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

HAEMATURIA ( 13 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 10 FDA reports)
DYSPNOEA ( 9 FDA reports)
ADENOIDAL HYPERTROPHY ( 8 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 8 FDA reports)
AUTISM ( 8 FDA reports)
CROUP INFECTIOUS ( 8 FDA reports)
DEPRESSION ( 8 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
LARYNGEAL STENOSIS ( 8 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 8 FDA reports)
VIRAL PHARYNGITIS ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
PAIN ( 7 FDA reports)
ANIMAL BITE ( 6 FDA reports)
ANXIETY ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 6 FDA reports)
BONE DISORDER ( 6 FDA reports)
COLON NEOPLASM ( 6 FDA reports)
CONGENITAL ANOMALY ( 6 FDA reports)
DECREASED INTEREST ( 6 FDA reports)
DEFAECATION URGENCY ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 6 FDA reports)
EDENTULOUS ( 6 FDA reports)
EMOTIONAL DISTRESS ( 6 FDA reports)
FACIAL PAIN ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
FISTULA ( 6 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
GINGIVAL ERYTHEMA ( 6 FDA reports)
GINGIVAL SWELLING ( 6 FDA reports)
GRANULOMA ( 6 FDA reports)
HYDRONEPHROSIS ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
IMPAIRED HEALING ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
LOCALISED INFECTION ( 6 FDA reports)
MALNUTRITION ( 6 FDA reports)
MASS ( 6 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 6 FDA reports)
METASTASES TO BONE ( 6 FDA reports)
OSTEOMYELITIS ( 6 FDA reports)
OSTEONECROSIS OF JAW ( 6 FDA reports)
OTITIS MEDIA CHRONIC ( 6 FDA reports)
PAIN IN JAW ( 6 FDA reports)
PANCREATIC NEOPLASM ( 6 FDA reports)
PLANTAR FASCIITIS ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
PROTHROMBIN TIME PROLONGED ( 6 FDA reports)
PURULENT DISCHARGE ( 6 FDA reports)
RASH PRURITIC ( 6 FDA reports)
RENAL ATROPHY ( 6 FDA reports)
SENSATION OF PRESSURE ( 6 FDA reports)
SWELLING FACE ( 6 FDA reports)
TRAUMATIC HAEMATOMA ( 6 FDA reports)
VOMITING ( 6 FDA reports)
ANASTOMOTIC LEAK ( 5 FDA reports)
COLONIC OBSTRUCTION ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
FAECALOMA ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
URETERIC OBSTRUCTION ( 5 FDA reports)
ATELECTASIS ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BRONCHITIS ACUTE ( 4 FDA reports)
CALCULUS URETERIC ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
EAR INFECTION ( 4 FDA reports)
FORCEPS DELIVERY ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
METAL POISONING ( 4 FDA reports)
METASTASES TO LUNG ( 4 FDA reports)
OEDEMA MUCOSAL ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
SEROSITIS ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
COMA ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
EXPOSURE TO TOXIC AGENT ( 3 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
INJURY ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
LEARNING DISABILITY ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
AMYLOIDOSIS ( 2 FDA reports)
AVERSION ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD MERCURY ABNORMAL ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARDIAC AMYLOIDOSIS ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
CREATINE URINE INCREASED ( 2 FDA reports)
CREATININE URINE INCREASED ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
FACTOR X DEFICIENCY ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
HAEMORRHAGIC DISEASE OF NEWBORN ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LEARNING DISORDER ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
METASTASES TO PERITONEUM ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
URINE CALCIUM INCREASED ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGENITAL ORAL MALFORMATION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEAR ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOETAL TOBACCO EXPOSURE ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
GASTROINTESTINAL DISORDER CONGENITAL ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PROLONGED LABOUR ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 1 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE MERCURY ABNORMAL ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAMIN K DECREASED ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)

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