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

DYSPNOEA ( 259 FDA reports)
ASTHMA ( 128 FDA reports)
PAIN ( 114 FDA reports)
DRUG INEFFECTIVE ( 106 FDA reports)
NAUSEA ( 104 FDA reports)
FATIGUE ( 95 FDA reports)
ANXIETY ( 94 FDA reports)
HEADACHE ( 92 FDA reports)
DIZZINESS ( 90 FDA reports)
COUGH ( 87 FDA reports)
BACK PAIN ( 85 FDA reports)
CHEST PAIN ( 76 FDA reports)
PRODUCT QUALITY ISSUE ( 76 FDA reports)
DRUG DOSE OMISSION ( 75 FDA reports)
HYPERTENSION ( 72 FDA reports)
OEDEMA PERIPHERAL ( 70 FDA reports)
VOMITING ( 70 FDA reports)
DEHYDRATION ( 67 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 66 FDA reports)
DIARRHOEA ( 66 FDA reports)
ABDOMINAL PAIN ( 64 FDA reports)
PAIN IN EXTREMITY ( 60 FDA reports)
ASTHENIA ( 59 FDA reports)
MUSCLE SPASMS ( 58 FDA reports)
PULMONARY EMBOLISM ( 58 FDA reports)
PRURITUS ( 57 FDA reports)
URINARY TRACT INFECTION ( 57 FDA reports)
PNEUMONIA ( 54 FDA reports)
DEPRESSION ( 52 FDA reports)
INSOMNIA ( 52 FDA reports)
DEEP VEIN THROMBOSIS ( 50 FDA reports)
OSTEOARTHRITIS ( 50 FDA reports)
CHEST DISCOMFORT ( 49 FDA reports)
FLUSHING ( 49 FDA reports)
BLOOD PRESSURE INCREASED ( 46 FDA reports)
STAPHYLOCOCCAL INFECTION ( 46 FDA reports)
WEIGHT DECREASED ( 46 FDA reports)
CONFUSIONAL STATE ( 45 FDA reports)
RENAL FAILURE ACUTE ( 45 FDA reports)
ERYTHEMA ( 44 FDA reports)
PALPITATIONS ( 44 FDA reports)
BRONCHITIS ( 43 FDA reports)
WHEEZING ( 43 FDA reports)
CONDITION AGGRAVATED ( 42 FDA reports)
HYPOTENSION ( 42 FDA reports)
OSTEONECROSIS OF JAW ( 42 FDA reports)
MUSCULAR WEAKNESS ( 41 FDA reports)
RASH ( 41 FDA reports)
CONSTIPATION ( 40 FDA reports)
FALL ( 40 FDA reports)
GAIT DISTURBANCE ( 40 FDA reports)
WEIGHT INCREASED ( 40 FDA reports)
DYSGEUSIA ( 39 FDA reports)
NO ADVERSE EVENT ( 38 FDA reports)
ABDOMINAL PAIN UPPER ( 37 FDA reports)
CHOLELITHIASIS ( 37 FDA reports)
FEELING ABNORMAL ( 37 FDA reports)
PLEURAL EFFUSION ( 37 FDA reports)
LOSS OF CONSCIOUSNESS ( 36 FDA reports)
MITRAL VALVE INCOMPETENCE ( 36 FDA reports)
PYREXIA ( 36 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 35 FDA reports)
PANCREATITIS ( 35 FDA reports)
VISUAL IMPAIRMENT ( 35 FDA reports)
ARTHRITIS ( 34 FDA reports)
PHARYNGEAL OEDEMA ( 34 FDA reports)
SYNCOPE ( 34 FDA reports)
OROPHARYNGEAL PAIN ( 33 FDA reports)
DEATH ( 32 FDA reports)
DYSURIA ( 32 FDA reports)
INJURY ( 32 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 32 FDA reports)
ANAEMIA ( 31 FDA reports)
BONE DISORDER ( 31 FDA reports)
SEPSIS ( 31 FDA reports)
SWELLING FACE ( 31 FDA reports)
ARTHRALGIA ( 30 FDA reports)
MEMORY IMPAIRMENT ( 30 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 30 FDA reports)
STRESS ( 30 FDA reports)
TOOTH ABSCESS ( 30 FDA reports)
ANAPHYLACTIC REACTION ( 29 FDA reports)
NEUROPATHY PERIPHERAL ( 29 FDA reports)
RESPIRATORY FAILURE ( 29 FDA reports)
TREMOR ( 29 FDA reports)
ANHEDONIA ( 28 FDA reports)
CHILLS ( 28 FDA reports)
HYPERSENSITIVITY ( 28 FDA reports)
NERVOUSNESS ( 28 FDA reports)
SINUSITIS ( 28 FDA reports)
BLOOD GLUCOSE INCREASED ( 27 FDA reports)
CEREBROVASCULAR ACCIDENT ( 27 FDA reports)
DIVERTICULUM ( 27 FDA reports)
DRY MOUTH ( 27 FDA reports)
HIATUS HERNIA ( 27 FDA reports)
LOBAR PNEUMONIA ( 27 FDA reports)
PARAESTHESIA ( 27 FDA reports)
PULMONARY CONGESTION ( 27 FDA reports)
SOMNOLENCE ( 27 FDA reports)
DECREASED APPETITE ( 26 FDA reports)
HYPERCALCAEMIA ( 26 FDA reports)
IMPAIRED HEALING ( 26 FDA reports)
MENTAL STATUS CHANGES ( 26 FDA reports)
MYOCARDIAL INFARCTION ( 26 FDA reports)
ORAL PAIN ( 26 FDA reports)
PLEURITIC PAIN ( 26 FDA reports)
TACHYCARDIA ( 26 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 26 FDA reports)
AMNESIA ( 25 FDA reports)
BONE PAIN ( 25 FDA reports)
HYPOAESTHESIA ( 25 FDA reports)
INFECTION ( 25 FDA reports)
THROAT TIGHTNESS ( 25 FDA reports)
DRUG HYPERSENSITIVITY ( 24 FDA reports)
HOT FLUSH ( 24 FDA reports)
NASAL CONGESTION ( 24 FDA reports)
OSTEONECROSIS ( 24 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 24 FDA reports)
BLOOD CALCIUM DECREASED ( 23 FDA reports)
CELLULITIS ( 23 FDA reports)
CHOLECYSTITIS CHRONIC ( 23 FDA reports)
DRUG EFFECT DECREASED ( 23 FDA reports)
DYSPHONIA ( 23 FDA reports)
MALAISE ( 23 FDA reports)
BLOOD CREATININE INCREASED ( 22 FDA reports)
FEELING HOT ( 22 FDA reports)
HYPERLIPIDAEMIA ( 22 FDA reports)
RESTLESS LEGS SYNDROME ( 22 FDA reports)
BURNING SENSATION ( 21 FDA reports)
CARDIOMYOPATHY ( 21 FDA reports)
DEVICE MALFUNCTION ( 21 FDA reports)
DIABETES MELLITUS ( 21 FDA reports)
EXOSTOSIS ( 21 FDA reports)
HAEMATURIA ( 21 FDA reports)
LYMPHADENOPATHY ( 21 FDA reports)
SPINAL FRACTURE ( 21 FDA reports)
ATELECTASIS ( 20 FDA reports)
ATRIAL FIBRILLATION ( 20 FDA reports)
BONE LESION ( 20 FDA reports)
BURSITIS ( 20 FDA reports)
EMPHYSEMA ( 20 FDA reports)
HYDRONEPHROSIS ( 20 FDA reports)
METASTASES TO BONE ( 20 FDA reports)
MUSCLE TWITCHING ( 20 FDA reports)
OSTEOPOROSIS ( 20 FDA reports)
SWOLLEN TONGUE ( 20 FDA reports)
TOOTH DISORDER ( 20 FDA reports)
AORTIC ANEURYSM ( 19 FDA reports)
BLOOD UREA INCREASED ( 19 FDA reports)
CARDIAC DISORDER ( 19 FDA reports)
CONTUSION ( 19 FDA reports)
DISABILITY ( 19 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 19 FDA reports)
HAEMOPTYSIS ( 19 FDA reports)
KYPHOSIS ( 19 FDA reports)
LOOSE TOOTH ( 19 FDA reports)
LUNG DISORDER ( 19 FDA reports)
LUNG NEOPLASM ( 19 FDA reports)
OSTEOMYELITIS ( 19 FDA reports)
POLYURIA ( 19 FDA reports)
RHINITIS ( 19 FDA reports)
SLEEP APNOEA SYNDROME ( 19 FDA reports)
VISION BLURRED ( 19 FDA reports)
ANEURYSM ( 18 FDA reports)
DENTAL CARIES ( 18 FDA reports)
DYSPHEMIA ( 18 FDA reports)
EPISTAXIS ( 18 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 18 FDA reports)
MYALGIA ( 18 FDA reports)
PANCYTOPENIA ( 18 FDA reports)
RHONCHI ( 18 FDA reports)
RIB FRACTURE ( 18 FDA reports)
ROAD TRAFFIC ACCIDENT ( 18 FDA reports)
TOOTHACHE ( 18 FDA reports)
AORTIC VALVE INCOMPETENCE ( 17 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 17 FDA reports)
CARPAL TUNNEL SYNDROME ( 17 FDA reports)
COORDINATION ABNORMAL ( 17 FDA reports)
DEAFNESS NEUROSENSORY ( 17 FDA reports)
DYSPHAGIA ( 17 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 17 FDA reports)
EXERCISE TOLERANCE DECREASED ( 17 FDA reports)
FISTULA ( 17 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 17 FDA reports)
GINGIVAL ULCERATION ( 17 FDA reports)
GINGIVITIS ( 17 FDA reports)
HAEMORRHOIDS ( 17 FDA reports)
HEARING AID USER ( 17 FDA reports)
HEART RATE INCREASED ( 17 FDA reports)
IRON DEFICIENCY ANAEMIA ( 17 FDA reports)
MASTICATION DISORDER ( 17 FDA reports)
OFF LABEL USE ( 17 FDA reports)
PRE-ECLAMPSIA ( 17 FDA reports)
PRIMARY SEQUESTRUM ( 17 FDA reports)
PULMONARY RADIATION INJURY ( 17 FDA reports)
RENAL CYST ( 17 FDA reports)
TELANGIECTASIA ( 17 FDA reports)
THYROID NEOPLASM ( 17 FDA reports)
BLOOD PRESSURE DECREASED ( 16 FDA reports)
BRUXISM ( 16 FDA reports)
CAESAREAN SECTION ( 16 FDA reports)
CANDIDIASIS ( 16 FDA reports)
CYSTITIS ( 16 FDA reports)
DROP ATTACKS ( 16 FDA reports)
DYSPEPSIA ( 16 FDA reports)
FEELING JITTERY ( 16 FDA reports)
OVERDOSE ( 16 FDA reports)
PERIODONTAL DISEASE ( 16 FDA reports)
POLYP COLORECTAL ( 16 FDA reports)
RESPIRATORY TRACT IRRITATION ( 16 FDA reports)
SCOLIOSIS ( 16 FDA reports)
SUICIDAL IDEATION ( 16 FDA reports)
SWELLING ( 16 FDA reports)
TOOTH EXTRACTION ( 16 FDA reports)
URTICARIA ( 16 FDA reports)
BLADDER NEOPLASM ( 15 FDA reports)
BREAST CANCER RECURRENT ( 15 FDA reports)
DEVICE RELATED INFECTION ( 15 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 15 FDA reports)
JAW OPERATION ( 15 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 15 FDA reports)
OEDEMA ( 15 FDA reports)
PANCREATITIS ACUTE ( 15 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 15 FDA reports)
SLEEP DISORDER ( 15 FDA reports)
TOOTH LOSS ( 15 FDA reports)
WHEELCHAIR USER ( 15 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 14 FDA reports)
DENTAL PLAQUE ( 14 FDA reports)
GINGIVAL EROSION ( 14 FDA reports)
GINGIVAL OEDEMA ( 14 FDA reports)
HYPERHIDROSIS ( 14 FDA reports)
ILEUS ( 14 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 14 FDA reports)
INCORRECT DOSE ADMINISTERED ( 14 FDA reports)
LETHARGY ( 14 FDA reports)
LIPOMA ( 14 FDA reports)
MENISCUS LESION ( 14 FDA reports)
SENSATION OF FOREIGN BODY ( 14 FDA reports)
TOOTH DEPOSIT ( 14 FDA reports)
TOOTH FRACTURE ( 14 FDA reports)
ADRENAL INSUFFICIENCY ( 13 FDA reports)
ALOPECIA ( 13 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 13 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 13 FDA reports)
DEVICE OCCLUSION ( 13 FDA reports)
DIPLOPIA ( 13 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
GALLBLADDER DISORDER ( 13 FDA reports)
GASTRITIS ( 13 FDA reports)
INJECTION SITE PAIN ( 13 FDA reports)
LIP SWELLING ( 13 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 13 FDA reports)
RHINITIS ALLERGIC ( 13 FDA reports)
SKIN DISCOLOURATION ( 13 FDA reports)
THROAT IRRITATION ( 13 FDA reports)
ABDOMINAL DISCOMFORT ( 12 FDA reports)
AGEUSIA ( 12 FDA reports)
BARRETT'S OESOPHAGUS ( 12 FDA reports)
BONE DENSITY DECREASED ( 12 FDA reports)
DEVICE FAILURE ( 12 FDA reports)
HEART RATE IRREGULAR ( 12 FDA reports)
HYPOXIA ( 12 FDA reports)
INFLAMMATION ( 12 FDA reports)
MEDICAL DEVICE COMPLICATION ( 12 FDA reports)
MUSCULOSKELETAL PAIN ( 12 FDA reports)
NEOPLASM MALIGNANT ( 12 FDA reports)
PATHOLOGICAL FRACTURE ( 12 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 12 FDA reports)
RESTLESSNESS ( 12 FDA reports)
VERTIGO ( 12 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 12 FDA reports)
APHONIA ( 11 FDA reports)
ARRHYTHMIA ( 11 FDA reports)
BALANCE DISORDER ( 11 FDA reports)
BONE DEBRIDEMENT ( 11 FDA reports)
CEREBRAL ISCHAEMIA ( 11 FDA reports)
DECREASED INTEREST ( 11 FDA reports)
DERMAL CYST ( 11 FDA reports)
ECONOMIC PROBLEM ( 11 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 11 FDA reports)
HYPERGLYCAEMIA ( 11 FDA reports)
INFLUENZA LIKE ILLNESS ( 11 FDA reports)
JOINT EFFUSION ( 11 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 11 FDA reports)
LIMB INJURY ( 11 FDA reports)
LUNG INFILTRATION ( 11 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 11 FDA reports)
MULTIPLE INJURIES ( 11 FDA reports)
MYOCARDIAL ISCHAEMIA ( 11 FDA reports)
PROTHROMBIN TIME PROLONGED ( 11 FDA reports)
THROMBOSIS ( 11 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 11 FDA reports)
TRANSAMINASES INCREASED ( 11 FDA reports)
UNEVALUABLE EVENT ( 11 FDA reports)
ABDOMINAL HERNIA ( 10 FDA reports)
ANGER ( 10 FDA reports)
BILIARY DYSKINESIA ( 10 FDA reports)
CARDIAC ARREST ( 10 FDA reports)
CARDIAC FAILURE ( 10 FDA reports)
CONVULSION ( 10 FDA reports)
CORONARY ARTERY BYPASS ( 10 FDA reports)
DRUG ADMINISTRATION ERROR ( 10 FDA reports)
EJECTION FRACTION DECREASED ( 10 FDA reports)
EMOTIONAL DISTRESS ( 10 FDA reports)
FEAR ( 10 FDA reports)
FLANK PAIN ( 10 FDA reports)
HAEMATOCHEZIA ( 10 FDA reports)
LEUKOPENIA ( 10 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 10 FDA reports)
MALIGNANT MELANOMA ( 10 FDA reports)
MUSCLE STRAIN ( 10 FDA reports)
NASOPHARYNGITIS ( 10 FDA reports)
OSTEOPENIA ( 10 FDA reports)
OXYGEN SATURATION DECREASED ( 10 FDA reports)
PRODUCTIVE COUGH ( 10 FDA reports)
RENAL FAILURE ( 10 FDA reports)
RESPIRATORY DISORDER ( 10 FDA reports)
RHEUMATOID ARTHRITIS ( 10 FDA reports)
SCIATICA ( 10 FDA reports)
THROMBOCYTOPENIA ( 10 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 10 FDA reports)
AGITATION ( 9 FDA reports)
BRONCHIOLITIS ( 9 FDA reports)
CAROTID ARTERY DISEASE ( 9 FDA reports)
CLOSTRIDIAL INFECTION ( 9 FDA reports)
DENTAL CARE ( 9 FDA reports)
DYSKINESIA ( 9 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 9 FDA reports)
HEPATIC CONGESTION ( 9 FDA reports)
HYPERCHOLESTEROLAEMIA ( 9 FDA reports)
HYPERPROTEINAEMIA ( 9 FDA reports)
HYPOALBUMINAEMIA ( 9 FDA reports)
HYPOPHAGIA ( 9 FDA reports)
HYPOTHYROIDISM ( 9 FDA reports)
ILL-DEFINED DISORDER ( 9 FDA reports)
LUNG INFECTION ( 9 FDA reports)
METASTASES TO SPINE ( 9 FDA reports)
METATARSALGIA ( 9 FDA reports)
MORTON'S NEUROMA ( 9 FDA reports)
NEUTROPENIA ( 9 FDA reports)
PERIARTHRITIS ( 9 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 9 FDA reports)
PLANTAR FASCIITIS ( 9 FDA reports)
POLLAKIURIA ( 9 FDA reports)
PSEUDOMONAL SEPSIS ( 9 FDA reports)
PYELOCALIECTASIS ( 9 FDA reports)
RENAL ATROPHY ( 9 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 9 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 9 FDA reports)
THIRST ( 9 FDA reports)
ABASIA ( 8 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 8 FDA reports)
ADRENAL DISORDER ( 8 FDA reports)
ANOREXIA ( 8 FDA reports)
AUTOIMMUNE HEPATITIS ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
CATHETER PLACEMENT ( 8 FDA reports)
CATHETER REMOVAL ( 8 FDA reports)
CHOLECYSTITIS ( 8 FDA reports)
CORONARY ARTERY DISEASE ( 8 FDA reports)
DISTURBANCE IN ATTENTION ( 8 FDA reports)
DRUG INTOLERANCE ( 8 FDA reports)
FEMALE STERILISATION ( 8 FDA reports)
GASTROINTESTINAL DISORDER ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
GLOSSODYNIA ( 8 FDA reports)
HAEMORRHAGE ( 8 FDA reports)
HEREDITARY ANGIOEDEMA ( 8 FDA reports)
HYPOAESTHESIA ORAL ( 8 FDA reports)
INCISIONAL DRAINAGE ( 8 FDA reports)
IRRITABILITY ( 8 FDA reports)
LOCAL SWELLING ( 8 FDA reports)
ORAL SURGERY ( 8 FDA reports)
PULMONARY HYPERTENSION ( 8 FDA reports)
SKIN LESION ( 8 FDA reports)
TOOTH INFECTION ( 8 FDA reports)
ACUTE RESPIRATORY FAILURE ( 7 FDA reports)
ADVERSE EVENT ( 7 FDA reports)
ANOSMIA ( 7 FDA reports)
ARTHROPATHY ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
BONE LOSS ( 7 FDA reports)
CHROMATURIA ( 7 FDA reports)
COAGULOPATHY ( 7 FDA reports)
CYANOSIS ( 7 FDA reports)
DIVERTICULUM INTESTINAL ( 7 FDA reports)
DRY SKIN ( 7 FDA reports)
DYSPNOEA EXERTIONAL ( 7 FDA reports)
ENDOCARDITIS ( 7 FDA reports)
ERUCTATION ( 7 FDA reports)
EYE SWELLING ( 7 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 7 FDA reports)
HALLUCINATION ( 7 FDA reports)
HIP FRACTURE ( 7 FDA reports)
JOINT SWELLING ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
MOOD SWINGS ( 7 FDA reports)
OEDEMA MOUTH ( 7 FDA reports)
POLYPECTOMY ( 7 FDA reports)
PROCEDURAL COMPLICATION ( 7 FDA reports)
PROTEINURIA ( 7 FDA reports)
RECTAL HAEMORRHAGE ( 7 FDA reports)
SPINAL COLUMN STENOSIS ( 7 FDA reports)
URINARY RETENTION ( 7 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 7 FDA reports)
WOUND ( 7 FDA reports)
ACCIDENTAL EXPOSURE ( 6 FDA reports)
AGGRESSION ( 6 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 6 FDA reports)
ANGINA UNSTABLE ( 6 FDA reports)
AORTIC STENOSIS ( 6 FDA reports)
ARTHROPOD BITE ( 6 FDA reports)
BILIARY COLIC ( 6 FDA reports)
BLINDNESS UNILATERAL ( 6 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 6 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
CATARACT ( 6 FDA reports)
CHOLESTASIS ( 6 FDA reports)
CHRONIC HEPATITIS ( 6 FDA reports)
EAR INFECTION ( 6 FDA reports)
EMOTIONAL DISORDER ( 6 FDA reports)
ENZYME ABNORMALITY ( 6 FDA reports)
ESCHAR ( 6 FDA reports)
EXPOSED BONE IN JAW ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
FIBROMYALGIA ( 6 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
IMPAIRED WORK ABILITY ( 6 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 6 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 6 FDA reports)
INJECTION SITE ERYTHEMA ( 6 FDA reports)
INJECTION SITE HAEMATOMA ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
KNEE ARTHROPLASTY ( 6 FDA reports)
LUNG NEOPLASM MALIGNANT ( 6 FDA reports)
MICTURITION URGENCY ( 6 FDA reports)
MOBILITY DECREASED ( 6 FDA reports)
MUSCLE INJURY ( 6 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 6 FDA reports)
MYOPATHY ( 6 FDA reports)
NECK PAIN ( 6 FDA reports)
NEPHROLITHIASIS ( 6 FDA reports)
NIGHT SWEATS ( 6 FDA reports)
NO THERAPEUTIC RESPONSE ( 6 FDA reports)
ORAL FUNGAL INFECTION ( 6 FDA reports)
PNEUMONIA KLEBSIELLA ( 6 FDA reports)
PRESYNCOPE ( 6 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
RASH GENERALISED ( 6 FDA reports)
RENAL DISORDER ( 6 FDA reports)
RESPIRATORY ARREST ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
SHOCK ( 6 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 6 FDA reports)
SPINAL OSTEOARTHRITIS ( 6 FDA reports)
SPONDYLOLISTHESIS ( 6 FDA reports)
STRESS CARDIOMYOPATHY ( 6 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 6 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 6 FDA reports)
TENSION ( 6 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 6 FDA reports)
VASCULITIS ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
WITHDRAWAL SYNDROME ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
AORTIC VALVE CALCIFICATION ( 5 FDA reports)
ATROPHIC VULVOVAGINITIS ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 5 FDA reports)
BRONCHOSPASM ( 5 FDA reports)
CARDIAC INFECTION ( 5 FDA reports)
CARDIAC STRESS TEST ( 5 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
CATHETERISATION CARDIAC ( 5 FDA reports)
COLD SWEAT ( 5 FDA reports)
DEFORMITY ( 5 FDA reports)
DEPRESSED MOOD ( 5 FDA reports)
DEVICE BREAKAGE ( 5 FDA reports)
EATING DISORDER ( 5 FDA reports)
ERYTHEMA NODOSUM ( 5 FDA reports)
EYE DISORDER ( 5 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HAEMORRHAGE URINARY TRACT ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HEPATOSPLENOMEGALY ( 5 FDA reports)
HYPOACUSIS ( 5 FDA reports)
HYSTERECTOMY ( 5 FDA reports)
INCISION SITE COMPLICATION ( 5 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 5 FDA reports)
INITIAL INSOMNIA ( 5 FDA reports)
INJECTION SITE REACTION ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
KIDNEY INFECTION ( 5 FDA reports)
LARYNGITIS ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
MOVEMENT DISORDER ( 5 FDA reports)
MUSCLE TIGHTNESS ( 5 FDA reports)
NEUROLOGICAL SYMPTOM ( 5 FDA reports)
NON-CARDIAC CHEST PAIN ( 5 FDA reports)
ORGAN FAILURE ( 5 FDA reports)
OROPHARYNGEAL BLISTERING ( 5 FDA reports)
ORTHOPNOEA ( 5 FDA reports)
PAIN IN JAW ( 5 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
PORTAL HYPERTENSION ( 5 FDA reports)
POST PROCEDURAL INFECTION ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
ROTATOR CUFF SYNDROME ( 5 FDA reports)
SKIN FISSURES ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
SUBCUTANEOUS ABSCESS ( 5 FDA reports)
SYNOVIAL CYST ( 5 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
UNDERDOSE ( 5 FDA reports)
URETHRAL SPASM ( 5 FDA reports)
URINARY INCONTINENCE ( 5 FDA reports)
VAGINAL HAEMORRHAGE ( 5 FDA reports)
VERTEBRAL WEDGING ( 5 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
ABDOMINAL WALL ABSCESS ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
APHAGIA ( 4 FDA reports)
APHASIA ( 4 FDA reports)
APPLICATION SITE RASH ( 4 FDA reports)
ASPIRATION ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
COMPRESSION FRACTURE ( 4 FDA reports)
CONCUSSION ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
DERMATITIS ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DISSOCIATION ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
DRY THROAT ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
FOETAL DISTRESS SYNDROME ( 4 FDA reports)
FRUSTRATION ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
FUNGAL SKIN INFECTION ( 4 FDA reports)
GASTRIC DISORDER ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
GESTATIONAL HYPERTENSION ( 4 FDA reports)
HAEMANGIOMA ( 4 FDA reports)
HAIR TEXTURE ABNORMAL ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HEAD INJURY ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 4 FDA reports)
INFLUENZA ( 4 FDA reports)
INFUSION SITE PRURITUS ( 4 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
KIDNEY FIBROSIS ( 4 FDA reports)
LACRIMATION INCREASED ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
LIGAMENT SPRAIN ( 4 FDA reports)
MACULAR DEGENERATION ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
MUCOUS STOOLS ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
ORAL DISCOMFORT ( 4 FDA reports)
OSTEOARTHROPATHY ( 4 FDA reports)
OVARIAN CYST ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
PANCREATITIS CHRONIC ( 4 FDA reports)
PARAESTHESIA ORAL ( 4 FDA reports)
PARANOIA ( 4 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 4 FDA reports)
PRODUCT CONTAMINATION ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
RADIOTHERAPY ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RASH PAPULAR ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 4 FDA reports)
RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
SALIVARY HYPERSECRETION ( 4 FDA reports)
SERUM SICKNESS ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SKIN WARM ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
TRANSPLANT FAILURE ( 4 FDA reports)
TUMOUR MARKER INCREASED ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
URINE FLOW DECREASED ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
WALKING AID USER ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ALVEOLITIS ALLERGIC ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ANOXIC ENCEPHALOPATHY ( 3 FDA reports)
APPENDICECTOMY ( 3 FDA reports)
APPETITE DISORDER ( 3 FDA reports)
APPLICATION SITE PAPULES ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CHOKING ( 3 FDA reports)
CHOLECYSTECTOMY ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 3 FDA reports)
COELIAC DISEASE ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
COLONIC POLYP ( 3 FDA reports)
COMPLEX PARTIAL SEIZURES ( 3 FDA reports)
CUSHING'S SYNDROME ( 3 FDA reports)
DEJA VU ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
EXCORIATION ( 3 FDA reports)
EYE DISCHARGE ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HALLUCINATIONS, MIXED ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPOAESTHESIA FACIAL ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 3 FDA reports)
INCOHERENT ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
JOINT DISLOCATION ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
LOWER EXTREMITY MASS ( 3 FDA reports)
LOWER LIMB FRACTURE ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 3 FDA reports)
MYOPIA ( 3 FDA reports)
NASAL DISCOMFORT ( 3 FDA reports)
NECK INJURY ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
ORAL MUCOSAL BLISTERING ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 3 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
POSTOPERATIVE ADHESION ( 3 FDA reports)
PRODUCT TASTE ABNORMAL ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PRURITUS GENITAL ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 3 FDA reports)
PULMONARY MYCOSIS ( 3 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 3 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
SCAR ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SELF-INJURIOUS IDEATION ( 3 FDA reports)
SEQUESTRECTOMY ( 3 FDA reports)
SINUS HEADACHE ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SKELETAL INJURY ( 3 FDA reports)
SKIN MASS ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
SOMNAMBULISM ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
SPLEEN CONGESTION ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
STERNAL FRACTURE ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
STRESS FRACTURE ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
SURGERY ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
TONGUE ULCERATION ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
VERTEBROPLASTY ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
VOCAL CORD DISORDER ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
WOUND SECRETION ( 3 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
ADRENAL MASS ( 2 FDA reports)
ADRENAL SUPPRESSION ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BACTERIAL RHINITIS ( 2 FDA reports)
BLADDER CANCER RECURRENT ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL INCREASED ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BONE FRAGMENTATION ( 2 FDA reports)
BONE GRAFT ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BREAST CALCIFICATIONS ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC ABLATION ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
COLITIS ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
DENTAL FISTULA ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DEVICE INEFFECTIVE ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
EAR PRURITUS ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 2 FDA reports)
ENDODONTIC PROCEDURE ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
GAMMOPATHY ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GENITAL HERPES ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GROWTH RETARDATION ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC ADENOMA ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE MACULE ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
JOINT HYPEREXTENSION ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIFE EXPECTANCY SHORTENED ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MOTION SICKNESS ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NAIL HYPERTROPHY ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
NODULE ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OPEN ANGLE GLAUCOMA ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PAPILLOMA VIRAL INFECTION ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PERIODONTITIS ( 2 FDA reports)
PHARYNGEAL ULCERATION ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POISONING ( 2 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 2 FDA reports)
PROSTATOMEGALY ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PSYCHOLOGICAL TRAUMA ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RECURRENT CANCER ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL MASS ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RHEUMATIC FEVER ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SINUS OPERATION ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN ODOUR ABNORMAL ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
TETANUS ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TOOTH EROSION ( 2 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALLERGIC OEDEMA ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APHAKIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CSF VOLUME INCREASED ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTURE WEARER ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE ISSUE ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DISACCHARIDE METABOLISM DISORDER ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXPLORATORY OPERATION ( 1 FDA reports)
EXPOSURE TO ALLERGEN ( 1 FDA reports)
EXPOSURE TO CONTAMINATED DEVICE ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE LACERATION ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRREGULAR SLEEP PHASE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASAL SEPTUM ULCERATION ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PASTEURELLA INFECTION ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PENILE BLISTER ( 1 FDA reports)
PERFORATION BILE DUCT ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPERM CONCENTRATION DECREASED ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
TIC ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TOOTH REPAIR ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
UVULA APLASIA ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VIRAL LOAD ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)

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