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

PAIN ( 61 FDA reports)
NAUSEA ( 48 FDA reports)
PULMONARY EMBOLISM ( 48 FDA reports)
CHOLECYSTITIS CHRONIC ( 47 FDA reports)
DYSPNOEA ( 43 FDA reports)
VOMITING ( 36 FDA reports)
DEEP VEIN THROMBOSIS ( 29 FDA reports)
DRUG INEFFECTIVE ( 29 FDA reports)
INJURY ( 29 FDA reports)
ANXIETY ( 28 FDA reports)
PNEUMONIA ( 25 FDA reports)
PRODUCT QUALITY ISSUE ( 25 FDA reports)
ABDOMINAL PAIN UPPER ( 24 FDA reports)
ASTHMA ( 22 FDA reports)
GALLBLADDER DISORDER ( 22 FDA reports)
DIARRHOEA ( 21 FDA reports)
FATIGUE ( 20 FDA reports)
BACK PAIN ( 19 FDA reports)
CHOLELITHIASIS ( 18 FDA reports)
EMOTIONAL DISTRESS ( 18 FDA reports)
COUGH ( 17 FDA reports)
DEPRESSION ( 17 FDA reports)
HEADACHE ( 17 FDA reports)
OEDEMA PERIPHERAL ( 17 FDA reports)
BLISTER ( 16 FDA reports)
PAIN IN EXTREMITY ( 16 FDA reports)
ASTHENIA ( 15 FDA reports)
CEREBROVASCULAR ACCIDENT ( 15 FDA reports)
CHOLECYSTITIS ( 15 FDA reports)
RASH GENERALISED ( 15 FDA reports)
ABDOMINAL PAIN ( 14 FDA reports)
ANHEDONIA ( 14 FDA reports)
CHEST PAIN ( 14 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 14 FDA reports)
PRURITUS ( 13 FDA reports)
SKIN EXFOLIATION ( 13 FDA reports)
URTICARIA ( 13 FDA reports)
BILIARY DYSKINESIA ( 12 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 12 FDA reports)
RASH PRURITIC ( 12 FDA reports)
WHEEZING ( 12 FDA reports)
CHOLECYSTECTOMY ( 11 FDA reports)
HYPOAESTHESIA ( 11 FDA reports)
MALAISE ( 11 FDA reports)
PYREXIA ( 11 FDA reports)
DIZZINESS ( 10 FDA reports)
HEART RATE INCREASED ( 10 FDA reports)
MUSCULOSKELETAL PAIN ( 10 FDA reports)
PLEURAL EFFUSION ( 10 FDA reports)
RENAL FAILURE ( 10 FDA reports)
SWOLLEN TONGUE ( 10 FDA reports)
ARTHRALGIA ( 9 FDA reports)
ATELECTASIS ( 9 FDA reports)
CHEST DISCOMFORT ( 9 FDA reports)
CHILLS ( 9 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
ECZEMA ( 9 FDA reports)
FEAR ( 9 FDA reports)
HYPERHIDROSIS ( 9 FDA reports)
HYPOXIA ( 9 FDA reports)
RENAL INJURY ( 9 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 9 FDA reports)
CHOKING ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
HYPERSENSITIVITY ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
BRONCHITIS ( 7 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 7 FDA reports)
CONSTIPATION ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
DYSPHONIA ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
GALLBLADDER INJURY ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 7 FDA reports)
MULTI-ORGAN FAILURE ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
RETCHING ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
THROMBOSIS ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
CEREBRAL INFARCTION ( 6 FDA reports)
DEATH ( 6 FDA reports)
FALL ( 6 FDA reports)
HEMIPARESIS ( 6 FDA reports)
INFLUENZA ( 6 FDA reports)
MENTAL DISORDER ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
STRESS ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
APHONIA ( 5 FDA reports)
BILIARY COLIC ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CHOLECYSTITIS ACUTE ( 5 FDA reports)
EMOTIONAL DISORDER ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
INFECTION ( 5 FDA reports)
INJECTION SITE ERYTHEMA ( 5 FDA reports)
NERVOUSNESS ( 5 FDA reports)
OROPHARYNGEAL PAIN ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PHARYNGEAL OEDEMA ( 5 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 5 FDA reports)
PULMONARY INFARCTION ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
UNEVALUABLE EVENT ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
APHASIA ( 4 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
AXILLARY PAIN ( 4 FDA reports)
CHOLESTEROSIS ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
FLANK PAIN ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
INJECTION SITE REACTION ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
MENSTRUATION IRREGULAR ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
PANCREATIC CARCINOMA ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PERIPHERAL ISCHAEMIA ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
SUBDURAL HAEMATOMA ( 4 FDA reports)
TREMOR ( 4 FDA reports)
ADVERSE REACTION ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ARTERIAL DISORDER ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CLAVICLE FRACTURE ( 3 FDA reports)
CONGENITAL AORTIC ANOMALY ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
FEAR OF DEATH ( 3 FDA reports)
FRACTURE NONUNION ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 3 FDA reports)
INJECTION SITE PAPULE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
LACERATION ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RESPIRATION ABNORMAL ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALCOHOL ABUSE ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
APPENDIX DISORDER ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
BED REST ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BONE GRAFT ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPAREUNIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ENCEPHALOMALACIA ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HAND AMPUTATION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYELITIS TRANSVERSE ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POISONING ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PSYCHOLOGICAL TRAUMA ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RASH ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD COUNT ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CERVIX DYSTOCIA ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHLAMYDIA TEST POSITIVE ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOETAL TOBACCO EXPOSURE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEARNING DISABILITY ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUPUS MYOCARDITIS ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOPERICARDITIS ( 1 FDA reports)
NASAL NEOPLASM ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PORCELAIN GALLBLADDER ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYLOROSPASM ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMEAR VAGINAL ABNORMAL ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ULCER ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VULVOVAGINITIS TRICHOMONAL ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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