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

COMPLETED SUICIDE ( 30 FDA reports)
AGITATION ( 22 FDA reports)
OVERDOSE ( 22 FDA reports)
SUICIDE ATTEMPT ( 21 FDA reports)
FATIGUE ( 20 FDA reports)
HEADACHE ( 20 FDA reports)
TREMOR ( 20 FDA reports)
NAUSEA ( 18 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 18 FDA reports)
ABNORMAL BEHAVIOUR ( 16 FDA reports)
CARDIAC ARREST ( 16 FDA reports)
DIZZINESS ( 16 FDA reports)
SUICIDAL IDEATION ( 16 FDA reports)
DRUG ABUSE ( 15 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 15 FDA reports)
SOMNOLENCE ( 15 FDA reports)
CONFUSIONAL STATE ( 13 FDA reports)
DISTURBANCE IN ATTENTION ( 13 FDA reports)
INSOMNIA ( 13 FDA reports)
RESPIRATORY ARREST ( 13 FDA reports)
AGGRESSION ( 12 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
FEELING ABNORMAL ( 12 FDA reports)
POISONING ( 12 FDA reports)
DEPRESSION ( 11 FDA reports)
IRRITABILITY ( 11 FDA reports)
PALPITATIONS ( 11 FDA reports)
VISION BLURRED ( 11 FDA reports)
ANXIETY ( 10 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
HYPERHIDROSIS ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
PRODUCT QUALITY ISSUE ( 9 FDA reports)
COMA ( 8 FDA reports)
DIARRHOEA ( 8 FDA reports)
DRY MOUTH ( 8 FDA reports)
DYSARTHRIA ( 8 FDA reports)
INTENTIONAL DRUG MISUSE ( 8 FDA reports)
MOOD SWINGS ( 8 FDA reports)
AMNESIA ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DEATH ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
FALL ( 7 FDA reports)
INTENTIONAL OVERDOSE ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
UNRESPONSIVE TO STIMULI ( 7 FDA reports)
ANGER ( 6 FDA reports)
ASTHENIA ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
DRUG EFFECT DECREASED ( 6 FDA reports)
DRUG SCREEN POSITIVE ( 6 FDA reports)
EUPHORIC MOOD ( 6 FDA reports)
HALLUCINATION ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
INTENTIONAL MISUSE ( 6 FDA reports)
MATERNAL USE OF ILLICIT DRUGS ( 6 FDA reports)
MEMORY IMPAIRMENT ( 6 FDA reports)
PAIN ( 6 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 6 FDA reports)
VAGINAL INFECTION ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DEVELOPMENTAL DELAY ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
INJURY ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
SUBSTANCE ABUSE ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
ACCIDENTAL POISONING ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
AMPHETAMINES ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BARBITURATES ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD ETHANOL INCREASED ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DRUG DEPENDENCE ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
FAMILY STRESS ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
IMPAIRED DRIVING ABILITY ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
MALAISE ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PREGNANCY WITH INJECTABLE CONTRACEPTIVE ( 4 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 4 FDA reports)
PULMONARY CONGESTION ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
URINE AMPHETAMINE POSITIVE ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ACCIDENTAL DEATH ( 3 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
MACULAR DEGENERATION ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PHYSICAL ASSAULT ( 3 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CRYING ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FEAR ( 2 FDA reports)
FOETAL GROWTH RESTRICTION ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
LUNG INJURY ( 2 FDA reports)
MANIA ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYOPIA ( 2 FDA reports)
NEONATAL ASPIRATION ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCOPRESIS ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EXCESSIVE MASTURBATION ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOW BIRTH WEIGHT BABY ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MENINGIOMA SURGERY ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OPTIC NERVE HYPOPLASIA ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POOR SUCKING REFLEX ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEXUAL ABUSE ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPASTIC PARALYSIS ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TIC ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TREMOR NEONATAL ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ULCER ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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