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

DYSPNOEA ( 49 FDA reports)
ASTHMA ( 36 FDA reports)
DRUG INEFFECTIVE ( 36 FDA reports)
NAUSEA ( 26 FDA reports)
PNEUMONIA ( 24 FDA reports)
VOMITING ( 23 FDA reports)
HYPOTENSION ( 22 FDA reports)
DIARRHOEA ( 20 FDA reports)
CONFUSIONAL STATE ( 19 FDA reports)
PYREXIA ( 19 FDA reports)
CONDITION AGGRAVATED ( 17 FDA reports)
DIZZINESS ( 17 FDA reports)
GRANULOCYTOPENIA ( 16 FDA reports)
HEADACHE ( 16 FDA reports)
OEDEMA PERIPHERAL ( 16 FDA reports)
ASTHENIA ( 15 FDA reports)
INSOMNIA ( 15 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 15 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 14 FDA reports)
ABDOMINAL PAIN ( 13 FDA reports)
CARDIAC ARREST ( 13 FDA reports)
CHEST DISCOMFORT ( 13 FDA reports)
AGITATION ( 12 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 12 FDA reports)
RASH ( 12 FDA reports)
FATIGUE ( 11 FDA reports)
URTICARIA ( 11 FDA reports)
ATRIAL FIBRILLATION ( 10 FDA reports)
BRONCHITIS ( 10 FDA reports)
BRONCHOSPASM ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
PARAESTHESIA ( 10 FDA reports)
RESPIRATORY FAILURE ( 10 FDA reports)
SINUS TACHYCARDIA ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
ANAEMIA ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
ERYTHEMA ( 9 FDA reports)
FALL ( 9 FDA reports)
MALAISE ( 9 FDA reports)
PAIN ( 9 FDA reports)
PULMONARY EMBOLISM ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
BLOOD GLUCOSE INCREASED ( 8 FDA reports)
BLOOD POTASSIUM INCREASED ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
COUGH ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
PRURITUS ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
SOMNOLENCE ( 8 FDA reports)
TREMOR ( 8 FDA reports)
WHEEZING ( 8 FDA reports)
AGEUSIA ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ARTHRALGIA ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
HYPOXIA ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
CHEST PAIN ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
AGGRESSION ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
CHILLS ( 5 FDA reports)
DELIRIUM ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
DUODENAL ULCER ( 5 FDA reports)
DYSGEUSIA ( 5 FDA reports)
EMPHYSEMA ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HAEMOLYSIS ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
ORGAN FAILURE ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PALLOR ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CAESAREAN SECTION ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FOETAL DISTRESS SYNDROME ( 4 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
LARYNGEAL OEDEMA ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
MELAENA ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
PULMONARY CONGESTION ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TACHYCARDIA FOETAL ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DEATH ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HERPES SIMPLEX ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
PERITONEAL DIALYSIS ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 3 FDA reports)
PREMATURE LABOUR ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ALVEOLITIS FIBROSING ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANIMAL SCRATCH ( 2 FDA reports)
APPLICATION SITE INFLAMMATION ( 2 FDA reports)
APPLICATION SITE MASS ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASTHMATIC CRISIS ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
AUTISM ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BREAKTHROUGH PAIN ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CRYING ( 2 FDA reports)
CULTURE THROAT POSITIVE ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PELVIC HAEMATOMA ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POISONING DELIBERATE ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THORACIC OUTLET SYNDROME ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
URINE KETONE BODY PRESENT ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADENOIDAL HYPERTROPHY ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANOREXIA NERVOSA ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE REPAIR ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AVERSION ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BLASTOCYSTIS INFECTION ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD KETONE BODY INCREASED ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE MARROW EOSINOPHILIC LEUKOCYTE COUNT INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FORCEPS DELIVERY ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYDROURETER ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTESTINAL STRANGULATION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 1 FDA reports)
LEARNING DISABILITY ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERISTALSIS VISIBLE ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLACENTA PRAEVIA ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEBORRHOEA ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
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SKIN WRINKLING ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBMANDIBULAR MASS ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRANSFERRIN INCREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE CYTOMEGALOVIRUS POSITIVE ( 1 FDA reports)
URINE MERCURY ABNORMAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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