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

CONVULSION ( 39 FDA reports)
EPILEPSY ( 29 FDA reports)
SOMNOLENCE ( 21 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 18 FDA reports)
NAUSEA ( 18 FDA reports)
DIZZINESS ( 17 FDA reports)
DRUG INEFFECTIVE ( 16 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
DIARRHOEA ( 13 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
FATIGUE ( 13 FDA reports)
VOMITING ( 13 FDA reports)
ASTHENIA ( 12 FDA reports)
CONFUSIONAL STATE ( 12 FDA reports)
DYSPNOEA ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
LOSS OF CONSCIOUSNESS ( 12 FDA reports)
FEELING ABNORMAL ( 11 FDA reports)
MALAISE ( 11 FDA reports)
TREMOR ( 10 FDA reports)
AGITATION ( 9 FDA reports)
FALL ( 9 FDA reports)
HEADACHE ( 9 FDA reports)
HYPERTENSION ( 9 FDA reports)
MULTIPLE DRUG OVERDOSE ( 9 FDA reports)
SMALL FOR DATES BABY ( 9 FDA reports)
COMA ( 8 FDA reports)
MUSCLE SPASMS ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
FEELING COLD ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
ANXIETY ( 6 FDA reports)
DEATH ( 6 FDA reports)
HALLUCINATION, AUDITORY ( 6 FDA reports)
HEPATIC ENZYME INCREASED ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
DRUG SCREEN POSITIVE ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
BRAIN OEDEMA ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
RASH ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
ACNE ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 3 FDA reports)
BRAIN SCAN ABNORMAL ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CHONDRODYSTROPHY ( 3 FDA reports)
COUGH ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
ENDOTRACHEAL INTUBATION ( 3 FDA reports)
FACE INJURY ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
INCOHERENT ( 3 FDA reports)
INTENTIONAL SELF-INJURY ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
THORACIC HAEMORRHAGE ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ACCIDENTAL POISONING ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALPERS' DISEASE ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
APATHY ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD URIC ACID ABNORMAL ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GASTROSTOMY ( 2 FDA reports)
GENE MUTATION ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INJECTION SITE DISCOLOURATION ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTESTINAL ULCER ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
POISONING ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUDDEN UNEXPLAINED DEATH IN EPILEPSY ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AURA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LAFORA'S MYOCLONIC EPILEPSY ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MARFAN'S SYNDROME ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS II ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIEMANN-PICK DISEASE ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OPTIC NERVE NEOPLASM ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOSYNTHESIS ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
RALES ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STAB WOUND ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TIC ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
ULCER ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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