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

DRUG EXPOSURE DURING PREGNANCY ( 24 FDA reports)
DIARRHOEA ( 22 FDA reports)
RASH ( 22 FDA reports)
HEADACHE ( 21 FDA reports)
FATIGUE ( 19 FDA reports)
NAUSEA ( 18 FDA reports)
VOMITING ( 18 FDA reports)
CHEST PAIN ( 15 FDA reports)
INJECTION SITE PAIN ( 15 FDA reports)
MEDICATION ERROR ( 15 FDA reports)
HYPERSENSITIVITY ( 14 FDA reports)
INJECTION SITE HAEMORRHAGE ( 14 FDA reports)
NASOPHARYNGITIS ( 13 FDA reports)
PYREXIA ( 13 FDA reports)
DEPRESSION ( 12 FDA reports)
LYMPHADENOPATHY ( 12 FDA reports)
NO ADVERSE EFFECT ( 12 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 11 FDA reports)
ANXIETY ( 11 FDA reports)
BACTERIAL INFECTION ( 11 FDA reports)
INFLUENZA LIKE ILLNESS ( 11 FDA reports)
INJECTION SITE ERYTHEMA ( 11 FDA reports)
INJECTION SITE INDURATION ( 11 FDA reports)
INJECTION SITE PRURITUS ( 11 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 11 FDA reports)
NYSTAGMUS ( 10 FDA reports)
SINUSITIS ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
BLOOD LACTIC ACID INCREASED ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
EYE MOVEMENT DISORDER ( 9 FDA reports)
MYOCARDIAL INFARCTION ( 9 FDA reports)
ORAL CANDIDIASIS ( 9 FDA reports)
CHILLS ( 8 FDA reports)
PRURITUS ( 8 FDA reports)
DEATH ( 7 FDA reports)
INJECTION SITE REACTION ( 7 FDA reports)
INJECTION SITE SWELLING ( 7 FDA reports)
RASH SCALY ( 7 FDA reports)
RENAL TUBULAR NECROSIS ( 7 FDA reports)
ACUTE PULMONARY OEDEMA ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 6 FDA reports)
CAESAREAN SECTION ( 6 FDA reports)
CSF PROTEIN INCREASED ( 6 FDA reports)
DYSKINESIA ( 6 FDA reports)
EYE DISORDER ( 6 FDA reports)
HYPOCALCAEMIA ( 6 FDA reports)
INJECTION SITE EXTRAVASATION ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 6 FDA reports)
ORAL HAIRY LEUKOPLAKIA ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
FACIAL WASTING ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
NEONATAL DISORDER ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
RENAL TUBULAR DISORDER ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 4 FDA reports)
CONGENITAL CLAVICULAR AGENESIS ( 4 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HEPATIC FIBROSIS ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
PAIN ( 4 FDA reports)
PREMATURE BABY ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
SENSE OF OPPRESSION ( 4 FDA reports)
VIRAL LOAD INCREASED ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ANOGENITAL DYSPLASIA ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CYST ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
HYPERTONIA NEONATAL ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LYMPHADENITIS ( 3 FDA reports)
MALAISE ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANOGENITAL WARTS ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
FANCONI SYNDROME ( 2 FDA reports)
FAT TISSUE INCREASED ( 2 FDA reports)
FOETAL DISTRESS SYNDROME ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GLARE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HIV WASTING SYNDROME ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
INJECTION SITE BURNING ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJECTION SITE MASS ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
MACROCYTOSIS ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
NODULE ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
OVERGROWTH BACTERIAL ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH SCARLATINIFORM ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
SCLERODERMA ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VIROLOGIC FAILURE ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD HIV RNA INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID ABNORMAL ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CATHETER SITE BRUISE ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CRYPTORCHISM ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FAT REDISTRIBUTION ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETOR HEPATICUS ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LACRIMATION DECREASED ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIPOATROPHY ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUROSYPHILIS ( 1 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PARAESTHESIA CIRCUMORAL ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCARLET FEVER ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYPHILIS ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIRAL LOAD DECREASED ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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