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

DIARRHOEA ( 453 FDA reports)
COLITIS ULCERATIVE ( 402 FDA reports)
NAUSEA ( 388 FDA reports)
CROHN'S DISEASE ( 380 FDA reports)
HEADACHE ( 368 FDA reports)
FATIGUE ( 365 FDA reports)
PAIN ( 313 FDA reports)
ABDOMINAL PAIN ( 294 FDA reports)
DRUG INEFFECTIVE ( 288 FDA reports)
ARTHRALGIA ( 285 FDA reports)
DYSPNOEA ( 285 FDA reports)
PYREXIA ( 276 FDA reports)
ANXIETY ( 265 FDA reports)
ANAEMIA ( 259 FDA reports)
VOMITING ( 246 FDA reports)
DIZZINESS ( 237 FDA reports)
WEIGHT DECREASED ( 235 FDA reports)
DEPRESSION ( 230 FDA reports)
COLITIS ( 229 FDA reports)
ASTHENIA ( 218 FDA reports)
CHEST PAIN ( 198 FDA reports)
INJECTION SITE PAIN ( 187 FDA reports)
PNEUMONIA ( 183 FDA reports)
OEDEMA PERIPHERAL ( 175 FDA reports)
BACK PAIN ( 172 FDA reports)
MALAISE ( 164 FDA reports)
FALL ( 160 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 160 FDA reports)
DEHYDRATION ( 158 FDA reports)
RASH ( 158 FDA reports)
INSOMNIA ( 153 FDA reports)
INFUSION RELATED REACTION ( 150 FDA reports)
HYPOAESTHESIA ( 149 FDA reports)
MYALGIA ( 147 FDA reports)
RECTAL HAEMORRHAGE ( 146 FDA reports)
URINARY TRACT INFECTION ( 140 FDA reports)
PARAESTHESIA ( 138 FDA reports)
PAIN IN EXTREMITY ( 136 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 127 FDA reports)
HAEMATOCHEZIA ( 127 FDA reports)
RENAL FAILURE ( 127 FDA reports)
COUGH ( 125 FDA reports)
HYPERTENSION ( 121 FDA reports)
WEIGHT INCREASED ( 119 FDA reports)
SEPSIS ( 118 FDA reports)
DEEP VEIN THROMBOSIS ( 117 FDA reports)
ABDOMINAL PAIN UPPER ( 116 FDA reports)
CONDITION AGGRAVATED ( 112 FDA reports)
SINUSITIS ( 111 FDA reports)
ERYTHEMA ( 106 FDA reports)
PULMONARY EMBOLISM ( 106 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 103 FDA reports)
PRURITUS ( 101 FDA reports)
INJECTION SITE ERYTHEMA ( 97 FDA reports)
IRRITABLE BOWEL SYNDROME ( 97 FDA reports)
MUSCLE SPASMS ( 97 FDA reports)
CELLULITIS ( 95 FDA reports)
PLEURAL EFFUSION ( 95 FDA reports)
URTICARIA ( 93 FDA reports)
GASTROINTESTINAL DISORDER ( 92 FDA reports)
DYSPHAGIA ( 91 FDA reports)
FEELING ABNORMAL ( 91 FDA reports)
HYPOTENSION ( 86 FDA reports)
ARTHRITIS ( 85 FDA reports)
OSTEOARTHRITIS ( 84 FDA reports)
HAEMOGLOBIN DECREASED ( 83 FDA reports)
MIGRAINE ( 83 FDA reports)
NEPHROLITHIASIS ( 83 FDA reports)
VISION BLURRED ( 83 FDA reports)
ASTHMA ( 81 FDA reports)
CHOLELITHIASIS ( 80 FDA reports)
DECREASED APPETITE ( 80 FDA reports)
DIABETES MELLITUS ( 80 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 80 FDA reports)
HYPERHIDROSIS ( 79 FDA reports)
MYOCARDIAL INFARCTION ( 79 FDA reports)
PANCREATITIS ( 79 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 78 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 77 FDA reports)
CHILLS ( 76 FDA reports)
INJURY ( 76 FDA reports)
OSTEOPOROSIS ( 76 FDA reports)
GAIT DISTURBANCE ( 75 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 75 FDA reports)
HEPATIC ENZYME INCREASED ( 74 FDA reports)
TREMOR ( 74 FDA reports)
OSTEOPENIA ( 73 FDA reports)
BONE PAIN ( 72 FDA reports)
CHEST DISCOMFORT ( 72 FDA reports)
FOOT FRACTURE ( 72 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 72 FDA reports)
INTESTINAL HAEMORRHAGE ( 71 FDA reports)
MUSCULAR WEAKNESS ( 71 FDA reports)
JOINT SWELLING ( 70 FDA reports)
CONSTIPATION ( 69 FDA reports)
LIP DRY ( 69 FDA reports)
BRONCHITIS ( 68 FDA reports)
INJECTION SITE HAEMATOMA ( 68 FDA reports)
THROMBOSIS ( 68 FDA reports)
HYPERSENSITIVITY ( 67 FDA reports)
LUNG DISORDER ( 67 FDA reports)
ALOPECIA ( 66 FDA reports)
CONVULSION ( 66 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 66 FDA reports)
LYMPHADENOPATHY ( 66 FDA reports)
NASAL CONGESTION ( 66 FDA reports)
SWELLING FACE ( 66 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 65 FDA reports)
EMOTIONAL DISTRESS ( 65 FDA reports)
MOUTH ULCERATION ( 65 FDA reports)
SWELLING ( 65 FDA reports)
FLUSHING ( 64 FDA reports)
GASTRITIS ( 64 FDA reports)
OSTEOMYELITIS ( 64 FDA reports)
ABDOMINAL DISTENSION ( 63 FDA reports)
DRY SKIN ( 62 FDA reports)
INFECTION ( 62 FDA reports)
OROPHARYNGEAL PAIN ( 61 FDA reports)
BLOOD PRESSURE INCREASED ( 60 FDA reports)
BONE DISORDER ( 60 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 59 FDA reports)
PANCYTOPENIA ( 59 FDA reports)
BLOOD GLUCOSE INCREASED ( 58 FDA reports)
HERPES ZOSTER ( 58 FDA reports)
PALPITATIONS ( 58 FDA reports)
ATELECTASIS ( 57 FDA reports)
HAEMORRHOIDS ( 57 FDA reports)
MULTI-ORGAN DISORDER ( 57 FDA reports)
RESPIRATORY FAILURE ( 57 FDA reports)
TACHYCARDIA ( 57 FDA reports)
CONFUSIONAL STATE ( 56 FDA reports)
OSTEONECROSIS OF JAW ( 56 FDA reports)
PLATELET COUNT INCREASED ( 56 FDA reports)
APPENDICITIS ( 55 FDA reports)
LOSS OF CONSCIOUSNESS ( 55 FDA reports)
NEUROPATHY PERIPHERAL ( 55 FDA reports)
RENAL FAILURE ACUTE ( 55 FDA reports)
STAPHYLOCOCCAL INFECTION ( 55 FDA reports)
HAEMORRHAGE ( 54 FDA reports)
MEMORY IMPAIRMENT ( 54 FDA reports)
OSTEITIS ( 54 FDA reports)
PERIODONTITIS ( 54 FDA reports)
THROMBOCYTOPENIA ( 54 FDA reports)
ACNE ( 53 FDA reports)
DENTAL CARIES ( 53 FDA reports)
NASOPHARYNGITIS ( 53 FDA reports)
STRESS ( 53 FDA reports)
SUICIDAL IDEATION ( 53 FDA reports)
TOOTH DISORDER ( 53 FDA reports)
HIATUS HERNIA ( 52 FDA reports)
INCORRECT DOSE ADMINISTERED ( 52 FDA reports)
STOMATITIS ( 52 FDA reports)
CEREBROVASCULAR ACCIDENT ( 51 FDA reports)
CONTUSION ( 51 FDA reports)
DRUG DOSE OMISSION ( 51 FDA reports)
INJECTION SITE HAEMORRHAGE ( 51 FDA reports)
ANAL FISTULA ( 50 FDA reports)
DRUG HYPERSENSITIVITY ( 50 FDA reports)
INFLUENZA LIKE ILLNESS ( 50 FDA reports)
PANIC ATTACK ( 50 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 49 FDA reports)
PAIN IN JAW ( 49 FDA reports)
HYPOKALAEMIA ( 48 FDA reports)
OSTEOLYSIS ( 48 FDA reports)
DYSGEUSIA ( 47 FDA reports)
OSTEONECROSIS ( 47 FDA reports)
RENAL DISORDER ( 47 FDA reports)
SOMNOLENCE ( 47 FDA reports)
LEUKOCYTOSIS ( 46 FDA reports)
METASTATIC NEOPLASM ( 46 FDA reports)
SYNCOPE ( 46 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 46 FDA reports)
VASCULITIS ( 46 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 46 FDA reports)
DEVICE FAILURE ( 45 FDA reports)
GINGIVITIS ( 45 FDA reports)
HEPATIC STEATOSIS ( 45 FDA reports)
CHOLECYSTITIS ( 44 FDA reports)
DYSPEPSIA ( 44 FDA reports)
GENERALISED OEDEMA ( 44 FDA reports)
LUNG NEOPLASM ( 44 FDA reports)
PELVIC FRACTURE ( 44 FDA reports)
ENTEROCOCCAL INFECTION ( 43 FDA reports)
HERNIA ( 43 FDA reports)
ILEUS ( 43 FDA reports)
INJECTION SITE PRURITUS ( 43 FDA reports)
ROTATOR CUFF SYNDROME ( 43 FDA reports)
SLEEP APNOEA SYNDROME ( 43 FDA reports)
TOOTH ABSCESS ( 43 FDA reports)
DEATH ( 42 FDA reports)
HEART RATE INCREASED ( 42 FDA reports)
HYPERGLYCAEMIA ( 42 FDA reports)
INJECTION SITE SWELLING ( 42 FDA reports)
PERIODONTAL DISEASE ( 42 FDA reports)
PNEUMONITIS ( 42 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 42 FDA reports)
UTERINE LEIOMYOMA ( 42 FDA reports)
VIRAL INFECTION ( 42 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 42 FDA reports)
BONE FRAGMENTATION ( 41 FDA reports)
INFLUENZA ( 41 FDA reports)
ADVERSE DRUG REACTION ( 40 FDA reports)
CANDIDIASIS ( 40 FDA reports)
CORONARY ARTERY DISEASE ( 40 FDA reports)
DYSURIA ( 40 FDA reports)
GASTROENTERITIS ( 40 FDA reports)
GINGIVAL INFECTION ( 40 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 40 FDA reports)
SPINAL OSTEOARTHRITIS ( 40 FDA reports)
ATRIAL FIBRILLATION ( 39 FDA reports)
ENTERITIS ( 39 FDA reports)
MUSCULOSKELETAL PAIN ( 39 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 39 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 39 FDA reports)
BONE EROSION ( 38 FDA reports)
FISTULA ( 38 FDA reports)
GINGIVAL PAIN ( 38 FDA reports)
IMPAIRED HEALING ( 38 FDA reports)
SKIN ULCER ( 38 FDA reports)
AFFECTIVE DISORDER ( 37 FDA reports)
CHOLECYSTITIS CHRONIC ( 37 FDA reports)
DIVERTICULITIS ( 37 FDA reports)
EXOSTOSIS ( 37 FDA reports)
ORAL CANDIDIASIS ( 37 FDA reports)
PERICARDIAL EFFUSION ( 37 FDA reports)
ABDOMINAL DISCOMFORT ( 36 FDA reports)
BLOOD PRESSURE DECREASED ( 36 FDA reports)
BREAST CANCER ( 36 FDA reports)
DEVICE MALFUNCTION ( 36 FDA reports)
HEPATIC FAILURE ( 36 FDA reports)
NIGHT SWEATS ( 36 FDA reports)
RENAL FAILURE CHRONIC ( 36 FDA reports)
VERTIGO ( 36 FDA reports)
DRUG DEPENDENCE ( 35 FDA reports)
SINUS TACHYCARDIA ( 35 FDA reports)
TOOTH EXTRACTION ( 35 FDA reports)
APPENDICECTOMY ( 34 FDA reports)
APTYALISM ( 34 FDA reports)
BLOOD POTASSIUM DECREASED ( 34 FDA reports)
BRONCHOPNEUMONIA ( 34 FDA reports)
BURNING SENSATION ( 34 FDA reports)
EPISTAXIS ( 34 FDA reports)
GINGIVAL SWELLING ( 34 FDA reports)
HALLUCINATION ( 34 FDA reports)
HEPATIC CIRRHOSIS ( 34 FDA reports)
HYPOGLYCAEMIA ( 34 FDA reports)
OESOPHAGITIS ( 34 FDA reports)
OLIGURIA ( 34 FDA reports)
PREGNANCY ( 34 FDA reports)
PROCTITIS ( 34 FDA reports)
TREATMENT NONCOMPLIANCE ( 34 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 33 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 33 FDA reports)
MALOCCLUSION ( 33 FDA reports)
POOR DENTAL CONDITION ( 33 FDA reports)
SCAR ( 33 FDA reports)
TOOTH INJURY ( 33 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 33 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 32 FDA reports)
CLOSTRIDIAL INFECTION ( 32 FDA reports)
DYSPNOEA EXERTIONAL ( 32 FDA reports)
ENDODONTIC PROCEDURE ( 32 FDA reports)
ESCHERICHIA INFECTION ( 32 FDA reports)
FEELING HOT ( 32 FDA reports)
FRACTURE ( 32 FDA reports)
GALLBLADDER DISORDER ( 32 FDA reports)
LUPUS-LIKE SYNDROME ( 32 FDA reports)
PYELONEPHRITIS ( 32 FDA reports)
SCAB ( 32 FDA reports)
ABASIA ( 31 FDA reports)
ARTERIOSCLEROSIS ( 31 FDA reports)
AUTOIMMUNE DISORDER ( 31 FDA reports)
BURSITIS ( 31 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 31 FDA reports)
FEAR ( 31 FDA reports)
NERVOUSNESS ( 31 FDA reports)
QUALITY OF LIFE DECREASED ( 31 FDA reports)
RHINORRHOEA ( 31 FDA reports)
WEGENER'S GRANULOMATOSIS ( 31 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 31 FDA reports)
ARTHROPATHY ( 30 FDA reports)
BALANCE DISORDER ( 30 FDA reports)
CHRONIC SINUSITIS ( 30 FDA reports)
DIVERTICULUM ( 30 FDA reports)
DRUG EFFECT DECREASED ( 30 FDA reports)
DRY MOUTH ( 30 FDA reports)
MALNUTRITION ( 30 FDA reports)
NECK PAIN ( 30 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 30 FDA reports)
ABDOMINAL PAIN LOWER ( 29 FDA reports)
CATARACT ( 29 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 29 FDA reports)
DISTURBANCE IN ATTENTION ( 29 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 29 FDA reports)
FLATULENCE ( 29 FDA reports)
HAEMANGIOMA ( 29 FDA reports)
HAEMATOCRIT DECREASED ( 29 FDA reports)
INJECTION SITE URTICARIA ( 29 FDA reports)
INTESTINAL OBSTRUCTION ( 29 FDA reports)
MAJOR DEPRESSION ( 29 FDA reports)
OTITIS EXTERNA ( 29 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 29 FDA reports)
PULPITIS DENTAL ( 29 FDA reports)
RENAL IMPAIRMENT ( 29 FDA reports)
ROAD TRAFFIC ACCIDENT ( 29 FDA reports)
SJOGREN'S SYNDROME ( 29 FDA reports)
VISUAL IMPAIRMENT ( 29 FDA reports)
ANOREXIA ( 28 FDA reports)
FACIAL NEURALGIA ( 28 FDA reports)
FLANK PAIN ( 28 FDA reports)
JOINT DISLOCATION ( 28 FDA reports)
MEDICATION RESIDUE ( 28 FDA reports)
OSTEITIS DEFORMANS ( 28 FDA reports)
RHEUMATOID ARTHRITIS ( 28 FDA reports)
SCLERODERMA ( 28 FDA reports)
THROAT IRRITATION ( 28 FDA reports)
THROMBOCYTOSIS ( 28 FDA reports)
FEELING COLD ( 27 FDA reports)
GASTRIC ULCER ( 27 FDA reports)
HUMERUS FRACTURE ( 27 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 27 FDA reports)
OCULAR HYPERAEMIA ( 27 FDA reports)
PERICARDITIS ( 27 FDA reports)
PERIRECTAL ABSCESS ( 27 FDA reports)
AMNESIA ( 26 FDA reports)
BLOOD CREATININE INCREASED ( 26 FDA reports)
BONE LOSS ( 26 FDA reports)
CARDIAC DISORDER ( 26 FDA reports)
DYSSTASIA ( 26 FDA reports)
FUNGAL INFECTION ( 26 FDA reports)
HOT FLUSH ( 26 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 26 FDA reports)
OEDEMA ( 26 FDA reports)
PROCTOCOLITIS ( 26 FDA reports)
SLEEP DISORDER ( 26 FDA reports)
TINNITUS ( 26 FDA reports)
TOOTHACHE ( 26 FDA reports)
UNEVALUABLE EVENT ( 26 FDA reports)
VITREOUS DETACHMENT ( 26 FDA reports)
ABORTION SPONTANEOUS ( 25 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 25 FDA reports)
AUTOIMMUNE HEPATITIS ( 25 FDA reports)
DRUG ERUPTION ( 25 FDA reports)
DRUG INTERACTION ( 25 FDA reports)
DYSPHONIA ( 25 FDA reports)
FOOT DEFORMITY ( 25 FDA reports)
INFLAMMATION ( 25 FDA reports)
LEUKOPENIA ( 25 FDA reports)
MENINGIOMA ( 25 FDA reports)
MUSCLE TWITCHING ( 25 FDA reports)
POLYP ( 25 FDA reports)
PULMONARY OEDEMA ( 25 FDA reports)
STREPTOCOCCAL INFECTION ( 25 FDA reports)
THROAT TIGHTNESS ( 25 FDA reports)
VAGINAL HAEMORRHAGE ( 25 FDA reports)
DEAFNESS ( 24 FDA reports)
DUODENITIS ( 24 FDA reports)
EXPOSED BONE IN JAW ( 24 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 24 FDA reports)
HOSPITALISATION ( 24 FDA reports)
INJECTION SITE REACTION ( 24 FDA reports)
OVERDOSE ( 24 FDA reports)
PLATELET COUNT DECREASED ( 24 FDA reports)
PSORIASIS ( 24 FDA reports)
RASH PRURITIC ( 24 FDA reports)
RETCHING ( 24 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 24 FDA reports)
SUICIDE ATTEMPT ( 24 FDA reports)
ACOUSTIC NEUROMA ( 23 FDA reports)
APHTHOUS STOMATITIS ( 23 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 23 FDA reports)
BONE DEBRIDEMENT ( 23 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 23 FDA reports)
EMPHYSEMA ( 23 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 23 FDA reports)
LEUKOENCEPHALOPATHY ( 23 FDA reports)
LUMBAR SPINAL STENOSIS ( 23 FDA reports)
NOCTURIA ( 23 FDA reports)
UMBILICAL HERNIA ( 23 FDA reports)
ANHEDONIA ( 22 FDA reports)
BASAL CELL CARCINOMA ( 22 FDA reports)
BLISTER ( 22 FDA reports)
BONE OPERATION ( 22 FDA reports)
DISEASE RECURRENCE ( 22 FDA reports)
ECZEMA ( 22 FDA reports)
ERUCTATION ( 22 FDA reports)
FEMUR FRACTURE ( 22 FDA reports)
FLUID RETENTION ( 22 FDA reports)
HAEMATURIA ( 22 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 22 FDA reports)
MENISCUS LESION ( 22 FDA reports)
MOBILITY DECREASED ( 22 FDA reports)
RAYNAUD'S PHENOMENON ( 22 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 21 FDA reports)
BONE DENSITY DECREASED ( 21 FDA reports)
CARDIOMEGALY ( 21 FDA reports)
CEREBRAL ATROPHY ( 21 FDA reports)
ENDOMETRIOSIS ( 21 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 21 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 21 FDA reports)
INJECTION SITE NODULE ( 21 FDA reports)
INJECTION SITE RASH ( 21 FDA reports)
IRRITABILITY ( 21 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 21 FDA reports)
NERVOUS SYSTEM DISORDER ( 21 FDA reports)
OFF LABEL USE ( 21 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 21 FDA reports)
SKIN EXFOLIATION ( 21 FDA reports)
SPINAL FRACTURE ( 21 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 21 FDA reports)
VISUAL DISTURBANCE ( 21 FDA reports)
WHEEZING ( 21 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 20 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 20 FDA reports)
CYANOSIS ( 20 FDA reports)
EAR INFECTION ( 20 FDA reports)
FOLLICULITIS ( 20 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 20 FDA reports)
HORDEOLUM ( 20 FDA reports)
INTERSTITIAL LUNG DISEASE ( 20 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 20 FDA reports)
LETHARGY ( 20 FDA reports)
MOOD ALTERED ( 20 FDA reports)
PEPTIC ULCER ( 20 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 20 FDA reports)
PYODERMA GANGRENOSUM ( 20 FDA reports)
SPINAL DISORDER ( 20 FDA reports)
SPLENOMEGALY ( 20 FDA reports)
WRIST FRACTURE ( 20 FDA reports)
ADENOCARCINOMA ( 19 FDA reports)
ADRENAL INSUFFICIENCY ( 19 FDA reports)
APHASIA ( 19 FDA reports)
ASCITES ( 19 FDA reports)
BONE ATROPHY ( 19 FDA reports)
BUNDLE BRANCH BLOCK ( 19 FDA reports)
COAGULOPATHY ( 19 FDA reports)
COLD SWEAT ( 19 FDA reports)
CRYING ( 19 FDA reports)
EYE LASER SURGERY ( 19 FDA reports)
HEPATITIS ( 19 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 19 FDA reports)
MOOD SWINGS ( 19 FDA reports)
MULTI-ORGAN FAILURE ( 19 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 19 FDA reports)
OVARIAN CYST RUPTURED ( 19 FDA reports)
PERIPHERAL COLDNESS ( 19 FDA reports)
POLLAKIURIA ( 19 FDA reports)
PREMATURE BABY ( 19 FDA reports)
PROTEINURIA ( 19 FDA reports)
PULMONARY FIBROSIS ( 19 FDA reports)
PURULENT DISCHARGE ( 19 FDA reports)
RASH MACULAR ( 19 FDA reports)
RESPIRATORY DISORDER ( 19 FDA reports)
SCAN BONE MARROW ABNORMAL ( 19 FDA reports)
TENSION HEADACHE ( 19 FDA reports)
TESTICULAR TORSION ( 19 FDA reports)
TUBERCULOSIS ( 19 FDA reports)
TYPE 2 DIABETES MELLITUS ( 19 FDA reports)
VAGINAL CANDIDIASIS ( 19 FDA reports)
ABSCESS ( 18 FDA reports)
ADVERSE EVENT ( 18 FDA reports)
ANAPHYLACTIC REACTION ( 18 FDA reports)
ANKLE FRACTURE ( 18 FDA reports)
ARRHYTHMIA ( 18 FDA reports)
COLITIS MICROSCOPIC ( 18 FDA reports)
CYSTITIS ( 18 FDA reports)
EAR PAIN ( 18 FDA reports)
ECZEMA INFECTED ( 18 FDA reports)
EXOPHTHALMOS ( 18 FDA reports)
GRAND MAL CONVULSION ( 18 FDA reports)
IRON DEFICIENCY ANAEMIA ( 18 FDA reports)
JAW DISORDER ( 18 FDA reports)
LICE INFESTATION ( 18 FDA reports)
LIGAMENT RUPTURE ( 18 FDA reports)
LOWER EXTREMITY MASS ( 18 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 18 FDA reports)
MALIGNANT MELANOMA ( 18 FDA reports)
MASTICATION DISORDER ( 18 FDA reports)
METASTASES TO BONE ( 18 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 18 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 18 FDA reports)
SYNOVITIS ( 18 FDA reports)
TENDONITIS ( 18 FDA reports)
TIBIA FRACTURE ( 18 FDA reports)
UPPER LIMB FRACTURE ( 18 FDA reports)
ABDOMINAL HERNIA ( 17 FDA reports)
ARTHRITIS ENTEROPATHIC ( 17 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
BLINDNESS ( 17 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 17 FDA reports)
BODY TEMPERATURE INCREASED ( 17 FDA reports)
DEFORMITY ( 17 FDA reports)
DEVICE RELATED INFECTION ( 17 FDA reports)
EYE PAIN ( 17 FDA reports)
FAECES DISCOLOURED ( 17 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 17 FDA reports)
HEAD INJURY ( 17 FDA reports)
HYPOACUSIS ( 17 FDA reports)
HYPOXIA ( 17 FDA reports)
INCREASED TENDENCY TO BRUISE ( 17 FDA reports)
LIPOMA ( 17 FDA reports)
MITRAL VALVE INCOMPETENCE ( 17 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 17 FDA reports)
NEOPLASM MALIGNANT ( 17 FDA reports)
NEPHRITIS INTERSTITIAL ( 17 FDA reports)
NEUTROPENIA ( 17 FDA reports)
PALLOR ( 17 FDA reports)
PARANOIA ( 17 FDA reports)
PELVIC ABSCESS ( 17 FDA reports)
THROMBOPHLEBITIS ( 17 FDA reports)
TOOTH LOSS ( 17 FDA reports)
VARICOSE VEIN ( 17 FDA reports)
ADRENAL DISORDER ( 16 FDA reports)
ANGINA PECTORIS ( 16 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 16 FDA reports)
BLEPHARITIS ( 16 FDA reports)
BLOOD POTASSIUM INCREASED ( 16 FDA reports)
BRADYCARDIA ( 16 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 16 FDA reports)
DISABILITY ( 16 FDA reports)
EATING DISORDER ( 16 FDA reports)
GASTROINTESTINAL INFECTION ( 16 FDA reports)
GRANULOMA ( 16 FDA reports)
HEART RATE IRREGULAR ( 16 FDA reports)
HYPONATRAEMIA ( 16 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 16 FDA reports)
INFERTILITY ( 16 FDA reports)
INJECTION SITE WARMTH ( 16 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 16 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 16 FDA reports)
LIMB DISCOMFORT ( 16 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 16 FDA reports)
MENIERE'S DISEASE ( 16 FDA reports)
MULTIPLE DRUG OVERDOSE ( 16 FDA reports)
MULTIPLE SCLEROSIS ( 16 FDA reports)
NASAL DRYNESS ( 16 FDA reports)
PILONIDAL CYST ( 16 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 16 FDA reports)
PROCTITIS ULCERATIVE ( 16 FDA reports)
RASH GENERALISED ( 16 FDA reports)
RHABDOMYOLYSIS ( 16 FDA reports)
SEPTIC SHOCK ( 16 FDA reports)
SINUS DISORDER ( 16 FDA reports)
SKIN DISORDER ( 16 FDA reports)
SKIN LESION ( 16 FDA reports)
SURGERY ( 16 FDA reports)
TONSILLITIS ( 16 FDA reports)
UTERINE ENLARGEMENT ( 16 FDA reports)
ANGER ( 15 FDA reports)
BLOOD SODIUM DECREASED ( 15 FDA reports)
CARDIAC FAILURE ( 15 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 15 FDA reports)
COLECTOMY ( 15 FDA reports)
COR PULMONALE CHRONIC ( 15 FDA reports)
CUSHINGOID ( 15 FDA reports)
DENTAL OPERATION ( 15 FDA reports)
ECCHYMOSIS ( 15 FDA reports)
ENCEPHALOPATHY ( 15 FDA reports)
EPISCLERITIS ( 15 FDA reports)
EUPHORIC MOOD ( 15 FDA reports)
FIBROMYALGIA ( 15 FDA reports)
GASTRODUODENITIS ( 15 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 15 FDA reports)
GLAUCOMA ( 15 FDA reports)
HYDROCEPHALUS ( 15 FDA reports)
ILEOSTOMY ( 15 FDA reports)
IMPAIRED DRIVING ABILITY ( 15 FDA reports)
INJECTION SITE PAPULE ( 15 FDA reports)
LARGE INTESTINAL ULCER ( 15 FDA reports)
LIMB INJURY ( 15 FDA reports)
LUNG INFILTRATION ( 15 FDA reports)
ONYCHOMYCOSIS ( 15 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 15 FDA reports)
POST PROCEDURAL COMPLICATION ( 15 FDA reports)
RADIUS FRACTURE ( 15 FDA reports)
RENAL CYST ( 15 FDA reports)
RESPIRATORY ARREST ( 15 FDA reports)
RIB FRACTURE ( 15 FDA reports)
SENSORY LOSS ( 15 FDA reports)
SKIN INFECTION ( 15 FDA reports)
SPEECH DISORDER ( 15 FDA reports)
VESTIBULAR NEURONITIS ( 15 FDA reports)
ABDOMINAL ABSCESS ( 14 FDA reports)
AGRANULOCYTOSIS ( 14 FDA reports)
ANGIOPATHY ( 14 FDA reports)
CEREBRAL ISCHAEMIA ( 14 FDA reports)
CIRCULATORY COLLAPSE ( 14 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 14 FDA reports)
DEMYELINATION ( 14 FDA reports)
DYSLIPIDAEMIA ( 14 FDA reports)
ELECTROLYTE IMBALANCE ( 14 FDA reports)
HEART RATE DECREASED ( 14 FDA reports)
HEPATOMEGALY ( 14 FDA reports)
LABORATORY TEST ABNORMAL ( 14 FDA reports)
LACERATION ( 14 FDA reports)
METATARSUS PRIMUS VARUS ( 14 FDA reports)
MUSCLE STRAIN ( 14 FDA reports)
PHARYNGITIS ( 14 FDA reports)
PLEURITIC PAIN ( 14 FDA reports)
POUCHITIS ( 14 FDA reports)
PROCTALGIA ( 14 FDA reports)
PRODUCT QUALITY ISSUE ( 14 FDA reports)
PRODUCTIVE COUGH ( 14 FDA reports)
RASH ERYTHEMATOUS ( 14 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 14 FDA reports)
SUBCUTANEOUS ABSCESS ( 14 FDA reports)
TOOTH FRACTURE ( 14 FDA reports)
TOOTH INFECTION ( 14 FDA reports)
UTERINE CANCER ( 14 FDA reports)
ABNORMAL DREAMS ( 13 FDA reports)
AGORAPHOBIA ( 13 FDA reports)
BACTERIAL INFECTION ( 13 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 13 FDA reports)
BLOOD IRON DECREASED ( 13 FDA reports)
BODY HEIGHT DECREASED ( 13 FDA reports)
CARDIAC ARREST ( 13 FDA reports)
CLAUSTROPHOBIA ( 13 FDA reports)
COELIAC DISEASE ( 13 FDA reports)
DISORIENTATION ( 13 FDA reports)
DISSEMINATED TUBERCULOSIS ( 13 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 13 FDA reports)
GRAFT VERSUS HOST DISEASE ( 13 FDA reports)
HYPERSOMNIA ( 13 FDA reports)
HYPERVENTILATION ( 13 FDA reports)
MENTAL DISORDER ( 13 FDA reports)
NASAL DISORDER ( 13 FDA reports)
POSTOPERATIVE ABSCESS ( 13 FDA reports)
PRECANCEROUS CELLS PRESENT ( 13 FDA reports)
PRIMARY SEQUESTRUM ( 13 FDA reports)
PULMONARY CONGESTION ( 13 FDA reports)
RASH PAPULAR ( 13 FDA reports)
RESPIRATORY TRACT CONGESTION ( 13 FDA reports)
SEBORRHOEIC KERATOSIS ( 13 FDA reports)
SINUS CONGESTION ( 13 FDA reports)
SKIN DISCOLOURATION ( 13 FDA reports)
SWOLLEN TONGUE ( 13 FDA reports)
SYNOVIAL CYST ( 13 FDA reports)
T-CELL LYMPHOMA ( 13 FDA reports)
THINKING ABNORMAL ( 13 FDA reports)
URINARY TRACT DISORDER ( 13 FDA reports)
VENOUS INSUFFICIENCY ( 13 FDA reports)
B-CELL LYMPHOMA ( 12 FDA reports)
BIPOLAR DISORDER ( 12 FDA reports)
BLOOD ALBUMIN DECREASED ( 12 FDA reports)
BLOOD BLISTER ( 12 FDA reports)
BLOOD GLUCOSE DECREASED ( 12 FDA reports)
BREAST CANCER FEMALE ( 12 FDA reports)
CEREBRAL HAEMORRHAGE ( 12 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 12 FDA reports)
DIVERTICULUM INTESTINAL ( 12 FDA reports)
EMOTIONAL DISORDER ( 12 FDA reports)
FAECAL INCONTINENCE ( 12 FDA reports)
FEELING OF DESPAIR ( 12 FDA reports)
GASTROINTESTINAL PAIN ( 12 FDA reports)
HYPERKALAEMIA ( 12 FDA reports)
HYPOPHAGIA ( 12 FDA reports)
HYPOVOLAEMIA ( 12 FDA reports)
INTESTINAL STENOSIS ( 12 FDA reports)
JOINT LOCK ( 12 FDA reports)
LACTIC ACIDOSIS ( 12 FDA reports)
MENORRHAGIA ( 12 FDA reports)
MUSCLE INJURY ( 12 FDA reports)
OSCILLOPSIA ( 12 FDA reports)
OXYGEN SATURATION DECREASED ( 12 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 12 FDA reports)
PERIANAL ABSCESS ( 12 FDA reports)
POLYP COLORECTAL ( 12 FDA reports)
PSYCHOTIC DISORDER ( 12 FDA reports)
RECTAL FISSURE ( 12 FDA reports)
RHINITIS ALLERGIC ( 12 FDA reports)
SIALOADENITIS ( 12 FDA reports)
STRESS FRACTURE ( 12 FDA reports)
UNRESPONSIVE TO STIMULI ( 12 FDA reports)
VISUAL ACUITY REDUCED ( 12 FDA reports)
VITREOUS FLOATERS ( 12 FDA reports)
ABNORMAL BEHAVIOUR ( 11 FDA reports)
ACINETOBACTER INFECTION ( 11 FDA reports)
AGGRESSION ( 11 FDA reports)
AGITATION ( 11 FDA reports)
BACK INJURY ( 11 FDA reports)
BACTERAEMIA ( 11 FDA reports)
BENIGN BREAST NEOPLASM ( 11 FDA reports)
BILIARY COLIC ( 11 FDA reports)
BLOOD BILIRUBIN INCREASED ( 11 FDA reports)
BLOOD UREA INCREASED ( 11 FDA reports)
BREAST PAIN ( 11 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 11 FDA reports)
CHOLECYSTECTOMY ( 11 FDA reports)
CORONARY ARTERY OCCLUSION ( 11 FDA reports)
CORONARY ARTERY STENOSIS ( 11 FDA reports)
DYSARTHRIA ( 11 FDA reports)
ENERGY INCREASED ( 11 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 11 FDA reports)
EXFOLIATIVE RASH ( 11 FDA reports)
EXTRASYSTOLES ( 11 FDA reports)
FEELING JITTERY ( 11 FDA reports)
HYDRONEPHROSIS ( 11 FDA reports)
HYPERLIPIDAEMIA ( 11 FDA reports)
ILL-DEFINED DISORDER ( 11 FDA reports)
INGUINAL HERNIA ( 11 FDA reports)
INTESTINAL ULCER ( 11 FDA reports)
JAUNDICE ( 11 FDA reports)
JOINT EFFUSION ( 11 FDA reports)
LOBAR PNEUMONIA ( 11 FDA reports)
LOCALISED INFECTION ( 11 FDA reports)
LOW TURNOVER OSTEOPATHY ( 11 FDA reports)
MACULAR DEGENERATION ( 11 FDA reports)
MOVEMENT DISORDER ( 11 FDA reports)
NODULE ( 11 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 11 FDA reports)
OPEN WOUND ( 11 FDA reports)
OPTIC NEURITIS ( 11 FDA reports)
ORAL INTAKE REDUCED ( 11 FDA reports)
PNEUMOTHORAX ( 11 FDA reports)
POLYDIPSIA ( 11 FDA reports)
POLYURIA ( 11 FDA reports)
RASH MACULO-PAPULAR ( 11 FDA reports)
RASH PUSTULAR ( 11 FDA reports)
SENSITIVITY OF TEETH ( 11 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 11 FDA reports)
TENDERNESS ( 11 FDA reports)
THERAPY NON-RESPONDER ( 11 FDA reports)
URINARY INCONTINENCE ( 11 FDA reports)
VAGINAL INFECTION ( 11 FDA reports)
WOUND ( 11 FDA reports)
WOUND INFECTION FUNGAL ( 11 FDA reports)
ABDOMINAL MASS ( 10 FDA reports)
ABSCESS DRAINAGE ( 10 FDA reports)
ACCIDENTAL OVERDOSE ( 10 FDA reports)
ANAL STENOSIS ( 10 FDA reports)
ANOGENITAL WARTS ( 10 FDA reports)
AUTOIMMUNE INNER EAR DISEASE ( 10 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 10 FDA reports)
BRONCHITIS CHRONIC ( 10 FDA reports)
COLONIC STENOSIS ( 10 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 10 FDA reports)
DIFFICULTY IN WALKING ( 10 FDA reports)
DISCOMFORT ( 10 FDA reports)
DISEASE PROGRESSION ( 10 FDA reports)
ENDOMETRIAL CANCER ( 10 FDA reports)
EOSINOPHILIA ( 10 FDA reports)
ERECTILE DYSFUNCTION ( 10 FDA reports)
EYE IRRITATION ( 10 FDA reports)
GASTROENTERITIS VIRAL ( 10 FDA reports)
HAND FRACTURE ( 10 FDA reports)
HEARING IMPAIRED ( 10 FDA reports)
HIP ARTHROPLASTY ( 10 FDA reports)
HYPERPLASIA ( 10 FDA reports)
HYPOMAGNESAEMIA ( 10 FDA reports)
HYPOTHYROIDISM ( 10 FDA reports)
ILEITIS ( 10 FDA reports)
IMMUNE SYSTEM DISORDER ( 10 FDA reports)
INTENTIONAL DRUG MISUSE ( 10 FDA reports)
KNEE ARTHROPLASTY ( 10 FDA reports)
LEUKAEMIA ( 10 FDA reports)
LIP EXFOLIATION ( 10 FDA reports)
LIPIDS INCREASED ( 10 FDA reports)
LIVER DISORDER ( 10 FDA reports)
LOWER LIMB FRACTURE ( 10 FDA reports)
MASS ( 10 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 10 FDA reports)
MENTAL STATUS CHANGES ( 10 FDA reports)
MICTURITION URGENCY ( 10 FDA reports)
ORAL HERPES ( 10 FDA reports)
ORAL PAIN ( 10 FDA reports)
ORTHOPNOEA ( 10 FDA reports)
PANCREATITIS ACUTE ( 10 FDA reports)
PERITONITIS BACTERIAL ( 10 FDA reports)
PHOTOPHOBIA ( 10 FDA reports)
PLEURISY ( 10 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 10 FDA reports)
PULMONARY TUBERCULOSIS ( 10 FDA reports)
RESTLESSNESS ( 10 FDA reports)
SOCIAL FEAR ( 10 FDA reports)
SPONDYLOARTHROPATHY ( 10 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 10 FDA reports)
THYROID CANCER ( 10 FDA reports)
THYROID DISORDER ( 10 FDA reports)
TINEA PEDIS ( 10 FDA reports)
TONGUE DISORDER ( 10 FDA reports)
URINARY RETENTION ( 10 FDA reports)
WOUND HAEMORRHAGE ( 10 FDA reports)
ACIDOSIS ( 9 FDA reports)
ACUTE CORONARY SYNDROME ( 9 FDA reports)
BLADDER CANCER ( 9 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 9 FDA reports)
BONE CYST ( 9 FDA reports)
BONE MARROW FAILURE ( 9 FDA reports)
CARCINOMA IN SITU OF SKIN ( 9 FDA reports)
CARDIAC MURMUR ( 9 FDA reports)
CHOLECYSTITIS ACUTE ( 9 FDA reports)
COLONIC OBSTRUCTION ( 9 FDA reports)
COMA ( 9 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 9 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 9 FDA reports)
DECREASED INTEREST ( 9 FDA reports)
DEFAECATION URGENCY ( 9 FDA reports)
DIALYSIS ( 9 FDA reports)
DRY EYE ( 9 FDA reports)
ENTEROCELE ( 9 FDA reports)
EYE HAEMORRHAGE ( 9 FDA reports)
FACIAL PALSY ( 9 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 9 FDA reports)
GOUT ( 9 FDA reports)
HAEMOLYTIC ANAEMIA ( 9 FDA reports)
HEPATIC ENCEPHALOPATHY ( 9 FDA reports)
HORMONE LEVEL ABNORMAL ( 9 FDA reports)
INCISION SITE COMPLICATION ( 9 FDA reports)
INJECTION SITE EXTRAVASATION ( 9 FDA reports)
INJECTION SITE INDURATION ( 9 FDA reports)
INSULIN RESISTANCE ( 9 FDA reports)
JOINT STIFFNESS ( 9 FDA reports)
LYMPHOHISTIOCYTOSIS ( 9 FDA reports)
LYMPHOMA ( 9 FDA reports)
MANIA ( 9 FDA reports)
METASTASES TO LIVER ( 9 FDA reports)
METRORRHAGIA ( 9 FDA reports)
MIDDLE INSOMNIA ( 9 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 9 FDA reports)
NICOTINE DEPENDENCE ( 9 FDA reports)
ORAL DISCOMFORT ( 9 FDA reports)
ORTHOSTATIC HYPOTENSION ( 9 FDA reports)
OVARIAN CYST ( 9 FDA reports)
PATELLA FRACTURE ( 9 FDA reports)
PELVIC PAIN ( 9 FDA reports)
PERIODONTAL INFECTION ( 9 FDA reports)
PROTEIN URINE PRESENT ( 9 FDA reports)
PULMONARY THROMBOSIS ( 9 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 9 FDA reports)
RENAL TUBULAR NECROSIS ( 9 FDA reports)
RESPIRATORY DISTRESS ( 9 FDA reports)
SARCOIDOSIS ( 9 FDA reports)
SENSORY DISTURBANCE ( 9 FDA reports)
SERUM SICKNESS ( 9 FDA reports)
SKIN REACTION ( 9 FDA reports)
SPINAL COMPRESSION FRACTURE ( 9 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 9 FDA reports)
STENOTROPHOMONAS INFECTION ( 9 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 9 FDA reports)
TEARFULNESS ( 9 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 9 FDA reports)
TONGUE ULCERATION ( 9 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 9 FDA reports)
ULNA FRACTURE ( 9 FDA reports)
VEIN DISORDER ( 9 FDA reports)
VENTRICULAR TACHYCARDIA ( 9 FDA reports)
VIITH NERVE PARALYSIS ( 9 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 9 FDA reports)
ABNORMAL FAECES ( 8 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 8 FDA reports)
ACTINIC KERATOSIS ( 8 FDA reports)
ANAL ABSCESS ( 8 FDA reports)
ANAL FISSURE ( 8 FDA reports)
ANURIA ( 8 FDA reports)
AQUEDUCTAL STENOSIS ( 8 FDA reports)
ASPERGILLOSIS ( 8 FDA reports)
ATRIAL FLUTTER ( 8 FDA reports)
BABESIOSIS ( 8 FDA reports)
BLINDNESS TRANSIENT ( 8 FDA reports)
BLOOD CORTISOL DECREASED ( 8 FDA reports)
BLOOD TEST ABNORMAL ( 8 FDA reports)
BLOOD URINE PRESENT ( 8 FDA reports)
BREAST CANCER METASTATIC ( 8 FDA reports)
CAESAREAN SECTION ( 8 FDA reports)
CALCULUS URETERIC ( 8 FDA reports)
CAROTID ARTERY STENOSIS ( 8 FDA reports)
CERVICAL DYSPLASIA ( 8 FDA reports)
CHOLESTASIS ( 8 FDA reports)
CHRONIC HEPATIC FAILURE ( 8 FDA reports)
COMPRESSION FRACTURE ( 8 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 8 FDA reports)
CYST ( 8 FDA reports)
DRUG ADMINISTRATION ERROR ( 8 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
DYSKINESIA ( 8 FDA reports)
ECONOMIC PROBLEM ( 8 FDA reports)
EXPIRED DRUG ADMINISTERED ( 8 FDA reports)
EYE PRURITUS ( 8 FDA reports)
EYE SWELLING ( 8 FDA reports)
EYELID PTOSIS ( 8 FDA reports)
FACIAL BONES FRACTURE ( 8 FDA reports)
FEBRILE NEUTROPENIA ( 8 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 8 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 8 FDA reports)
GASTRIC DISORDER ( 8 FDA reports)
GINGIVAL RECESSION ( 8 FDA reports)
HAEMATEMESIS ( 8 FDA reports)
HAEMOLYSIS ( 8 FDA reports)
HEPATIC CYST ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
HEPATOTOXICITY ( 8 FDA reports)
HODGKIN'S DISEASE ( 8 FDA reports)
HYPOAESTHESIA ORAL ( 8 FDA reports)
HYPOCALCAEMIA ( 8 FDA reports)
HYSTERECTOMY ( 8 FDA reports)
INJECTION SITE IRRITATION ( 8 FDA reports)
INTRA-UTERINE DEATH ( 8 FDA reports)
JUGULAR VEIN THROMBOSIS ( 8 FDA reports)
KIDNEY INFECTION ( 8 FDA reports)
KYPHOSIS ( 8 FDA reports)
LIP SWELLING ( 8 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 8 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 8 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 8 FDA reports)
MYOCARDIAL ISCHAEMIA ( 8 FDA reports)
NEUTROPHIL COUNT INCREASED ( 8 FDA reports)
ODONTOGENIC CYST ( 8 FDA reports)
ORAL TORUS ( 8 FDA reports)
OSTEOSCLEROSIS ( 8 FDA reports)
OVERWEIGHT ( 8 FDA reports)
PAIN OF SKIN ( 8 FDA reports)
PERITONITIS ( 8 FDA reports)
PHARYNGEAL OEDEMA ( 8 FDA reports)
PNEUMONIA ASPIRATION ( 8 FDA reports)
PREMATURE LABOUR ( 8 FDA reports)
PROTHROMBIN TIME PROLONGED ( 8 FDA reports)
PSYCHIATRIC SYMPTOM ( 8 FDA reports)
SKIN CANCER ( 8 FDA reports)
SKIN PAPILLOMA ( 8 FDA reports)
SPUTUM DISCOLOURED ( 8 FDA reports)
STOMACH DISCOMFORT ( 8 FDA reports)
TRISMUS ( 8 FDA reports)
VENTRICULAR DYSFUNCTION ( 8 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 8 FDA reports)
VOMITING IN PREGNANCY ( 8 FDA reports)
ACUTE RESPIRATORY FAILURE ( 7 FDA reports)
APATHY ( 7 FDA reports)
APHAGIA ( 7 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 7 FDA reports)
ATRIAL TACHYCARDIA ( 7 FDA reports)
BACK DISORDER ( 7 FDA reports)
BEDRIDDEN ( 7 FDA reports)
BILIARY DYSKINESIA ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
BREAST CANCER IN SITU ( 7 FDA reports)
BREAST MASS ( 7 FDA reports)
BRONCHOSPASM ( 7 FDA reports)
CHEST X-RAY ABNORMAL ( 7 FDA reports)
COGNITIVE DISORDER ( 7 FDA reports)
DRUG ABUSER ( 7 FDA reports)
DYSMENORRHOEA ( 7 FDA reports)
EJECTION FRACTION DECREASED ( 7 FDA reports)
ERYTHEMA MULTIFORME ( 7 FDA reports)
ERYTHEMA NODOSUM ( 7 FDA reports)
FIBRIN D DIMER INCREASED ( 7 FDA reports)
FURUNCLE ( 7 FDA reports)
GALLBLADDER INJURY ( 7 FDA reports)
GINGIVAL ULCERATION ( 7 FDA reports)
GOITRE ( 7 FDA reports)
HAEMATOMA INFECTION ( 7 FDA reports)
HAEMODIALYSIS ( 7 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 7 FDA reports)
HERPES VIRUS INFECTION ( 7 FDA reports)
HISTOPLASMOSIS ( 7 FDA reports)
HYPERAESTHESIA ( 7 FDA reports)
HYPERCOAGULATION ( 7 FDA reports)
HYPOTONIA ( 7 FDA reports)
ILEAL STENOSIS ( 7 FDA reports)
INITIAL INSOMNIA ( 7 FDA reports)
INJECTION SITE DISCOLOURATION ( 7 FDA reports)
INJECTION SITE MASS ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 7 FDA reports)
IUCD COMPLICATION ( 7 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 7 FDA reports)
LISTERIA SEPSIS ( 7 FDA reports)
LIVER ABSCESS ( 7 FDA reports)
LOCAL SWELLING ( 7 FDA reports)
LOCALISED OSTEOARTHRITIS ( 7 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
MACULAR OEDEMA ( 7 FDA reports)
MALABSORPTION ( 7 FDA reports)
MEDICATION ERROR ( 7 FDA reports)
MENSTRUATION IRREGULAR ( 7 FDA reports)
METASTASES TO LUNG ( 7 FDA reports)
NECROSIS ( 7 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 7 FDA reports)
NYSTAGMUS ( 7 FDA reports)
OESOPHAGEAL DISORDER ( 7 FDA reports)
PNEUMOMEDIASTINUM ( 7 FDA reports)
PNEUMONIA MYCOPLASMAL ( 7 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 7 FDA reports)
PORTAL HYPERTENSION ( 7 FDA reports)
PROCEDURAL PAIN ( 7 FDA reports)
PROTEIN TOTAL DECREASED ( 7 FDA reports)
PRURITUS GENERALISED ( 7 FDA reports)
PSORIATIC ARTHROPATHY ( 7 FDA reports)
RECTAL ABSCESS ( 7 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 7 FDA reports)
RESTLESS LEGS SYNDROME ( 7 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 7 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 7 FDA reports)
SINUS BRADYCARDIA ( 7 FDA reports)
SNEEZING ( 7 FDA reports)
STEVENS-JOHNSON SYNDROME ( 7 FDA reports)
TELANGIECTASIA ( 7 FDA reports)
TENDON DISORDER ( 7 FDA reports)
TENOSYNOVITIS ( 7 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 7 FDA reports)
WOUND INFECTION ( 7 FDA reports)
ABDOMINAL TENDERNESS ( 6 FDA reports)
ABORTION INDUCED ( 6 FDA reports)
ABSCESS ORAL ( 6 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 6 FDA reports)
APHONIA ( 6 FDA reports)
APPENDIX DISORDER ( 6 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 6 FDA reports)
AXILLARY MASS ( 6 FDA reports)
BLADDER PROLAPSE ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
CARDIOMYOPATHY ( 6 FDA reports)
CHOLANGIOGRAM ( 6 FDA reports)
CHOLANGITIS ( 6 FDA reports)
CHOLANGITIS SCLEROSING ( 6 FDA reports)
COLON CANCER ( 6 FDA reports)
COLON CANCER METASTATIC ( 6 FDA reports)
COLONIC POLYP ( 6 FDA reports)
CONDYLOMA ACUMINATUM ( 6 FDA reports)
CORNEAL DYSTROPHY ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
DERMATITIS ( 6 FDA reports)
DIVERTICULAR HERNIA ( 6 FDA reports)
EJACULATION DISORDER ( 6 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 6 FDA reports)
EYELID CYST ( 6 FDA reports)
FAECALOMA ( 6 FDA reports)
FAMILY STRESS ( 6 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 6 FDA reports)
FRACTURE MALUNION ( 6 FDA reports)
FUNGAL SKIN INFECTION ( 6 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
HAEMOPTYSIS ( 6 FDA reports)
HEART RATE ABNORMAL ( 6 FDA reports)
HEMIPLEGIA ( 6 FDA reports)
HEPATIC VEIN STENOSIS ( 6 FDA reports)
HERPES SIMPLEX ( 6 FDA reports)
HIP FRACTURE ( 6 FDA reports)
HYPERCALCAEMIA ( 6 FDA reports)
HYPERCHOLESTEROLAEMIA ( 6 FDA reports)
HYPERMETROPIA ( 6 FDA reports)
IMPAIRED WORK ABILITY ( 6 FDA reports)
INCISIONAL DRAINAGE ( 6 FDA reports)
INCORRECT STORAGE OF DRUG ( 6 FDA reports)
INCREASED APPETITE ( 6 FDA reports)
INTERMITTENT CLAUDICATION ( 6 FDA reports)
INTESTINAL FISTULA ( 6 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 6 FDA reports)
LACRIMATION INCREASED ( 6 FDA reports)
LUNG NEOPLASM MALIGNANT ( 6 FDA reports)
LYMPHOEDEMA ( 6 FDA reports)
MASTITIS ( 6 FDA reports)
MENINGITIS LISTERIA ( 6 FDA reports)
MUSCLE ATROPHY ( 6 FDA reports)
MUSCLE RUPTURE ( 6 FDA reports)
MYOPATHY ( 6 FDA reports)
NECROTISING FASCIITIS ( 6 FDA reports)
NEPHROPATHY ( 6 FDA reports)
NEUTROPENIC SEPSIS ( 6 FDA reports)
NO THERAPEUTIC RESPONSE ( 6 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 6 FDA reports)
ODYNOPHAGIA ( 6 FDA reports)
OPTIC NEUROPATHY ( 6 FDA reports)
PAPILLOMA ( 6 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 6 FDA reports)
PETECHIAE ( 6 FDA reports)
PHOTOSENSITIVITY REACTION ( 6 FDA reports)
POSTURE ABNORMAL ( 6 FDA reports)
PREMATURE DELIVERY ( 6 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 6 FDA reports)
PSEUDOPOLYP ( 6 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 6 FDA reports)
RENAL INJURY ( 6 FDA reports)
RESPIRATORY RATE INCREASED ( 6 FDA reports)
SACROILIITIS ( 6 FDA reports)
SELF ESTEEM DECREASED ( 6 FDA reports)
SKIN ATROPHY ( 6 FDA reports)
SPINA BIFIDA OCCULTA ( 6 FDA reports)
SPINAL DEFORMITY ( 6 FDA reports)
SQUAMOUS CELL CARCINOMA ( 6 FDA reports)
SUBDURAL HAEMATOMA ( 6 FDA reports)
SUDDEN DEATH ( 6 FDA reports)
THYROID NEOPLASM ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
ULCER HAEMORRHAGE ( 6 FDA reports)
URINE OUTPUT DECREASED ( 6 FDA reports)
UROSEPSIS ( 6 FDA reports)
WITHDRAWAL SYNDROME ( 6 FDA reports)
ABSCESS INTESTINAL ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 5 FDA reports)
ADRENAL MASS ( 5 FDA reports)
AGEUSIA ( 5 FDA reports)
AMENORRHOEA ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
AORTIC VALVE INCOMPETENCE ( 5 FDA reports)
APLASTIC ANAEMIA ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 5 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 5 FDA reports)
BONE LESION ( 5 FDA reports)
BONE SCAN ABNORMAL ( 5 FDA reports)
BREAST TENDERNESS ( 5 FDA reports)
BRONCHIECTASIS ( 5 FDA reports)
BRONCHITIS ACUTE ( 5 FDA reports)
BUNION ( 5 FDA reports)
CALCIUM METABOLISM DISORDER ( 5 FDA reports)
CATARACT NUCLEAR ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
CERVICITIS ( 5 FDA reports)
CHONDROPATHY ( 5 FDA reports)
CHORIOAMNIONITIS ( 5 FDA reports)
CHROMATURIA ( 5 FDA reports)
COLECTOMY TOTAL ( 5 FDA reports)
COLOSTOMY ( 5 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 5 FDA reports)
CONDUCTION DISORDER ( 5 FDA reports)
CONJUNCTIVITIS ( 5 FDA reports)
CORONARY ANGIOPLASTY ( 5 FDA reports)
CORONARY ARTERY THROMBOSIS ( 5 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 5 FDA reports)
DARK CIRCLES UNDER EYES ( 5 FDA reports)
DEMENTIA ( 5 FDA reports)
DEPRESSIVE SYMPTOM ( 5 FDA reports)
DERMATITIS CONTACT ( 5 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 5 FDA reports)
DIABETIC ULCER ( 5 FDA reports)
DIASTOLIC DYSFUNCTION ( 5 FDA reports)
DILATATION VENTRICULAR ( 5 FDA reports)
DIPLOPIA ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 5 FDA reports)
EMBOLIC STROKE ( 5 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 5 FDA reports)
GENERALISED ANXIETY DISORDER ( 5 FDA reports)
GINGIVAL BLEEDING ( 5 FDA reports)
GINGIVAL OEDEMA ( 5 FDA reports)
GROIN PAIN ( 5 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 5 FDA reports)
HAEMORRHAGIC ANAEMIA ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 5 FDA reports)
HEPATOSPLENOMEGALY ( 5 FDA reports)
HERNIA HIATUS REPAIR ( 5 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 5 FDA reports)
HYPERADRENOCORTICISM ( 5 FDA reports)
HYPERKERATOSIS ( 5 FDA reports)
HYPOSMIA ( 5 FDA reports)
ILEUS PARALYTIC ( 5 FDA reports)
IMMUNOSUPPRESSION ( 5 FDA reports)
INCOHERENT ( 5 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 5 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 5 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 5 FDA reports)
INTESTINAL PERFORATION ( 5 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 5 FDA reports)
JOINT INJURY ( 5 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 5 FDA reports)
JOINT SPRAIN ( 5 FDA reports)
KIDNEY FIBROSIS ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
LOOSE TOOTH ( 5 FDA reports)
LYMPH NODE PAIN ( 5 FDA reports)
MASTECTOMY ( 5 FDA reports)
MELANOCYTIC NAEVUS ( 5 FDA reports)
METASTASES TO SPINE ( 5 FDA reports)
MITRAL VALVE PROLAPSE ( 5 FDA reports)
MONOCYTE COUNT INCREASED ( 5 FDA reports)
MUCOUS STOOLS ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
MUSCLE RIGIDITY ( 5 FDA reports)
MYOCARDITIS ( 5 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 5 FDA reports)
MYOSITIS ( 5 FDA reports)
NAIL DISORDER ( 5 FDA reports)
NASAL DISCOMFORT ( 5 FDA reports)
NEEDLE ISSUE ( 5 FDA reports)
NEPHROCALCINOSIS ( 5 FDA reports)
NEURILEMMOMA ( 5 FDA reports)
NEURODERMATITIS ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER ( 5 FDA reports)
OBESITY ( 5 FDA reports)
OESOPHAGEAL STENOSIS ( 5 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 5 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 5 FDA reports)
PAROTID DUCT OBSTRUCTION ( 5 FDA reports)
PELVIC VENOUS THROMBOSIS ( 5 FDA reports)
PERIOSTITIS ( 5 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 5 FDA reports)
PERNICIOUS ANAEMIA ( 5 FDA reports)
PHOTOPSIA ( 5 FDA reports)
PLANTAR FASCIITIS ( 5 FDA reports)
POLYARTHRITIS ( 5 FDA reports)
PRESYNCOPE ( 5 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 5 FDA reports)
PROSTATE CANCER ( 5 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
PYURIA ( 5 FDA reports)
QUADRIPLEGIA ( 5 FDA reports)
RECTAL CANCER ( 5 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
RENAL PAIN ( 5 FDA reports)
RENAL TUBULAR ATROPHY ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
RETINAL VEIN THROMBOSIS ( 5 FDA reports)
SEASONAL ALLERGY ( 5 FDA reports)
SENSATION OF FOREIGN BODY ( 5 FDA reports)
SKIN TIGHTNESS ( 5 FDA reports)
SPINAL CORD COMPRESSION ( 5 FDA reports)
STENT PLACEMENT ( 5 FDA reports)
STOOL ANALYSIS ABNORMAL ( 5 FDA reports)
THERMAL BURN ( 5 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 5 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 5 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 5 FDA reports)
URINE ODOUR ABNORMAL ( 5 FDA reports)
VAGINAL DISCHARGE ( 5 FDA reports)
VENOUS INJURY ( 5 FDA reports)
VESTIBULAR DISORDER ( 5 FDA reports)
VITAMIN D DECREASED ( 5 FDA reports)
VULVOVAGINAL DRYNESS ( 5 FDA reports)
ABDOMINAL ADHESIONS ( 4 FDA reports)
ABDOMINAL INFECTION ( 4 FDA reports)
ACUTE PSYCHOSIS ( 4 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 4 FDA reports)
ANAEMIA MACROCYTIC ( 4 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 4 FDA reports)
ANAL ATRESIA ( 4 FDA reports)
ANTI-PLATELET ANTIBODY ( 4 FDA reports)
ANTIBODY TEST POSITIVE ( 4 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 4 FDA reports)
ARTERIAL BYPASS OPERATION ( 4 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 4 FDA reports)
ARTERITIS ( 4 FDA reports)
ASTIGMATISM ( 4 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 4 FDA reports)
BACTERIAL SEPSIS ( 4 FDA reports)
BACTERIAL TEST POSITIVE ( 4 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
BLOOD CULTURE POSITIVE ( 4 FDA reports)
BRAIN ABSCESS ( 4 FDA reports)
BRAIN NEOPLASM ( 4 FDA reports)
BREAST ABSCESS ( 4 FDA reports)
BREAST MICROCALCIFICATION ( 4 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 4 FDA reports)
CALCINOSIS ( 4 FDA reports)
CARDIAC TAMPONADE ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 4 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 4 FDA reports)
CLAVICLE FRACTURE ( 4 FDA reports)
CNS VENTRICULITIS ( 4 FDA reports)
COLON NEOPLASM ( 4 FDA reports)
COMPARTMENT SYNDROME ( 4 FDA reports)
CONGENITAL HEARING DISORDER ( 4 FDA reports)
CULTURE POSITIVE ( 4 FDA reports)
DEAFNESS NEUROSENSORY ( 4 FDA reports)
DEPENDENCE ( 4 FDA reports)
DEVICE BREAKAGE ( 4 FDA reports)
DIABETIC FOOT ( 4 FDA reports)
DRUG DISPENSING ERROR ( 4 FDA reports)
DRUG LEVEL DECREASED ( 4 FDA reports)
DRUG RESISTANCE ( 4 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 4 FDA reports)
ENDOCARDITIS ( 4 FDA reports)
ENDOTRACHEAL INTUBATION ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
EXTRADURAL HAEMATOMA ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
EYELID OEDEMA ( 4 FDA reports)
FAILURE TO THRIVE ( 4 FDA reports)
FISTULA DISCHARGE ( 4 FDA reports)
FLUID INTAKE REDUCED ( 4 FDA reports)
FOETAL DISORDER ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
FOREIGN BODY TRAUMA ( 4 FDA reports)
FORMICATION ( 4 FDA reports)
GALLBLADDER PAIN ( 4 FDA reports)
GANGRENE ( 4 FDA reports)
GESTATIONAL DIABETES ( 4 FDA reports)
GLIOBLASTOMA MULTIFORME ( 4 FDA reports)
GLOMERULONEPHRITIS ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 4 FDA reports)
GYNAECOMASTIA ( 4 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 4 FDA reports)
HELICOBACTER INFECTION ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HUNGER ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
INCISION SITE INFECTION ( 4 FDA reports)
INCISIONAL HERNIA ( 4 FDA reports)
INFLAMMATORY MARKER INCREASED ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 4 FDA reports)
INTESTINAL OPERATION ( 4 FDA reports)
INTESTINAL RESECTION ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
KNEE OPERATION ( 4 FDA reports)
LACUNAR INFARCTION ( 4 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 4 FDA reports)
LARGE INTESTINE PERFORATION ( 4 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 4 FDA reports)
LEG AMPUTATION ( 4 FDA reports)
LEUKOPLAKIA ( 4 FDA reports)
LIGAMENT SPRAIN ( 4 FDA reports)
LISTERIOSIS ( 4 FDA reports)
LIVER TRANSPLANT ( 4 FDA reports)
LIVER TRANSPLANT REJECTION ( 4 FDA reports)
LYME DISEASE ( 4 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MARROW HYPERPLASIA ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
MENINGITIS CHEMICAL ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MORBID THOUGHTS ( 4 FDA reports)
MULTIPLE ALLERGIES ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MUSCULOSKELETAL DISORDER ( 4 FDA reports)
NEOPLASM PROGRESSION ( 4 FDA reports)
NEPHROPATHY TOXIC ( 4 FDA reports)
NEPHROSCLEROSIS ( 4 FDA reports)
NERVE COMPRESSION ( 4 FDA reports)
NERVE INJURY ( 4 FDA reports)
NEURALGIA ( 4 FDA reports)
NEUROPATHY ( 4 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
NON-CARDIAC CHEST PAIN ( 4 FDA reports)
OLIGOMENORRHOEA ( 4 FDA reports)
ONYCHOMADESIS ( 4 FDA reports)
OROPHARYNGEAL BLISTERING ( 4 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 4 FDA reports)
OVARIAN CANCER ( 4 FDA reports)
PANCREATITIS CHRONIC ( 4 FDA reports)
PANIC REACTION ( 4 FDA reports)
PAPILLOEDEMA ( 4 FDA reports)
PERONEAL NERVE PALSY ( 4 FDA reports)
PLACENTAL DISORDER ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
POOR VENOUS ACCESS ( 4 FDA reports)
PORTAL VEIN THROMBOSIS ( 4 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 4 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 4 FDA reports)
PROCEDURAL COMPLICATION ( 4 FDA reports)
PRODUCT TASTE ABNORMAL ( 4 FDA reports)
PSYCHOLOGICAL TRAUMA ( 4 FDA reports)
PULMONARY HAEMORRHAGE ( 4 FDA reports)
PULMONARY MASS ( 4 FDA reports)
PURULENCE ( 4 FDA reports)
RED BLOOD CELL ABNORMALITY ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
RETINOPATHY ( 4 FDA reports)
RHINITIS ( 4 FDA reports)
ROSACEA ( 4 FDA reports)
SCOLIOSIS ( 4 FDA reports)
SEDATION ( 4 FDA reports)
SHOULDER PAIN ( 4 FDA reports)
SIGMOIDITIS ( 4 FDA reports)
SINUS HEADACHE ( 4 FDA reports)
SINUS OPERATION ( 4 FDA reports)
SKIN BURNING SENSATION ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SPINAL COLUMN STENOSIS ( 4 FDA reports)
SPINAL FUSION SURGERY ( 4 FDA reports)
SUBILEUS ( 4 FDA reports)
SUPRAPUBIC PAIN ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
TARDIVE DYSKINESIA ( 4 FDA reports)
TEMPERATURE INTOLERANCE ( 4 FDA reports)
TENDON INJURY ( 4 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
TUBERCULIN TEST POSITIVE ( 4 FDA reports)
ULCERATIVE KERATITIS ( 4 FDA reports)
URINE ABNORMALITY ( 4 FDA reports)
UVULOPALATOPHARYNGOPLASTY ( 4 FDA reports)
VENOUS THROMBOSIS ( 4 FDA reports)
VITAMIN D DEFICIENCY ( 4 FDA reports)
VULVOVAGINAL DISCOMFORT ( 4 FDA reports)
ACCIDENT ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
ACUTE SINUSITIS ( 3 FDA reports)
ADVERSE REACTION ( 3 FDA reports)
ALCOHOL POISONING ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 3 FDA reports)
ALVEOLITIS ( 3 FDA reports)
ALVEOLITIS ALLERGIC ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 3 FDA reports)
ANAL HAEMORRHAGE ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 3 FDA reports)
AORTIC DILATATION ( 3 FDA reports)
AORTIC VALVE SCLEROSIS ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
ARTHROPOD BITE ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
ATHEROSCLEROSIS ( 3 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BLOOD CALCIUM ABNORMAL ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
BLOOD COUNT ABNORMAL ( 3 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 3 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 3 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 3 FDA reports)
BONE DENSITY INCREASED ( 3 FDA reports)
BRAIN MASS ( 3 FDA reports)
BREAST CALCIFICATIONS ( 3 FDA reports)
BREAST SWELLING ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
CARDIAC ENZYMES INCREASED ( 3 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 3 FDA reports)
CATHETER RELATED COMPLICATION ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 3 FDA reports)
CHANGE OF BOWEL HABIT ( 3 FDA reports)
CHEILITIS ( 3 FDA reports)
CHOLESTEATOMA ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
COLITIS COLLAGENOUS ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
COLONIC FISTULA ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 3 FDA reports)
CONVERSION DISORDER ( 3 FDA reports)
CRYOGLOBULINAEMIA ( 3 FDA reports)
CUTANEOUS VASCULITIS ( 3 FDA reports)
CYSTITIS NONINFECTIVE ( 3 FDA reports)
DEBRIDEMENT ( 3 FDA reports)
DERMAL CYST ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DIABETIC COMA ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 3 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
DYSPAREUNIA ( 3 FDA reports)
DYSPLASIA ( 3 FDA reports)
EAR CONGESTION ( 3 FDA reports)
EJACULATION FAILURE ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
ENTEROVESICAL FISTULA ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ( 3 FDA reports)
EPIGASTRIC DISCOMFORT ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 3 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FACIAL PARESIS ( 3 FDA reports)
FAECES HARD ( 3 FDA reports)
FEAR OF DEATH ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 3 FDA reports)
GALLBLADDER ENLARGEMENT ( 3 FDA reports)
GALLBLADDER OPERATION ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
GENITAL RASH ( 3 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 3 FDA reports)
GLOSSITIS ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
GRIP STRENGTH DECREASED ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEPATIC LESION ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HERPES OESOPHAGITIS ( 3 FDA reports)
HYPERACUSIS ( 3 FDA reports)
HYPERPARATHYROIDISM ( 3 FDA reports)
HYPERPHAGIA ( 3 FDA reports)
HYPOGONADISM ( 3 FDA reports)
HYPOVENTILATION ( 3 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
INTRACRANIAL ANEURYSM ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
JAW OPERATION ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
LABYRINTHITIS ( 3 FDA reports)
LARYNGITIS ( 3 FDA reports)
LEFT ATRIAL DILATATION ( 3 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 3 FDA reports)
LICHENOID KERATOSIS ( 3 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 3 FDA reports)
LISTERIA ENCEPHALITIS ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 3 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
MERALGIA PARAESTHETICA ( 3 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 3 FDA reports)
METASTASES TO KIDNEY ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
METASTASES TO PERITONEUM ( 3 FDA reports)
METASTASIS ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MULTIPLE MYELOMA ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
MYCOPLASMA INFECTION ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
NATURAL KILLER-CELL LEUKAEMIA ( 3 FDA reports)
NEONATAL DISORDER ( 3 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NEUROMA ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
NOCARDIOSIS ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 3 FDA reports)
OESOPHAGEAL PAIN ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
ORAL DISORDER ( 3 FDA reports)
OTITIS MEDIA ( 3 FDA reports)
OVARIAN DISORDER ( 3 FDA reports)
OVARIAN MASS ( 3 FDA reports)
OVERGROWTH BACTERIAL ( 3 FDA reports)
PAIN EXACERBATED ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 3 FDA reports)
PEPTIC ULCER REACTIVATED ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PERITONEAL TUBERCULOSIS ( 3 FDA reports)
PERSONALITY CHANGE ( 3 FDA reports)
PHARYNGEAL ULCERATION ( 3 FDA reports)
PHLEBITIS SUPERFICIAL ( 3 FDA reports)
PILOERECTION ( 3 FDA reports)
PLACENTAL NECROSIS ( 3 FDA reports)
PNEUMONIA ASPERGILLUS ( 3 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
POSTNASAL DRIP ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PRECANCEROUS SKIN LESION ( 3 FDA reports)
PROCEDURAL NAUSEA ( 3 FDA reports)
PROCEDURAL VOMITING ( 3 FDA reports)
PROSTATOMEGALY ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PULMONARY GRANULOMA ( 3 FDA reports)
PULMONARY VASCULAR DISORDER ( 3 FDA reports)
PURPURA ( 3 FDA reports)
QRS AXIS ABNORMAL ( 3 FDA reports)
RALES ( 3 FDA reports)
RASH VESICULAR ( 3 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 3 FDA reports)
RENAL MASS ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
RENAL VASCULITIS ( 3 FDA reports)
RENAL VEIN THROMBOSIS ( 3 FDA reports)
RHINITIS SEASONAL ( 3 FDA reports)
SALIVARY GLAND CANCER ( 3 FDA reports)
SALPINGITIS ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
SCRATCH ( 3 FDA reports)
SEBORRHOEIC DERMATITIS ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
SEPTIC EMBOLUS ( 3 FDA reports)
SEQUESTRECTOMY ( 3 FDA reports)
SEROMA ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SHOULDER ARTHROPLASTY ( 3 FDA reports)
SKIN IRRITATION ( 3 FDA reports)
SKIN LACERATION ( 3 FDA reports)
SKIN MASS ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SKIN ODOUR ABNORMAL ( 3 FDA reports)
SMALL FOR DATES BABY ( 3 FDA reports)
SMEAR CERVIX ABNORMAL ( 3 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 3 FDA reports)
SPERM COUNT DECREASED ( 3 FDA reports)
SPINAL CORD DISORDER ( 3 FDA reports)
SPLENIC ARTERY ANEURYSM ( 3 FDA reports)
SPLENIC VEIN THROMBOSIS ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
TESTIS CANCER ( 3 FDA reports)
TETANUS ( 3 FDA reports)
THERAPY REGIMEN CHANGED ( 3 FDA reports)
TONSIL CANCER ( 3 FDA reports)
TONSILLECTOMY ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TRACHEOBRONCHITIS ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
TRIGGER FINGER ( 3 FDA reports)
TUNNEL VISION ( 3 FDA reports)
ULCER ( 3 FDA reports)
URETERIC OBSTRUCTION ( 3 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
VAGINAL MYCOSIS ( 3 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 3 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 3 FDA reports)
WALKING AID USER ( 3 FDA reports)
WEIGHT LOSS POOR ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
WISDOM TEETH REMOVAL ( 3 FDA reports)
5-HYDROXYINDOLACETIC ACID IN URINE INCREASED ( 2 FDA reports)
ABDOMINAL HERNIA REPAIR ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABNORMAL LABOUR ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ACID FAST BACILLI INFECTION ( 2 FDA reports)
ACROCHORDON ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ALCOHOL INTOLERANCE ( 2 FDA reports)
ALOPECIA AREATA ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
ANAL SPHINCTER ATONY ( 2 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANIMAL BITE ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
ANTITHROMBIN III INCREASED ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
AVERSION ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BILIARY TRACT INFECTION ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLASTOCYSTIS INFECTION ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BODY MASS INDEX DECREASED ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRADYCARDIA FOETAL ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BREAST ENLARGEMENT ( 2 FDA reports)
BREAST LUMP REMOVAL ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BRONCHIAL DISORDER ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
BURSITIS INFECTIVE ( 2 FDA reports)
BUTTOCK PAIN ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARCINOID SYNDROME ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIAC OPERATION ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHEST WALL PAIN ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHOROID MELANOMA ( 2 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 2 FDA reports)
COCCIDIOIDOMYCOSIS ( 2 FDA reports)
COCCYDYNIA ( 2 FDA reports)
COLON ADENOMA ( 2 FDA reports)
COLON CANCER STAGE IV ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 2 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONNECTIVE TISSUE DISORDER ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CONTRAST MEDIA ALLERGY ( 2 FDA reports)
CORONARY ARTERY REOCCLUSION ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DEVICE DISLOCATION ( 2 FDA reports)
DIABETIC COMPLICATION ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 2 FDA reports)
DUODENITIS HAEMORRHAGIC ( 2 FDA reports)
DYSHIDROSIS ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
EAR HAEMORRHAGE ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
EMBOLISM ARTERIAL ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENCEPHALOMALACIA ( 2 FDA reports)
ENTEROBACTER INFECTION ( 2 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 2 FDA reports)
EPIDIDYMITIS ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FIBRIN ABNORMAL ( 2 FDA reports)
FIBROADENOMA OF BREAST ( 2 FDA reports)
FIBROUS HISTIOCYTOMA ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOETAL GROWTH RETARDATION ( 2 FDA reports)
FOOD INTERACTION ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GAMMOPATHY ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 2 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 2 FDA reports)
GLOMERULONEPHROPATHY ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMOGLOBINURIA ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEAD AND NECK CANCER ( 2 FDA reports)
HEPATIC CANCER METASTATIC ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HUMAN BITE ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFANT ( 2 FDA reports)
INFECTED CYST ( 2 FDA reports)
INFUSION SITE CELLULITIS ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INFUSION SITE INFECTION ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
INGUINAL HERNIA REPAIR ( 2 FDA reports)
INJECTION SITE DISCOMFORT ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTRACRANIAL HYPOTENSION ( 2 FDA reports)
INTRAOCULAR MELANOMA ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
IUD MIGRATION ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LATENT TUBERCULOSIS ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIP DISCOLOURATION ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MENINGITIS TUBERCULOUS ( 2 FDA reports)
MENOMETRORRHAGIA ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
MESENTERIC PANNICULITIS ( 2 FDA reports)
METAMORPHOPSIA ( 2 FDA reports)
MIDDLE EAR DISORDER ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MONOCLONAL GAMMOPATHY ( 2 FDA reports)
MONOCYTOSIS ( 2 FDA reports)
MONONEUROPATHY MULTIPLEX ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCULAR DYSTROPHY ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NAIL PIGMENTATION ( 2 FDA reports)
NARCOTIC INTOXICATION ( 2 FDA reports)
NASOPHARYNGEAL CANCER ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NEPHROBLASTOMA ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NEUROENDOCRINE TUMOUR ( 2 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 2 FDA reports)
NUCHAL RIGIDITY ( 2 FDA reports)
OBSTRUCTED LABOUR ( 2 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 2 FDA reports)
OESTROGEN DEFICIENCY ( 2 FDA reports)
OOPHORECTOMY ( 2 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 2 FDA reports)
ORCHITIS ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PELVIC FLUID COLLECTION ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PERITONEAL ABSCESS ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PNEUMOCOCCAL INFECTION ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PNEUMOCONIOSIS ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYCHONDRITIS ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
POST PROCEDURAL NAUSEA ( 2 FDA reports)
POST PROCEDURAL PNEUMONIA ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
POSTPARTUM DEPRESSION ( 2 FDA reports)
POSTRENAL FAILURE ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PROCTITIS HAEMORRHAGIC ( 2 FDA reports)
PROCTOCOLECTOMY ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PROTEIN C INCREASED ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PSEUDOCYST ( 2 FDA reports)
PSYCHOTIC BEHAVIOUR ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY ARTERY DILATATION ( 2 FDA reports)
PULMONARY CALCIFICATION ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PULMONARY SEPSIS ( 2 FDA reports)
PUS IN STOOL ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
RADICULITIS LUMBOSACRAL ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RECTAL TENESMUS ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
RED MAN SYNDROME ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SALMONELLOSIS ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SEXUAL ASSAULT VICTIM ( 2 FDA reports)
SINUSITIS BACTERIAL ( 2 FDA reports)
SKIN FRAGILITY ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SMALL INTESTINAL RESECTION ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SNORING ( 2 FDA reports)
SOFT TISSUE DISORDER ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPERM CONCENTRATION DECREASED ( 2 FDA reports)
SPERM COUNT ZERO ( 2 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 2 FDA reports)
SPLENIC INFECTION ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
TACHYCARDIA FOETAL ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TESTICULAR PAIN ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THYROID MASS ( 2 FDA reports)
TIC ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 2 FDA reports)
TRAUMATIC FRACTURE ( 2 FDA reports)
TWIN PREGNANCY ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URINARY HESITATION ( 2 FDA reports)
URINARY TRACT MALFORMATION ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
UTERINE INFECTION ( 2 FDA reports)
UTERINE PROLAPSE ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VESICOURETERIC REFLUX ( 2 FDA reports)
VIRAEMIA ( 2 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 2 FDA reports)
VITAMIN B12 DECREASED ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
VITAMIN B12 INCREASED ( 2 FDA reports)
VITAMIN E DEFICIENCY ( 2 FDA reports)
VITILIGO ( 2 FDA reports)
VULVAL ABSCESS ( 2 FDA reports)
WOUND ABSCESS ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABSCESS OF EXTERNAL AUDITORY MEATUS ( 1 FDA reports)
ABSCESS RUPTURE ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ACTINOMYCOSIS ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE HAEMORRHAGIC OEDEMA OF INFANCY ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADNEXA UTERI CYST ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
AIDS RELATED COMPLICATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALLERGIC MYOCARDITIS ( 1 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 1 FDA reports)
ALVEOLAR OSTEITIS ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANAL INJURY ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANGIOSCLEROSIS ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANOGENITAL DYSPLASIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARRESTED LABOUR ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
B PRECURSOR TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BARTHOLIN'S CYST ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BIOPSY LUNG ABNORMAL ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 1 FDA reports)
BLOOD THROMBOPLASTIN ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE DECALCIFICATION ( 1 FDA reports)
BONE FORMATION INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW EOSINOPHILIC LEUKOCYTE COUNT INCREASED ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST DISORDER MALE ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BUCCAL POLYP ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 1 FDA reports)
CARCINOID TUMOUR PULMONARY ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATARACT CORTICAL ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHOROIDAL DETACHMENT ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL THYMUS ABSENCE ( 1 FDA reports)
CONJUNCTIVAL PRIMARY ACQUIRED MELANOSIS ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DEATH OF SPOUSE ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DIVERTICULUM DUODENAL ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG CLEARANCE INCREASED ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUBIN-JOHNSON SYNDROME ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENTEROCOLONIC FISTULA ( 1 FDA reports)
ENZYME INHIBITION ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 1 FDA reports)
EPIDURAL LIPOMATOSIS ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXPOSURE TO NOISE ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FAT REDISTRIBUTION ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FEMALE GENITAL-DIGESTIVE TRACT FISTULA ( 1 FDA reports)
FIBRIN D DIMER DECREASED ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC FISTULA ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC HYPOMOTILITY ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 1 FDA reports)
GASTROENTERITIS NONINFECTIOUS ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL DYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVAL GRAFT ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMORRHAGE IN PREGNANCY ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEART SOUNDS ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEAVY EXPOSURE TO ULTRAVIOLET LIGHT ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HISTONE ANTIBODY POSITIVE ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HYDROCELE ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPERVITAMINOSIS ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEAL FISTULA ( 1 FDA reports)
ILEOCOLOSTOMY ( 1 FDA reports)
ILIAC VEIN THROMBOSIS ( 1 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPLANT SITE IRRITATION ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INFERTILITY MALE ( 1 FDA reports)
INFLAMMATORY PAIN ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE PARAESTHESIA ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INSOMNIA RELATED TO ANOTHER MENTAL CONDITION ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
IRITIS ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 1 FDA reports)
LARGE INTESTINAL STRICTURE ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNGOMALACIA ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LOCALISED SKIN REACTION ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MALIGNANT PALATE NEOPLASM ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MECHANICAL URTICARIA ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ACQUIRED ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 1 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEONATAL ASPHYXIA ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODAL OSTEOARTHRITIS ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OCULAR NEOPLASM ( 1 FDA reports)
OEDEMATOUS PANCREATITIS ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL IRRITATION ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
ORGASMIC SENSATION DECREASED ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARASPINAL ABSCESS ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIANAL ERYTHEMA ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERIPANCREATIC FLUID COLLECTION ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOTOSENSITIVE RASH ( 1 FDA reports)
PHYLLODES TUMOUR ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLACENTA PRAEVIA ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POROKERATOSIS ( 1 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POSTINFARCTION ANGINA ( 1 FDA reports)
POSTOPERATIVE HETEROTOPIC CALCIFICATION ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY TEST POSITIVE ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROLONGED LABOUR ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATIC CALCIFICATION ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATIC PAIN ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSYCHOGENIC ERECTILE DYSFUNCTION ( 1 FDA reports)
PTERYGIUM ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY COCCIDIOIDES ( 1 FDA reports)
PULMONARY FUNCTION TEST INCREASED ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL FISTULA REPAIR ( 1 FDA reports)
RECTAL LESION ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
REPAIR OF IMPERFORATE RECTUM ( 1 FDA reports)
REPETITIVE STRAIN INJURY ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCHAMBERG'S DISEASE ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SCROTAL GANGRENE ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 1 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOULDER DEFORMITY ( 1 FDA reports)
SHUNT MALFUNCTION ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SPERM COUNT ABNORMAL ( 1 FDA reports)
SPERMATOCELE ( 1 FDA reports)
SPERMATOZOA ABNORMAL ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STAPHYLOCOCCAL IMPETIGO ( 1 FDA reports)
STARING ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STICKY SKIN ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUPERNUMERARY NIPPLE ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TEETH BRITTLE ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TESTICULAR ATROPHY ( 1 FDA reports)
TESTICULAR GERM CELL CANCER METASTATIC ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
TETANY ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THIRST ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOSED VARICOSE VEIN ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROID CYST ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOOTH IMPACTED ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICHOSPORON INFECTION ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TUBERCULOSIS OF CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
TUMOUR COMPRESSION ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY TRACT ABSCESS ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINARY TRACT PAIN ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE MASS ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
UTERINE RUPTURE ( 1 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICOCELE ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASECTOMY ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VESICAL FISTULA ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITAMIN A INCREASED ( 1 FDA reports)
VITAMIN C DEFICIENCY ( 1 FDA reports)
VULVAR DYSPLASIA ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use