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

HYPERTENSION ( 33 FDA reports)
ANXIETY ( 31 FDA reports)
PAIN IN EXTREMITY ( 29 FDA reports)
ANGIOEDEMA ( 28 FDA reports)
DEFORMITY ( 28 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 28 FDA reports)
CEREBRAL ISCHAEMIA ( 27 FDA reports)
DYSPNOEA ( 27 FDA reports)
HOT FLUSH ( 27 FDA reports)
SWELLING ( 27 FDA reports)
SWOLLEN TONGUE ( 27 FDA reports)
OEDEMA PERIPHERAL ( 26 FDA reports)
EMOTIONAL DISTRESS ( 25 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 25 FDA reports)
HYPOPHAGIA ( 25 FDA reports)
OEDEMA MOUTH ( 25 FDA reports)
ORAL PAIN ( 25 FDA reports)
TOOTH ABSCESS ( 25 FDA reports)
URINARY TRACT INFECTION ( 25 FDA reports)
AMNESIA ( 24 FDA reports)
ARTHRITIS ( 24 FDA reports)
BIOPSY TONGUE ABNORMAL ( 24 FDA reports)
BONE DISORDER ( 24 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 24 FDA reports)
DECREASED INTEREST ( 24 FDA reports)
DEEP VEIN THROMBOSIS ( 24 FDA reports)
GINGIVAL ERYTHEMA ( 24 FDA reports)
GINGIVAL SWELLING ( 24 FDA reports)
GINGIVAL ULCERATION ( 24 FDA reports)
LEUKOCYTOSIS ( 24 FDA reports)
LIFE EXPECTANCY SHORTENED ( 24 FDA reports)
MICTURITION URGENCY ( 24 FDA reports)
MONONUCLEOSIS SYNDROME ( 24 FDA reports)
NEOPLASM MALIGNANT ( 24 FDA reports)
ONYCHOMYCOSIS ( 24 FDA reports)
PERIODONTITIS ( 24 FDA reports)
POLYP ( 24 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 24 FDA reports)
SOFT TISSUE INFECTION ( 24 FDA reports)
VAGINAL HAEMORRHAGE ( 24 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 23 FDA reports)
ADNEXA UTERI MASS ( 22 FDA reports)
OSTEONECROSIS OF JAW ( 22 FDA reports)
OSTEOPENIA ( 22 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 22 FDA reports)
UTERINE ENLARGEMENT ( 22 FDA reports)
UTERINE LEIOMYOMA ( 22 FDA reports)
UTERINE POLYP ( 22 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 21 FDA reports)
ATROPHIC VULVOVAGINITIS ( 20 FDA reports)
COITAL BLEEDING ( 20 FDA reports)
DERMATITIS ATOPIC ( 20 FDA reports)
ECZEMA ( 20 FDA reports)
FALL ( 20 FDA reports)
FOOT DEFORMITY ( 20 FDA reports)
FOREIGN BODY IN EYE ( 20 FDA reports)
HAEMORRHOIDS ( 20 FDA reports)
HYPERLIPIDAEMIA ( 20 FDA reports)
LUMBAR SPINAL STENOSIS ( 20 FDA reports)
SCIATICA ( 20 FDA reports)
TENDON INJURY ( 20 FDA reports)
DEPRESSION ( 18 FDA reports)
FOLLICULITIS ( 18 FDA reports)
SKIN PAPILLOMA ( 18 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 17 FDA reports)
INTESTINAL HAEMORRHAGE ( 17 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 16 FDA reports)
DRY SKIN ( 16 FDA reports)
RECTAL HAEMORRHAGE ( 16 FDA reports)
CHEST PAIN ( 15 FDA reports)
COLITIS ( 15 FDA reports)
CONFUSIONAL STATE ( 15 FDA reports)
DIZZINESS ( 15 FDA reports)
GASTROINTESTINAL DISORDER ( 15 FDA reports)
LIP DRY ( 15 FDA reports)
MULTI-ORGAN DISORDER ( 15 FDA reports)
CROHN'S DISEASE ( 14 FDA reports)
DRUG INEFFECTIVE ( 14 FDA reports)
SPONDYLOLISTHESIS ( 14 FDA reports)
URTICARIA ( 14 FDA reports)
ANAEMIA ( 12 FDA reports)
JOINT INJURY ( 12 FDA reports)
MALNUTRITION ( 12 FDA reports)
MUSCLE INJURY ( 12 FDA reports)
BLOOD POTASSIUM DECREASED ( 11 FDA reports)
COLITIS ULCERATIVE ( 11 FDA reports)
INJURY ( 11 FDA reports)
CORNEAL ABRASION ( 10 FDA reports)
DUODENAL ULCER ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
NASOPHARYNGITIS ( 10 FDA reports)
OCULAR HYPERAEMIA ( 10 FDA reports)
VOMITING ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
ASTHENIA ( 9 FDA reports)
DENTAL CARIES ( 9 FDA reports)
GASTRITIS EROSIVE ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
ABNORMAL BEHAVIOUR ( 8 FDA reports)
BALANCE DISORDER ( 8 FDA reports)
CARDIOMYOPATHY ( 8 FDA reports)
CATARACT ( 8 FDA reports)
COUGH ( 8 FDA reports)
PAIN ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
DIPLOPIA ( 7 FDA reports)
DYSKINESIA ( 7 FDA reports)
ENDODONTIC PROCEDURE ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
MELAENA ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
RESTLESSNESS ( 7 FDA reports)
TARDIVE DYSKINESIA ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
AGGRESSION ( 6 FDA reports)
AMENORRHOEA ( 6 FDA reports)
ANAPHYLACTIC SHOCK ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
BONE DEBRIDEMENT ( 6 FDA reports)
BUNION OPERATION ( 6 FDA reports)
CATHETER PLACEMENT ( 6 FDA reports)
CONJUNCTIVITIS VIRAL ( 6 FDA reports)
DEBRIDEMENT ( 6 FDA reports)
DELUSION ( 6 FDA reports)
DRUG DEPENDENCE ( 6 FDA reports)
FOOT OPERATION ( 6 FDA reports)
GENITOURINARY TRACT INFECTION ( 6 FDA reports)
HAEMORRHAGE ( 6 FDA reports)
HALLUCINATION, AUDITORY ( 6 FDA reports)
HYPERPHAGIA ( 6 FDA reports)
JOINT ARTHROPLASTY ( 6 FDA reports)
LACRIMATION INCREASED ( 6 FDA reports)
LOGORRHOEA ( 6 FDA reports)
LYMPHADENECTOMY ( 6 FDA reports)
MALAISE ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
OSTEOTOMY ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
PHOTOSENSITIVITY REACTION ( 6 FDA reports)
TOE OPERATION ( 6 FDA reports)
TOOTH EXTRACTION ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
VISUAL IMPAIRMENT ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
BRONCHITIS ACUTE ( 5 FDA reports)
CEREBROVASCULAR ACCIDENT ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEART RATE IRREGULAR ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
STOMACH DISCOMFORT ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
UTERINE DILATION AND CURETTAGE ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ABSCESS ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DEATH ( 4 FDA reports)
EPIGASTRIC DISCOMFORT ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
LACTOSE INTOLERANCE ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TENOSYNOVITIS ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
VENTRICULAR HYPERTROPHY ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
AGITATION ( 3 FDA reports)
AORTIC DISSECTION ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
COLON OPERATION ( 3 FDA reports)
CRYING ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DISABILITY ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
FEAR ( 3 FDA reports)
GUN SHOT WOUND ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
INFECTION ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RASH ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
SPLENECTOMY ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
TEMPORAL ARTERITIS ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
AMPHETAMINES POSITIVE ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GASTROINTESTINAL INJURY ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MENINGEAL DISORDER ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PERICARDIAL HAEMORRHAGE ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SNORING ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABORTION SPONTANEOUS INCOMPLETE ( 1 FDA reports)
ACANTHOLYSIS ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADENOIDAL HYPERTROPHY ( 1 FDA reports)
ADENOIDITIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CYST ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DELUSION OF REFERENCE ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HIGH FREQUENCY ABLATION ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODAL OSTEOARTHRITIS ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCLERAL CYST ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROID CYST ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTH REPAIR ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRENDELENBURG'S SYMPTOM ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
ULCER ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VULVA INJURY ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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