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

DRUG INEFFECTIVE ( 443 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 378 FDA reports)
FATIGUE ( 280 FDA reports)
ASTHENIA ( 218 FDA reports)
DYSPNOEA ( 205 FDA reports)
WEIGHT DECREASED ( 174 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 171 FDA reports)
HEADACHE ( 168 FDA reports)
DIZZINESS ( 160 FDA reports)
NAUSEA ( 160 FDA reports)
PAIN ( 148 FDA reports)
ERECTILE DYSFUNCTION ( 147 FDA reports)
OEDEMA PERIPHERAL ( 144 FDA reports)
ANXIETY ( 143 FDA reports)
DIARRHOEA ( 127 FDA reports)
FEELING ABNORMAL ( 124 FDA reports)
MYOCARDIAL INFARCTION ( 123 FDA reports)
BACK PAIN ( 118 FDA reports)
ARTHRALGIA ( 117 FDA reports)
DEPRESSION ( 117 FDA reports)
WEIGHT INCREASED ( 107 FDA reports)
INSOMNIA ( 102 FDA reports)
ACNE ( 101 FDA reports)
ABDOMINAL PAIN ( 93 FDA reports)
VOMITING ( 93 FDA reports)
PAIN IN EXTREMITY ( 91 FDA reports)
ANAEMIA ( 88 FDA reports)
ALOPECIA ( 86 FDA reports)
PYREXIA ( 86 FDA reports)
MYALGIA ( 85 FDA reports)
DEEP VEIN THROMBOSIS ( 84 FDA reports)
PULMONARY EMBOLISM ( 84 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 82 FDA reports)
FLUSHING ( 82 FDA reports)
BONE DISORDER ( 81 FDA reports)
LIBIDO DECREASED ( 79 FDA reports)
ACCIDENTAL EXPOSURE ( 78 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 78 FDA reports)
HYPERHIDROSIS ( 78 FDA reports)
PRURITUS ( 78 FDA reports)
ATRIAL FIBRILLATION ( 76 FDA reports)
CHEST PAIN ( 76 FDA reports)
PROSTATE CANCER ( 76 FDA reports)
INCORRECT DOSE ADMINISTERED ( 75 FDA reports)
FALL ( 74 FDA reports)
RASH ( 74 FDA reports)
OSTEONECROSIS OF JAW ( 70 FDA reports)
SOMNOLENCE ( 70 FDA reports)
HAIR GROWTH ABNORMAL ( 69 FDA reports)
BLOOD GLUCOSE INCREASED ( 68 FDA reports)
HYPERTENSION ( 67 FDA reports)
LOSS OF CONSCIOUSNESS ( 66 FDA reports)
PNEUMONIA ( 66 FDA reports)
CHEST DISCOMFORT ( 64 FDA reports)
HYPOAESTHESIA ( 64 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 64 FDA reports)
COUGH ( 61 FDA reports)
ERYTHEMA ( 61 FDA reports)
CONSTIPATION ( 60 FDA reports)
PARAESTHESIA ( 60 FDA reports)
URTICARIA ( 60 FDA reports)
DYSPEPSIA ( 59 FDA reports)
INJURY ( 59 FDA reports)
PAIN IN JAW ( 59 FDA reports)
PALPITATIONS ( 58 FDA reports)
MALAISE ( 57 FDA reports)
OSTEONECROSIS ( 57 FDA reports)
HYPOTENSION ( 56 FDA reports)
NERVOUSNESS ( 54 FDA reports)
RENAL FAILURE ACUTE ( 54 FDA reports)
SINUSITIS ( 54 FDA reports)
DEATH ( 53 FDA reports)
DYSURIA ( 53 FDA reports)
BLOOD PRESSURE INCREASED ( 52 FDA reports)
OSTEOMYELITIS ( 52 FDA reports)
SPINAL OSTEOARTHRITIS ( 52 FDA reports)
AGGRESSION ( 51 FDA reports)
CEREBROVASCULAR ACCIDENT ( 51 FDA reports)
GAIT DISTURBANCE ( 51 FDA reports)
SLEEP APNOEA SYNDROME ( 51 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 49 FDA reports)
DECREASED INTEREST ( 49 FDA reports)
ATELECTASIS ( 48 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 48 FDA reports)
GYNAECOMASTIA ( 47 FDA reports)
NEUROPATHY PERIPHERAL ( 47 FDA reports)
TOOTH EXTRACTION ( 46 FDA reports)
DRUG EFFECT DECREASED ( 45 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 45 FDA reports)
HIRSUTISM ( 45 FDA reports)
DEHYDRATION ( 44 FDA reports)
OSTEOARTHRITIS ( 44 FDA reports)
MUSCULAR WEAKNESS ( 43 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 42 FDA reports)
MUSCULOSKELETAL PAIN ( 42 FDA reports)
NOCTURIA ( 42 FDA reports)
RENAL FAILURE ( 42 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 42 FDA reports)
THROMBOSIS ( 42 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 41 FDA reports)
URINARY TRACT INFECTION ( 41 FDA reports)
ABDOMINAL PAIN UPPER ( 40 FDA reports)
OFF LABEL USE ( 40 FDA reports)
HEART RATE INCREASED ( 39 FDA reports)
HOT FLUSH ( 39 FDA reports)
PLEURAL EFFUSION ( 39 FDA reports)
PRECOCIOUS PUBERTY ( 38 FDA reports)
STRESS ( 38 FDA reports)
POLLAKIURIA ( 37 FDA reports)
SYNCOPE ( 37 FDA reports)
CELLULITIS ( 36 FDA reports)
CHILLS ( 36 FDA reports)
CONFUSIONAL STATE ( 36 FDA reports)
DECREASED APPETITE ( 36 FDA reports)
FLATULENCE ( 36 FDA reports)
HEPATIC STEATOSIS ( 36 FDA reports)
MUSCLE SPASMS ( 36 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 36 FDA reports)
APPLICATION SITE RASH ( 35 FDA reports)
DRUG DOSE OMISSION ( 35 FDA reports)
DRY MOUTH ( 35 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 35 FDA reports)
ANGER ( 34 FDA reports)
CORONARY ARTERY DISEASE ( 34 FDA reports)
PANCREATITIS ( 34 FDA reports)
MEMORY IMPAIRMENT ( 33 FDA reports)
MUSCLE DISORDER ( 33 FDA reports)
NECK PAIN ( 33 FDA reports)
ABDOMINAL DISCOMFORT ( 32 FDA reports)
APPLICATION SITE REACTION ( 32 FDA reports)
HYPERSENSITIVITY ( 32 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 32 FDA reports)
BACTERIAL INFECTION ( 31 FDA reports)
HAEMOGLOBIN DECREASED ( 31 FDA reports)
INFLUENZA ( 31 FDA reports)
OSTEOPENIA ( 31 FDA reports)
SOFT TISSUE DISORDER ( 31 FDA reports)
SUICIDAL IDEATION ( 31 FDA reports)
CONDITION AGGRAVATED ( 30 FDA reports)
PRODUCT QUALITY ISSUE ( 30 FDA reports)
PROSTATOMEGALY ( 30 FDA reports)
BRONCHITIS ( 29 FDA reports)
CONTUSION ( 29 FDA reports)
EMOTIONAL DISTRESS ( 29 FDA reports)
PANCYTOPENIA ( 29 FDA reports)
PROTHROMBIN TIME PROLONGED ( 29 FDA reports)
AMNESIA ( 28 FDA reports)
ANGINA PECTORIS ( 28 FDA reports)
ARTHRITIS ( 28 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 28 FDA reports)
HAEMOGLOBIN INCREASED ( 28 FDA reports)
HIP ARTHROPLASTY ( 28 FDA reports)
HYPERLIPIDAEMIA ( 28 FDA reports)
INFECTION ( 28 FDA reports)
JOINT SWELLING ( 28 FDA reports)
WHEEZING ( 28 FDA reports)
ANHEDONIA ( 27 FDA reports)
COMPRESSION FRACTURE ( 27 FDA reports)
CONVULSION ( 27 FDA reports)
DIABETES MELLITUS ( 27 FDA reports)
DYSGEUSIA ( 27 FDA reports)
FEELING HOT ( 27 FDA reports)
HAEMATOCRIT INCREASED ( 27 FDA reports)
HYPOPHAGIA ( 27 FDA reports)
LETHARGY ( 27 FDA reports)
ORAL PAIN ( 27 FDA reports)
TREMOR ( 27 FDA reports)
DRUG INTERACTION ( 26 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 26 FDA reports)
SINUS TACHYCARDIA ( 26 FDA reports)
TESTICULAR PAIN ( 26 FDA reports)
UMBILICAL HERNIA ( 26 FDA reports)
VISION BLURRED ( 26 FDA reports)
ABDOMINAL DISTENSION ( 25 FDA reports)
DISTURBANCE IN ATTENTION ( 25 FDA reports)
EMPHYSEMA ( 25 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 25 FDA reports)
INFLAMMATION ( 25 FDA reports)
LIBIDO INCREASED ( 25 FDA reports)
LOSS OF LIBIDO ( 25 FDA reports)
MUSCLE STRAIN ( 25 FDA reports)
OEDEMA ( 25 FDA reports)
PRESYNCOPE ( 25 FDA reports)
RENAL IMPAIRMENT ( 25 FDA reports)
SEPSIS ( 25 FDA reports)
SKIN EXFOLIATION ( 25 FDA reports)
TACHYCARDIA ( 25 FDA reports)
AGITATION ( 24 FDA reports)
ARTERIOSCLEROSIS ( 24 FDA reports)
BLOOD POTASSIUM DECREASED ( 24 FDA reports)
CARDIAC ARREST ( 24 FDA reports)
LEUKOCYTOSIS ( 24 FDA reports)
PANCREATITIS ACUTE ( 24 FDA reports)
RENAL DISORDER ( 24 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 23 FDA reports)
BLOOD GLUCOSE DECREASED ( 23 FDA reports)
CONJUNCTIVITIS ( 23 FDA reports)
DEBRIDEMENT ( 23 FDA reports)
DYSARTHRIA ( 23 FDA reports)
GINGIVAL BLEEDING ( 23 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 23 FDA reports)
LIPIDS INCREASED ( 23 FDA reports)
METASTASES TO BONE ( 23 FDA reports)
NEOPLASM MALIGNANT ( 23 FDA reports)
NEPHROLITHIASIS ( 23 FDA reports)
SEXUAL DYSFUNCTION ( 23 FDA reports)
TACHYARRHYTHMIA ( 23 FDA reports)
BACK DISORDER ( 22 FDA reports)
FRACTURED SACRUM ( 22 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 22 FDA reports)
IRRITABILITY ( 22 FDA reports)
OSTEOPOROSIS ( 22 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 22 FDA reports)
TESTICULAR ATROPHY ( 22 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 21 FDA reports)
CARDIOVASCULAR DISORDER ( 21 FDA reports)
CATARACT ( 21 FDA reports)
CORONARY ARTERY OCCLUSION ( 21 FDA reports)
DRY SKIN ( 21 FDA reports)
FEBRILE NEUTROPENIA ( 21 FDA reports)
HERPES ZOSTER ( 21 FDA reports)
HYPOCALCAEMIA ( 21 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 21 FDA reports)
MUSCLE TWITCHING ( 21 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 21 FDA reports)
PERITONEAL DISORDER ( 21 FDA reports)
PLASMACYTOSIS ( 21 FDA reports)
ROAD TRAFFIC ACCIDENT ( 21 FDA reports)
UNEVALUABLE EVENT ( 21 FDA reports)
APPLICATION SITE DISCOLOURATION ( 20 FDA reports)
BURNING SENSATION ( 20 FDA reports)
DEFORMITY ( 20 FDA reports)
FACET JOINT SYNDROME ( 20 FDA reports)
GASTRITIS ( 20 FDA reports)
LIFE EXPECTANCY SHORTENED ( 20 FDA reports)
LUNG NEOPLASM ( 20 FDA reports)
TOOTHACHE ( 20 FDA reports)
VISUAL IMPAIRMENT ( 20 FDA reports)
APPLICATION SITE PRURITUS ( 19 FDA reports)
BLOOD POTASSIUM INCREASED ( 19 FDA reports)
CANCER PAIN ( 19 FDA reports)
CARDIOMEGALY ( 19 FDA reports)
CARDIOMYOPATHY ( 19 FDA reports)
DYSPNOEA EXERTIONAL ( 19 FDA reports)
ENDODONTIC PROCEDURE ( 19 FDA reports)
HAEMATOCHEZIA ( 19 FDA reports)
IMPAIRED HEALING ( 19 FDA reports)
LEFT ATRIAL DILATATION ( 19 FDA reports)
LUMBAR RADICULOPATHY ( 19 FDA reports)
LYMPHADENOPATHY ( 19 FDA reports)
MEDICATION ERROR ( 19 FDA reports)
MOOD ALTERED ( 19 FDA reports)
NERVE COMPRESSION ( 19 FDA reports)
NEURALGIA ( 19 FDA reports)
PERIPHERAL EMBOLISM ( 19 FDA reports)
POST HERPETIC NEURALGIA ( 19 FDA reports)
RENAL ISCHAEMIA ( 19 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 19 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 19 FDA reports)
URINARY HESITATION ( 19 FDA reports)
BLOOD CREATININE INCREASED ( 18 FDA reports)
CARDIAC VALVE ABSCESS ( 18 FDA reports)
COORDINATION ABNORMAL ( 18 FDA reports)
ECONOMIC PROBLEM ( 18 FDA reports)
JAW DISORDER ( 18 FDA reports)
NIGHT SWEATS ( 18 FDA reports)
PLATELET COUNT DECREASED ( 18 FDA reports)
SKIN IRRITATION ( 18 FDA reports)
SWELLING FACE ( 18 FDA reports)
VISUAL DISTURBANCE ( 18 FDA reports)
APPLICATION SITE PAIN ( 17 FDA reports)
ARRHYTHMIA ( 17 FDA reports)
ASTHMA ( 17 FDA reports)
BREAST TENDERNESS ( 17 FDA reports)
CEREBRAL ATROPHY ( 17 FDA reports)
DYSAESTHESIA ( 17 FDA reports)
EYE PAIN ( 17 FDA reports)
FISTULA ( 17 FDA reports)
HEPATOMEGALY ( 17 FDA reports)
INCORRECT STORAGE OF DRUG ( 17 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 17 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 17 FDA reports)
LIVER DISORDER ( 17 FDA reports)
MOOD SWINGS ( 17 FDA reports)
ONYCHOMYCOSIS ( 17 FDA reports)
ORAL CANDIDIASIS ( 17 FDA reports)
PITUITARY TUMOUR ( 17 FDA reports)
PRODUCTIVE COUGH ( 17 FDA reports)
PULMONARY HYPERTENSION ( 17 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 17 FDA reports)
SENSITIVITY OF TEETH ( 17 FDA reports)
TESTICULAR SWELLING ( 17 FDA reports)
THROMBOCYTOPENIA ( 17 FDA reports)
URINARY RETENTION ( 17 FDA reports)
ANOREXIA ( 16 FDA reports)
ARTHROPATHY ( 16 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 16 FDA reports)
CARDIAC FAILURE ( 16 FDA reports)
COLITIS ISCHAEMIC ( 16 FDA reports)
DYSPHAGIA ( 16 FDA reports)
EPIDIDYMITIS ( 16 FDA reports)
HYDROCELE ( 16 FDA reports)
HYPERCHOLESTEROLAEMIA ( 16 FDA reports)
JOINT CREPITATION ( 16 FDA reports)
LOCALISED INFECTION ( 16 FDA reports)
MENTAL DISORDER ( 16 FDA reports)
NASOPHARYNGITIS ( 16 FDA reports)
NEUTROPENIA ( 16 FDA reports)
OSTEOLYSIS ( 16 FDA reports)
PHLEBITIS ( 16 FDA reports)
POLYCYTHAEMIA ( 16 FDA reports)
SKIN BURNING SENSATION ( 16 FDA reports)
SKIN DISCOLOURATION ( 16 FDA reports)
SPINAL FRACTURE ( 16 FDA reports)
TOOTH DEPOSIT ( 16 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 16 FDA reports)
WOUND DEHISCENCE ( 16 FDA reports)
ATRIAL FLUTTER ( 15 FDA reports)
DERMAL CYST ( 15 FDA reports)
DRUG HYPERSENSITIVITY ( 15 FDA reports)
ENERGY INCREASED ( 15 FDA reports)
ESSENTIAL TREMOR ( 15 FDA reports)
HAEMATEMESIS ( 15 FDA reports)
HYPOXIA ( 15 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 15 FDA reports)
MUSCLE ATROPHY ( 15 FDA reports)
PRIMARY HYPOGONADISM ( 15 FDA reports)
PULMONARY CONGESTION ( 15 FDA reports)
STAPHYLOCOCCAL INFECTION ( 15 FDA reports)
TENDONITIS ( 15 FDA reports)
THROMBOCYTOSIS ( 15 FDA reports)
ABNORMAL DREAMS ( 14 FDA reports)
BALANCE DISORDER ( 14 FDA reports)
DISABILITY ( 14 FDA reports)
DIVERTICULUM ( 14 FDA reports)
ENLARGED CLITORIS ( 14 FDA reports)
FORAMEN MAGNUM STENOSIS ( 14 FDA reports)
GINGIVAL PAIN ( 14 FDA reports)
HAEMATOCRIT DECREASED ( 14 FDA reports)
MENTAL IMPAIRMENT ( 14 FDA reports)
MICTURITION URGENCY ( 14 FDA reports)
ORAL DISCOMFORT ( 14 FDA reports)
PITUITARY TUMOUR BENIGN ( 14 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 14 FDA reports)
POST PROCEDURAL COMPLICATION ( 14 FDA reports)
PULMONARY OEDEMA ( 14 FDA reports)
RADICULAR PAIN ( 14 FDA reports)
SWELLING ( 14 FDA reports)
SWOLLEN TONGUE ( 14 FDA reports)
URINARY INCONTINENCE ( 14 FDA reports)
URINE FLOW DECREASED ( 14 FDA reports)
ABASIA ( 13 FDA reports)
ABNORMAL BEHAVIOUR ( 13 FDA reports)
ADRENAL DISORDER ( 13 FDA reports)
CARDIAC DISORDER ( 13 FDA reports)
CHOLELITHIASIS ( 13 FDA reports)
DYSTROPHIC CALCIFICATION ( 13 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 13 FDA reports)
HYPERTRICHOSIS ( 13 FDA reports)
INJECTION SITE HAEMORRHAGE ( 13 FDA reports)
LOOSE TOOTH ( 13 FDA reports)
MENTAL STATUS CHANGES ( 13 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 13 FDA reports)
MYELODYSPLASTIC SYNDROME ( 13 FDA reports)
ORCHITIS ( 13 FDA reports)
PERSONALITY CHANGE ( 13 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 13 FDA reports)
RESPIRATORY TRACT INFECTION ( 13 FDA reports)
RETINAL DETACHMENT ( 13 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 13 FDA reports)
TENDERNESS ( 13 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 13 FDA reports)
TOOTH FRACTURE ( 13 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 13 FDA reports)
VENOUS OCCLUSION ( 13 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 12 FDA reports)
APPLICATION SITE ERYTHEMA ( 12 FDA reports)
APPLICATION SITE IRRITATION ( 12 FDA reports)
BLOOD PRESSURE DECREASED ( 12 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 12 FDA reports)
DRUG ADMINISTRATION ERROR ( 12 FDA reports)
GLOSSODYNIA ( 12 FDA reports)
HIP FRACTURE ( 12 FDA reports)
ILL-DEFINED DISORDER ( 12 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 12 FDA reports)
KIDNEY INFECTION ( 12 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 12 FDA reports)
MENSTRUAL DISORDER ( 12 FDA reports)
MENSTRUATION IRREGULAR ( 12 FDA reports)
METASTASES TO LIVER ( 12 FDA reports)
MOBILITY DECREASED ( 12 FDA reports)
MOUTH HAEMORRHAGE ( 12 FDA reports)
MYOCARDIAL ISCHAEMIA ( 12 FDA reports)
OVERDOSE ( 12 FDA reports)
PORTAL VEIN THROMBOSIS ( 12 FDA reports)
PRURITUS GENERALISED ( 12 FDA reports)
RETINAL DISORDER ( 12 FDA reports)
SENSORY DISTURBANCE ( 12 FDA reports)
SINUS DISORDER ( 12 FDA reports)
ABSCESS ( 11 FDA reports)
ANKLE FRACTURE ( 11 FDA reports)
BLOOD BILIRUBIN INCREASED ( 11 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 11 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 11 FDA reports)
DYSPHONIA ( 11 FDA reports)
EPICONDYLITIS ( 11 FDA reports)
FORMICATION ( 11 FDA reports)
HEAD INJURY ( 11 FDA reports)
HEART RATE DECREASED ( 11 FDA reports)
HEART RATE IRREGULAR ( 11 FDA reports)
HIATUS HERNIA ( 11 FDA reports)
LIBIDO DISORDER ( 11 FDA reports)
LUMBAR SPINAL STENOSIS ( 11 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 11 FDA reports)
MEDICATION RESIDUE ( 11 FDA reports)
MIDDLE INSOMNIA ( 11 FDA reports)
RESTLESSNESS ( 11 FDA reports)
ROTATOR CUFF SYNDROME ( 11 FDA reports)
SINUS CONGESTION ( 11 FDA reports)
SLEEP DISORDER ( 11 FDA reports)
SPINAL DISORDER ( 11 FDA reports)
SPONTANEOUS PENILE ERECTION ( 11 FDA reports)
TINNITUS ( 11 FDA reports)
VIRAL INFECTION ( 11 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 11 FDA reports)
ACROMEGALY ( 10 FDA reports)
ANAL FISTULA ( 10 FDA reports)
APHASIA ( 10 FDA reports)
BLINDNESS TRANSIENT ( 10 FDA reports)
BONE SCAN ABNORMAL ( 10 FDA reports)
CEREBRAL INFARCTION ( 10 FDA reports)
COMPLETED SUICIDE ( 10 FDA reports)
CORNEAL ABRASION ( 10 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 10 FDA reports)
DELIRIUM ( 10 FDA reports)
DENTAL DISCOMFORT ( 10 FDA reports)
DERMATITIS CONTACT ( 10 FDA reports)
DIABETIC RETINOPATHY ( 10 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 10 FDA reports)
EPIPHYSES PREMATURE FUSION ( 10 FDA reports)
EYE OPERATION ( 10 FDA reports)
FLOPPY IRIS SYNDROME ( 10 FDA reports)
GASTROINTESTINAL DISORDER ( 10 FDA reports)
HAEMOPTYSIS ( 10 FDA reports)
HEPATIC CYST ( 10 FDA reports)
HYPERCOAGULATION ( 10 FDA reports)
HYPOAESTHESIA FACIAL ( 10 FDA reports)
INJECTION SITE PAIN ( 10 FDA reports)
LACUNAR INFARCTION ( 10 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 10 FDA reports)
MULTIPLE INJURIES ( 10 FDA reports)
PERIODONTAL DISEASE ( 10 FDA reports)
SCROTAL SWELLING ( 10 FDA reports)
SPONDYLOARTHROPATHY ( 10 FDA reports)
ABORTION SPONTANEOUS ( 9 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 9 FDA reports)
APATHY ( 9 FDA reports)
APPLICATION SITE DRYNESS ( 9 FDA reports)
BLOOD OESTROGEN INCREASED ( 9 FDA reports)
BLOOD UREA INCREASED ( 9 FDA reports)
BLOOD URINE PRESENT ( 9 FDA reports)
BONE LESION ( 9 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 9 FDA reports)
BREAST ENLARGEMENT ( 9 FDA reports)
CARDIAC FLUTTER ( 9 FDA reports)
CHOLECYSTECTOMY ( 9 FDA reports)
ENCEPHALOMALACIA ( 9 FDA reports)
EPISTAXIS ( 9 FDA reports)
FEAR ( 9 FDA reports)
FLUID RETENTION ( 9 FDA reports)
GINGIVAL RECESSION ( 9 FDA reports)
GLIOSIS ( 9 FDA reports)
HALLUCINATION ( 9 FDA reports)
HEAT EXHAUSTION ( 9 FDA reports)
HEPATITIS ( 9 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 9 FDA reports)
HYPERPLASIA ( 9 FDA reports)
HYPOGEUSIA ( 9 FDA reports)
ILEUS PARALYTIC ( 9 FDA reports)
INCREASED APPETITE ( 9 FDA reports)
LEUKOPENIA ( 9 FDA reports)
LIMB INJURY ( 9 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 9 FDA reports)
NASAL ODOUR ( 9 FDA reports)
OESOPHAGITIS ( 9 FDA reports)
PAROTID GLAND ENLARGEMENT ( 9 FDA reports)
PILONIDAL CYST ( 9 FDA reports)
POIKILOCYTOSIS ( 9 FDA reports)
PRIMARY SEQUESTRUM ( 9 FDA reports)
RENAL CYST ( 9 FDA reports)
RESPIRATORY DISORDER ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
SALIVARY GLAND PAIN ( 9 FDA reports)
SKIN CANCER ( 9 FDA reports)
SKIN REACTION ( 9 FDA reports)
SPONDYLOPATHY TRAUMATIC ( 9 FDA reports)
SQUAMOUS CELL CARCINOMA ( 9 FDA reports)
SUFFOCATION FEELING ( 9 FDA reports)
TYPE 2 DIABETES MELLITUS ( 9 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 9 FDA reports)
VARICES OESOPHAGEAL ( 9 FDA reports)
VISUAL ACUITY REDUCED ( 9 FDA reports)
WITHDRAWAL SYNDROME ( 9 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 8 FDA reports)
BLISTER ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
BLOOD PROLACTIN INCREASED ( 8 FDA reports)
BRONCHIAL DISORDER ( 8 FDA reports)
COMPLEX PARTIAL SEIZURES ( 8 FDA reports)
CORONARY ARTERY BYPASS ( 8 FDA reports)
DERMATITIS ( 8 FDA reports)
DISORIENTATION ( 8 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 8 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 8 FDA reports)
ERECTION INCREASED ( 8 FDA reports)
EXPIRED DRUG ADMINISTERED ( 8 FDA reports)
FAECES DISCOLOURED ( 8 FDA reports)
HALLUCINATION, AUDITORY ( 8 FDA reports)
HEPATIC ENZYME INCREASED ( 8 FDA reports)
HYPERSOMNIA ( 8 FDA reports)
HYPOGONADISM ( 8 FDA reports)
HYPONATRAEMIA ( 8 FDA reports)
INFLUENZA LIKE ILLNESS ( 8 FDA reports)
LUNG INFILTRATION ( 8 FDA reports)
MENORRHAGIA ( 8 FDA reports)
MICROANGIOPATHY ( 8 FDA reports)
MITRAL VALVE INCOMPETENCE ( 8 FDA reports)
ODONTOGENIC CYST ( 8 FDA reports)
ORAL INFECTION ( 8 FDA reports)
PANIC ATTACK ( 8 FDA reports)
POOR QUALITY SLEEP ( 8 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 8 FDA reports)
PUPILS UNEQUAL ( 8 FDA reports)
RASH MACULAR ( 8 FDA reports)
RASH PRURITIC ( 8 FDA reports)
SENSORY LOSS ( 8 FDA reports)
SLUGGISHNESS ( 8 FDA reports)
STENT PLACEMENT ( 8 FDA reports)
SUBCUTANEOUS ABSCESS ( 8 FDA reports)
SURGERY ( 8 FDA reports)
TENDON RUPTURE ( 8 FDA reports)
THROAT IRRITATION ( 8 FDA reports)
THYROID CANCER ( 8 FDA reports)
TRISMUS ( 8 FDA reports)
ACUTE CORONARY SYNDROME ( 7 FDA reports)
ANOGENITAL WARTS ( 7 FDA reports)
BENIGN NEOPLASM ( 7 FDA reports)
BLOOD CALCIUM DECREASED ( 7 FDA reports)
BLOOD SODIUM DECREASED ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
BREAST PAIN ( 7 FDA reports)
CANDIDIASIS ( 7 FDA reports)
CAROTID ARTERY OCCLUSION ( 7 FDA reports)
DACRYOCYSTITIS INFECTIVE ( 7 FDA reports)
DENTAL CARIES ( 7 FDA reports)
DIHYDROTESTOSTERONE INCREASED ( 7 FDA reports)
DIPLOPIA ( 7 FDA reports)
DRUG PRESCRIBING ERROR ( 7 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 7 FDA reports)
EAR INFECTION ( 7 FDA reports)
EMOTIONAL DISORDER ( 7 FDA reports)
EYE SWELLING ( 7 FDA reports)
FEELING JITTERY ( 7 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 7 FDA reports)
HYPERCALCAEMIA ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
INTERMITTENT CLAUDICATION ( 7 FDA reports)
KNEE ARTHROPLASTY ( 7 FDA reports)
KYPHOSIS ( 7 FDA reports)
LOWER LIMB FRACTURE ( 7 FDA reports)
LUNG INFECTION ( 7 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 7 FDA reports)
MANIA ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
MUCOSAL INFLAMMATION ( 7 FDA reports)
NASAL CONGESTION ( 7 FDA reports)
NASAL DRYNESS ( 7 FDA reports)
NERVE ROOT INJURY LUMBAR ( 7 FDA reports)
OPEN WOUND ( 7 FDA reports)
OSTEOTOMY ( 7 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 7 FDA reports)
PERICARDIAL EFFUSION ( 7 FDA reports)
PERIPHERAL COLDNESS ( 7 FDA reports)
PHOTOSENSITIVITY REACTION ( 7 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 7 FDA reports)
PROTEIN URINE PRESENT ( 7 FDA reports)
RADIATION INJURY ( 7 FDA reports)
RENAL FAILURE CHRONIC ( 7 FDA reports)
RESTLESS LEGS SYNDROME ( 7 FDA reports)
SEBORRHOEIC KERATOSIS ( 7 FDA reports)
SHOULDER PAIN ( 7 FDA reports)
SPERM CONCENTRATION DECREASED ( 7 FDA reports)
TESTIS CANCER ( 7 FDA reports)
TONGUE DISORDER ( 7 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 7 FDA reports)
URTICARIA CHOLINERGIC ( 7 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 7 FDA reports)
VITREOUS FLOATERS ( 7 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 7 FDA reports)
WEIGHT LOSS POOR ( 7 FDA reports)
ACTINIC KERATOSIS ( 6 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 6 FDA reports)
BLOOD PRESSURE ABNORMAL ( 6 FDA reports)
BODY TEMPERATURE DECREASED ( 6 FDA reports)
CHORIORETINOPATHY ( 6 FDA reports)
COLONIC POLYP ( 6 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 6 FDA reports)
DECREASED ACTIVITY ( 6 FDA reports)
DRUG INTOLERANCE ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
EJACULATION FAILURE ( 6 FDA reports)
EUPHORIC MOOD ( 6 FDA reports)
FEELING COLD ( 6 FDA reports)
GINGIVAL INFECTION ( 6 FDA reports)
GINGIVITIS ( 6 FDA reports)
GOUT ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
HOSTILITY ( 6 FDA reports)
HYPERACUSIS ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 6 FDA reports)
INTENTIONAL DRUG MISUSE ( 6 FDA reports)
INTENTIONAL OVERDOSE ( 6 FDA reports)
INTESTINAL OBSTRUCTION ( 6 FDA reports)
JOINT INJURY ( 6 FDA reports)
MONOPARESIS ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
NOCTURNAL DYSPNOEA ( 6 FDA reports)
OBESITY ( 6 FDA reports)
OEDEMA MOUTH ( 6 FDA reports)
PALLOR ( 6 FDA reports)
PARANOIA ( 6 FDA reports)
PAROSMIA ( 6 FDA reports)
PENILE SIZE REDUCED ( 6 FDA reports)
PSYCHOTIC DISORDER ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
RASH GENERALISED ( 6 FDA reports)
RASH PAPULAR ( 6 FDA reports)
RESPIRATORY RATE INCREASED ( 6 FDA reports)
RETINAL VEIN OCCLUSION ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
SKIN DISORDER ( 6 FDA reports)
SKIN ODOUR ABNORMAL ( 6 FDA reports)
SPINAL HAEMANGIOMA ( 6 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 6 FDA reports)
SUICIDE ATTEMPT ( 6 FDA reports)
TENSION ( 6 FDA reports)
THINKING ABNORMAL ( 6 FDA reports)
TREATMENT NONCOMPLIANCE ( 6 FDA reports)
UNRESPONSIVE TO STIMULI ( 6 FDA reports)
URINARY TRACT DISORDER ( 6 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
VIRILISM ( 6 FDA reports)
WOUND ( 6 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 5 FDA reports)
ADENOCARCINOMA ( 5 FDA reports)
AMAUROSIS FUGAX ( 5 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
ANKYLOSING SPONDYLITIS ( 5 FDA reports)
AORTIC VALVE INCOMPETENCE ( 5 FDA reports)
APPLICATION SITE URTICARIA ( 5 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
BASAL CELL CARCINOMA ( 5 FDA reports)
BLADDER DISORDER ( 5 FDA reports)
BLINDNESS ( 5 FDA reports)
CAROTID ARTERY DISEASE ( 5 FDA reports)
COGNITIVE DISORDER ( 5 FDA reports)
CORONARY ARTERY STENOSIS ( 5 FDA reports)
CRYING ( 5 FDA reports)
CYST ( 5 FDA reports)
DEAFNESS ( 5 FDA reports)
DENTAL PROSTHESIS USER ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DEVICE LEAKAGE ( 5 FDA reports)
DRUG DISPENSING ERROR ( 5 FDA reports)
DRY EYE ( 5 FDA reports)
DYSKINESIA ( 5 FDA reports)
EJECTION FRACTION DECREASED ( 5 FDA reports)
ENTEROCOLITIS ( 5 FDA reports)
EXOSTOSIS ( 5 FDA reports)
EYE HAEMORRHAGE ( 5 FDA reports)
EYE IRRITATION ( 5 FDA reports)
FIBROMYALGIA ( 5 FDA reports)
FLATBACK SYNDROME ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
HAIR COLOUR CHANGES ( 5 FDA reports)
HAIR TEXTURE ABNORMAL ( 5 FDA reports)
HEARING IMPAIRED ( 5 FDA reports)
HYPERTONIA ( 5 FDA reports)
HYPOGONADISM MALE ( 5 FDA reports)
IMPAIRED DRIVING ABILITY ( 5 FDA reports)
INCONTINENCE ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
INTRACARDIAC THROMBUS ( 5 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
MALIGNANT MELANOMA ( 5 FDA reports)
MULTIPLE MYELOMA ( 5 FDA reports)
MUSCLE FATIGUE ( 5 FDA reports)
NAIL DYSTROPHY ( 5 FDA reports)
NEOPLASM RECURRENCE ( 5 FDA reports)
NIPPLE PAIN ( 5 FDA reports)
OESOPHAGEAL STENOSIS ( 5 FDA reports)
ORGANISING PNEUMONIA ( 5 FDA reports)
OTORRHOEA ( 5 FDA reports)
PANCREATIC CYST ( 5 FDA reports)
PARKINSON'S DISEASE ( 5 FDA reports)
PENIS DISORDER ( 5 FDA reports)
PLATELET COUNT INCREASED ( 5 FDA reports)
PLEURAL FIBROSIS ( 5 FDA reports)
PRODUCT PHYSICAL ISSUE ( 5 FDA reports)
PSYCHIATRIC SYMPTOM ( 5 FDA reports)
RADIOTHERAPY ( 5 FDA reports)
RENAL INJURY ( 5 FDA reports)
SEMEN VOLUME DECREASED ( 5 FDA reports)
SERUM FERRITIN INCREASED ( 5 FDA reports)
SKIN INJURY ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
THERAPY NON-RESPONDER ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 5 FDA reports)
TONGUE COATED ( 5 FDA reports)
VARICOSE VEIN RUPTURED ( 5 FDA reports)
VENTRICULAR ARRHYTHMIA ( 5 FDA reports)
VISUAL FIELD DEFECT ( 5 FDA reports)
WRIST FRACTURE ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
ADRENAL ADENOMA ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
AFFECTIVE DISORDER ( 4 FDA reports)
AKATHISIA ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ANEURYSM ( 4 FDA reports)
ANGIOPATHY ( 4 FDA reports)
AORTIC VALVE REPLACEMENT ( 4 FDA reports)
BEHCET'S SYNDROME ( 4 FDA reports)
BILIARY DILATATION ( 4 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 4 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 4 FDA reports)
BLOOD IRON DECREASED ( 4 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 4 FDA reports)
BLOOD MAGNESIUM DECREASED ( 4 FDA reports)
BLOOD TESTOSTERONE FREE DECREASED ( 4 FDA reports)
BLOOD TESTOSTERONE FREE INCREASED ( 4 FDA reports)
BODY HEIGHT ABOVE NORMAL ( 4 FDA reports)
BONE DENSITY DECREASED ( 4 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 4 FDA reports)
BONE LOSS ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
COLON CANCER ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DILATATION VENTRICULAR ( 4 FDA reports)
DISCOMFORT ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
DRUG LEVEL THERAPEUTIC ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
EJACULATION DISORDER ( 4 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 4 FDA reports)
ELEVATED MOOD ( 4 FDA reports)
FLANK PAIN ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
GENITAL DISORDER MALE ( 4 FDA reports)
GENITAL RASH ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
HAEMANGIOMA ( 4 FDA reports)
HAEMANGIOMA OF LIVER ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HYPERAESTHESIA ( 4 FDA reports)
HYPOAESTHESIA ORAL ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
INCREASED TENDENCY TO BRUISE ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
LABORATORY TEST ABNORMAL ( 4 FDA reports)
LACRIMATION INCREASED ( 4 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
LIMB DEFORMITY ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
MALE SEXUAL DYSFUNCTION ( 4 FDA reports)
MALNUTRITION ( 4 FDA reports)
MASS ( 4 FDA reports)
MENINGIOMA ( 4 FDA reports)
MENSTRUATION DELAYED ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER ( 4 FDA reports)
ODYNOPHAGIA ( 4 FDA reports)
OESOPHAGEAL CARCINOMA ( 4 FDA reports)
OESOPHAGEAL PAIN ( 4 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 4 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 4 FDA reports)
OROPHARYNGEAL SWELLING ( 4 FDA reports)
ORTHOPNOEA ( 4 FDA reports)
PARAESTHESIA ORAL ( 4 FDA reports)
PHYSICAL ASSAULT ( 4 FDA reports)
POLYP ( 4 FDA reports)
PROCTITIS ( 4 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
RALES ( 4 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
SARCOPENIA ( 4 FDA reports)
SCAR ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 4 FDA reports)
SHOULDER OPERATION ( 4 FDA reports)
SIALOADENITIS ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
SUDDEN ONSET OF SLEEP ( 4 FDA reports)
TACHYPHRENIA ( 4 FDA reports)
TERMINAL INSOMNIA ( 4 FDA reports)
THIRST ( 4 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
TOOTH DISORDER ( 4 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
UPPER LIMB FRACTURE ( 4 FDA reports)
WEIGHT FLUCTUATION ( 4 FDA reports)
WOUND DEBRIDEMENT ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ADJUSTMENT DISORDER ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
AORTIC RUPTURE ( 3 FDA reports)
AORTIC VALVE SCLEROSIS ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
APPLICATION SITE SWELLING ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BACK INJURY ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD CORTICOSTERONE DECREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
BLOOD TEST ABNORMAL ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BURNING MOUTH SYNDROME ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CELLULITIS STREPTOCOCCAL ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CEREBROSPINAL FLUID RHINORRHOEA ( 3 FDA reports)
CHOKING ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
COMA ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
CROHN'S DISEASE ( 3 FDA reports)
DACRYOCYSTITIS ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
DYSLIPIDAEMIA ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
FOOD ALLERGY ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GENITAL BURNING SENSATION ( 3 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 3 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 3 FDA reports)
GROIN PAIN ( 3 FDA reports)
GROWTH RETARDATION ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HERNIA ( 3 FDA reports)
HORMONE LEVEL ABNORMAL ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERVIGILANCE ( 3 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 3 FDA reports)
IMPATIENCE ( 3 FDA reports)
INFERTILITY ( 3 FDA reports)
INFERTILITY MALE ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INTESTINAL HAEMORRHAGE ( 3 FDA reports)
INTRACRANIAL HYPOTENSION ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LIPOHYPERTROPHY ( 3 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LYME DISEASE ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MAJOR DEPRESSION ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 3 FDA reports)
MILIA ( 3 FDA reports)
MONOCYTE COUNT INCREASED ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
MULTIPLE FRACTURES ( 3 FDA reports)
MUSCLE MASS ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MUSCULOSKELETAL DISORDER ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
NAIL DISORDER ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
NEUROPATHIC ULCER ( 3 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 3 FDA reports)
OCCULT BLOOD POSITIVE ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
OESOPHAGEAL DISCOMFORT ( 3 FDA reports)
OESOPHAGEAL SPASM ( 3 FDA reports)
ORAL SURGERY ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PANCREAS INFECTION ( 3 FDA reports)
PANCREATIC DISORDER ( 3 FDA reports)
PANCREATITIS CHRONIC ( 3 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 3 FDA reports)
PARESIS ( 3 FDA reports)
PAROTID DUCT OBSTRUCTION ( 3 FDA reports)
PATHOLOGICAL GAMBLING ( 3 FDA reports)
PENILE HAEMORRHAGE ( 3 FDA reports)
PERIORBITAL CELLULITIS ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PHLEBITIS SUPERFICIAL ( 3 FDA reports)
PHOTOPSIA ( 3 FDA reports)
PITUITARY HAEMORRHAGE ( 3 FDA reports)
PRECANCEROUS SKIN LESION ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PROSTATITIS ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PSORIATIC ARTHROPATHY ( 3 FDA reports)
PULMONARY THROMBOSIS ( 3 FDA reports)
PURULENT DISCHARGE ( 3 FDA reports)
REFLUX GASTRITIS ( 3 FDA reports)
REGURGITATION ( 3 FDA reports)
RENAL CANCER ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
RETCHING ( 3 FDA reports)
RETICULOCYTE COUNT DECREASED ( 3 FDA reports)
RETINAL INJURY ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
SCOLIOSIS ( 3 FDA reports)
SCROTAL CYST ( 3 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 3 FDA reports)
SELF-INJURIOUS IDEATION ( 3 FDA reports)
SEMEN DISCOLOURATION ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
SKIN TIGHTNESS ( 3 FDA reports)
SPERM COUNT ZERO ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
SYNCOPE VASOVAGAL ( 3 FDA reports)
TESTICULAR DISORDER ( 3 FDA reports)
THYROXINE INCREASED ( 3 FDA reports)
TIBIA FRACTURE ( 3 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 3 FDA reports)
URINARY BLADDER RUPTURE ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 3 FDA reports)
WEGENER'S GRANULOMATOSIS ( 3 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ADRENAL CARCINOMA ( 2 FDA reports)
ADVANCED SLEEP PHASE ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANGIOGRAM ABNORMAL ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
APPLICATION SITE VESICLES ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BINGE EATING ( 2 FDA reports)
BIPOLAR II DISORDER ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD OESTROGEN DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD TESTOSTERONE ( 2 FDA reports)
BLOOD TESTOSTERONE FREE ABNORMAL ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 2 FDA reports)
BODY HEIGHT INCREASED ( 2 FDA reports)
BONE DEBRIDEMENT ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BREAST CANCER IN SITU ( 2 FDA reports)
BRONCHIAL IRRITATION ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CAFE AU LAIT SPOTS ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CAUSTIC INJURY ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 2 FDA reports)
CERUMEN IMPACTION ( 2 FDA reports)
CERVICAL SPINAL STENOSIS ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHILDHOOD DISINTEGRATIVE DISORDER ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
COLON CANCER STAGE 0 ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CRANIOPHARYNGIOMA ( 2 FDA reports)
DEAFNESS TRANSITORY ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
EPIDIDYMAL CYST ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
EXPOSURE VIA PARTNER ( 2 FDA reports)
FAT TISSUE INCREASED ( 2 FDA reports)
FEAR OF FALLING ( 2 FDA reports)
FEELING GUILTY ( 2 FDA reports)
FEELINGS OF WORTHLESSNESS ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GENITAL ERYTHEMA ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMANGIOPERICYTOMA ( 2 FDA reports)
HAEMATOSPERMIA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMORRHAGE URINARY TRACT ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HYPERANDROGENISM ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOPNOEA ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
IMPULSE-CONTROL DISORDER ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INSTILLATION SITE ABNORMAL SENSATION ( 2 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INTRASPINAL ABSCESS ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LAPAROSCOPIC SURGERY ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 2 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MONARTHRITIS ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MORBID THOUGHTS ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MYOSITIS OSSIFICANS ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NASAL INFLAMMATION ( 2 FDA reports)
NEOPLASM PROSTATE ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OTITIS MEDIA ACUTE ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARASPINAL ABSCESS ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PENILE DISCHARGE ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
PENILE SWELLING ( 2 FDA reports)
PERISTALSIS VISIBLE ( 2 FDA reports)
PITUITARY TUMOUR RECURRENT ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POLYMEDICATION ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PRODUCT LABEL ISSUE ( 2 FDA reports)
PRODUCT ODOUR ABNORMAL ( 2 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 2 FDA reports)
PROMISCUITY ( 2 FDA reports)
PROSTATE CANCER STAGE II ( 2 FDA reports)
PROSTATE CANCER STAGE IV ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROSTATE INFECTION ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RECTAL CANCER STAGE 0 ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RETICULOCYTE COUNT INCREASED ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCHIZOID PERSONALITY DISORDER ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SEASONAL ALLERGY ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SECONDARY HYPOGONADISM ( 2 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SEXUAL OFFENCE ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SIGNET-RING CELL CARCINOMA ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SKIN WRINKLING ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TENDON INJURY ( 2 FDA reports)
TESTICULAR NEOPLASM ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THROMBECTOMY ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
THYROID PAIN ( 2 FDA reports)
THYROIDITIS ( 2 FDA reports)
TOBACCO ABUSE ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TOOTH IMPACTED ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TOOTH REPAIR ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
URINARY SEDIMENT PRESENT ( 2 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 2 FDA reports)
VARICOCELE ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
WEIGHT ABNORMAL ( 2 FDA reports)
WEIGHT LOSS DIET ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ADRENAL HAEMORRHAGE ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
AGITATED DEPRESSION ( 1 FDA reports)
AIDS RELATED COMPLICATION ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
APPLICATION SITE PERSPIRATION ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ASPERMIA ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AUTOIMMUNE PANCREATITIS ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BENIGN NEOPLASM OF TESTIS ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER HYPERTROPHY ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD LUTEINISING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN TUMOUR OPERATION ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST ATROPHY ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNION ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARCINOID TUMOUR PULMONARY ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CARTILAGE ATROPHY ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHEMICAL BURNS OF EYE ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
DACRYOCYSTORHINOSTOMY ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DENTAL CARE ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPIPHYSIOLYSIS ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
EXPOSURE VIA DIRECT CONTACT ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOLLICULAR THYROID CANCER ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GASTRIC BANDING ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HIV WASTING SYNDROME ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRITIS ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LENS DISLOCATION ( 1 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MACULE ( 1 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONONEURITIS ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
OSCILLOPSIA ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
OVULATION DISORDER ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARAPHILIA ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PELVIC NEOPLASM ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PENIS CARCINOMA ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERICARDITIS ADHESIVE ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PIGMENT NEPHROPATHY ( 1 FDA reports)
PLACENTA PRAEVIA ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT RECONSTITUTION ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROGESTERONE DECREASED ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROLACTINOMA ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROSTATIC CALCIFICATION ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC PAIN ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SEX HORMONE BINDING GLOBULIN INCREASED ( 1 FDA reports)
SEXUAL ACTIVITY INCREASED ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SLIPPED FEMORAL EPIPHYSIS ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPERM CONCENTRATION ZERO ( 1 FDA reports)
SPERM COUNT DECREASED ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TESTIS DISCOMFORT ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TONGUE ATROPHY ( 1 FDA reports)
TONGUE CANCER METASTATIC ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR DYSSYNCHRONY ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIOLENT IDEATION ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
VULVOVAGINAL SWELLING ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WITHDRAWAL HYPERTENSION ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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