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

DRUG EXPOSURE DURING PREGNANCY ( 21 FDA reports)
DYSPNOEA ( 15 FDA reports)
DRUG INEFFECTIVE ( 14 FDA reports)
INFECTION ( 12 FDA reports)
ASTHMA ( 11 FDA reports)
PNEUMONIA ( 11 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 10 FDA reports)
APNOEA ( 10 FDA reports)
COLLAPSE OF LUNG ( 10 FDA reports)
DIZZINESS ( 10 FDA reports)
EATING DISORDER ( 10 FDA reports)
HYPOTENSION ( 10 FDA reports)
HYPOXIA ( 10 FDA reports)
IMMUNOGLOBULINS DECREASED ( 10 FDA reports)
INTESTINAL PERFORATION ( 10 FDA reports)
LUNG INJURY ( 10 FDA reports)
PREMATURE BABY ( 10 FDA reports)
PULMONARY OEDEMA ( 10 FDA reports)
RESPIRATORY DISORDER ( 10 FDA reports)
RESPIRATORY DISTRESS ( 10 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 10 FDA reports)
NAUSEA ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
PAIN ( 7 FDA reports)
PULMONARY VALVE STENOSIS ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ATRIAL SEPTAL DEFECT ( 6 FDA reports)
BALANCE DISORDER ( 6 FDA reports)
MALAISE ( 6 FDA reports)
RASH ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
ANXIETY ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
COARCTATION OF THE AORTA ( 4 FDA reports)
COLOBOMA ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
DYSMORPHISM ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
FALL ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
OCULOAURICULOVERTEBRAL DYSPLASIA ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
APPLICATION SITE PAIN ( 3 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHOLECYSTITIS CHRONIC ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CONGENITAL SCOLIOSIS ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEMIVERTEBRA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
VERTICAL TALUS ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
APPLICATION SITE SCAR ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISABILITY ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJURY ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PULMONARY HYPOPLASIA ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TRACHEAL STENOSIS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL EYELID MALFORMATION ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYANOSIS NEONATAL ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KOUNIS SYNDROME ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TENSION ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VICTIM OF SEXUAL ABUSE ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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