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

NAUSEA ( 37 FDA reports)
DRUG INEFFECTIVE ( 34 FDA reports)
DIZZINESS ( 32 FDA reports)
PRURITUS ( 31 FDA reports)
COMPLETED SUICIDE ( 29 FDA reports)
PAIN ( 28 FDA reports)
BLOOD PRESSURE INCREASED ( 26 FDA reports)
VOMITING ( 26 FDA reports)
ASTHENIA ( 24 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 23 FDA reports)
DYSPNOEA ( 21 FDA reports)
FLUSHING ( 20 FDA reports)
FEELING ABNORMAL ( 17 FDA reports)
DIARRHOEA ( 16 FDA reports)
FEELING HOT ( 15 FDA reports)
HEADACHE ( 15 FDA reports)
OEDEMA PERIPHERAL ( 15 FDA reports)
VISION BLURRED ( 15 FDA reports)
CEREBROVASCULAR ACCIDENT ( 14 FDA reports)
INJECTION SITE PAIN ( 13 FDA reports)
MALAISE ( 13 FDA reports)
ANGIOEDEMA ( 12 FDA reports)
DEPRESSION ( 12 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 12 FDA reports)
RASH ( 12 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
FATIGUE ( 11 FDA reports)
PSORIASIS ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
ARTHRALGIA ( 10 FDA reports)
BACK PAIN ( 10 FDA reports)
BLOOD GLUCOSE INCREASED ( 10 FDA reports)
CARDIAC ARREST ( 10 FDA reports)
DEATH ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
PLEURAL EFFUSION ( 10 FDA reports)
PRODUCT QUALITY ISSUE ( 10 FDA reports)
ABDOMINAL DISTENSION ( 9 FDA reports)
ANXIETY ( 9 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
CHEST PAIN ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
HEART RATE INCREASED ( 9 FDA reports)
MUSCULAR WEAKNESS ( 9 FDA reports)
TACHYCARDIA ( 9 FDA reports)
UNRESPONSIVE TO STIMULI ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
BLOOD PRESSURE DECREASED ( 8 FDA reports)
CHEST DISCOMFORT ( 8 FDA reports)
COLITIS ( 8 FDA reports)
DEEP VEIN THROMBOSIS ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
INJECTION SITE MASS ( 8 FDA reports)
MEMORY IMPAIRMENT ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
SENSORY DISTURBANCE ( 8 FDA reports)
SKIN BURNING SENSATION ( 8 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 7 FDA reports)
PRURITUS GENERALISED ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
SWOLLEN TONGUE ( 7 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
BALANCE DISORDER ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
BRONCHITIS ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
COUGH ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
INJURY ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
OROPHARYNGEAL PAIN ( 6 FDA reports)
POISONING ( 6 FDA reports)
SKIN DISCOLOURATION ( 6 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
VISUAL IMPAIRMENT ( 6 FDA reports)
AMNESIA ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
DYSSTASIA ( 5 FDA reports)
EMOTIONAL DISTRESS ( 5 FDA reports)
FALL ( 5 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HEART RATE DECREASED ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
HYPOTHYROIDISM ( 5 FDA reports)
INCOHERENT ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
MASS ( 5 FDA reports)
MENISCUS LESION ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
NEPHROPATHY ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PRURITUS GENITAL ( 5 FDA reports)
SKIN EXFOLIATION ( 5 FDA reports)
SKIN TIGHTNESS ( 5 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ACROCHORDON ( 4 FDA reports)
ACUTE SINUSITIS ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 4 FDA reports)
DEFORMITY ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ( 4 FDA reports)
MUSCLE TIGHTNESS ( 4 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PLASMACYTOMA ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SKIN HYPERPIGMENTATION ( 4 FDA reports)
SKIN INDURATION ( 4 FDA reports)
SKIN PLAQUE ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
TENDERNESS ( 4 FDA reports)
TREMOR ( 4 FDA reports)
UROSEPSIS ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHOKING ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMORRHAGE URINARY TRACT ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPOAESTHESIA FACIAL ( 3 FDA reports)
ILEUS ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
INJECTION SITE SCAB ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
PANCREATITIS CHRONIC ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
APPLICATION SITE HAEMATOMA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CATAPLEXY ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CRYING ( 2 FDA reports)
CYST ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DEVICE MISUSE ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 2 FDA reports)
HYPERMAGNESAEMIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PSEUDOCYST ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WHITE CLOT SYNDROME ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMA ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INSULIN C-PEPTIDE DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRANASAL HYPOAESTHESIA ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MICROVASCULAR ANGINA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NODULE ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST THROMBOTIC SYNDROME ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRODUCT COMMINGLING ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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