)
DYSLIPIDAEMIA ( 6 FDA reports)
EAR IRRIGATION ( 6 FDA reports)
ECCHYMOSIS ( 6 FDA reports)
ENCEPHALOMALACIA ( 6 FDA reports)
EYELID INFECTION ( 6 FDA reports)
FAILURE TO THRIVE ( 6 FDA reports)
FREE PROSTATE-SPECIFIC ANTIGEN DECREASED ( 6 FDA reports)
GALLBLADDER DISORDER ( 6 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 6 FDA reports)
GENERALISED OEDEMA ( 6 FDA reports)
GENITAL DISCOMFORT ( 6 FDA reports)
GLIOSIS ( 6 FDA reports)
HAEMORRHAGIC ANAEMIA ( 6 FDA reports)
HAIR COLOUR CHANGES ( 6 FDA reports)
HEAT EXHAUSTION ( 6 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 6 FDA reports)
HEPATOCELLULAR INJURY ( 6 FDA reports)
HYPERAESTHESIA ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
HYPERREFLEXIA ( 6 FDA reports)
HYPERTHYROIDISM ( 6 FDA reports)
HYPOGEUSIA ( 6 FDA reports)
HYPOREFLEXIA ( 6 FDA reports)
INCREASED APPETITE ( 6 FDA reports)
INHALATION THERAPY ( 6 FDA reports)
INJECTION SITE HAEMATOMA ( 6 FDA reports)
INJECTION SITE HAEMORRHAGE ( 6 FDA reports)
ISCHAEMIC STROKE ( 6 FDA reports)
JOINT ARTHROPLASTY ( 6 FDA reports)
JOINT STIFFNESS ( 6 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 6 FDA reports)
LABORATORY TEST ABNORMAL ( 6 FDA reports)
LEUKAEMIA ( 6 FDA reports)
LIPIDS INCREASED ( 6 FDA reports)
LOCALISED INFECTION ( 6 FDA reports)
MACULAR SCAR ( 6 FDA reports)
MENINGITIS ( 6 FDA reports)
METASTATIC NEOPLASM ( 6 FDA reports)
MOBILITY DECREASED ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
NASAL ODOUR ( 6 FDA reports)
NEOPLASM PROSTATE ( 6 FDA reports)
NON-CARDIAC CHEST PAIN ( 6 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 6 FDA reports)
OESOPHAGEAL DISCOMFORT ( 6 FDA reports)
PAINFUL ERECTION ( 6 FDA reports)
PARAPARESIS ( 6 FDA reports)
PAROTID GLAND ENLARGEMENT ( 6 FDA reports)
PERIODONTAL DISEASE ( 6 FDA reports)
PLEURISY ( 6 FDA reports)
POLYNEUROPATHY ( 6 FDA reports)
POLYPECTOMY ( 6 FDA reports)
POST PROCEDURAL COMPLICATION ( 6 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 6 FDA reports)
PROTEIN TOTAL DECREASED ( 6 FDA reports)
PSORIASIS ( 6 FDA reports)
PULMONARY THROMBOSIS ( 6 FDA reports)
SALIVARY GLAND PAIN ( 6 FDA reports)
SENSATION OF HEAVINESS ( 6 FDA reports)
SKIN HAEMORRHAGE ( 6 FDA reports)
SKIN INFECTION ( 6 FDA reports)
SPONDYLOPATHY TRAUMATIC ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
SUBMANDIBULAR MASS ( 6 FDA reports)
SUBRETINAL FIBROSIS ( 6 FDA reports)
SUNBURN ( 6 FDA reports)
TENDON GRAFT ( 6 FDA reports)
TESTICULAR DISORDER ( 6 FDA reports)
THERMAL BURN ( 6 FDA reports)
TONGUE ULCERATION ( 6 FDA reports)
URINARY BLADDER POLYP ( 6 FDA reports)
URINE ANALYSIS ABNORMAL ( 6 FDA reports)
VASCULAR CALCIFICATION ( 6 FDA reports)
VASCULAR PURPURA ( 6 FDA reports)
VITREOUS DEGENERATION ( 6 FDA reports)
WRONG DRUG ADMINISTERED ( 6 FDA reports)
ACNE ( 5 FDA reports)
ANKLE FRACTURE ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 5 FDA reports)
AORTIC VALVE SCLEROSIS ( 5 FDA reports)
ASTHENOPIA ( 5 FDA reports)
BLOOD ALBUMIN DECREASED ( 5 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
BLOOD PROLACTIN INCREASED ( 5 FDA reports)
BODY TEMPERATURE DECREASED ( 5 FDA reports)
BONE GRAFT ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 5 FDA reports)
CEREBRAL ISCHAEMIA ( 5 FDA reports)
COAGULOPATHY ( 5 FDA reports)
COORDINATION ABNORMAL ( 5 FDA reports)
CREPITATIONS ( 5 FDA reports)
CULTURE URINE POSITIVE ( 5 FDA reports)
CYTOLYTIC HEPATITIS ( 5 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 5 FDA reports)
DEMENTIA WITH LEWY BODIES ( 5 FDA reports)
DERMATITIS ALLERGIC ( 5 FDA reports)
DRY THROAT ( 5 FDA reports)
DYSPAREUNIA ( 5 FDA reports)
EATING DISORDER ( 5 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 5 FDA reports)
EMOTIONAL DISORDER ( 5 FDA reports)
ENTEROCOLITIS ( 5 FDA reports)
EYE INFECTION ( 5 FDA reports)
FAECES HARD ( 5 FDA reports)
FLUID OVERLOAD ( 5 FDA reports)
GASTROINTESTINAL PAIN ( 5 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 5 FDA reports)
HAEMOLYSIS ( 5 FDA reports)
HAEMORRHAGE URINARY TRACT ( 5 FDA reports)
HEPATIC ENZYME ABNORMAL ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
HERNIA ( 5 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
HORMONE THERAPY ( 5 FDA reports)
HOSPITALISATION ( 5 FDA reports)
HYPERCOAGULATION ( 5 FDA reports)
HYPOVOLAEMIA ( 5 FDA reports)
IMMOBILE ( 5 FDA reports)
IMPAIRED DRIVING ABILITY ( 5 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 5 FDA reports)
INTENTIONAL OVERDOSE ( 5 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 5 FDA reports)
JOINT DISLOCATION ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
MALIGNANT TUMOUR EXCISION ( 5 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 5 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 5 FDA reports)
MONOCYTE COUNT INCREASED ( 5 FDA reports)
MOUTH ULCERATION ( 5 FDA reports)
MUSCLE ENZYME INCREASED ( 5 FDA reports)
MUSCLE FATIGUE ( 5 FDA reports)
MUSCLE SPASTICITY ( 5 FDA reports)
MYOCLONUS ( 5 FDA reports)
NERVOUS SYSTEM DISORDER ( 5 FDA reports)
NEUROPATHY ( 5 FDA reports)
NIGHT BLINDNESS ( 5 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 5 FDA reports)
PANIC ATTACK ( 5 FDA reports)
PETECHIAE ( 5 FDA reports)
PHIMOSIS ( 5 FDA reports)
PHOTOSENSITIVITY REACTION ( 5 FDA reports)
PORTAL VEIN THROMBOSIS ( 5 FDA reports)
POSTNASAL DRIP ( 5 FDA reports)
PROSTATE INDURATION ( 5 FDA reports)
RADICAL MASTECTOMY ( 5 FDA reports)
RALES ( 5 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 5 FDA reports)
RHONCHI ( 5 FDA reports)
SECRETION DISCHARGE ( 5 FDA reports)
SERUM FERRITIN INCREASED ( 5 FDA reports)
SHOCK ( 5 FDA reports)
SKIN ODOUR ABNORMAL ( 5 FDA reports)
SLUGGISHNESS ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
SYNOVITIS ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
TONGUE DISORDER ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 5 FDA reports)
TUMOUR MARKER INCREASED ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
URETHRAL DISCHARGE ( 5 FDA reports)
URETHRAL OBSTRUCTION ( 5 FDA reports)
URINE KETONE BODY PRESENT ( 5 FDA reports)
VASECTOMY ( 5 FDA reports)
WITHDRAWAL SYNDROME ( 5 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 4 FDA reports)
ACUTE PRERENAL FAILURE ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
ADENOCARCINOMA PANCREAS ( 4 FDA reports)
ADVERSE REACTION ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
ANAL PRURITUS ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 4 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 4 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 4 FDA reports)
ARTHRITIS BACTERIAL ( 4 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
ATROPHY ( 4 FDA reports)
BACK DISORDER ( 4 FDA reports)
BARRETT'S OESOPHAGUS ( 4 FDA reports)
BIOPSY BONE ( 4 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BREAST CYST ( 4 FDA reports)
BREAST NEOPLASM ( 4 FDA reports)
BREATH SOUNDS ABNORMAL ( 4 FDA reports)
BURSITIS ( 4 FDA reports)
CALCULUS URETERIC ( 4 FDA reports)
CARBON DIOXIDE DECREASED ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 4 FDA reports)
CHEST X-RAY ABNORMAL ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
CLONUS ( 4 FDA reports)
COLITIS ( 4 FDA reports)
COLITIS ISCHAEMIC ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
CONGENITAL KNEE DEFORMITY ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
CORONARY ARTERY STENOSIS ( 4 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 4 FDA reports)
CRYING ( 4 FDA reports)
DANDRUFF ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
DRUG ABUSE ( 4 FDA reports)
DRUG DEPENDENCE ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
ENTEROCOCCAL SEPSIS ( 4 FDA reports)
FIBRIN D DIMER INCREASED ( 4 FDA reports)
FLOPPY IRIS SYNDROME ( 4 FDA reports)
FRUSTRATION ( 4 FDA reports)
GASTROENTERITIS VIRAL ( 4 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
GUILLAIN-BARRE SYNDROME ( 4 FDA reports)
HAEMOLYTIC ANAEMIA ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HAIR TEXTURE ABNORMAL ( 4 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HODGKIN'S DISEASE ( 4 FDA reports)
HYDROCEPHALUS ( 4 FDA reports)
HYPERCREATININAEMIA ( 4 FDA reports)
HYPERPROTEINAEMIA ( 4 FDA reports)
HYPERTONIC BLADDER ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
HYPOTONIA ( 4 FDA reports)
IMPAIRED SELF-CARE ( 4 FDA reports)
INCORRECT STORAGE OF DRUG ( 4 FDA reports)
INJECTION SITE BRUISING ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
LIBIDO INCREASED ( 4 FDA reports)
LIP OEDEMA ( 4 FDA reports)
LOBAR PNEUMONIA ( 4 FDA reports)
LUNG CANCER METASTATIC ( 4 FDA reports)
LUNG INJURY ( 4 FDA reports)
MALIGNANT MELANOMA ( 4 FDA reports)
METASTASES TO SKIN ( 4 FDA reports)
MICTURITION FREQUENCY DECREASED ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MITRAL VALVE PROLAPSE ( 4 FDA reports)
MUCOUS STOOLS ( 4 FDA reports)
MYOPIA ( 4 FDA reports)
NASAL DRYNESS ( 4 FDA reports)
NEEDLE ISSUE ( 4 FDA reports)
NEOPLASM ( 4 FDA reports)
NERVE COMPRESSION ( 4 FDA reports)
NIPPLE SWELLING ( 4 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 4 FDA reports)
NUCHAL RIGIDITY ( 4 FDA reports)
OPISTHOTONUS ( 4 FDA reports)
OROPHARYNGEAL SPASM ( 4 FDA reports)
OVERWEIGHT ( 4 FDA reports)
PAINFUL RESPIRATION ( 4 FDA reports)
PANCREATIC CYST ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PAROSMIA ( 4 FDA reports)
PENIS DEVIATION ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
PLATELET COUNT INCREASED ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
PROCEDURAL COMPLICATION ( 4 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 4 FDA reports)
PROSTATE INFECTION ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
RECTAL DISCHARGE ( 4 FDA reports)
RENAL PAIN ( 4 FDA reports)
RENAL TUBULAR NECROSIS ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 4 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 4 FDA reports)
SALIVARY HYPERSECRETION ( 4 FDA reports)
SCROTAL DISORDER ( 4 FDA reports)
SINUS CONGESTION ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
SKIN WRINKLING ( 4 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 4 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 4 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
TALIPES ( 4 FDA reports)
THERAPEUTIC PROCEDURE ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
THINKING ABNORMAL ( 4 FDA reports)
THYROID DISORDER ( 4 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 4 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 4 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 4 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 4 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 4 FDA reports)
VENOUS INSUFFICIENCY ( 4 FDA reports)
VENTRICULAR DYSFUNCTION ( 4 FDA reports)
VESTIBULAR NEURONITIS ( 4 FDA reports)
WOUND CLOSURE ( 4 FDA reports)
ABDOMINAL HERNIA ( 3 FDA reports)
ABDOMINAL SYMPTOM ( 3 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACTINOMYCOSIS ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 3 FDA reports)
AMYLOIDOSIS ( 3 FDA reports)
ANGIOGRAM ABNORMAL ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 3 FDA reports)
AXILLARY PAIN ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BACTERIURIA ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BENIGN GASTRIC NEOPLASM ( 3 FDA reports)
BIPOLAR I DISORDER ( 3 FDA reports)
BLADDER NECK OBSTRUCTION ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD COUNT ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD DISORDER ( 3 FDA reports)
BLOOD IRON DECREASED ( 3 FDA reports)
BLOOD IRON INCREASED ( 3 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 3 FDA reports)
BLOOD TESTOSTERONE FREE DECREASED ( 3 FDA reports)
BODY HEIGHT DECREASED ( 3 FDA reports)
BONE SCAN ABNORMAL ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
BREAST HYPERPLASIA ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
CALCULUS BLADDER ( 3 FDA reports)
CAPILLARY DISORDER ( 3 FDA reports)
CARDIAC OPERATION ( 3 FDA reports)
CARPAL TUNNEL SYNDROME ( 3 FDA reports)
CEREBROVASCULAR SPASM ( 3 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
COCCYDYNIA ( 3 FDA reports)
COELIAC ARTERY STENOSIS ( 3 FDA reports)
CONCUSSION ( 3 FDA reports)
CREATININE RENAL CLEARANCE ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CRYPTORCHISM ( 3 FDA reports)
CSF PROTEIN INCREASED ( 3 FDA reports)
CUSHINGOID ( 3 FDA reports)
CUTIS LAXA ( 3 FDA reports)
DEAFNESS NEUROSENSORY ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DERMATITIS CONTACT ( 3 FDA reports)
DIARRHOEA INFECTIOUS ( 3 FDA reports)
DIHYDROTESTOSTERONE INCREASED ( 3 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 3 FDA reports)
DIVERTICULUM INTESTINAL ( 3 FDA reports)
DIZZINESS EXERTIONAL ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
DRUG LEVEL DECREASED ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
ENURESIS ( 3 FDA reports)
ESSENTIAL HYPERTENSION ( 3 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 3 FDA reports)
EXPIRED DRUG ADMINISTERED ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
EYE DISCHARGE ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
FACIAL BONES FRACTURE ( 3 FDA reports)
FAMILY STRESS ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FIBROSIS ( 3 FDA reports)
FOOD INTERACTION ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
FULL BLOOD COUNT DECREASED ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GENITAL BURNING SENSATION ( 3 FDA reports)
GENITAL DISORDER MALE ( 3 FDA reports)
GENITAL PAIN ( 3 FDA reports)
HAIR DISORDER ( 3 FDA reports)
HEART VALVE INCOMPETENCE ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HYPERTENSIVE CRISIS ( 3 FDA reports)
HYPOAESTHESIA FACIAL ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
HYPOSPADIAS ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INFARCTION ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INTENSIVE CARE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 3 FDA reports)
INTESTINAL DILATATION ( 3 FDA reports)
IRIS DISORDER ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
LABILE HYPERTENSION ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LENTIGO ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LIBIDO DISORDER ( 3 FDA reports)
LIGAMENT LAXITY ( 3 FDA reports)
LIVE BIRTH ( 3 FDA reports)
LIVER INJURY ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
LYMPHADENECTOMY ( 3 FDA reports)
MALE SEXUAL DYSFUNCTION ( 3 FDA reports)
MALIGNANT MELANOMA IN SITU ( 3 FDA reports)
MASS ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 3 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 3 FDA reports)
METASTASES TO PERITONEUM ( 3 FDA reports)
MIDDLE EAR EFFUSION ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 3 FDA reports)
MYCOPLASMA INFECTION ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NECK INJURY ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
NODULE ( 3 FDA reports)
OEDEMA GENITAL ( 3 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
ORAL SURGERY ( 3 FDA reports)
PALLIATIVE CARE ( 3 FDA reports)
PANCREATITIS CHRONIC ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PARKINSONISM ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PERONEAL NERVE PALSY ( 3 FDA reports)
PERSONALITY CHANGE ( 3 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 3 FDA reports)
PLATELET DISORDER ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PRESBYOPIA ( 3 FDA reports)
PROCTITIS ( 3 FDA reports)
PRODUCT ODOUR ABNORMAL ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ( 3 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 3 FDA reports)
PRURITUS GENITAL ( 3 FDA reports)
PULMONARY MASS ( 3 FDA reports)
PYELOCALIECTASIS ( 3 FDA reports)
RADIOTHERAPY ( 3 FDA reports)
RASH VESICULAR ( 3 FDA reports)
RAYNAUD'S PHENOMENON ( 3 FDA reports)
RECTAL SPASM ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RESPIRATORY THERAPY ( 3 FDA reports)
RESUSCITATION ( 3 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
RHINITIS ALLERGIC ( 3 FDA reports)
SINUS HEADACHE ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SKIN NODULE ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
SNORING ( 3 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 3 FDA reports)
SOCIAL PROBLEM ( 3 FDA reports)
SOMNAMBULISM ( 3 FDA reports)
SPERM COUNT ZERO ( 3 FDA reports)
SPINAL CORD COMPRESSION ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
SUBDURAL HAEMORRHAGE ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
TEMPORAL ARTERITIS ( 3 FDA reports)
TENDON DISORDER ( 3 FDA reports)
TESTIS DISCOMFORT ( 3 FDA reports)
TINEA CRURIS ( 3 FDA reports)
TOE OPERATION ( 3 FDA reports)
TONGUE BLACK HAIRY ( 3 FDA reports)
TONGUE DISCOLOURATION ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
ULCER ( 3 FDA reports)
URETHRAL DISORDER ( 3 FDA reports)
URETHRAL PAIN ( 3 FDA reports)
VENTRICULAR HYPOKINESIA ( 3 FDA reports)
VISCERAL PAIN ( 3 FDA reports)
WOUND HAEMORRHAGE ( 3 FDA reports)
ABSCESS NECK ( 2 FDA reports)
ACUTE LUNG INJURY ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
ADRENAL ADENOMA ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANKYLOGLOSSIA ACQUIRED ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASTHMATIC CRISIS ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
AZOOSPERMIA ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
BICUSPID AORTIC VALVE ( 2 FDA reports)
BLADDER DILATATION ( 2 FDA reports)
BLADDER INJURY ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD TESTOSTERONE FREE INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRAIN STEM HAEMORRHAGE ( 2 FDA reports)
BREAST DISCHARGE ( 2 FDA reports)
BREAST DISORDER MALE ( 2 FDA reports)
BREAST FIBROSIS ( 2 FDA reports)
BREAST INFLAMMATION ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
BRONCHOSCOPY NORMAL ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
BULIMIA NERVOSA ( 2 FDA reports)
BURNS SECOND DEGREE ( 2 FDA reports)
CARDIAC ANEURYSM ( 2 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CEREBRAL HYPOPERFUSION ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CHRONIC LEUKAEMIA ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 2 FDA reports)
CORONARY ARTERY SURGERY ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
CYSTITIS NONINFECTIVE ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRUG LEVEL ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
EAR PRURITUS ( 2 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 2 FDA reports)
EXTERNAL EAR PAIN ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
EYES SUNKEN ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
FEMINISATION ACQUIRED ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GAMMOPATHY ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GENITAL LESION ( 2 FDA reports)
GLARE ( 2 FDA reports)
GUN SHOT WOUND ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HEAD DEFORMITY ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
IMPULSE-CONTROL DISORDER ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INFERTILITY ( 2 FDA reports)
INFERTILITY MALE ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INGROWING NAIL ( 2 FDA reports)
INJECTION SITE DISCOMFORT ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INSTILLATION SITE PAIN ( 2 FDA reports)
INTERCEPTED MEDICATION ERROR ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
LABYRINTHITIS ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MALE ORGASMIC DISORDER ( 2 FDA reports)
MAMMOGRAM ABNORMAL ( 2 FDA reports)
MANIA ( 2 FDA reports)
MANTLE CELL LYMPHOMA ( 2 FDA reports)
MARITAL PROBLEM ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTATIC GASTRIC CANCER ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MIXED LIVER INJURY ( 2 FDA reports)
MONOCLONAL GAMMOPATHY ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MUSCULAR DYSTROPHY ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
NIPPLE EXUDATE BLOODY ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OSTECTOMY ( 2 FDA reports)
OTITIS MEDIA ACUTE ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PALMAR ERYTHEMA ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PAROTID GLAND INFLAMMATION ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 2 FDA reports)
PHOTOSENSITIVE RASH ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYGLANDULAR DISORDER ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
POOR VENOUS ACCESS ( 2 FDA reports)
PREGNANCY OF PARTNER ( 2 FDA reports)
PREMATURE EJACULATION ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PROSTATE CANCER STAGE I ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RECALL PHENOMENON ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL CANCER METASTATIC ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RETINAL OEDEMA ( 2 FDA reports)
RETINITIS PIGMENTOSA ( 2 FDA reports)
RETINOIC ACID SYNDROME ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SCAB ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SCROTAL ERYTHEMA ( 2 FDA reports)
SCROTAL OEDEMA ( 2 FDA reports)
SEMEN ANALYSIS ABNORMAL ( 2 FDA reports)
SEMEN VISCOSITY ABNORMAL ( 2 FDA reports)
SEMEN VISCOSITY DECREASED ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SEPSIS SYNDROME ( 2 FDA reports)
SERUM FERRITIN NORMAL ( 2 FDA reports)
SHOULDER OPERATION ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SPERM CONCENTRATION ZERO ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SWEAT GLAND INFECTION ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
TESTICULAR ABSCESS ( 2 FDA reports)
TESTIS CANCER ( 2 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TOOTH INJURY ( 2 FDA reports)
TOOTH REPAIR ( 2 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 2 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 2 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
URETERAL DISORDER ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
URINARY TRACT PAIN ( 2 FDA reports)
URINE ABNORMALITY ( 2 FDA reports)
VACCINATION COMPLICATION ( 2 FDA reports)
VASCULAR INJURY ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
WEIGHT LOSS POOR ( 2 FDA reports)
WHIPLASH INJURY ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADRENAL CYST ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANHIDROSIS ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APATHY ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILE OUTPUT DECREASED ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLADDER CANCER STAGE 0, WITH CANCER IN SITU ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLADDER STENOSIS ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD LUTEINISING HORMONE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD OESTROGEN INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE NORMAL ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST DISCOLOURATION ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BREAST OPERATION ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUBONIC PLAGUE ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
BURNING MOUTH SYNDROME ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC MASSAGE ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVICAL ROOT PAIN ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHLOASMA ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGENITAL GENITAL MALFORMATION MALE ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEFORMITY THORAX ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE CAPTURING ISSUE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EPIDERMAL NAEVUS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXCESSIVE MASTURBATION ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EXPOSURE VIA SEMEN ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FACIAL DYSMORPHISM ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GENERAL ANAESTHESIA ( 1 FDA reports)
GENITAL CYST ( 1 FDA reports)
GENITAL ERYTHEMA ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GENITAL SWELLING ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE II ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GROWTH OF EYELASHES ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEARING AID USER ( 1 FDA reports)
HELMINTHIC INFECTION ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS E ANTIBODY ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYDROCELE ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INFUSION SITE INDURATION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRIS HYPERPIGMENTATION ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABORATORY TEST ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIGAMENT PAIN ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE ABNORMAL ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT NIPPLE NEOPLASM MALE ( 1 FDA reports)
MALIGNANT SPLENIC NEOPLASM ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
METASTASES TO PROSTATE ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MILIA ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOUTH CYST ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYOCARDIAL OEDEMA ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
MYOGLOBIN BLOOD DECREASED ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAIL BED INFLAMMATION ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESTRADIOL DECREASED ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
ORGASMIC SENSATION DECREASED ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVERSENSING ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PENILE CURVATURE ( 1 FDA reports)
PENILE DISCHARGE ( 1 FDA reports)
PENILE ERYTHEMA ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PHYSICAL TESTICLE EXAMINATION ABNORMAL ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PREHYPERTENSION ( 1 FDA reports)
PREMATURE AGEING ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT STERILITY LACKING ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROMISCUITY ( 1 FDA reports)
PROSTATE CANCER STAGE IV ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RADICULAR SYNDROME ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL EXAMINATION ABNORMAL ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
REDUCED BLADDER CAPACITY ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESIDUAL URINE VOLUME INCREASED ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESPIROVIRUS TEST POSITIVE ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCROTAL HAEMATOCOELE ( 1 FDA reports)
SEMEN ABNORMAL ( 1 FDA reports)
SEMEN VOLUME ABNORMAL ( 1 FDA reports)
SEMEN VOLUME INCREASED ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOLAR URTICARIA ( 1 FDA reports)
SPERM CONCENTRATION DECREASED ( 1 FDA reports)
SPERMATOZOA ABNORMAL ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENITIS ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STARING ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STENT-GRAFT MALFUNCTION ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STRANGULATED HERNIA REPAIR ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SYMPTOM MASKED ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
TABLET ISSUE ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENSION ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TESTICULAR OEDEMA ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TIC ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
ULTRASOUND SCAN ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
URETERAL NEOPLASM ( 1 FDA reports)
URETERECTOMY ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URETHRAL INJURY ( 1 FDA reports)
URETHRITIS NONINFECTIVE ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENOUS HAEMORRHAGE ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS PRESSURE JUGULAR ABNORMAL ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VIRILISM ( 1 FDA reports)
VIRUS URINE TEST POSITIVE ( 1 FDA reports)
VOCAL CORD POLYP ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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