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

ALCOHOL USE ( 135 FDA reports)
SUICIDE ATTEMPT ( 116 FDA reports)
OVERDOSE ( 99 FDA reports)
MULTIPLE DRUG OVERDOSE ( 94 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 71 FDA reports)
DRUG ABUSER ( 63 FDA reports)
LOSS OF CONSCIOUSNESS ( 63 FDA reports)
COMA ( 55 FDA reports)
SOMNOLENCE ( 54 FDA reports)
ALCOHOL POISONING ( 53 FDA reports)
VOMITING ( 53 FDA reports)
INTENTIONAL OVERDOSE ( 52 FDA reports)
POLYSUBSTANCE ABUSE ( 52 FDA reports)
DEPRESSION ( 46 FDA reports)
DRUG DEPENDENCE ( 46 FDA reports)
SUICIDAL IDEATION ( 44 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 43 FDA reports)
HYPOTENSION ( 39 FDA reports)
NAUSEA ( 39 FDA reports)
DRUG INEFFECTIVE ( 36 FDA reports)
ACCIDENTAL OVERDOSE ( 34 FDA reports)
FALL ( 33 FDA reports)
AGITATION ( 31 FDA reports)
ANXIETY ( 31 FDA reports)
DRUG TOXICITY ( 31 FDA reports)
INTENTIONAL MISUSE ( 31 FDA reports)
ROAD TRAFFIC ACCIDENT ( 30 FDA reports)
HYPERHIDROSIS ( 28 FDA reports)
INSOMNIA ( 28 FDA reports)
PAIN ( 28 FDA reports)
BLOOD ALCOHOL INCREASED ( 27 FDA reports)
DRUG INTERACTION ( 27 FDA reports)
AGGRESSION ( 26 FDA reports)
FEELING ABNORMAL ( 26 FDA reports)
SUBSTANCE ABUSE ( 26 FDA reports)
TACHYCARDIA ( 26 FDA reports)
TREMOR ( 26 FDA reports)
COMPLETED SUICIDE ( 25 FDA reports)
CONVULSION ( 25 FDA reports)
ALCOHOLISM ( 23 FDA reports)
ALCOHOL INTERACTION ( 22 FDA reports)
INCORRECT DOSE ADMINISTERED ( 22 FDA reports)
CONDITION AGGRAVATED ( 21 FDA reports)
DIZZINESS ( 21 FDA reports)
DYSPNOEA ( 21 FDA reports)
HEADACHE ( 21 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 21 FDA reports)
AMNESIA ( 20 FDA reports)
CARDIAC ARREST ( 20 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 20 FDA reports)
PSYCHOTIC DISORDER ( 20 FDA reports)
DRUG SCREEN POSITIVE ( 19 FDA reports)
FATIGUE ( 19 FDA reports)
METABOLIC ACIDOSIS ( 19 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 18 FDA reports)
DIARRHOEA ( 18 FDA reports)
DISTURBANCE IN ATTENTION ( 18 FDA reports)
CONFUSIONAL STATE ( 17 FDA reports)
IRRITABILITY ( 17 FDA reports)
MEMORY IMPAIRMENT ( 17 FDA reports)
ABDOMINAL PAIN ( 16 FDA reports)
ABNORMAL BEHAVIOUR ( 15 FDA reports)
DRUG ABUSE ( 15 FDA reports)
HYPOKALAEMIA ( 15 FDA reports)
INTENTIONAL DRUG MISUSE ( 15 FDA reports)
INTENTIONAL SELF-INJURY ( 15 FDA reports)
RHABDOMYOLYSIS ( 15 FDA reports)
SELF-MEDICATION ( 15 FDA reports)
SINUS TACHYCARDIA ( 15 FDA reports)
SYNCOPE ( 15 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 15 FDA reports)
ASTHENIA ( 14 FDA reports)
DEPRESSED MOOD ( 14 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 14 FDA reports)
MALAISE ( 14 FDA reports)
RESPIRATORY ARREST ( 14 FDA reports)
WEIGHT DECREASED ( 14 FDA reports)
WEIGHT INCREASED ( 14 FDA reports)
BACK PAIN ( 13 FDA reports)
PARANOIA ( 13 FDA reports)
PULMONARY OEDEMA ( 13 FDA reports)
BALANCE DISORDER ( 12 FDA reports)
BLOOD PRESSURE DECREASED ( 12 FDA reports)
CRYING ( 12 FDA reports)
EMOTIONAL DISTRESS ( 12 FDA reports)
HEAD INJURY ( 12 FDA reports)
HYPOGLYCAEMIA ( 12 FDA reports)
INFLUENZA LIKE ILLNESS ( 12 FDA reports)
MUSCLE SPASMS ( 12 FDA reports)
NERVOUSNESS ( 12 FDA reports)
PARAESTHESIA ( 12 FDA reports)
PULMONARY CONGESTION ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
ASPIRATION ( 11 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
HALLUCINATION ( 11 FDA reports)
MOOD SWINGS ( 11 FDA reports)
MYDRIASIS ( 11 FDA reports)
OXYGEN SATURATION DECREASED ( 11 FDA reports)
PALPITATIONS ( 11 FDA reports)
SLEEP DISORDER ( 11 FDA reports)
ABNORMAL DREAMS ( 10 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
ERECTILE DYSFUNCTION ( 10 FDA reports)
GRAND MAL CONVULSION ( 10 FDA reports)
HEART RATE INCREASED ( 10 FDA reports)
HEPATIC FAILURE ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
HYPOAESTHESIA ( 10 FDA reports)
RESPIRATORY DEPRESSION ( 10 FDA reports)
RESTLESSNESS ( 10 FDA reports)
ANGER ( 9 FDA reports)
BLOOD GLUCOSE INCREASED ( 9 FDA reports)
DELUSION ( 9 FDA reports)
DIALYSIS ( 9 FDA reports)
HEPATIC STEATOSIS ( 9 FDA reports)
LACERATION ( 9 FDA reports)
LACTIC ACIDOSIS ( 9 FDA reports)
NIGHTMARE ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
UNRESPONSIVE TO STIMULI ( 9 FDA reports)
VERTIGO ( 9 FDA reports)
ACCIDENT ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
DISORIENTATION ( 8 FDA reports)
DYSARTHRIA ( 8 FDA reports)
HOMICIDAL IDEATION ( 8 FDA reports)
MAJOR DEPRESSION ( 8 FDA reports)
MIOSIS ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
SHOCK ( 8 FDA reports)
TREATMENT NONCOMPLIANCE ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
ANGIONEUROTIC OEDEMA ( 7 FDA reports)
ANHEDONIA ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
BLOOD GLUCOSE DECREASED ( 7 FDA reports)
DRUG LEVEL INCREASED ( 7 FDA reports)
HALLUCINATION, AUDITORY ( 7 FDA reports)
HALLUCINATION, VISUAL ( 7 FDA reports)
HEPATIC CIRRHOSIS ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
IMPAIRED DRIVING ABILITY ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
MEDICATION ERROR ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
RASH ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
SPEECH DISORDER ( 7 FDA reports)
SUDDEN DEATH ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ACCIDENTAL DEATH ( 6 FDA reports)
ACUTE HEPATIC FAILURE ( 6 FDA reports)
AFFECTIVE DISORDER ( 6 FDA reports)
APNOEA ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 6 FDA reports)
BLOOD SODIUM DECREASED ( 6 FDA reports)
BODY TEMPERATURE INCREASED ( 6 FDA reports)
CARBON MONOXIDE POISONING ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
HYPOTHERMIA ( 6 FDA reports)
INJURY ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 6 FDA reports)
MUSCLE TWITCHING ( 6 FDA reports)
PALLOR ( 6 FDA reports)
PETIT MAL EPILEPSY ( 6 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 6 FDA reports)
RESPIRATORY RATE INCREASED ( 6 FDA reports)
STRESS ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ACIDOSIS ( 5 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
ALCOHOL ABUSE ( 5 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 5 FDA reports)
BLOOD CALCIUM DECREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
BLOOD PH DECREASED ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
BODY TEMPERATURE DECREASED ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
DEATH ( 5 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
DRUG EFFECT DECREASED ( 5 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 5 FDA reports)
ENCEPHALOPATHY ( 5 FDA reports)
EYE ROLLING ( 5 FDA reports)
FEELING DRUNK ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
GUN SHOT WOUND ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HOMICIDE ( 5 FDA reports)
HOSTILITY ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
INJURY ASPHYXIATION ( 5 FDA reports)
MANIA ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
PERSONALITY CHANGE ( 5 FDA reports)
POISONING ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
PROTHROMBIN TIME PROLONGED ( 5 FDA reports)
PULMONARY HAEMORRHAGE ( 5 FDA reports)
PULSE ABSENT ( 5 FDA reports)
RIB FRACTURE ( 5 FDA reports)
SPLEEN CONGESTION ( 5 FDA reports)
THINKING ABNORMAL ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
WITHDRAWAL SYNDROME ( 5 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 4 FDA reports)
ACCIDENT AT WORK ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
ALCOHOL INTOLERANCE ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 4 FDA reports)
ATAXIA ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD LACTIC ACID INCREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
COLON INJURY ( 4 FDA reports)
COLONIC ATONY ( 4 FDA reports)
COMPARTMENT SYNDROME ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DRUG TOLERANCE ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
FAECAL INCONTINENCE ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HAND FRACTURE ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
HEPATOCELLULAR DAMAGE ( 4 FDA reports)
ILLUSION ( 4 FDA reports)
INCOHERENT ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
NODULE ( 4 FDA reports)
NYSTAGMUS ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PANIC DISORDER ( 4 FDA reports)
PHYSICAL ASSAULT ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 4 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RESPIRATORY ACIDOSIS ( 4 FDA reports)
RESPIRATORY RATE DECREASED ( 4 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 4 FDA reports)
SEXUAL DYSFUNCTION ( 4 FDA reports)
SKIN LACERATION ( 4 FDA reports)
SPINAL FRACTURE ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
APATHY ( 3 FDA reports)
APGAR SCORE LOW ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
APPLICATION SITE SWELLING ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
AURA ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
BIPOLAR I DISORDER ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CHEST INJURY ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CHORIORETINOPATHY ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
COMA SCALE ABNORMAL ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 3 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
ERECTION INCREASED ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
EXERCISE TOLERANCE DECREASED ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
FEAR ( 3 FDA reports)
FLASHBACK ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERLACTACIDAEMIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
IMPRISONMENT ( 3 FDA reports)
IMPULSIVE BEHAVIOUR ( 3 FDA reports)
INFECTION ( 3 FDA reports)
IUCD COMPLICATION ( 3 FDA reports)
JUDGEMENT IMPAIRED ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
LIBIDO DECREASED ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 3 FDA reports)
MEAN CELL VOLUME INCREASED ( 3 FDA reports)
METRORRHAGIA ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MURDER ( 3 FDA reports)
MUSCLE CRAMP ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
OBSESSIVE THOUGHTS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PARTIAL SEIZURES ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SLEEP WALKING ( 3 FDA reports)
SLUGGISHNESS ( 3 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 3 FDA reports)
SOCIAL PROBLEM ( 3 FDA reports)
STILLBIRTH ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 3 FDA reports)
UPPER LIMB FRACTURE ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
UTERINE RUPTURE ( 3 FDA reports)
VICTIM OF HOMICIDE ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACTIVATION SYNDROME ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ALCOHOLIC PANCREATITIS ( 2 FDA reports)
ANOXIC ENCEPHALOPATHY ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
ANURIA ( 2 FDA reports)
APPLICATION SITE WARMTH ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHLAMYDIAL INFECTION ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
COMMINUTED FRACTURE ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISINHIBITION ( 2 FDA reports)
DISLOCATION OF VERTEBRA ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DIVORCED ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
FASCIOTOMY ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HANGOVER ( 2 FDA reports)
HEPATIC RUPTURE ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG INJURY ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MARITAL PROBLEM ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OCCUPATIONAL PHYSICAL PROBLEM ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
POLYTRAUMATISM ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
POSTURING ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RETINAL VEIN OCCLUSION ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SNORING ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPLEEN DISORDER ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
STARING ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
TENSION ( 2 FDA reports)
TESTICULAR ATROPHY ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
UMBILICAL CORD AROUND NECK ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
YAWNING ( 2 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
ALCOHOLIC ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BIOPSY STOMACH ABNORMAL ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLEEDING PERIPARTUM ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGENITAL TONGUE ANOMALY ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CRIME ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSKINESIA NEONATAL ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPROSODY ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
ERYTHROPSIA ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GYNAECOLOGICAL CHLAMYDIA INFECTION ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JEALOUS DELUSION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MOANING ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEAR DROWNING ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCCUPATIONAL PROBLEM ENVIRONMENTAL ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPIATES ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PANCREATIC INJURY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PAPILLARY THYROID CANCER ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POLYMEDICATION ( 1 FDA reports)
PORPHYRIA ACUTE ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY WITH INJECTABLE CONTRACEPTIVE ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PYROGLUTAMATE INCREASED ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
RADICULAR PAIN ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
REYE'S SYNDROME ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SEXUAL ABUSE ( 1 FDA reports)
SEXUAL ASSAULT VICTIM ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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