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

PAIN ( 463 FDA reports)
DRUG INEFFECTIVE ( 398 FDA reports)
NAUSEA ( 387 FDA reports)
FATIGUE ( 275 FDA reports)
ANXIETY ( 270 FDA reports)
DYSPNOEA ( 264 FDA reports)
VOMITING ( 261 FDA reports)
HEADACHE ( 245 FDA reports)
ABDOMINAL PAIN UPPER ( 220 FDA reports)
PULMONARY EMBOLISM ( 215 FDA reports)
DIZZINESS ( 212 FDA reports)
DEEP VEIN THROMBOSIS ( 208 FDA reports)
DEPRESSION ( 202 FDA reports)
CHOLELITHIASIS ( 191 FDA reports)
DIARRHOEA ( 189 FDA reports)
CHEST PAIN ( 177 FDA reports)
CHOLECYSTITIS CHRONIC ( 177 FDA reports)
BACK PAIN ( 172 FDA reports)
INJURY ( 172 FDA reports)
ARTHRALGIA ( 171 FDA reports)
ASTHENIA ( 164 FDA reports)
OEDEMA PERIPHERAL ( 163 FDA reports)
PAIN IN EXTREMITY ( 163 FDA reports)
INSOMNIA ( 161 FDA reports)
ANAEMIA ( 149 FDA reports)
ABDOMINAL PAIN ( 137 FDA reports)
PARAESTHESIA ( 137 FDA reports)
PYREXIA ( 130 FDA reports)
WEIGHT DECREASED ( 129 FDA reports)
RASH ( 128 FDA reports)
HYPOAESTHESIA ( 127 FDA reports)
CONDITION AGGRAVATED ( 124 FDA reports)
FALL ( 123 FDA reports)
PRURITUS ( 117 FDA reports)
EMOTIONAL DISTRESS ( 116 FDA reports)
GALLBLADDER DISORDER ( 114 FDA reports)
BONE DISORDER ( 109 FDA reports)
SOMNOLENCE ( 106 FDA reports)
MALAISE ( 102 FDA reports)
GAIT DISTURBANCE ( 100 FDA reports)
OSTEONECROSIS OF JAW ( 100 FDA reports)
CEREBROVASCULAR ACCIDENT ( 98 FDA reports)
MYALGIA ( 96 FDA reports)
ABDOMINAL DISCOMFORT ( 93 FDA reports)
CONSTIPATION ( 93 FDA reports)
HYPERTENSION ( 91 FDA reports)
RENAL FAILURE ACUTE ( 88 FDA reports)
WEIGHT INCREASED ( 88 FDA reports)
FEELING ABNORMAL ( 87 FDA reports)
RENAL FAILURE ( 85 FDA reports)
URTICARIA ( 85 FDA reports)
INCORRECT DOSE ADMINISTERED ( 81 FDA reports)
HYPERSENSITIVITY ( 79 FDA reports)
THROMBOSIS ( 78 FDA reports)
ERYTHEMA ( 76 FDA reports)
ANHEDONIA ( 75 FDA reports)
DECREASED APPETITE ( 75 FDA reports)
OVERDOSE ( 75 FDA reports)
OSTEOARTHRITIS ( 74 FDA reports)
PNEUMONIA ( 73 FDA reports)
URINARY TRACT INFECTION ( 73 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 71 FDA reports)
MUSCULOSKELETAL PAIN ( 71 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 70 FDA reports)
SWELLING ( 67 FDA reports)
ABDOMINAL DISTENSION ( 66 FDA reports)
IRRITABLE BOWEL SYNDROME ( 66 FDA reports)
PLEURAL EFFUSION ( 66 FDA reports)
COLITIS ULCERATIVE ( 65 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 65 FDA reports)
METASTASES TO BONE ( 65 FDA reports)
MUSCLE SPASMS ( 64 FDA reports)
HYPOTENSION ( 63 FDA reports)
VISION BLURRED ( 63 FDA reports)
BILIARY DYSKINESIA ( 62 FDA reports)
STRESS ( 62 FDA reports)
DEHYDRATION ( 61 FDA reports)
DRUG EFFECT DECREASED ( 61 FDA reports)
MIGRAINE ( 61 FDA reports)
CHILLS ( 60 FDA reports)
FLUSHING ( 60 FDA reports)
ATELECTASIS ( 59 FDA reports)
BLOOD PRESSURE INCREASED ( 58 FDA reports)
DYSPHAGIA ( 58 FDA reports)
UNEVALUABLE EVENT ( 58 FDA reports)
SWELLING FACE ( 57 FDA reports)
CONTUSION ( 56 FDA reports)
CONVULSION ( 56 FDA reports)
CROHN'S DISEASE ( 56 FDA reports)
DYSPEPSIA ( 56 FDA reports)
HYPERHIDROSIS ( 56 FDA reports)
INFECTION ( 55 FDA reports)
INJECTION SITE PAIN ( 55 FDA reports)
TOOTH EXTRACTION ( 55 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 54 FDA reports)
FEAR ( 54 FDA reports)
JOINT SWELLING ( 54 FDA reports)
MUSCULAR WEAKNESS ( 54 FDA reports)
CHEST DISCOMFORT ( 53 FDA reports)
COUGH ( 53 FDA reports)
OSTEOMYELITIS ( 53 FDA reports)
TREMOR ( 53 FDA reports)
PALPITATIONS ( 52 FDA reports)
PRODUCT QUALITY ISSUE ( 52 FDA reports)
RECTAL HAEMORRHAGE ( 52 FDA reports)
ARTHRITIS ( 51 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 51 FDA reports)
BONE PAIN ( 50 FDA reports)
CHOLECYSTITIS ( 50 FDA reports)
NEPHROLITHIASIS ( 50 FDA reports)
CONFUSIONAL STATE ( 49 FDA reports)
DENTAL CARIES ( 49 FDA reports)
INJECTION SITE ERYTHEMA ( 49 FDA reports)
MYOCARDIAL INFARCTION ( 49 FDA reports)
PANCREATITIS ( 49 FDA reports)
TACHYCARDIA ( 49 FDA reports)
DEATH ( 48 FDA reports)
NECK PAIN ( 48 FDA reports)
PAIN IN JAW ( 48 FDA reports)
SINUSITIS ( 48 FDA reports)
DIABETES MELLITUS ( 47 FDA reports)
HOT FLUSH ( 47 FDA reports)
FEELING HOT ( 46 FDA reports)
LOOSE TOOTH ( 46 FDA reports)
SPINAL OSTEOARTHRITIS ( 46 FDA reports)
COELIAC DISEASE ( 45 FDA reports)
HYPOAESTHESIA ORAL ( 45 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 45 FDA reports)
DRUG INTERACTION ( 44 FDA reports)
GASTRITIS ( 44 FDA reports)
INFLUENZA LIKE ILLNESS ( 44 FDA reports)
NERVOUSNESS ( 44 FDA reports)
NEUROPATHY PERIPHERAL ( 44 FDA reports)
POLLAKIURIA ( 44 FDA reports)
RENAL IMPAIRMENT ( 44 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 43 FDA reports)
BLOOD GLUCOSE INCREASED ( 43 FDA reports)
COLITIS ( 42 FDA reports)
HIATUS HERNIA ( 42 FDA reports)
SYNCOPE ( 42 FDA reports)
TOOTH LOSS ( 42 FDA reports)
HEART RATE INCREASED ( 41 FDA reports)
LYMPHADENOPATHY ( 41 FDA reports)
NIGHT SWEATS ( 41 FDA reports)
OSTEONECROSIS ( 41 FDA reports)
RENAL CYST ( 41 FDA reports)
TOOTH ABSCESS ( 41 FDA reports)
BRONCHITIS ( 40 FDA reports)
GASTROINTESTINAL DISORDER ( 40 FDA reports)
OSTEOPOROSIS ( 40 FDA reports)
VISUAL IMPAIRMENT ( 40 FDA reports)
CELLULITIS ( 39 FDA reports)
DISTURBANCE IN ATTENTION ( 39 FDA reports)
DYSGEUSIA ( 39 FDA reports)
HAEMATURIA ( 39 FDA reports)
RENAL INJURY ( 39 FDA reports)
TOOTH FRACTURE ( 39 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 39 FDA reports)
CHOLECYSTITIS ACUTE ( 38 FDA reports)
EYE SWELLING ( 38 FDA reports)
VERTIGO ( 38 FDA reports)
CARDIOMEGALY ( 37 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 37 FDA reports)
DECREASED INTEREST ( 37 FDA reports)
DYSURIA ( 36 FDA reports)
FLATULENCE ( 36 FDA reports)
IMPAIRED HEALING ( 36 FDA reports)
ASTHMA ( 35 FDA reports)
BALANCE DISORDER ( 35 FDA reports)
MASTICATION DISORDER ( 35 FDA reports)
MENTAL DISORDER ( 35 FDA reports)
CARDIAC MURMUR ( 34 FDA reports)
DRUG ADMINISTRATION ERROR ( 34 FDA reports)
INFLAMMATION ( 34 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 34 FDA reports)
MULTI-ORGAN FAILURE ( 34 FDA reports)
OEDEMA ( 34 FDA reports)
ORAL PAIN ( 34 FDA reports)
ABASIA ( 33 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 33 FDA reports)
BREAST CANCER ( 33 FDA reports)
CHOLECYSTECTOMY ( 33 FDA reports)
DISABILITY ( 33 FDA reports)
EPISTAXIS ( 33 FDA reports)
INJECTION SITE HAEMATOMA ( 33 FDA reports)
LOSS OF CONSCIOUSNESS ( 33 FDA reports)
SLEEP DISORDER ( 33 FDA reports)
SUICIDAL IDEATION ( 33 FDA reports)
TOOTHACHE ( 33 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 32 FDA reports)
BLISTER ( 32 FDA reports)
BURNING SENSATION ( 32 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 32 FDA reports)
PANCYTOPENIA ( 32 FDA reports)
ARTHROPATHY ( 31 FDA reports)
GLOSSODYNIA ( 31 FDA reports)
HERPES ZOSTER ( 31 FDA reports)
HYPERLIPIDAEMIA ( 31 FDA reports)
HYPONATRAEMIA ( 31 FDA reports)
THROAT IRRITATION ( 31 FDA reports)
WHEEZING ( 31 FDA reports)
AMNESIA ( 30 FDA reports)
DRY SKIN ( 30 FDA reports)
LIP SWELLING ( 30 FDA reports)
RASH ERYTHEMATOUS ( 30 FDA reports)
RASH MACULAR ( 30 FDA reports)
RIB FRACTURE ( 30 FDA reports)
SPINAL COMPRESSION FRACTURE ( 30 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 29 FDA reports)
MASS ( 29 FDA reports)
NASOPHARYNGITIS ( 29 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 29 FDA reports)
BONE LESION ( 28 FDA reports)
EYE PAIN ( 28 FDA reports)
MITRAL VALVE INCOMPETENCE ( 28 FDA reports)
NEUTROPENIA ( 28 FDA reports)
PANIC ATTACK ( 28 FDA reports)
POLYP ( 28 FDA reports)
SPEECH DISORDER ( 28 FDA reports)
ALOPECIA ( 27 FDA reports)
HEPATIC ENZYME INCREASED ( 27 FDA reports)
HYPOPHAGIA ( 27 FDA reports)
LUNG NEOPLASM ( 27 FDA reports)
ROAD TRAFFIC ACCIDENT ( 27 FDA reports)
AGITATION ( 26 FDA reports)
BLOOD PRESSURE DECREASED ( 26 FDA reports)
DRUG HYPERSENSITIVITY ( 26 FDA reports)
DYSPNOEA EXERTIONAL ( 26 FDA reports)
HEAD INJURY ( 26 FDA reports)
MOUTH ULCERATION ( 26 FDA reports)
OVARIAN CYST ( 26 FDA reports)
URINARY INCONTINENCE ( 26 FDA reports)
DEFORMITY ( 25 FDA reports)
DISCOMFORT ( 25 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 25 FDA reports)
JAUNDICE ( 25 FDA reports)
LETHARGY ( 25 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 25 FDA reports)
MEMORY IMPAIRMENT ( 25 FDA reports)
PHOTOPHOBIA ( 25 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 25 FDA reports)
ARTERIOSCLEROSIS ( 24 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 24 FDA reports)
CATARACT ( 24 FDA reports)
EAR PAIN ( 24 FDA reports)
FAECES DISCOLOURED ( 24 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 24 FDA reports)
HAEMATOCHEZIA ( 24 FDA reports)
HEPATIC STEATOSIS ( 24 FDA reports)
IRRITABILITY ( 24 FDA reports)
ORAL DISCOMFORT ( 24 FDA reports)
OSTEOSCLEROSIS ( 24 FDA reports)
TINNITUS ( 24 FDA reports)
ABNORMAL DREAMS ( 23 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 23 FDA reports)
ATRIAL FIBRILLATION ( 23 FDA reports)
DEBRIDEMENT ( 23 FDA reports)
DEPRESSED MOOD ( 23 FDA reports)
DISORIENTATION ( 23 FDA reports)
HAEMOGLOBIN DECREASED ( 23 FDA reports)
HEMIPARESIS ( 23 FDA reports)
HEPATOMEGALY ( 23 FDA reports)
HYPOKALAEMIA ( 23 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 23 FDA reports)
TOOTH DISORDER ( 23 FDA reports)
VAGINAL HAEMORRHAGE ( 23 FDA reports)
BILIARY COLIC ( 22 FDA reports)
BONE DENSITY DECREASED ( 22 FDA reports)
CARDIAC ARREST ( 22 FDA reports)
CYSTITIS ( 22 FDA reports)
EMOTIONAL DISORDER ( 22 FDA reports)
HAEMATEMESIS ( 22 FDA reports)
INFLUENZA ( 22 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 22 FDA reports)
STAPHYLOCOCCAL INFECTION ( 22 FDA reports)
THROMBOCYTOPENIA ( 22 FDA reports)
APHTHOUS STOMATITIS ( 21 FDA reports)
BONE DEBRIDEMENT ( 21 FDA reports)
CARDIAC DISORDER ( 21 FDA reports)
HAEMORRHAGE ( 21 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 21 FDA reports)
LUNG DISORDER ( 21 FDA reports)
MUSCLE STRAIN ( 21 FDA reports)
PHARYNGEAL OEDEMA ( 21 FDA reports)
PLEURITIC PAIN ( 21 FDA reports)
PNEUMOTHORAX ( 21 FDA reports)
PULMONARY INFARCTION ( 21 FDA reports)
RHINITIS ALLERGIC ( 21 FDA reports)
ROTATOR CUFF SYNDROME ( 21 FDA reports)
SEPSIS ( 21 FDA reports)
STEVENS-JOHNSON SYNDROME ( 21 FDA reports)
ABSCESS ( 20 FDA reports)
BLOOD CREATININE INCREASED ( 20 FDA reports)
CARPAL TUNNEL SYNDROME ( 20 FDA reports)
CORONARY ARTERY DISEASE ( 20 FDA reports)
DIVERTICULUM ( 20 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 20 FDA reports)
GALLBLADDER INJURY ( 20 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 20 FDA reports)
HAEMORRHOIDS ( 20 FDA reports)
MENISCUS LESION ( 20 FDA reports)
MOBILITY DECREASED ( 20 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 20 FDA reports)
PLATELET COUNT DECREASED ( 20 FDA reports)
RASH PRURITIC ( 20 FDA reports)
RHEUMATOID ARTHRITIS ( 20 FDA reports)
SWOLLEN TONGUE ( 20 FDA reports)
BLOOD BILIRUBIN INCREASED ( 19 FDA reports)
BREAST CANCER METASTATIC ( 19 FDA reports)
CAESAREAN SECTION ( 19 FDA reports)
DEAFNESS ( 19 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 19 FDA reports)
DYSARTHRIA ( 19 FDA reports)
FLUID RETENTION ( 19 FDA reports)
GASTRIC DISORDER ( 19 FDA reports)
NEURALGIA ( 19 FDA reports)
RHINORRHOEA ( 19 FDA reports)
SINUS DISORDER ( 19 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 19 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 19 FDA reports)
BLINDNESS ( 18 FDA reports)
BLOOD POTASSIUM DECREASED ( 18 FDA reports)
EATING DISORDER ( 18 FDA reports)
FIBROMYALGIA ( 18 FDA reports)
FUNGAL INFECTION ( 18 FDA reports)
HEPATITIS ( 18 FDA reports)
ILL-DEFINED DISORDER ( 18 FDA reports)
ORAL HERPES ( 18 FDA reports)
OSTEOLYSIS ( 18 FDA reports)
PROTEINURIA ( 18 FDA reports)
RESPIRATORY DISTRESS ( 18 FDA reports)
ULCER ( 18 FDA reports)
ASCITES ( 17 FDA reports)
BARRETT'S OESOPHAGUS ( 17 FDA reports)
CANDIDIASIS ( 17 FDA reports)
CYST ( 17 FDA reports)
HYPOTHYROIDISM ( 17 FDA reports)
INTESTINAL OBSTRUCTION ( 17 FDA reports)
JOINT STIFFNESS ( 17 FDA reports)
LIBIDO DECREASED ( 17 FDA reports)
MENSTRUATION IRREGULAR ( 17 FDA reports)
MENTAL STATUS CHANGES ( 17 FDA reports)
MOOD SWINGS ( 17 FDA reports)
MULTIPLE MYELOMA ( 17 FDA reports)
OESOPHAGITIS ( 17 FDA reports)
ORAL SURGERY ( 17 FDA reports)
OROPHARYNGEAL PAIN ( 17 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 17 FDA reports)
PULMONARY HYPERTENSION ( 17 FDA reports)
PYELOCALIECTASIS ( 17 FDA reports)
RESTLESS LEGS SYNDROME ( 17 FDA reports)
SCAR ( 17 FDA reports)
SKIN DISCOLOURATION ( 17 FDA reports)
SLEEP APNOEA SYNDROME ( 17 FDA reports)
STOMATITIS ( 17 FDA reports)
COMPRESSION FRACTURE ( 16 FDA reports)
DRY MOUTH ( 16 FDA reports)
EPICONDYLITIS ( 16 FDA reports)
FOREIGN BODY ( 16 FDA reports)
GASTRIC ULCER ( 16 FDA reports)
HAEMANGIOMA OF LIVER ( 16 FDA reports)
HYPOXIA ( 16 FDA reports)
IMPAIRED WORK ABILITY ( 16 FDA reports)
INTENTIONAL DRUG MISUSE ( 16 FDA reports)
JOINT EFFUSION ( 16 FDA reports)
MELAENA ( 16 FDA reports)
NEOPLASM MALIGNANT ( 16 FDA reports)
PROCEDURAL PAIN ( 16 FDA reports)
RETCHING ( 16 FDA reports)
SINUS TACHYCARDIA ( 16 FDA reports)
TENDERNESS ( 16 FDA reports)
VISUAL ACUITY REDUCED ( 16 FDA reports)
ANAPHYLACTIC REACTION ( 15 FDA reports)
ANGINA PECTORIS ( 15 FDA reports)
CRYING ( 15 FDA reports)
DIVERTICULUM INTESTINAL ( 15 FDA reports)
ECZEMA ( 15 FDA reports)
EMPHYSEMA ( 15 FDA reports)
EYE HAEMORRHAGE ( 15 FDA reports)
GINGIVAL INFECTION ( 15 FDA reports)
HAND FRACTURE ( 15 FDA reports)
ILEUS ( 15 FDA reports)
LEUKOCYTOSIS ( 15 FDA reports)
OBESITY ( 15 FDA reports)
OFF LABEL USE ( 15 FDA reports)
ORAL INFECTION ( 15 FDA reports)
PLEURISY ( 15 FDA reports)
PRODUCTIVE COUGH ( 15 FDA reports)
PRURITUS GENERALISED ( 15 FDA reports)
RESPIRATORY ARREST ( 15 FDA reports)
SKIN EXFOLIATION ( 15 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 15 FDA reports)
TENDONITIS ( 15 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 15 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 15 FDA reports)
ACCIDENTAL OVERDOSE ( 14 FDA reports)
BASAL CELL CARCINOMA ( 14 FDA reports)
BRADYCARDIA ( 14 FDA reports)
DEVICE RELATED INFECTION ( 14 FDA reports)
DYSPHONIA ( 14 FDA reports)
EAR INFECTION ( 14 FDA reports)
EXOSTOSIS ( 14 FDA reports)
GINGIVAL PAIN ( 14 FDA reports)
INJECTION SITE HAEMORRHAGE ( 14 FDA reports)
INTESTINAL HAEMORRHAGE ( 14 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 14 FDA reports)
KELOID SCAR ( 14 FDA reports)
LACERATION ( 14 FDA reports)
LIFE EXPECTANCY SHORTENED ( 14 FDA reports)
LIPOMA ( 14 FDA reports)
MICTURITION URGENCY ( 14 FDA reports)
MULTI-ORGAN DISORDER ( 14 FDA reports)
NO ADVERSE EVENT ( 14 FDA reports)
NONSPECIFIC REACTION ( 14 FDA reports)
PHARYNGITIS ( 14 FDA reports)
PHYSICAL DISABILITY ( 14 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 14 FDA reports)
SCOLIOSIS ( 14 FDA reports)
SURGERY ( 14 FDA reports)
ACNE ( 13 FDA reports)
AGRANULOCYTOSIS ( 13 FDA reports)
ATRIAL FLUTTER ( 13 FDA reports)
CEREBRAL HAEMORRHAGE ( 13 FDA reports)
CEREBRAL INFARCTION ( 13 FDA reports)
CHROMATURIA ( 13 FDA reports)
COORDINATION ABNORMAL ( 13 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 13 FDA reports)
ENDODONTIC PROCEDURE ( 13 FDA reports)
FEELING COLD ( 13 FDA reports)
FISTULA ( 13 FDA reports)
GINGIVAL RECESSION ( 13 FDA reports)
HALLUCINATION ( 13 FDA reports)
HYPERSOMNIA ( 13 FDA reports)
INGUINAL HERNIA ( 13 FDA reports)
JAW OPERATION ( 13 FDA reports)
LACRIMATION INCREASED ( 13 FDA reports)
MAJOR DEPRESSION ( 13 FDA reports)
METASTASES TO SPINE ( 13 FDA reports)
NASAL CONGESTION ( 13 FDA reports)
NIGHTMARE ( 13 FDA reports)
PARAESTHESIA ORAL ( 13 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 13 FDA reports)
POOR QUALITY SLEEP ( 13 FDA reports)
PREGNANCY ( 13 FDA reports)
PSYCHOTIC DISORDER ( 13 FDA reports)
RASH GENERALISED ( 13 FDA reports)
RESPIRATORY DISORDER ( 13 FDA reports)
RESPIRATORY FAILURE ( 13 FDA reports)
RESTLESSNESS ( 13 FDA reports)
SKIN BURNING SENSATION ( 13 FDA reports)
SNEEZING ( 13 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 13 FDA reports)
VIRAL INFECTION ( 13 FDA reports)
WOUND DEHISCENCE ( 13 FDA reports)
ABORTION SPONTANEOUS ( 12 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 12 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 12 FDA reports)
AORTIC VALVE INCOMPETENCE ( 12 FDA reports)
BLOOD SODIUM DECREASED ( 12 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 12 FDA reports)
BONE MARROW FAILURE ( 12 FDA reports)
CEREBRAL ISCHAEMIA ( 12 FDA reports)
CERVICAL DYSPLASIA ( 12 FDA reports)
COGNITIVE DISORDER ( 12 FDA reports)
COLONIC POLYP ( 12 FDA reports)
CYTOLYTIC HEPATITIS ( 12 FDA reports)
FEBRILE NEUTROPENIA ( 12 FDA reports)
FEELING JITTERY ( 12 FDA reports)
FURUNCLE ( 12 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 12 FDA reports)
HAEMATOCRIT DECREASED ( 12 FDA reports)
HAEMOPTYSIS ( 12 FDA reports)
LEUKOPENIA ( 12 FDA reports)
LUNG INFILTRATION ( 12 FDA reports)
MALNUTRITION ( 12 FDA reports)
METABOLIC ACIDOSIS ( 12 FDA reports)
MULTIPLE SCLEROSIS ( 12 FDA reports)
MUSCLE TWITCHING ( 12 FDA reports)
NOCTURIA ( 12 FDA reports)
OROPHARYNGEAL BLISTERING ( 12 FDA reports)
OSTEITIS ( 12 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 12 FDA reports)
PARALYSIS ( 12 FDA reports)
SACROILIITIS ( 12 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 12 FDA reports)
SPINAL FRACTURE ( 12 FDA reports)
TOOTH DEPOSIT ( 12 FDA reports)
VERTEBROPLASTY ( 12 FDA reports)
VULVOVAGINAL DRYNESS ( 12 FDA reports)
ACTINOMYCOSIS ( 11 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 11 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 11 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 11 FDA reports)
APHASIA ( 11 FDA reports)
ARTERY DISSECTION ( 11 FDA reports)
BILE DUCT STONE ( 11 FDA reports)
BLADDER DILATATION ( 11 FDA reports)
BLINDNESS UNILATERAL ( 11 FDA reports)
BLOOD GLUCOSE DECREASED ( 11 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 11 FDA reports)
BURSITIS ( 11 FDA reports)
CYANOSIS ( 11 FDA reports)
DENTURE WEARER ( 11 FDA reports)
DYSMENORRHOEA ( 11 FDA reports)
FACIAL PAIN ( 11 FDA reports)
FAILURE TO THRIVE ( 11 FDA reports)
GINGIVITIS ( 11 FDA reports)
HEPATIC FAILURE ( 11 FDA reports)
HERPES SIMPLEX ( 11 FDA reports)
HODGKIN'S DISEASE ( 11 FDA reports)
HYPERCHOLESTEROLAEMIA ( 11 FDA reports)
HYPOVOLAEMIA ( 11 FDA reports)
JAW DISORDER ( 11 FDA reports)
LARYNGOCELE ( 11 FDA reports)
METASTASES TO LIVER ( 11 FDA reports)
OCULAR HYPERAEMIA ( 11 FDA reports)
ORAL DISORDER ( 11 FDA reports)
OSTEOPENIA ( 11 FDA reports)
OTITIS MEDIA ( 11 FDA reports)
PELVIC PAIN ( 11 FDA reports)
PERICARDIAL EFFUSION ( 11 FDA reports)
PHOTOPSIA ( 11 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 11 FDA reports)
RENAL DISORDER ( 11 FDA reports)
SKIN DISORDER ( 11 FDA reports)
SKIN IRRITATION ( 11 FDA reports)
SKIN LACERATION ( 11 FDA reports)
SUICIDE ATTEMPT ( 11 FDA reports)
THINKING ABNORMAL ( 11 FDA reports)
TONSILLITIS ( 11 FDA reports)
URINARY RETENTION ( 11 FDA reports)
VITAMIN B12 DEFICIENCY ( 11 FDA reports)
ABDOMINAL PAIN LOWER ( 10 FDA reports)
ABDOMINAL TENDERNESS ( 10 FDA reports)
AGGRESSION ( 10 FDA reports)
ANGER ( 10 FDA reports)
APHAGIA ( 10 FDA reports)
ARRHYTHMIA ( 10 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 10 FDA reports)
BILE DUCT OBSTRUCTION ( 10 FDA reports)
BLOOD CULTURE POSITIVE ( 10 FDA reports)
BLOOD DISORDER ( 10 FDA reports)
BRUXISM ( 10 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 10 FDA reports)
COAGULOPATHY ( 10 FDA reports)
COLLAPSE OF LUNG ( 10 FDA reports)
DENTAL CARE ( 10 FDA reports)
DERMATOMYOSITIS ( 10 FDA reports)
DISEASE PROGRESSION ( 10 FDA reports)
DRUG TOXICITY ( 10 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 10 FDA reports)
GINGIVAL DISORDER ( 10 FDA reports)
GINGIVAL ULCERATION ( 10 FDA reports)
HAEMARTHROSIS ( 10 FDA reports)
HIP ARTHROPLASTY ( 10 FDA reports)
HIP FRACTURE ( 10 FDA reports)
HYPERCALCAEMIA ( 10 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 10 FDA reports)
HYPERGLYCAEMIA ( 10 FDA reports)
HYPOAESTHESIA FACIAL ( 10 FDA reports)
IMPAIRED DRIVING ABILITY ( 10 FDA reports)
IRON DEFICIENCY ANAEMIA ( 10 FDA reports)
KYPHOSIS ( 10 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 10 FDA reports)
MENORRHAGIA ( 10 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 10 FDA reports)
MITRAL VALVE PROLAPSE ( 10 FDA reports)
NASAL POLYPS ( 10 FDA reports)
OTITIS EXTERNA ( 10 FDA reports)
PERIODONTAL DISEASE ( 10 FDA reports)
PULMONARY OEDEMA ( 10 FDA reports)
RESPIRATORY TRACT INFECTION ( 10 FDA reports)
SCOTOMA ( 10 FDA reports)
SEASONAL ALLERGY ( 10 FDA reports)
SINUS CONGESTION ( 10 FDA reports)
SKIN LESION ( 10 FDA reports)
SKIN PAPILLOMA ( 10 FDA reports)
SPINAL DEFORMITY ( 10 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 10 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 10 FDA reports)
VENOUS THROMBOSIS ( 10 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 9 FDA reports)
ACUTE RESPIRATORY FAILURE ( 9 FDA reports)
ANAPHYLACTIC SHOCK ( 9 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 9 FDA reports)
BLOOD AMYLASE INCREASED ( 9 FDA reports)
BREAST TENDERNESS ( 9 FDA reports)
CARDIOMYOPATHY ( 9 FDA reports)
CERVICAL SPINAL STENOSIS ( 9 FDA reports)
CHOLESTEROSIS ( 9 FDA reports)
DERMATITIS ( 9 FDA reports)
DIASTOLIC DYSFUNCTION ( 9 FDA reports)
DIPLOPIA ( 9 FDA reports)
DRUG DOSE OMISSION ( 9 FDA reports)
DRUG INTOLERANCE ( 9 FDA reports)
DYSPAREUNIA ( 9 FDA reports)
ERECTILE DYSFUNCTION ( 9 FDA reports)
FIBROUS HISTIOCYTOMA ( 9 FDA reports)
GASTRIC HAEMORRHAGE ( 9 FDA reports)
GINGIVAL SWELLING ( 9 FDA reports)
GOITRE ( 9 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 9 FDA reports)
HYPERKALAEMIA ( 9 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 9 FDA reports)
INJECTION SITE RASH ( 9 FDA reports)
INTENTIONAL OVERDOSE ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 9 FDA reports)
LARYNGEAL OEDEMA ( 9 FDA reports)
LIP DRY ( 9 FDA reports)
LOBAR PNEUMONIA ( 9 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 9 FDA reports)
MIDDLE INSOMNIA ( 9 FDA reports)
ORTHOSTATIC HYPOTENSION ( 9 FDA reports)
OXYGEN SATURATION DECREASED ( 9 FDA reports)
PARANOIA ( 9 FDA reports)
PATHOLOGICAL FRACTURE ( 9 FDA reports)
PERIODONTITIS ( 9 FDA reports)
PERIPHERAL COLDNESS ( 9 FDA reports)
RENAL FAILURE CHRONIC ( 9 FDA reports)
RETINAL VEIN OCCLUSION ( 9 FDA reports)
SCIATICA ( 9 FDA reports)
SINUS BRADYCARDIA ( 9 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 9 FDA reports)
SYNOVIAL CYST ( 9 FDA reports)
TONGUE DISORDER ( 9 FDA reports)
ADENOCARCINOMA ( 8 FDA reports)
ANGIOEDEMA ( 8 FDA reports)
ANGIOPATHY ( 8 FDA reports)
ANXIETY DISORDER ( 8 FDA reports)
APPETITE DISORDER ( 8 FDA reports)
ARTHROPOD BITE ( 8 FDA reports)
AXILLARY MASS ( 8 FDA reports)
BACTERIAL TEST NEGATIVE ( 8 FDA reports)
BLOOD UREA INCREASED ( 8 FDA reports)
BONE NEOPLASM MALIGNANT ( 8 FDA reports)
BONE OPERATION ( 8 FDA reports)
BRAIN OEDEMA ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 8 FDA reports)
CHEILITIS ( 8 FDA reports)
DYSKINESIA ( 8 FDA reports)
EARLY SATIETY ( 8 FDA reports)
EROSIVE DUODENITIS ( 8 FDA reports)
EXERCISE TOLERANCE DECREASED ( 8 FDA reports)
EYE IRRITATION ( 8 FDA reports)
FACE OEDEMA ( 8 FDA reports)
FOOT FRACTURE ( 8 FDA reports)
GASTRIC POLYPS ( 8 FDA reports)
GASTROINTESTINAL PAIN ( 8 FDA reports)
GRANULOCYTOPENIA ( 8 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 8 FDA reports)
HYPOTHERMIA ( 8 FDA reports)
IMMUNOSUPPRESSION ( 8 FDA reports)
INCONTINENCE ( 8 FDA reports)
INJECTION SITE REACTION ( 8 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 8 FDA reports)
MALIGNANT MELANOMA ( 8 FDA reports)
MENSTRUAL DISORDER ( 8 FDA reports)
MIGRAINE WITH AURA ( 8 FDA reports)
MUCOSAL ULCERATION ( 8 FDA reports)
NERVE INJURY ( 8 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 8 FDA reports)
OPEN FRACTURE ( 8 FDA reports)
OPEN REDUCTION OF FRACTURE ( 8 FDA reports)
PANCOAST'S TUMOUR ( 8 FDA reports)
PAROTID GLAND ENLARGEMENT ( 8 FDA reports)
PELVIC VENOUS THROMBOSIS ( 8 FDA reports)
PERIODONTAL DESTRUCTION ( 8 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 8 FDA reports)
PLATELET COUNT INCREASED ( 8 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 8 FDA reports)
POST PROCEDURAL COMPLICATION ( 8 FDA reports)
POSTPARTUM DEPRESSION ( 8 FDA reports)
PROSTATE CANCER ( 8 FDA reports)
PROSTATE CANCER METASTATIC ( 8 FDA reports)
PULMONARY THROMBOSIS ( 8 FDA reports)
RADIOTHERAPY ( 8 FDA reports)
RASH PAPULAR ( 8 FDA reports)
RED BLOOD CELLS URINE ( 8 FDA reports)
REFLUX LARYNGITIS ( 8 FDA reports)
RESPIRATORY RATE INCREASED ( 8 FDA reports)
SENSITIVITY OF TEETH ( 8 FDA reports)
SEXUAL DYSFUNCTION ( 8 FDA reports)
SHOCK ( 8 FDA reports)
SOFT TISSUE DISORDER ( 8 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 8 FDA reports)
THROMBOCYTOSIS ( 8 FDA reports)
TYPE 2 DIABETES MELLITUS ( 8 FDA reports)
URINE ANALYSIS ( 8 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 8 FDA reports)
WHITE BLOOD CELL COUNT ( 8 FDA reports)
ABDOMINAL ABSCESS ( 7 FDA reports)
ACUTE SINUSITIS ( 7 FDA reports)
ALLERGY TO ANIMAL ( 7 FDA reports)
APNOEA ( 7 FDA reports)
BASEDOW'S DISEASE ( 7 FDA reports)
BLADDER DYSFUNCTION ( 7 FDA reports)
BLADDER NEOPLASM ( 7 FDA reports)
BLADDER PROLAPSE ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 7 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 7 FDA reports)
BLOOD URINE PRESENT ( 7 FDA reports)
BREAST MASS ( 7 FDA reports)
BREATH SOUNDS ABNORMAL ( 7 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 7 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 7 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 7 FDA reports)
CONGENITAL ANOMALY ( 7 FDA reports)
DENTAL FISTULA ( 7 FDA reports)
DRUG ABUSE ( 7 FDA reports)
DRUG SCREEN POSITIVE ( 7 FDA reports)
DRY THROAT ( 7 FDA reports)
EJECTION FRACTION DECREASED ( 7 FDA reports)
EPIGASTRIC DISCOMFORT ( 7 FDA reports)
EXCORIATION ( 7 FDA reports)
EXPIRED DRUG ADMINISTERED ( 7 FDA reports)
FLANK PAIN ( 7 FDA reports)
GLAUCOMA ( 7 FDA reports)
HAEMATOMA ( 7 FDA reports)
HEART RATE IRREGULAR ( 7 FDA reports)
HYDRONEPHROSIS ( 7 FDA reports)
HYPOMAGNESAEMIA ( 7 FDA reports)
INCREASED TENDENCY TO BRUISE ( 7 FDA reports)
JOINT INSTABILITY ( 7 FDA reports)
LIMB INJURY ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
LOCALISED INFECTION ( 7 FDA reports)
LUMBAR RADICULOPATHY ( 7 FDA reports)
LUMBAR SPINAL STENOSIS ( 7 FDA reports)
LUNG INFECTION ( 7 FDA reports)
METASTATIC NEOPLASM ( 7 FDA reports)
MOOD ALTERED ( 7 FDA reports)
MULTIPLE INJURIES ( 7 FDA reports)
NYSTAGMUS ( 7 FDA reports)
OCCULT BLOOD POSITIVE ( 7 FDA reports)
ONYCHOMYCOSIS ( 7 FDA reports)
PAIN OF SKIN ( 7 FDA reports)
PAROSMIA ( 7 FDA reports)
PATHOLOGICAL GAMBLING ( 7 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 7 FDA reports)
PERSONALITY CHANGE ( 7 FDA reports)
PREMATURE BABY ( 7 FDA reports)
PRESYNCOPE ( 7 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 7 FDA reports)
PURULENCE ( 7 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 7 FDA reports)
SEBORRHOEIC KERATOSIS ( 7 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 7 FDA reports)
SENSATION OF FOREIGN BODY ( 7 FDA reports)
SENSATION OF HEAVINESS ( 7 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 7 FDA reports)
TENDON RUPTURE ( 7 FDA reports)
THIRST ( 7 FDA reports)
THROAT TIGHTNESS ( 7 FDA reports)
TOOTH IMPACTED ( 7 FDA reports)
TOOTH INFECTION ( 7 FDA reports)
UNRESPONSIVE TO STIMULI ( 7 FDA reports)
UTERINE HAEMORRHAGE ( 7 FDA reports)
UTERINE LEIOMYOMA ( 7 FDA reports)
VARICELLA ( 7 FDA reports)
VARICOSE VEIN ( 7 FDA reports)
WHEELCHAIR USER ( 7 FDA reports)
WOUND DRAINAGE ( 7 FDA reports)
ACCIDENT ( 6 FDA reports)
ACCIDENTAL EXPOSURE ( 6 FDA reports)
ADVERSE DRUG REACTION ( 6 FDA reports)
ANOREXIA ( 6 FDA reports)
APATHY ( 6 FDA reports)
APPENDICECTOMY ( 6 FDA reports)
ARTHRITIS BACTERIAL ( 6 FDA reports)
BLINDNESS TRANSIENT ( 6 FDA reports)
BLOOD FOLATE INCREASED ( 6 FDA reports)
BONE EROSION ( 6 FDA reports)
BREAST CANCER RECURRENT ( 6 FDA reports)
BREAST FIBROSIS ( 6 FDA reports)
BREAST NECROSIS ( 6 FDA reports)
BREATH ODOUR ( 6 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 6 FDA reports)
CHAPPED LIPS ( 6 FDA reports)
CIRCULATORY COLLAPSE ( 6 FDA reports)
COLD SWEAT ( 6 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 6 FDA reports)
CYSTOCELE ( 6 FDA reports)
DECUBITUS ULCER ( 6 FDA reports)
DENTAL PLAQUE ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DILATATION ATRIAL ( 6 FDA reports)
DRUG ERUPTION ( 6 FDA reports)
DUODENAL ULCER ( 6 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 6 FDA reports)
DYSGRAPHIA ( 6 FDA reports)
DYSPHEMIA ( 6 FDA reports)
DYSSTASIA ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 6 FDA reports)
EYE DISORDER ( 6 FDA reports)
FACET JOINT SYNDROME ( 6 FDA reports)
FACIAL NERVE DISORDER ( 6 FDA reports)
FACIAL PARESIS ( 6 FDA reports)
FIBULA FRACTURE ( 6 FDA reports)
FLUID OVERLOAD ( 6 FDA reports)
FOOD CRAVING ( 6 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
GENITAL HERPES ( 6 FDA reports)
GINGIVAL EROSION ( 6 FDA reports)
GINGIVAL OEDEMA ( 6 FDA reports)
HEART DISEASE CONGENITAL ( 6 FDA reports)
HEPATITIS CHOLESTATIC ( 6 FDA reports)
HOMICIDAL IDEATION ( 6 FDA reports)
HORMONE LEVEL ABNORMAL ( 6 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 6 FDA reports)
HYPOACUSIS ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
ILEUS PARALYTIC ( 6 FDA reports)
IMMUNODEFICIENCY ( 6 FDA reports)
INCOHERENT ( 6 FDA reports)
INJECTION SITE SWELLING ( 6 FDA reports)
JOINT INJURY ( 6 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 6 FDA reports)
MULTIPLE ALLERGIES ( 6 FDA reports)
MUSCLE INJURY ( 6 FDA reports)
MYOPATHY ( 6 FDA reports)
NECROTISING FASCIITIS ( 6 FDA reports)
NODULE ON EXTREMITY ( 6 FDA reports)
OBSTRUCTIVE UROPATHY ( 6 FDA reports)
OEDEMA MOUTH ( 6 FDA reports)
OPTIC NEURITIS ( 6 FDA reports)
ORAL CANDIDIASIS ( 6 FDA reports)
PALLOR ( 6 FDA reports)
PANCREATITIS CHRONIC ( 6 FDA reports)
PANIC REACTION ( 6 FDA reports)
PERICARDITIS ( 6 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 6 FDA reports)
PETECHIAE ( 6 FDA reports)
PHOTOSENSITIVITY REACTION ( 6 FDA reports)
PORTAL VEIN THROMBOSIS ( 6 FDA reports)
POST PROCEDURAL HAEMATOMA ( 6 FDA reports)
PRIMARY SEQUESTRUM ( 6 FDA reports)
PSORIASIS ( 6 FDA reports)
PYODERMA GANGRENOSUM ( 6 FDA reports)
RALES ( 6 FDA reports)
RECTOCELE ( 6 FDA reports)
RENAL PAIN ( 6 FDA reports)
RETINAL DETACHMENT ( 6 FDA reports)
RETINAL HAEMORRHAGE ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
SECRETION DISCHARGE ( 6 FDA reports)
SEDATION ( 6 FDA reports)
SINUS ARRHYTHMIA ( 6 FDA reports)
SOFT TISSUE INFLAMMATION ( 6 FDA reports)
SPINAL CORD COMPRESSION ( 6 FDA reports)
SPLENOMEGALY ( 6 FDA reports)
SPUTUM DISCOLOURED ( 6 FDA reports)
SUDDEN DEATH ( 6 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 6 FDA reports)
SYNOVITIS ( 6 FDA reports)
TACHYPNOEA ( 6 FDA reports)
THOUGHT BLOCKING ( 6 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
THYROTOXIC CRISIS ( 6 FDA reports)
TONGUE ULCERATION ( 6 FDA reports)
TONSILLAR HYPERTROPHY ( 6 FDA reports)
TYPE 1 DIABETES MELLITUS ( 6 FDA reports)
VEIN DISORDER ( 6 FDA reports)
VIITH NERVE PARALYSIS ( 6 FDA reports)
VISUAL DISTURBANCE ( 6 FDA reports)
VITAMIN B12 INCREASED ( 6 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
ABNORMAL SENSATION IN EYE ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ADRENAL ADENOMA ( 5 FDA reports)
ADRENAL GLAND CANCER METASTATIC ( 5 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
ANKLE FRACTURE ( 5 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 5 FDA reports)
ANURIA ( 5 FDA reports)
AORTIC ANEURYSM ( 5 FDA reports)
AORTIC CALCIFICATION ( 5 FDA reports)
ATAXIA ( 5 FDA reports)
ATRIAL SEPTAL DEFECT ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 5 FDA reports)
BILE DUCT STENOSIS ( 5 FDA reports)
BIOPSY THYMUS GLAND ABNORMAL ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 5 FDA reports)
BLOOD MAGNESIUM INCREASED ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 5 FDA reports)
BODY TEMPERATURE INCREASED ( 5 FDA reports)
BONE FORMATION INCREASED ( 5 FDA reports)
BONE FRAGMENTATION ( 5 FDA reports)
BRAIN MIDLINE SHIFT ( 5 FDA reports)
BREAST HYPERPLASIA ( 5 FDA reports)
BREAST PAIN ( 5 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
CACHEXIA ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
CARDIOGENIC SHOCK ( 5 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 5 FDA reports)
CHOLANGITIS SCLEROSING ( 5 FDA reports)
COLITIS ISCHAEMIC ( 5 FDA reports)
COLON ADENOMA ( 5 FDA reports)
COLONIC STENOSIS ( 5 FDA reports)
CORONARY ARTERY STENOSIS ( 5 FDA reports)
COSTOCHONDRITIS ( 5 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 5 FDA reports)
DERMAL CYST ( 5 FDA reports)
DEVELOPMENTAL DELAY ( 5 FDA reports)
DRY EYE ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
EMBOLISM VENOUS ( 5 FDA reports)
ENTERITIS ( 5 FDA reports)
EROSIVE OESOPHAGITIS ( 5 FDA reports)
FEMUR FRACTURE ( 5 FDA reports)
FISTULA DISCHARGE ( 5 FDA reports)
FOOD ALLERGY ( 5 FDA reports)
FRACTURE ( 5 FDA reports)
GASTROENTERITIS VIRAL ( 5 FDA reports)
GASTROINTESTINAL INJURY ( 5 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 5 FDA reports)
GENITAL LESION ( 5 FDA reports)
GINGIVAL BLEEDING ( 5 FDA reports)
GINGIVAL OPERATION ( 5 FDA reports)
GLOSSITIS ( 5 FDA reports)
GOUT ( 5 FDA reports)
GROIN PAIN ( 5 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 5 FDA reports)
HAEMORRHAGIC ANAEMIA ( 5 FDA reports)
HEART RATE DECREASED ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
HERNIA ( 5 FDA reports)
HUNGER ( 5 FDA reports)
HYPERAESTHESIA ( 5 FDA reports)
HYPERCOAGULATION ( 5 FDA reports)
HYPERNATRAEMIA ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
HYPOALBUMINAEMIA ( 5 FDA reports)
HYPOCALCAEMIA ( 5 FDA reports)
HYPOKINESIA ( 5 FDA reports)
HYPOVENTILATION ( 5 FDA reports)
INNER EAR DISORDER ( 5 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 5 FDA reports)
INTESTINAL POLYP ( 5 FDA reports)
IRITIS ( 5 FDA reports)
ISCHAEMIC STROKE ( 5 FDA reports)
JAW FRACTURE ( 5 FDA reports)
KAWASAKI'S DISEASE ( 5 FDA reports)
KNEE ARTHROPLASTY ( 5 FDA reports)
LARGE INTESTINAL ULCER ( 5 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
LIPOATROPHY ( 5 FDA reports)
LIVER INJURY ( 5 FDA reports)
LOCALISED OEDEMA ( 5 FDA reports)
LOSS OF PROPRIOCEPTION ( 5 FDA reports)
LYMPHADENITIS ( 5 FDA reports)
METABOLIC ALKALOSIS ( 5 FDA reports)
METASTASES TO SKIN ( 5 FDA reports)
METASTASES TO THE MEDIASTINUM ( 5 FDA reports)
METRORRHAGIA ( 5 FDA reports)
MICTURITION FREQUENCY DECREASED ( 5 FDA reports)
MIOSIS ( 5 FDA reports)
MOUTH HAEMORRHAGE ( 5 FDA reports)
MOVEMENT DISORDER ( 5 FDA reports)
MUCOSAL INFLAMMATION ( 5 FDA reports)
MUSCLE ATROPHY ( 5 FDA reports)
MUSCLE DISORDER ( 5 FDA reports)
MUSCLE TIGHTNESS ( 5 FDA reports)
MYELOMA RECURRENCE ( 5 FDA reports)
NEOPLASM PROGRESSION ( 5 FDA reports)
NERVE COMPRESSION ( 5 FDA reports)
NERVOUS SYSTEM DISORDER ( 5 FDA reports)
NEURODERMATITIS ( 5 FDA reports)
NON-CARDIAC CHEST PAIN ( 5 FDA reports)
OLIGOMENORRHOEA ( 5 FDA reports)
OVERWEIGHT ( 5 FDA reports)
PEPTIC ULCER ( 5 FDA reports)
PERIORBITAL OEDEMA ( 5 FDA reports)
PEYRONIE'S DISEASE ( 5 FDA reports)
PHLEBITIS ( 5 FDA reports)
PHONOPHOBIA ( 5 FDA reports)
PNEUMOCOCCAL INFECTION ( 5 FDA reports)
PNEUMONIA VIRAL ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
POST PROCEDURAL FISTULA ( 5 FDA reports)
PROSTATITIS ( 5 FDA reports)
PROSTATOMEGALY ( 5 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 5 FDA reports)
PULMONARY CONGESTION ( 5 FDA reports)
PULMONARY VASCULAR DISORDER ( 5 FDA reports)
QUALITY OF LIFE DECREASED ( 5 FDA reports)
RADICAL MASTECTOMY ( 5 FDA reports)
RADICULOPATHY ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RASH SCARLATINIFORM ( 5 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 5 FDA reports)
RENAL ARTERY STENOSIS ( 5 FDA reports)
RENAL CANCER METASTATIC ( 5 FDA reports)
RHINITIS ( 5 FDA reports)
RIGHT ATRIAL DILATATION ( 5 FDA reports)
SEROMA ( 5 FDA reports)
SERUM FERRITIN INCREASED ( 5 FDA reports)
SHOULDER OPERATION ( 5 FDA reports)
SINUS HEADACHE ( 5 FDA reports)
SKIN WARM ( 5 FDA reports)
SOFT TISSUE INJURY ( 5 FDA reports)
SPINAL COLUMN STENOSIS ( 5 FDA reports)
SPONDYLOLYSIS ( 5 FDA reports)
SPUTUM PURULENT ( 5 FDA reports)
STREPTOCOCCAL SEPSIS ( 5 FDA reports)
TEMPERATURE INTOLERANCE ( 5 FDA reports)
TENSION ( 5 FDA reports)
TESTICULAR PAIN ( 5 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 5 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
TUBERCULOSIS ( 5 FDA reports)
TUNNEL VISION ( 5 FDA reports)
UNDERWEIGHT ( 5 FDA reports)
URETHRAL CARBUNCLE ( 5 FDA reports)
URINE ODOUR ABNORMAL ( 5 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 5 FDA reports)
VASCULITIS ( 5 FDA reports)
VENA CAVA THROMBOSIS ( 5 FDA reports)
VENOUS STENOSIS ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
VESTIBULAR DISORDER ( 5 FDA reports)
VITAMIN D DECREASED ( 5 FDA reports)
WISDOM TEETH REMOVAL ( 5 FDA reports)
WRIST FRACTURE ( 5 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 4 FDA reports)
AMENORRHOEA ( 4 FDA reports)
ANAL ABSCESS ( 4 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 4 FDA reports)
APPENDICITIS ( 4 FDA reports)
ASPIRATION JOINT ( 4 FDA reports)
ASPIRATION PLEURAL CAVITY ( 4 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 4 FDA reports)
AZOTAEMIA ( 4 FDA reports)
BACK INJURY ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BEDRIDDEN ( 4 FDA reports)
BLADDER DISORDER ( 4 FDA reports)
BLOOD COUNT ABNORMAL ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
BLOOD IRON DECREASED ( 4 FDA reports)
BLOOD PRESSURE ABNORMAL ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
BONE TRIMMING ( 4 FDA reports)
BRACHIAL PLEXOPATHY ( 4 FDA reports)
BREAST CANCER FEMALE ( 4 FDA reports)
BREAST OEDEMA ( 4 FDA reports)
BRONCHOSPASM ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CERUMEN IMPACTION ( 4 FDA reports)
CERVICAL CYST ( 4 FDA reports)
CERVICITIS ( 4 FDA reports)
CHEST INJURY ( 4 FDA reports)
CHOKING ( 4 FDA reports)
CHOLECYSTITIS INFECTIVE ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 4 FDA reports)
COMA ( 4 FDA reports)
CONCUSSION ( 4 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
CORNEAL DISORDER ( 4 FDA reports)
CORONARY ANGIOPLASTY ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
CULTURE URINE POSITIVE ( 4 FDA reports)
CUSHING'S SYNDROME ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DENTAL OPERATION ( 4 FDA reports)
DEVICE MALFUNCTION ( 4 FDA reports)
DIABETES INSIPIDUS ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DIET REFUSAL ( 4 FDA reports)
DILATATION VENTRICULAR ( 4 FDA reports)
DYSLEXIA ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
ENCEPHALOMALACIA ( 4 FDA reports)
ENERGY INCREASED ( 4 FDA reports)
ERUCTATION ( 4 FDA reports)
EXOPHTHALMOS ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
FACIAL BONES FRACTURE ( 4 FDA reports)
FASCIITIS ( 4 FDA reports)
FEEDING DISORDER ( 4 FDA reports)
FOLLICULITIS ( 4 FDA reports)
FORMICATION ( 4 FDA reports)
FUMBLING ( 4 FDA reports)
FUSOBACTERIUM INFECTION ( 4 FDA reports)
GALLBLADDER PERFORATION ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 4 FDA reports)
GESTATIONAL HYPERTENSION ( 4 FDA reports)
HAEMODYNAMIC INSTABILITY ( 4 FDA reports)
HAEMORRHAGIC STROKE ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
HIDRADENITIS ( 4 FDA reports)
HORNER'S SYNDROME ( 4 FDA reports)
HYPERKERATOSIS ( 4 FDA reports)
HYPERSEXUALITY ( 4 FDA reports)
HYPOSPADIAS ( 4 FDA reports)
HYSTERECTOMY ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 4 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 4 FDA reports)
INGROWING NAIL ( 4 FDA reports)
INJECTION SITE EXTRAVASATION ( 4 FDA reports)
INJECTION SITE MASS ( 4 FDA reports)
INJECTION SITE NODULE ( 4 FDA reports)
JOINT ARTHROPLASTY ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
MASTECTOMY ( 4 FDA reports)
MEDIASTINAL DISORDER ( 4 FDA reports)
MEDICATION RESIDUE ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
METASTASES TO LUNG ( 4 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 4 FDA reports)
MUSCULOSKELETAL DISORDER ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
MYOPIA ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NASAL ULCER ( 4 FDA reports)
NECK INJURY ( 4 FDA reports)
NEPHROTIC SYNDROME ( 4 FDA reports)
NERVE BLOCK ( 4 FDA reports)
OCCULT BLOOD ( 4 FDA reports)
OPIATES POSITIVE ( 4 FDA reports)
ORGAN FAILURE ( 4 FDA reports)
PANCREATIC CYST ( 4 FDA reports)
PANCREATIC ENZYMES INCREASED ( 4 FDA reports)
PANCREATIC NEOPLASM ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PELVIC ABSCESS ( 4 FDA reports)
PERIARTHRITIS ( 4 FDA reports)
PERINEAL LACERATION ( 4 FDA reports)
PERINEURIAL CYST ( 4 FDA reports)
PERIPHERAL ISCHAEMIA ( 4 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 4 FDA reports)
PNEUMONIA BACTERIAL ( 4 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
POSTOPERATIVE ILEUS ( 4 FDA reports)
POSTPARTUM HAEMORRHAGE ( 4 FDA reports)
PROCTOCOLITIS ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PULMONARY ARTERY DILATATION ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
PULMONARY GRANULOMA ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 4 FDA reports)
RENAL TUBULAR NECROSIS ( 4 FDA reports)
SCARLET FEVER ( 4 FDA reports)
SCRATCH ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SPINAL DISORDER ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 4 FDA reports)
STRESS FRACTURE ( 4 FDA reports)
SUPERINFECTION ( 4 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 4 FDA reports)
TARDIVE DYSKINESIA ( 4 FDA reports)
THYROID DISORDER ( 4 FDA reports)
THYROID NEOPLASM ( 4 FDA reports)
TOBACCO ABUSE ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 4 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 4 FDA reports)
URINE ABNORMALITY ( 4 FDA reports)
URINE FLOW DECREASED ( 4 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 4 FDA reports)
VENTRICULAR HYPERTROPHY ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
WEIGHT FLUCTUATION ( 4 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
ABDOMINAL SYMPTOM ( 3 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 3 FDA reports)
ABSCESS INTESTINAL ( 3 FDA reports)
ABSCESS NECK ( 3 FDA reports)
ABSCESS ORAL ( 3 FDA reports)
ADDISON'S DISEASE ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
ALVEOLOPLASTY ( 3 FDA reports)
AMBLYOPIA ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANAL FISTULA ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANORECTAL DISCOMFORT ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
BIOPSY BONE MARROW ( 3 FDA reports)
BLADDER SPASM ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD BICARBONATE INCREASED ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BONE CYST ( 3 FDA reports)
BONE SCAN ABNORMAL ( 3 FDA reports)
BRAIN HERNIATION ( 3 FDA reports)
BRAIN NEOPLASM ( 3 FDA reports)
BREAST CANCER IN SITU ( 3 FDA reports)
CARDIAC PACEMAKER INSERTION ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CATARACT OPERATION ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
CATHETERISATION CARDIAC ( 3 FDA reports)
CELLULITIS STREPTOCOCCAL ( 3 FDA reports)
CEREBROVASCULAR DISORDER ( 3 FDA reports)
CERVIX CARCINOMA ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CHORIORETINAL DISORDER ( 3 FDA reports)
CHORIORETINOPATHY ( 3 FDA reports)
CHRONIC HEPATITIS ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 3 FDA reports)
COLON POLYPECTOMY ( 3 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 3 FDA reports)
CONJUNCTIVITIS VIRAL ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
DEATH OF RELATIVE ( 3 FDA reports)
DENERVATION ATROPHY ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG LABEL CONFUSION ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
EAR DISORDER ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 3 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 3 FDA reports)
ERYSIPELAS ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
ERYTHEMA NODOSUM ( 3 FDA reports)
EUPHORIC MOOD ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
FANCONI SYNDROME ACQUIRED ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
FOOD INTOLERANCE ( 3 FDA reports)
FOOD POISONING ( 3 FDA reports)
GALLBLADDER PAIN ( 3 FDA reports)
GASTROENTERITIS RADIATION ( 3 FDA reports)
GENERALISED ANXIETY DISORDER ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
GRIP STRENGTH DECREASED ( 3 FDA reports)
GYNAECOMASTIA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HEAD TITUBATION ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATIC LESION ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HEPATIC PAIN ( 3 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
HIGH-PITCHED CRYING ( 3 FDA reports)
HOSPICE CARE ( 3 FDA reports)
HYPERACUSIS ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPERCHLORHYDRIA ( 3 FDA reports)
HYPERPHAGIA ( 3 FDA reports)
HYPOMENORRHOEA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
ILEITIS ( 3 FDA reports)
IMMUNE SYSTEM DISORDER ( 3 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 3 FDA reports)
INCISIONAL DRAINAGE ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INFUSION SITE PAIN ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
INJECTION SITE IRRITATION ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
INJECTION SITE WARMTH ( 3 FDA reports)
INTERCOSTAL RETRACTION ( 3 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTESTINAL MASS ( 3 FDA reports)
INTRAOCULAR LENS IMPLANT ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
JAUNDICE NEONATAL ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
LARYNGEAL CYST ( 3 FDA reports)
LEARNING DISORDER ( 3 FDA reports)
LIGAMENT SPRAIN ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
LIP HAEMORRHAGE ( 3 FDA reports)
LIPODYSTROPHY ACQUIRED ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LOW TURNOVER OSTEOPATHY ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MAXILLOFACIAL OPERATION ( 3 FDA reports)
MEDIASTINAL BIOPSY ( 3 FDA reports)
MEDIASTINAL MASS ( 3 FDA reports)
MENINGIOMA ( 3 FDA reports)
METASTASES TO PLEURA ( 3 FDA reports)
MICROCYTIC ANAEMIA ( 3 FDA reports)
MUCOSAL HAEMORRHAGE ( 3 FDA reports)
MUSCLE ABSCESS ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
NASAL FLARING ( 3 FDA reports)
NASAL OBSTRUCTION ( 3 FDA reports)
NASAL SEPTUM DEVIATION ( 3 FDA reports)
NEPHRECTOMY ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
OCULAR HYPERTENSION ( 3 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 3 FDA reports)
OESOPHAGITIS ULCERATIVE ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
OSTEOMYELITIS ACUTE ( 3 FDA reports)
OTORRHOEA ( 3 FDA reports)
PANCREATIC DISORDER ( 3 FDA reports)
PARANASAL CYST ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PAROTITIS ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PHARYNGEAL INFLAMMATION ( 3 FDA reports)
PILONIDAL CYST ( 3 FDA reports)
PLATELET COUNT ABNORMAL ( 3 FDA reports)
PLATELET DISORDER ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
POST STROKE DEPRESSION ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
PREGNANCY TEST POSITIVE ( 3 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 3 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA STAGE II ( 3 FDA reports)
PROCTITIS ULCERATIVE ( 3 FDA reports)
PROTEIN C DECREASED ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 3 FDA reports)
PULMONARY HYPOPLASIA ( 3 FDA reports)
PULMONARY VALVE STENOSIS ( 3 FDA reports)
RENAL COLIC ( 3 FDA reports)
RETINAL DISORDER ( 3 FDA reports)
RETINOPATHY HYPERTENSIVE ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
RIB DEFORMITY ( 3 FDA reports)
SCAB ( 3 FDA reports)
SCLERAL DISCOLOURATION ( 3 FDA reports)
SENSORY LOSS ( 3 FDA reports)
SEQUESTRECTOMY ( 3 FDA reports)
SKIN CANCER ( 3 FDA reports)
SKIN NEOPLASM EXCISION ( 3 FDA reports)
SNORING ( 3 FDA reports)
SPINAL CORD INJURY ( 3 FDA reports)
STRESS ULCER ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
TERMINAL INSOMNIA ( 3 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 3 FDA reports)
THYROID MASS ( 3 FDA reports)
TIBIA FRACTURE ( 3 FDA reports)
TOBACCO USER ( 3 FDA reports)
TRIGGER FINGER ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
URINARY TRACT DISORDER ( 3 FDA reports)
URINE OUTPUT INCREASED ( 3 FDA reports)
UTERINE CANCER ( 3 FDA reports)
VASCULAR GRAFT OCCLUSION ( 3 FDA reports)
VASCULAR INSUFFICIENCY ( 3 FDA reports)
VASCULAR PURPURA ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
VOCAL CORD PARALYSIS ( 3 FDA reports)
VOCAL CORD THICKENING ( 3 FDA reports)
VULVOVAGINAL DISCOMFORT ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
WOUND HAEMORRHAGE ( 3 FDA reports)
ZYGOMYCOSIS ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABORTION THREATENED ( 2 FDA reports)
ACANTHOMA ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACOUSTIC NEUROMA ( 2 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 2 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADENOMA BENIGN ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
ADRENAL NEOPLASM ( 2 FDA reports)
AFTERBIRTH PAIN ( 2 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
AMPHETAMINES POSITIVE ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANIMAL BITE ( 2 FDA reports)
ANKLE OPERATION ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
APHONIA ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 2 FDA reports)
ARRESTED LABOUR ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BACTEROIDES INFECTION ( 2 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BILE OUTPUT INCREASED ( 2 FDA reports)
BILIARY TRACT OPERATION ( 2 FDA reports)
BIOPSY STOMACH ( 2 FDA reports)
BLADDER DISCOMFORT ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD HOMOCYSTEINE DECREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BORDERLINE GLAUCOMA ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRAIN INJURY ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
BURNING MOUTH SYNDROME ( 2 FDA reports)
BURNS SECOND DEGREE ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 2 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CAROTID ARTERY DISSECTION ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CAROTID ARTERY THROMBOSIS ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COAGULATION FACTOR IX LEVEL DECREASED ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COLON CANCER STAGE II ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CORNEAL LESION ( 2 FDA reports)
CRANIAL NERVE DISORDER ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DEVICE RELATED SEPSIS ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSPLASTIC NAEVUS ( 2 FDA reports)
DYSPRAXIA ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EPIPHYSEAL INJURY ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EXCESSIVE EYE BLINKING ( 2 FDA reports)
EXPOSED BONE IN JAW ( 2 FDA reports)
EYE ABSCESS ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
EYE OPERATION COMPLICATION ( 2 FDA reports)
EYELASH DISCOLOURATION ( 2 FDA reports)
EYELID BLEEDING ( 2 FDA reports)
EYELID CYST ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
EYELID RETRACTION ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FAT INTOLERANCE ( 2 FDA reports)
FAT TISSUE INCREASED ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEAR OF DISEASE ( 2 FDA reports)
FEEDING TUBE COMPLICATION ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GAIT SPASTIC ( 2 FDA reports)
GALLBLADDER ENLARGEMENT ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GIANOTTI-CROSTI SYNDROME ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAEMORRHOID OPERATION ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEPATECTOMY ( 2 FDA reports)
HEPATITIS VIRAL ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HIGH RISK PREGNANCY ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HORDEOLUM ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOVITAMINOSIS ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
IMPRISONMENT ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INFUSION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE DRYNESS ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTESTINAL ULCER PERFORATION ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
JUGULAR VEIN THROMBOSIS ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
LIMB OPERATION ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MACROCYTOSIS ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MAMMOGRAM ABNORMAL ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
MAY-THURNER SYNDROME ( 2 FDA reports)
MEDIASTINAL CYST ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MEDICAL DIET ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MELANOSIS COLI ( 2 FDA reports)
MENIERE'S DISEASE ( 2 FDA reports)
MENOMETRORRHAGIA ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MENSTRUATION DELAYED ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MURPHY'S SIGN POSITIVE ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NODULE ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORBITAL INFECTION ( 2 FDA reports)
ORBITAL OEDEMA ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
PAPILLOMA ( 2 FDA reports)
PARAPSORIASIS ( 2 FDA reports)
PELVIC FLUID COLLECTION ( 2 FDA reports)
PENILE OEDEMA ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
PENILE SWELLING ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PERITONSILLAR ABSCESS ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 2 FDA reports)
PHARYNGEAL ABSCESS ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PHOBIA ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
POLYCYSTIC OVARIES ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POST CONCUSSION SYNDROME ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PREMENSTRUAL SYNDROME ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PRODUCT LABEL CONFUSION ( 2 FDA reports)
PRODUCT LABEL ISSUE ( 2 FDA reports)
PRODUCT SIZE ISSUE ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PROSTATE INFECTION ( 2 FDA reports)
PROSTATIC ACID PHOSPHATASE INCREASED ( 2 FDA reports)
PROSTATIC PAIN ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PROTEIN TOTAL ABNORMAL ( 2 FDA reports)
PSOAS ABSCESS ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PSYCHOTIC BEHAVIOUR ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
RADIATION SKIN INJURY ( 2 FDA reports)
RADIUS FRACTURE ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL VEIN THROMBOSIS ( 2 FDA reports)
RESORPTION BONE INCREASED ( 2 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
RETROPERITONEAL CANCER ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SKIN DISCOMFORT ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SMOKER ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 2 FDA reports)
SPIDER VEIN ( 2 FDA reports)
SPONDYLOLISTHESIS ( 2 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUPERINFECTION BACTERIAL ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
TEMPORAL ARTERITIS ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
THYROXINE FREE INCREASED ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TOOTH EROSION ( 2 FDA reports)
TOXIC OPTIC NEUROPATHY ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 2 FDA reports)
TRICUSPID VALVE STENOSIS ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URETHRAL SYNDROME ( 2 FDA reports)
URINARY HESITATION ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VAGINAL INFECTION ( 2 FDA reports)
VAGINAL SWELLING ( 2 FDA reports)
VASCULAR COMPLICATION ASSOCIATED WITH DEVICE ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VIRAL PHARYNGITIS ( 2 FDA reports)
VIRAL RASH ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VULVOVAGINAL PAIN ( 2 FDA reports)
WALKING AID USER ( 2 FDA reports)
WHIPLASH INJURY ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABNORMAL LABOUR ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALVEOLAR OSTEITIS ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMPUTATION STUMP PAIN ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
AURA ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BAROTITIS MEDIA ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BASILAR ARTERY THROMBOSIS ( 1 FDA reports)
BEHAVIOURAL AND PSYCHIATRIC SYMPTOMS OF DEMENTIA ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY THYROID GLAND ABNORMAL ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER HYPERTROPHY ( 1 FDA reports)
BLADDER IRRITATION ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD UREA ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE CALLUS EXCESSIVE ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST HAEMORRHAGE ( 1 FDA reports)
BREAST PROSTHESIS USER ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCIUM DEFICIENCY ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CAPSULE ISSUE ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
CERVICAL ROOT PAIN ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHONDROPLASTY ( 1 FDA reports)
CHOROID MELANOMA ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COITAL BLEEDING ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLOBOMA ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONGENITAL ANOMALY IN OFFSPRING ( 1 FDA reports)
CONGENITAL AORTIC STENOSIS ( 1 FDA reports)
CONGENITAL MITRAL VALVE STENOSIS ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
CRYSTAL ARTHROPATHY ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE INTOLERANCE ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIAPHRAGMATIC INJURY ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DUODENAL SCARRING ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ECZEMA INFECTED ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FEAR OF NEEDLES ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEMALE GENITAL OPERATION ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOETAL MALPRESENTATION ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FORAMEN MAGNUM STENOSIS ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRANULOCYTES MATURATION ARREST ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEART VALVE STENOSIS ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC ADENOMA ( 1 FDA reports)
HEPATIC AMOEBIASIS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HETEROPHORIA ( 1 FDA reports)
HETEROTAXIA ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
INABILITY TO CRAWL ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARGE INTESTINAL STRICTURE ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIPOSARCOMA ( 1 FDA reports)
LIPOSUCTION ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MASTOCYTOSIS ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO PELVIS ( 1 FDA reports)
METASTATIC PAIN ( 1 FDA reports)
MITRAL VALVE DISEASE MIXED ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE MASS ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEEDLE TRACK MARKS ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEPHRITIS AUTOIMMUNE ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL MASS ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPTIC NERVE CUPPING ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
ORAL CAVITY FISTULA ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN ABSCESS ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PAGET'S DISEASE OF THE BREAST ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARAPHARYNGEAL ABSCESS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PELVIC PROLAPSE ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHARYNGOTONSILLITIS ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PHYSIOTHERAPY ( 1 FDA reports)
PLACENTAL INFARCTION ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 1 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST THROMBOTIC SYNDROME ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT COMMINGLING ( 1 FDA reports)
PRODUCT DOSAGE FORM ISSUE ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROSTATIC CALCIFICATION ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY ATRESIA ( 1 FDA reports)
PULMONARY ARTERY STENOSIS ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY OEDEMA NEONATAL ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PYELECTASIA ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADICULAR PAIN ( 1 FDA reports)
RADICULITIS CERVICAL ( 1 FDA reports)
READING REHABILITATION ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL CANCER STAGE IV ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
REVERSE TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SALIVA DISCOLOURATION ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SECONDARY SEQUESTRUM ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SOCIAL ALCOHOL DRINKER ( 1 FDA reports)
SOLITARY KIDNEY ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPLINT APPLICATION ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 1 FDA reports)
SYMBLEPHARON ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TESTICULAR HAEMORRHAGE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THREATENED LABOUR ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
TIC ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE PRURITUS ( 1 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TRACHEOMALACIA ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
UHTHOFF'S PHENOMENON ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
UTERINE INFLAMMATION ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VASCULAR HEADACHE ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENOUS THROMBOSIS IN PREGNANCY ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VERTEBRAL WEDGING ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VOCAL CORD ATROPHY ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
VULVOVAGINITIS TRICHOMONAL ( 1 FDA reports)
WEST NILE VIRAL INFECTION ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
YAWNING ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use