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

DRUG INEFFECTIVE ( 42 FDA reports)
HYPOTENSION ( 37 FDA reports)
HEADACHE ( 30 FDA reports)
PARAESTHESIA ( 25 FDA reports)
DIZZINESS ( 22 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 22 FDA reports)
CONFUSIONAL STATE ( 19 FDA reports)
PAIN ( 17 FDA reports)
ANXIETY ( 16 FDA reports)
MALAISE ( 16 FDA reports)
DYSPNOEA ( 15 FDA reports)
ANAESTHETIC COMPLICATION ( 14 FDA reports)
COMA ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
ARTHRITIS ( 13 FDA reports)
PARANOIA ( 13 FDA reports)
SUICIDAL IDEATION ( 13 FDA reports)
TREMOR ( 13 FDA reports)
ABNORMAL DREAMS ( 12 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 12 FDA reports)
CARDIO-RESPIRATORY ARREST ( 12 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 12 FDA reports)
DRY MOUTH ( 12 FDA reports)
INFLUENZA LIKE ILLNESS ( 12 FDA reports)
SENSORY DISTURBANCE ( 12 FDA reports)
FIBROMYALGIA ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
WEIGHT DECREASED ( 11 FDA reports)
BRONCHOPNEUMONIA ( 10 FDA reports)
CYST ( 10 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 10 FDA reports)
GRIP STRENGTH DECREASED ( 10 FDA reports)
HYPERPHAGIA ( 10 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 10 FDA reports)
MENISCUS LESION ( 10 FDA reports)
NERVE INJURY ( 10 FDA reports)
PLEURITIC PAIN ( 10 FDA reports)
RASH MACULAR ( 10 FDA reports)
ROAD TRAFFIC ACCIDENT ( 10 FDA reports)
SKIN CANCER ( 10 FDA reports)
DRUG ADMINISTRATION ERROR ( 9 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 9 FDA reports)
MOBILITY DECREASED ( 9 FDA reports)
SPONDYLITIS ( 9 FDA reports)
BRONCHITIS ( 8 FDA reports)
HYPERAEMIA ( 8 FDA reports)
MYOCARDIAL ISCHAEMIA ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
POST PROCEDURAL COMPLICATION ( 8 FDA reports)
VIRAL INFECTION ( 8 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
BRAIN INJURY ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
ANAPHYLACTIC REACTION ( 6 FDA reports)
ANAPHYLACTIC SHOCK ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
EPILEPSY ( 6 FDA reports)
FALL ( 6 FDA reports)
HEAD INJURY ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
INTENTIONAL DRUG MISUSE ( 6 FDA reports)
MEMORY IMPAIRMENT ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ADVERSE EVENT ( 5 FDA reports)
DERMATITIS ALLERGIC ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
DYSTONIA ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
RECTAL ABSCESS ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
HIP ARTHROPLASTY ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PROCEDURAL COMPLICATION ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CHOLECYSTITIS CHRONIC ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
NO ADVERSE EVENT ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
STRESS ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABORTION THREATENED ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BRAIN COMPRESSION ( 2 FDA reports)
CATAPLEXY ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
DEATH ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FEAR ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPEREMESIS GRAVIDARUM ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NORMAL DELIVERY ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN ABNORMAL ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONGENITAL GENITAL MALFORMATION ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG DELIVERY DEVICE REMOVAL ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MECONIUM STAIN ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NODULE ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
UMBILICAL CORD ABNORMALITY ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
URETERAL NECROSIS ( 1 FDA reports)
UTERINE INFLAMMATION ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND ( 1 FDA reports)

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